The University of Queensland

Genetic correlation between cortical gray matter thickness and white matter connections

Shen, Kaikai, Dore, Vincent, Fripp, Jurgen, Rose, Stephen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2018). Genetic correlation between cortical gray matter thickness and white matter connections. Imaging genetics. (pp. 85-100) edited by Adrian Dalca, Kayhan Batmanghelich, Mert Sabuncu and Li Shen. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-813968-4.00005-5

Direction of causation models

Gillespie, Nathan A. and Martin, Nicholas G. (2014). Direction of causation models. Wiley StatsRef: Statistics Reference Online. (pp. *-*) Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06685

Multiple stages classification of Alzheimer’s disease based on structural brain networks using generalized low rank approximations (GLRAM)

Zhan, L., Nie, Z., Ye, J., Wang, Y., Jin, Y., Jahanshad, N., Prasad, G., de Zubicaray, G. I., McMahan, K. L., Martin, N. G., Wright, M. J. and Thompson, P. M. (2014). Multiple stages classification of Alzheimer’s disease based on structural brain networks using generalized low rank approximations (GLRAM). Computational diffusion MRI: MICCAI Workshop, Boston, MA, USA, September 2014. (pp. 35-44) edited by Lauren O'Donnell, Gemma Nedjati-Gilani, Yogesh Rathi, Marco Reisert and Torben Schneider. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-11182-7_4

Multivariate genetic analysis

Gillespie, Nathan A. and Martin, Nicholas G. (2014). Multivariate genetic analysis. Wiley StatsRef: statistics reference online. Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06468

Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families

Eaves, Lindon J., Hatemi, Peter K., Heath, Andrew C. and Martin, Nicholas G. (2011). Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families. Man is by nature a political animal: evolution, biology, and politics. (pp. 101-184) edited by Peter K. Hatemi and Rose McDermott. Chicago, IL, United States: University of Chicago Press. doi: 10.7208/chicago/9780226319117.003.0005

Genetic and Environmental Influences on Sexual Orientation

Khytam Dawood, J. Michael Bailey and Nicholas G. Martin (2009). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics. (pp. 269-279) edited by Kim, Yong-Kyu. United Sates: Springer New York. doi: 10.1007/978-0-387-76727-7_19

Neuroticism as a genetic marker for mood and anxiety

Gillespie, N. A. and Martin, N. G. (2006). Neuroticism as a genetic marker for mood and anxiety. Biology of Personality & Individual Differences. (pp. 225-250) edited by T. Canli. New York, U.S.A.: Guilford Press.

Genetic covariance between processing speed and IQ

Luciano, M., Wright, M. J., Smith, G. A., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2003). Genetic covariance between processing speed and IQ. Behavior genetics in the postgenomic era. (pp. 163-182) edited by Robert Plomin, John C. Defries, Ian W. Craig and Peter McGuffin. Washington, DC, USA: APA Books.

Gene-environment interactions

Boomsma, D. I. and Martin, N. G. (2002). Gene-environment interactions. Biological Psychiatry. (pp. 181-187) edited by H. D'haenen, J. A. den Boer and P. Willner. New York: John Wiley & Sons Ltd.

Biological and cultural inheritance of stature and attitudes

Eaves, Lindon J., Heath, A., Martin, Nicholas G., Neale, Michael C., Meyer, J. M., Silberg, J. L., Corey, Linda, Truett, Kimberley and Walters, Ellen (1999). Biological and cultural inheritance of stature and attitudes. Personality and Psychopathology. (pp. 269-308) edited by C. Robert Cloninger. Washington: American Psychiatric Press.

Gene-environment interaction and twin studies

Martin, N. G. (1999). Gene-environment interaction and twin studies. Advances in Twin and Sib-pair Analysis. (pp. 143-150) edited by Tim D. Spector, Harold Snieder and Alex J. MacGregor. London: Greenwich Medical Media Ltd.

Genetic and environmental structure of personality

Heath, A., Madden, P. A., Cloninger, C. R. and Martin, N. G. (1999). Genetic and environmental structure of personality. Personality and Psychopathology. (pp. 343-367) edited by C. Robert Cloninger. Washington, U.S.A.: American Psychiatric Press.

Insights into the genetic basis of human dental variation from statistical modelling analyses

Dempsey, P. J., Townsend, G. C. and Martin, N. G. (1999). Insights into the genetic basis of human dental variation from statistical modelling analyses. Perspectives in Human Biology. (pp. 9-18) edited by Loren Knapp. Nedlands: The University of Western Australia.

Genetic determinants of thyroid function in children

Mulder, Tessa A, Campbell, Purdey J, Taylor, Peter N, Peeters, Robin P, Wilson, Scott G, Medici, Marco, Dayan, Colin, Jaddoe, Vincent V W, Walsh, John P, Martin, Nicholas G, Tiemeier, Henning and Korevaar, Tim I M (2023). Genetic determinants of thyroid function in children. European Journal of Endocrinology, 189 (2), 164-174. doi: 10.1093/ejendo/lvad086

The Effect of Genetic Predisposition to Alzheimer’s Disease and Related Traits on Recruitment Bias in a Study of Cognitive Aging

Gomez, Lina M., Mitchell, Brittany L., McAloney, Kerrie, Adsett, Jessica, Garden, Natalie, Wood, Madeline, Diaz-Torres, Santiago, Garcia-Marin, Luis M., Breakspear, Michael, Martin, Nicholas G. and Lupton, Michelle K. (2023). The Effect of Genetic Predisposition to Alzheimer’s Disease and Related Traits on Recruitment Bias in a Study of Cognitive Aging. Twin Research and Human Genetics, 26 (3), 1-6. doi: 10.1017/thg.2023.26

Rare genetic variants underlie outlying levels of DNA methylation and gene-expression

Chundru, V. Kartik, Marioni, Riccardo E., Pendergast, James G. D., Lin, Tian, Beveridge, Allan J., Martin, Nicholas G, Montgomery, Grant W., Hume, David A., Deary, Ian J., Visscher, Peter M., Wray, Naomi R. and McRae, Allan F. (2023). Rare genetic variants underlie outlying levels of DNA methylation and gene-expression. Human Molecular Genetics, 32 (11), 1912-1921. doi: 10.1093/hmg/ddad028

The association between sleep restlessness and neuroimaging biomarkers of Alzheimer’s Disease in mid‐life to older adults and patients

Kholghi, Mahnoosh, Fazlollahi, Amir, Lupton, Michelle K, Bourgeat, Pierrick, Zhang, Qing, Martin, Nicholas G, Breakspear, Michael, Fripp, Jurgen and PISA (Prospective Imaging Study of Aging: Genes, Brain and Behaviour) (2023). The association between sleep restlessness and neuroimaging biomarkers of Alzheimer’s Disease in mid‐life to older adults and patients. Alzheimer's & Dementia, 19 (S2). doi: 10.1002/alz.062017

Author Correction: The power of genetic diversity in genome-wide association studies of lipids

Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium (2023). Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature, 618 (7965), E19-E20. doi: 10.1038/s41586-023-06194-2

Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis users

Johnson, Emma C., Colbert, Sarah M.C., Jeffries, Paul W., Tillman, Rebecca, Bigdeli, Tim B., Karcher, Nicole R., Chan, Grace, Kuperman, Samuel, Meyers, Jacquelyn L., Nurnberger, John I., Plawecki, Martin H., Degenhardt, Louisa, Martin, Nicholas G., Kamarajan, Chella, Schuckit, Marc A., Murray, Robin M., Dick, Danielle M., Edenberg, Howard J., D’Souza, Deepak Cyril, Di Forti, Marta, Porjesz, Bernice, Nelson, Elliot C. and Agrawal, Arpana (2023). Associations between cannabis use, polygenic liability for schizophrenia, and cannabis-related experiences in a sample of cannabis users. Schizophrenia Bulletin, 49 (3), 778-787. doi: 10.1093/schbul/sbac196

Genome-wide association studies identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations

Peng, Fuduan, Xiong, Ziyi, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Wu, Sijie, Adhikari, Kaustubh, Chen, Yan, Li, Yi, Gonzalez-José, Rolando, Schüler-Faccini, Lavinia, Bortolini, Maria-Cátira, Acuña-Alonzo, Victor, Canizales-Quinteros, Samuel, Gallo, Carla, Poletti, Giovanni, Bedoya, Gabriel, Rothhammer, Francisco, Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Ruiz-Linares, Andrés, Wang, Sijia, Walsh, Susan, Spector, Timothy D., Martin, Nicholas G., Kayser, Manfred and Liu, Fan (2023). Genome-wide association studies identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations. Journal of Investigative Dermatology, 143 (7), 1317-1322.e11. doi: 10.1016/j.jid.2022.11.026

Specificity in genetic and environmental risk for prescription opioid misuse and heroin use

Dash, Genevieve F., Gizer, Ian R., Martin, Nicholas G. and Slutske, Wendy S. (2023). Specificity in genetic and environmental risk for prescription opioid misuse and heroin use. Psychological Medicine, 107 (2). doi: 10.1017/s003329172300034x

Genetic and shared environmental factors explain the association between adolescent polysubstance use and high school noncompletion

Davis, Christal N., Gizer, Ian R., Agrawal, Arpana, Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2023). Genetic and shared environmental factors explain the association between adolescent polysubstance use and high school noncompletion. Psychology of Addictive Behaviors. doi: 10.1037/adb0000915

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K. ... The 23andMe Research Team (2023). The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nature Genetics, 55 (3), 423-436. doi: 10.1038/s41588-023-01323-z

Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring

Campos, Adrian I., Ingold, Nathan, Huang, Yunru, Mitchell, Brittany L., Kho, Pik-Fang, Han, Xikun, García-Marín, Luis M., Ong, Jue-Sheng, 23andMe Research Team, Law, Matthew H., Yokoyama, Jennifer S., Martin, Nicholas G., Dong, Xianjun, Cuellar-Partida, Gabriel, MacGregor, Stuart, Aslibekyan, Stella and Rentería, Miguel E. (2023). Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep, 46 (3) zsac308, 1-14. doi: 10.1093/sleep/zsac308

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2023). Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 55 (3), 520-520. doi: 10.1038/s41588-023-01336-8

Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9

Weihs, Antoine, Chaker, Layal, Martin, Tiphaine Christiane, Braun, Kim V.E., Campbell, Purdey J, Cox, Simon R, Fornage, Myriam, Gieger, Christian, Grabe, Hans J, Grallert, Harald, Harris, Sarah E, Kühnel, Brigitte, Marioni, Riccardo E, Martin, Nicholas G, McCartney, Daniel L, McRae, Allan F, Meisinger, Christa, Meurs, Joyce van, Nano, Jana, Nauck, Matthias, Peters, Annette, Prokisch, Holger, Roden, Michael, Selvin, Elizabeth, Beekman, Marian, van Heemst, Diana, Slagboom, Eline P, Swenson, Brenton R, Tin, Adrienne ... Teumer, Alexander (2023). Epigenome-wide association study reveals CpG sites associated with thyroid function and regulatory effects on KLF9. Thyroid (ja), 301-311. doi: 10.1089/thy.2022.0373

Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts

Silventoinen, Karri, Piirtola, Maarit, Jelenkovic, Aline, Sund, Reijo, Tarnoki, Adam D., Tarnoki, David L., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Gatz, Margaret, Butler, David A., Lee, Jooyeon, Lee, Soo Ji, Sung, Joohon, Franz, Carol E., Kremen, William S., Lyons, Michael J., Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Tynelius, Per, Rasmussen, Finn, Martin, Nicholas G., Medland, Sarah E. ... Kaprio, Jaakko (2022). Smoking remains associated with education after controlling for social background and genetic factors in a study of 18 twin cohorts. Scientific Reports, 12 (1) 13148, 1-9. doi: 10.1038/s41598-022-17536-x

Discovery of 42 genome-wide significant loci associated with dyslexia

Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D., Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Filshtein, Teresa, Fletez-Brant, Kipper, Freyman, Will, Gandhi, Pooja M., Heilbron, Karl, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn ... Quantitative Trait Working Group of the GenLang Consortium (2022). Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11), 1621-1629. doi: 10.1038/s41588-022-01192-y

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Tielbeek, Jorim J., Uffelmann, Emil, Williams, Benjamin S., Colodro-Conde, Lucía, Gagnon, Éloi, Mallard, Travis T., Levitt, Brandt E., Jansen, Philip R., Johansson, Ada, Sallis, Hannah M., Pistis, Giorgio, Saunders, Gretchen R. B., Allegrini, Andrea G., Rimfeld, Kaili, Konte, Bettina, Klein, Marieke, Hartmann, Annette M., Salvatore, Jessica E., Nolte, Ilja M., Demontis, Ditte, Malmberg, Anni L. K., Burt, S. Alexandra, Savage, Jeanne E., Sugden, Karen, Poulton, Richie, Harris, Kathleen Mullan, Vrieze, Scott, McGue, Matt, Iacono, William G. ... Spit for Science Working Group (2022). Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis. Molecular Psychiatry, 27 (11), 4453-4463. doi: 10.1038/s41380-022-01793-3

Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use

Davis, Christal N., Gizer, Ian R., Colodro-Conde, Lucía, Statham, Dixie J., Martin, Nicholas G. and Slutske, Wendy S. (2022). Educational attainment polygenic scores: examining evidence for gene–environment interplay with adolescent alcohol, tobacco and cannabis use. Twin Research and Human Genetics, 25 (4-5), 187-195. doi: 10.1017/thg.2022.33

Self-reported impact of developmental stuttering across the lifespan

Boyce, Jessica O., Jackson, Victoria E., van Reyk, Olivia, Parker, Richard, Vogel, Adam P., Eising, Else, Horton, Sarah E., Gillespie, Nathan A., Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie and Morgan, Angela T. (2022). Self-reported impact of developmental stuttering across the lifespan. Developmental Medicine and Child Neurology, 64 (10), 1297-1306. doi: 10.1111/dmcn.15211

Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Agee, Michelle, Alipanahi, Babak ... the 23andMe Research Team (2022). Author correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 13 (1) 5543, 5543. doi: 10.1038/s41467-022-33222-y

Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention

Wang, Zhe, Emmerich, Andrew, Pillon, Nicolas J., Moore, Tim, Hemerich, Daiane, Cornelis, Marilyn C., Mazzaferro, Eugenia, Broos, Siacia, Ahluwalia, Tarunveer S., Bartz, Traci M., Bentley, Amy R., Bielak, Lawrence F., Chong, Mike, Chu, Audrey Y., Berry, Diane, Dorajoo, Rajkumar, Dueker, Nicole D., Kasbohm, Elisa, Feenstra, Bjarke, Feitosa, Mary F., Gieger, Christian, Graff, Mariaelisa, Hall, Leanne M., Haller, Toomas, Hartwig, Fernando P., Hillis, David A., Huikari, Ville, Heard-Costa, Nancy, Holzapfel, Christina ... Lifelines Cohort Study (2022). Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature Genetics, 54 (9), 1332-1344. doi: 10.1038/s41588-022-01165-1

Phenome-wide screening of the putative causal determinants of depression using genetic data

Aman, Asma M., García-Marín, Luis M., Thorp, Jackson G., Campos, Adrian I., Cuellar-Partida, Gabriel, Martin, Nicholas G.. and Rentería, Miguel E. (2022). Phenome-wide screening of the putative causal determinants of depression using genetic data. Human Molecular Genetics, 31 (17), 2887-2898. doi: 10.1093/hmg/ddac081

Polygenic influences associated with adolescent cognitive skills

Mitchell, Brittany L., Hansell, Narelle K., McAloney, Kerrie, Martin, Nicholas G., Wright, Margaret J., Renteria, Miguel E. and Grasby, Katrina L. (2022). Polygenic influences associated with adolescent cognitive skills. Intelligence, 94 101680, 1-9. doi: 10.1016/j.intell.2022.101680

Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts

Silventoinen, Karri, Li, Weilong, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Aaltonen, Sari, Piirtola, Maarit, Sugawara, Masumi, Tanaka, Mami, Matsumoto, Satoko, Baker, Laura A., Tuvblad, Catherine, Tynelius, Per, Rasmussen, Finn, Craig, Jeffrey M., Saffery, Richard, Willemsen, Gonneke, Bartels, Meike, van Beijsterveldt, Catharina E. M., Martin, Nicholas G., Medland, Sarah E., Montgomery, Grant W., Lichtenstein, Paul, Krueger, Robert F., McGue, Matt, Pahlen, Shandell, Christensen, Kaare, Skytthe, Axel, Kyvik, Kirsten O. ... Kaprio, Jaakko (2022). Changing genetic architecture of body mass index from infancy to early adulthood: an individual based pooled analysis of 25 twin cohorts. International Journal of Obesity, 46 (10), 1901-1909. doi: 10.1038/s41366-022-01202-3

Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

Campos, Adrian I., Byrne, Enda M., Iorfino, Frank, Fabbri, Chiara, Hickie, Ian B., Lewis, Cathryn M., Wray, Naomi R., Medland, Sarah E., Rentería, Miguel E. and Martin, Nicholas G. (2022). Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 189 (6), 196-206. doi: 10.1002/ajmg.b.32913

Co-inheritance of variation in all-cause mortality and biochemical risk factors

Whitfield, John B., Colodro-Conde, Lucía, Zhu, Gu, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G (2022). Co-inheritance of variation in all-cause mortality and biochemical risk factors. Twin Research and Human Genetics, 25 (3), 1-8. doi: 10.1017/thg.2022.25

Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings

Hansell, Narelle K., Strike, Lachlan T., van Eijk, Liza, O'Callaghan, Victoria, Martin, Nicholas G., de Zubicaray, Greig I., Thompson, Paul M., McMahon, Katie L. and Wright, Margaret J. (2022). Genetic specificity of hippocampal subfield volumes, relative to hippocampal formation, identified in 2148 young adult twins and siblings. Twin Research and Human Genetics, 25 (3), 129-139. doi: 10.1017/thg.2022.20

Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression

Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Bennett, Elizabeth, Mackle, Tracey, Guintivano, Jerry, Hickie, Ian B, Colodro-Conde, Lucia, Medland, Sarah E, Martin, Nick, Wray, Naomi and Byrne, Enda (2022). Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression. BMJ Open, 12 (8) e059300, 1-7. doi: 10.1136/bmjopen-2021-059300

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Winkler, Thomas W., Rasheed, Humaira, Teumer, Alexander, Gorski, Mathias, Rowan, Bryce X., Stanzick, Kira J., Thomas, Laurent F., Tin, Adrienne, Hoppmann, Anselm, Chu, Audrey Y., Tayo, Bamidele, Thio, Chris H. L., Cusi, Daniele, Chai, Jin-Fang, Sieber, Karsten B., Horn, Katrin, Li, Man, Scholz, Markus, Cocca, Massimiliano, Wuttke, Matthias, van der Most, Peter J., Yang, Qiong, Ghasemi, Sahar, Nutile, Teresa, Li, Yong, Pontali, Giulia, Günther, Felix, Dehghan, Abbas, Correa, Adolfo ... VA Million Veteran Program (2022). Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. Communications Biology, 5 (1) 580, 1-20. doi: 10.1038/s42003-022-03448-z

Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults

Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Parker, Richard, Park, Shin Ho, Couvy-Duchesne, Baptiste, Mitchell, Brittany, Byrne, Enda M., Hermens, Daniel F., Medland, Sarah E., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2022). Dynamic networks of psychological symptoms, impairment, substance use, and social support: the evolution of psychopathology among emerging adults. European Psychiatry, 65 (1) e32, 1-24. doi: 10.1192/j.eurpsy.2022.23

The heritability of twinning in seven large historic pedigrees

Duffy, David L. and Martin, Nicholas G. (2022). The heritability of twinning in seven large historic pedigrees. Twin Research and Human Genetics, 25 (2), 1-4. doi: 10.1017/thg.2022.14

Lindon Eaves: a personal memoir

Martin, Nick (2022). Lindon Eaves: a personal memoir. Twin Research and Human Genetics, 25 (2), 97-100. doi: 10.1017/thg.2022.13

Mapping anorexia nervosa genes to clinical phenotypes

Johnson, Jessica S., Cote, Alanna C., Dobbyn, Amanda, Sloofman, Laura G., Xu, Jiayi, Cotter, Liam, Charney, Alexander W., Birgegård, Andreas, Jordan, Jennifer, Kennedy, Martin, Landén, Mikaél, Maguire, Sarah L., Martin, Nicholas G., Mortensen, Preben Bo, Thornton, Laura M., Bulik, Cynthia M., Huckins, Laura M. and Eating Disorders Working Group of the Psychiatric Genomics Consortium (2022). Mapping anorexia nervosa genes to clinical phenotypes. Psychological Medicine, 53 (6), 1-15. doi: 10.1017/s0033291721004554

Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences

Dash, Genevieve F., Martin, Nicholas G. and Slutske, Wendy S. (2022). Childhood maltreatment and disordered gambling in adulthood: Disentangling causal and familial influences. Psychological Medicine, 52 (5), 1-10. doi: 10.1017/S0033291720002743

Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information

Maihofer, Adam X., Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Denckla, Christy A., Ketema, Elizabeth, Morey, Rajendra A., Polimanti, Renato, Ratanatharathorn, Andrew, Torres, Katy, Wingo, Aliza P., Zai, Clement C., Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Borglum, Anders D., Babic, Dragan, Bμkvad-Hansen, Marie, Baker, Dewleen G., Beckham, Jean C., Bierut, Laura J., Bisson, Jonathan I., Boks, Marco P. ... Nievergelt, Caroline M. (2022). Enhancing discovery of genetic variants for PTSD through integration of quantitative phenotypes and trauma exposure information. Biological Psychiatry, 91 (7), 626-636. doi: 10.1016/j.biopsych.2021.09.020

Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression

Kiewa, Jacqueline, Meltzer‐Brody, Samantha, Milgrom, Jeanette, Guintivano, Jerry, Hickie, Ian B., Whiteman, David C., Olsen, Catherine M., Colodro‐Conde, Lucía, Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Byrne, Enda M. (2022). Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression. Depression and Anxiety, 39 (3), 182-191. doi: 10.1002/da.23232

Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use

Rabinowitz, Jill A., Campos, Adrian I., Ong, Jue-Sheng, García-Marín, Luis M., Alcauter, Sarael, Mitchell, Brittany L, Grasby, Katrina L, Cuéllar-Partida, Gabriel, Gillespie, Nathan A, Huhn, Andrew S, Martin, Nicholas G, Thompson, Paul M, Medland, Sarah E, Maher, Brion S and Rentería, Miguel E (2022). Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use. Cerebral Cortex, 32 (4), 796-807. doi: 10.1093/cercor/bhab243

Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay

Finkel, Deborah, Zavala, Catalina, Franz, Carol E., Pahlen, Shandell, Gatz, Margaret, Pedersen, Nancy L., Finch, Brian K., Dahl Aslan, Anna, Catts, Vibeke S., Ericsson, Malin, Krueger, Robert F., Martin, Nicholas G., Mohan, Adith, Mosing, Miriam A., Prescott, Carol A. and Whitfield, Keith E. (2022). Financial strain moderates genetic influences on self-rated health: support for diathesis–stress model of gene–environment interplay. Biodemography and Social Biology, 67 (1), 1-13. doi: 10.1080/19485565.2022.2037069

Genome-wide association meta-analysis identifies 29 new acne susceptibility loci

Mitchell, Brittany L., Saklatvala, Jake R., Dand, Nick, Hagenbeek, Fiona A., Li, Xin, Min, Josine L., Thomas, Laurent, Bartels, Meike, Jan Hottenga, Jouke, Lupton, Michelle K., Boomsma, Dorret I., Dong, Xianjun, Hveem, Kristian, Løset, Mari, Martin, Nicholas G., Barker, Jonathan N., Han, Jiali, Smith, Catherine H., Rentería, Miguel E. and Simpson, Michael A. (2022). Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. Nature Communications, 13 (1) 702, 702. doi: 10.1038/s41467-022-28252-5

Australian Parkinson’s Genetics Study (APGS): pilot (n=1532)

Bivol, Svetlana, Mellick, George D., Gratten, Jacob, Parker, Richard, Mulcahy, Aoibhe, Mosley, Philip E., Poortvliet, Peter C., Campos, Adrian I., Mitchell, Brittany L., Garcia-Marin, Luis M., Cross, Simone, Ferguson, Mary, Lind, Penelope A., Loesch, Danuta Z., Visscher, Peter M., Medland, Sarah E., Scherzer, Clemens R., Martin, Nicholas G. and Rentería, Miguel E. (2022). Australian Parkinson’s Genetics Study (APGS): pilot (n=1532). BMJ Open, 12 (2) e052032, e052032. doi: 10.1136/bmjopen-2021-052032

Early effects of amyloid-β on structural and vascular brain changes in mid-life cognitively unimpaired individuals

Fazlollahi, Amir, Xia, Ying, Lupton, Michelle K., Raniga, Parnesh, Bourgeat, Pierrick, Martin, Nick, Dore, Vincent, Rose, Stephen, Salvado, Olivier, Breakspear, Michael and Fripp, Jurgen (2022). Early effects of amyloid-β on structural and vascular brain changes in mid-life cognitively unimpaired individuals. Alzheimer's and dementia : the journal of the Alzheimer's Association, 17, 1-3. doi: 10.1002/alz.052681

Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study

Campos, Adrian I., Byrne, Enda M., Mitchell, Brittany L., Wray, Naomi R., Lind, Penelope A., Licinio, Julio, Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2022). Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study. The Pharmacogenomics Journal, 22 (2), 130-135. doi: 10.1038/s41397-022-00267-7

Limb development genes underlie variation in human fingerprint patterns

Li, Jinxi, Glover, James D., Zhang, Haiguo, Peng, Meifang, Tan, Jingze, Mallick, Chandana Basu, Hou, Dan, Yang, Yajun, Wu, Sijie, Liu, Yu, Peng, Qianqian, Zheng, Shijie C., Crosse, Edie I., Medvinsky, Alexander, Anderson, Richard A., Brown, Helen, Yuan, Ziyu, Zhou, Shen, Xu, Yanqing, Kemp, John P., Ho, Yvonne Y.W., Loesch, Danuta Z., Wang, Lizhong, Li, Yingxiang, Tang, Senwei, Wu, Xiaoli, Walters, Robin G., Lin, Kuang, Meng, Ruogu ... Wang, Sijia (2022). Limb development genes underlie variation in human fingerprint patterns. Cell, 185 (1), 95-112.e18. doi: 10.1016/j.cell.2021.12.008

An Epidemiologic, Longitudinal, and Discordant-Twin Study of the Association Between Gambling Disorder and Suicidal Behaviors

Slutske, Wendy S., Davis, Christal N., Lynskey, Michael T., Heath, Andrew C. and Martin, Nicholas G. (2022). An Epidemiologic, Longitudinal, and Discordant-Twin Study of the Association Between Gambling Disorder and Suicidal Behaviors. Clinical Psychological Science, 10 (5), 901-919. doi: 10.1177/21677026211062599

The power of genetic diversity in genome-wide association studies of lipids

Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium* (2021). The power of genetic diversity in genome-wide association studies of lipids. Nature, 600 (7890), 675-679. doi: 10.1038/s41586-021-04064-3

Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: a polygenic risk score analysis

Melhuish Beaupre, Lindsay M., Tiwari, Arun K., Gonçalves, Vanessa F., Zai, Clement C., Marshe, Victoria S., Lewis, Cathryn M., Martin, Nicholas G., McIntosh, Andrew M., Adams, Mark J., Baune, Bernhard T., Levinson, Doug F., Boomsma, Dorret I., Penninx, Brenda W. J. H., Breen, Gerome, Hamilton, Steve, Awasthi, Swapnil, Ripke, Stephan, Jones, Lisa, Jones, Ian, Byrne, Enda M., Hickie, Ian B., Potash, James P., Shi, Jianxin, Weissman, Myrna M., Milaneschi, Yuri, Shyn, Stanley I., Geus, Eco J. C. de, Willemsen, Gonneke, Brown, Gregory M. and Kennedy, James L. (2021). Potential genetic overlap between insomnia and sleep symptoms in major depressive disorder: a polygenic risk score analysis. Frontiers in Psychiatry, 12 734077, 734077. doi: 10.3389/fpsyt.2021.734077

Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2)

Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasés, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C. ... Børglum, Anders D. (2021). Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder (Nature Communications, (2021), 12, 1, (576), 10.1038/s41467-020-20443-2). Nature Communications, 12 (1) 1166. doi: 10.1038/s41467-021-21566-w

Phenome-wide analysis highlights putative causal relationships between self-reported migraine and other complex traits

García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide analysis highlights putative causal relationships between self-reported migraine and other complex traits. Journal of Headache and Pain, 22 (1) 66, 66. doi: 10.1186/s10194-021-01284-w

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C. ... ADHD Working Group of the Psychiatric Genomics Consortium (PGC) (2021). Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nature Communications, 12 (1) 576. doi: 10.1038/s41467-020-20443-2

The Eating Disorders Genetics Initiative (EDGI): study protocol

Bulik, Cynthia M., Thornton, Laura M., Parker, Richard, Kennedy, Hannah, Baker, Jessica H., MacDermod, Casey, Guintivano, Jerry, Cleland, Lana, Miller, Allison L., Harper, Lauren, Larsen, Janne T., Yilmaz, Zeynep, Grove, Jakob, Sullivan, Patrick F., Petersen, Liselotte V., Jordan, Jennifer, Kennedy, Martin A. and Martin, Nicholas G. (2021). The Eating Disorders Genetics Initiative (EDGI): study protocol. BMC Psychiatry, 21 (1) 234. doi: 10.1186/s12888-021-03212-3

Big Five personality traits and illicit drug use: Specificity in trait–drug associations

Dash, Genevieve F., Martin, Nicholas G. and Slutske, Wendy S. (2021). Big Five personality traits and illicit drug use: Specificity in trait–drug associations. Psychology of Addictive Behaviors, 37 (2), 318-330. doi: 10.1037/adb0000793

Understanding genetic risk factors for common side effects of antidepressant medications

Campos, Adrian I., Mulcahy, Aoibhe, Thorp, Jackson G., Wray, Naomi R., Byrne, Enda M., Lind, Penelope A., Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B. and Rentería, Miguel E. (2021). Understanding genetic risk factors for common side effects of antidepressant medications. Communications Medicine, 1 (1) 45, 1-10. doi: 10.1038/s43856-021-00046-8

Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study

Arends, Rachel M., Pasman, Joëlle A., Verweij, Karin J.H., Derks, Eske M., Gordon, Scott D., Hickie, Ian, Thomas, Nathaniel S., Aliev, Fazil, Zietsch, Brendan P., van der Zee, Matthijs D., Mitchell, Brittany L., Martin, Nicholas G., Dick, Danielle M., Gillespie, Nathan A., de Geus, Eco J.C., Boomsma, Dorret I., Schellekens, Arnt F.A. and Vink, Jacqueline M. (2021). Associations between the CADM2 gene, substance use, risky sexual behavior, and self-control: A phenome-wide association study. Addiction Biology, 26 (6) e13015, e13015. doi: 10.1111/adb.13015

The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypes

Mitchell, Brittany L., Campos, Adrian I., Whiteman, David C., Olsen, Catherine M., Gordon, Scott D., Walker, Adam J., Dean, Olivia M., Berk, Michael, Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Martin, Nicholas G. and Byrne, Enda M. (2021). The Australian Genetics of Depression Study: new risk loci and dissecting heterogeneity between subtypes. Biological Psychiatry, 92 (3), 227-235. doi: 10.1016/j.biopsych.2021.10.021

Genetic and environmental influences on perceived social support: differences by sex and relationship

Coventry, William L., Gillespie, Nathan A., Heath, Andrew C. and Martin, Nicholas G. (2021). Genetic and environmental influences on perceived social support: differences by sex and relationship. Twin Research and Human Genetics, 24 (5), 251-263. doi: 10.1017/thg.2021.43

Genetic and environmental influences on sleep-wake behaviours in adolescence

O'Callaghan, Victoria S., Hansell, Narelle K., Guo, Wei, Carpenter, Joanne S., Shou, Haochang, Strike, Lachlan T., Crouse, Jacob J., McAloney, Kerrie, McMahon, Katie L., Byrne, Enda M., Burns, Jane M., Martin, Nicholas G., Hickie, Ian B., Merikangas, Kathleen R. and Wright, Margaret J. (2021). Genetic and environmental influences on sleep-wake behaviours in adolescence. Sleep Advances, 2 (1). doi: 10.1093/sleepadvances/zpab018

Association and genetic overlap between clinical chemistry tests and migraine

Tanha, Hamzeh M, Martin, Nicholas G, Whitfield, John B, Nyholt, Dale R, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S, Palta, Priit, Esko, Tonu, Pers, Tune H, Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A, Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M, Kallela, Mikko, Freilinger, Tobias M, Ran, Caroline, Gordon, Scott G, Stam, Anine H, Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H H ... Palotie, Aarno (2021). Association and genetic overlap between clinical chemistry tests and migraine. Cephalalgia, 41 (11-12), 1208-1221. doi: 10.1177/03331024211018131

Genetic correlation analysis does not associate male pattern baldness with COVID-19

Tanha, Hamzeh M., Medland, Sarah, Martin, Nicholas G. and Nyholt, Dale R. (2021). Genetic correlation analysis does not associate male pattern baldness with COVID-19. Journal of the American Academy of Dermatology, 85 (4), 971-973. doi: 10.1016/j.jaad.2021.05.009

Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight

Beck, Jeffrey J., Pool, René, Van De Weijer, Margot, Chen, Xu, Krapohl, Eva, Gordon, Scott D., Nygaard, Marianne, Debrabant, Birgit, Palviainen, Teemu, Van Der Zee, Matthijs D., Baselmans, Bart, Finnicum, Casey T., Yi, Lu, Lundström, Sebastian, Van Beijsterveldt, Toos, Christiansen, Lene, Heikkilä, Kauko, Kittelsrud, Julie, Loukola, Anu, Ollikainen, Miina, Christensen, Kaare, Martin, Nicholas G., Plomin, Robert, Nivard, Michel, Bartels, Meike, Dolan, Conor, Willemsen, Gonneke, De Geus, Eco, Almqvist, Catarina ... Hottenga, Jouke-Jan (2021). Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight. Human Molecular Genetics, 30 (19), 1894-1905. doi: 10.1093/hmg/ddab121

Identical twins carry a persistent epigenetic signature of early genome programming

van Dongen, Jenny, Gordon, Scott D., McRae, Allan F., Odintsova, Veronika V., Mbarek, Hamdi, Breeze, Charles E., Sugden, Karen, Lundgren, Sara, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hagenbeek, Fiona A., van Beijsterveldt, Catharina E. M., Jan Hottenga, Jouke, Tsai, Pei-Chien, van Dongen, Jenny, Hottenga, Jouke-Jan, McRae, Allan F., Sugden, Karen, Castillo-Fernandez, Juan E., Hannon, Eilis, Moffitt, Terrie E., Hottenga, Jouke-Jan, de Geus, Eco J. C., Spector, Timothy D., Min, Josine L., Hemani, Gibran, Ehli, Erik A., Paul, Franziska ... Genetics of DNA Methylation Consortium (2021). Identical twins carry a persistent epigenetic signature of early genome programming. Nature Communications, 12 (1) 5618, 5618. doi: 10.1038/s41467-021-25583-7

Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression

Martin, Joanna, Asjadi, Kimiya, Hubbard, Leon, Kendall, Kimberley, Pardiñas, Antonio F., Jermy, Bradley, Lewis, Cathryn M., Baune, Bernhard T., Boomsma, Dorret I., Hamilton, Steven P., Lucae, Susanne, Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Mehta, Divya, Mors, Ole, Mullins, Niamh, Penninx, Brenda W. J. H., Preisig, Martin, Rietschel, Marcella, Jones, Ian, Walters, James T. R., Rice, Frances, Thapar, Anita, O’Donovan, Michael and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2021). Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. PLoS One, 16 (9) e0248254, e0248254. doi: 10.1371/journal.pone.0248254

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Min, Josine L., Hemani, Gibran, Hannon, Eilis, Dekkers, Koen F., Castillo-Fernandez, Juan, Luijk, René, Carnero-Montoro, Elena, Lawson, Daniel J., Burrows, Kimberley, Suderman, Matthew, Bretherick, Andrew D., Richardson, Tom G., Klughammer, Johanna, Iotchkova, Valentina, Sharp, Gemma, Al Khleifat, Ahmad, Shatunov, Aleksey, Iacoangeli, Alfredo, McArdle, Wendy L., Ho, Karen M., Kumar, Ashish, Söderhäll, Cilla, Soriano-Tárraga, Carolina, Giralt-Steinhauer, Eva, Kazmi, Nabila, Mason, Dan, McRae, Allan F., Corcoran, David L., Sugden, Karen ... BIOS Consortium (2021). Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Nature Genetics, 53 (9), 1311-1321. doi: 10.1038/s41588-021-00923-x

Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis

Tapmeier, Thomas T., Rahmioglu, Nilufer, Lin, Jianghai, De Leo, Bianca, Obendorf, Maik, Raveendran, Muthuswamy, Fischer, Oliver M., Bafligil, Cemsel, Guo, Manman, Harris, Ronald Alan, Hess-Stumpp, Holger, Laux-Biehlmann, Alexis, Lowy, Ernesto, Lunter, Gerton, Malzahn, Jessica, Martin, Nicholas G., Martinez, Fernando O., Manek, Sanjiv, Mesch, Stefanie, Montgomery, Grant W., Morris, Andrew P., Nagel, Jens, Simmons, Heather A., Brocklebank, Denise, Shang, Catherine, Treloar, Susan, Wells, Graham, Becker, Christian M., Oppermann, Udo ... Zondervan, Krina T. (2021). Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis. Science Translational Medicine, 13 (608) eabd6469, 1-12. doi: 10.1126/scitranslmed.abd6469

Phantom epistasis between unlinked loci

Hemani, Gibran, Powell, Joseph E., Wang, Huanwei, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Goddard, Michael E., Gibson, Greg, Yang, Jian and Visscher, Peter M. (2021). Phantom epistasis between unlinked loci. Nature, 596 (7871), E1-E3. doi: 10.1038/s41586-021-03765-z

Polygenic risk scores derived from varying definitions of depression and risk of depression

Mitchell, Brittany L., Thorp, Jackson G., Wu, Yeda, Campos, Adrian I., Nyholt, Dale R., Gordon, Scott D., Whiteman, David C., Olsen, Catherine M., Hickie, Ian B., Martin, Nicholas G., Medland, Sarah E., Wray, Naomi R. and Byrne, Enda M. (2021). Polygenic risk scores derived from varying definitions of depression and risk of depression. JAMA Psychiatry, 78 (10), 1152-1160. doi: 10.1001/jamapsychiatry.2021.1988

Genetic insights into biological mechanisms governing human ovarian ageing

Ruth, Katherine S., Day, Felix R., Hussain, Jazib, Martínez-Marchal, Ana, Aiken, Catherine E., Azad, Ajuna, Thompson, Deborah J., Knoblochova, Lucie, Abe, Hironori, Tarry-Adkins, Jane L., Gonzalez, Javier Martin, Fontanillas, Pierre, Claringbould, Annique, Bakker, Olivier B., Sulem, Patrick, Walters, Robin G., Terao, Chikashi, Turon, Sandra, Horikoshi, Momoko, Lin, Kuang, Onland-Moret, N. Charlotte, Sankar, Aditya, Hertz, Emil Peter Thrane, Timshel, Pascal N., Shukla, Vallari, Borup, Rehannah, Olsen, Kristina W., Aguilera, Paula, Ferrer-Roda, Mònica ... Perry, John R. B. (2021). Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872), 393-397. doi: 10.1038/s41586-021-03779-7

Genetic susceptibility to pneumonia: a GWAS meta-analysis between the UK Biobank and FinnGen

Campos, Adrian I., Kho, Pik, Vazquez-Prada, Karla X., García-Marín, Luis M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Genetic susceptibility to pneumonia: a GWAS meta-analysis between the UK Biobank and FinnGen. Twin Research and Human Genetics, 24 (3), 145-154. doi: 10.1017/thg.2021.27

Genetic association study of childhood aggression across raters, instruments, and age

Ip, Hill F., van der Laan, Camiel M., Krapohl, Eva M. L., Brikell, Isabell, Sánchez-Mora, Cristina, Nolte, Ilja M., St Pourcain, Beate, Bolhuis, Koen, Palviainen, Teemu, Zafarmand, Hadi, Colodro-Conde, Lucía, Gordon, Scott, Zayats, Tetyana, Aliev, Fazil, Jiang, Chang, Wang, Carol A., Saunders, Gretchen, Karhunen, Ville, Hammerschlag, Anke R., Adkins, Daniel E., Border, Richard, Peterson, Roseann E., Prinz, Joseph A., Thiering, Elisabeth, Seppälä, Ilkka, Vilor-Tejedor, Natàlia, Ahluwalia, Tarunveer S., Day, Felix R., Hottenga, Jouke-Jan ... Boomsma, Dorret I. (2021). Genetic association study of childhood aggression across raters, instruments, and age. Translational Psychiatry, 11 (1) 413, 413. doi: 10.1038/s41398-021-01480-x

Genetic risk for chronic pain is associated with lower antidepressant effectiveness: converging evidence for a depression subtype

Campos, Adrián I., Ngo, Trung Thanh, Medland, Sarah E., Wray, Naomi R., Hickie, Ian B., Byrne, Enda M., Martin, Nicholas G. and Rentería, Miguel E. (2021). Genetic risk for chronic pain is associated with lower antidepressant effectiveness: converging evidence for a depression subtype. Australian and New Zealand Journal of Psychiatry, 56 (9), 1-10. doi: 10.1177/00048674211031491

Using monozygotic twins to dissect common genes in posttraumatic stress disorder and migraine

Bainomugisa, Charlotte K., Sutherland, Heidi G., Parker, Richard, Mcrae, Allan F., Haupt, Larisa M., Griffiths, Lyn R., Heath, Andrew, Nelson, Elliot C., Wright, Margaret J., Hickie, Ian B., Martin, Nicholas G., Nyholt, Dale R. and Mehta, Divya (2021). Using monozygotic twins to dissect common genes in posttraumatic stress disorder and migraine. Frontiers in Neuroscience, 15 678350, 678350. doi: 10.3389/fnins.2021.678350

Early expressions of psychopathology and risk associated with trans-diagnostic transition to mood and psychotic disorders in adolescents and young adults

Scott, Jan, Crouse, Jacob J., Ho, Nicholas, Iorfino, Frank, Martin, Nicholas, Parker, Richard, McGrath, John, Gillespie, Nathan A., Medland, Sarah and Hickie, Ian B. (2021). Early expressions of psychopathology and risk associated with trans-diagnostic transition to mood and psychotic disorders in adolescents and young adults. PLoS ONE, 16 (6 June) e0252550, 1-17. doi: 10.1371/journal.pone.0252550

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Mullins, Niamh, Forstner, Andreas J., O'Connell, Kevin S., Coombes, Brandon, Coleman, Jonathan R I, Qiao, Zhen, Als, Thomas D., Bigdeli, Tim B., Børte, Sigrid, Bryois, Julien, Charney, Alexander W., Drange, Ole Kristian, Gandal, Michael J., Hagenaars, Saskia P., Ikeda, Masashi, Kamitaki, Nolan, Kim, Minsoo, Krebs, Kristi, Panagiotaropoulou, Georgia, Schilder, Brian M., Sloofman, Laura G., Steinberg, Stacy, Trubetskoy, Vassily, Winsvold, Bendik S., Won, Hong-Hee, Abramova, Liliya, Adorjan, Kristina, Agerbo, Esben, Al Eissa, Mariam ... Andreassen, Ole A. (2021). Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Nature genetics, 53 (6), 817-829. doi: 10.1038/s41588-021-00857-4

Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity

García-Marín, Luis M., Campos, Adrián I., Kho, Pik-Fang, Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity. Human Genetics, 140 (8), 1253-1265. doi: 10.1007/s00439-021-02298-9

Correction to: The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption

Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). Correction to: The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (4), 441-442. doi: 10.1007/s10519-021-10065-9

Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults

Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Martin, Nicholas G., Couvy-Duchesne, Baptiste, Hermens, Daniel F., Parker, Richard, Gillespie, Nathan A., Medland, Sarah E. and Hickie, Ian B. (2021). Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults. Translational Psychiatry, 11 (1) 285, 285. doi: 10.1038/s41398-021-01390-y

The association between genetically determined ABO blood types and major depressive disorder

Garvert, Linda, Baune, Bernhard T, Berger, Klaus, Boomsma, Dorret I, Breen, Gerome, Greinacher, Andreas, Hamilton, Steven P, Levinson, Douglas F, Lewis, Cathryn M, Lucae, Susanne, Magnusson, Patrik K E, Martin, Nicholas G, McIntosh, Andrew M, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W J H, Perlis, Roy H, Pistis, Giorgio, Potash, James B, Preisig, Martin, Rietschel, Marcella, Shi, Jianxin, Smoller, Jordan W, Tiemeier, Henning, Uher, Rudolf, Völker, Uwe, Völzke, Henry, Weissman, Myrna M, Grabe, Hans J and Van der Auwera, Sandra (2021). The association between genetically determined ABO blood types and major depressive disorder. Psychiatry Research, 299 113837, 113837. doi: 10.1016/j.psychres.2021.113837

Typologies of illicit drug use in mid-adulthood: a quasi-longitudinal latent class analysis in a community-based sample of twins

Dash, Genevieve F., Martin, Nicholas G., Agrawal, Arpana, Lynskey, Michael T. and Slutske, Wendy S. (2021). Typologies of illicit drug use in mid-adulthood: a quasi-longitudinal latent class analysis in a community-based sample of twins. Addiction, 116 (5), 1101-1112. doi: 10.1111/add.15225

Epigenome-wide association study of thyroid function traits identifies novel associations of fT3 with KLF9 and DOT1L

Lafontaine, Nicole, Campbell, Purdey J., Castillo-Fernandez, Juan E., Mullin, Shelby, Lim, Ee Mun, Kendrew, Phillip, Lewer, Michelle, Brown, Suzanne J., Huang, Rae-Chi, Melton, Phillip E., Mori, Trevor A., Beilin, Lawrence J., Dudbridge, Frank, Spector, Tim D., Wright, Margaret J., Martin, Nicholas G., McRae, Allan F., Panicker, Vijay, Zhu, Gu, Walsh, John P., Bell, Jordana T. and Wilson, Scott G. (2021). Epigenome-wide association study of thyroid function traits identifies novel associations of fT3 with KLF9 and DOT1L. The Journal of Clinical Endocrinology and Metabolism, 106 (5), e2191-e2202. doi: 10.1210/clinem/dgaa975

Symptom-level modelling unravels the shared genetic architecture of anxiety and depression

Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary F., An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2021). Symptom-level modelling unravels the shared genetic architecture of anxiety and depression. Nature Human Behaviour, 5 (10), 1432-1442. doi: 10.1038/s41562-021-01094-9

Comorbid chronic pain and depression: shared risk factors and differential antidepressant effectiveness

Roughan, William H., Campos, Adrián I., García-Marín, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung Thanh, Martin, Nicholas G. and Rentería, Miguel E. (2021). Comorbid chronic pain and depression: shared risk factors and differential antidepressant effectiveness. Frontiers in Psychiatry, 12 643609, 1-13. doi: 10.3389/fpsyt.2021.643609

'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers

Loesch, Danuta Z., Duffy, David L., Martin, Nicholas G., Tassone, Flora, Atkinson, Anna and Storey, Elsdon (2021). 'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers. Twin Research and Human Genetics, 24 (2), 95-102. doi: 10.1017/thg.2021.10

Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts

Campos, Adrian I., Thompson, Paul M., Veltman, Dick J., Pozzi, Elena, van Veltzen, Laura S., Jahanshad, Neda, Adams, Mark J., Baune, Bernhard T., Berger, Klaus, Brosch, Katharina, Bülow, Robin, Connolly, Colm G., Dannlowski, Udo, Davey, Christopher G., de Zubicaray, Greig I., Dima, Danai, Erwin-Grabner, Tracy, Evans, Jennifer W., Fu, Cynthia H.Y., Gotlib, Ian H., Goya-Maldonado, Roberto, Grabe, Hans J., Grotegerd, Dominik, Harris, Matthew A., Harrison, Ben J., Hatton, Sean N., Hermesdorf, Marco, Hickie, Ian B., Ho, Tiffany C. ... Rentería, Miguel E. (2021). Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts. Biological Psychiatry, 90 (4), 243-252. doi: 10.1016/j.biopsych.2021.03.015

Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color

Simcoe, Mark, Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Hemani, Gibran, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Vuckovic, Dragana, Girotto, Giorgia, Sala, Cinzia, Catamo, Eulalia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex, Wu, Wenting, Kraft, Peter, Hammond, Christopher J., Shi, Yuan, Chen, Yan ... the International Visible Trait Genetics Consortium (2021). Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Science Advances, 7 (11) abd1239, eabd1239. doi: 10.1126/sciadv.abd1239

Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes

Sherva, Richard, Zhu, Congcong, Wetherill, Leah, Edenberg, Howard J., Johnson, Emma, Degenhardt, Louisa, Agrawal, Arpana, Martin, Nicholas G., Nelson, Elliot, Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2021). Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Exploration of Medicine, 2 (1), 60-73. doi: 10.37349/emed.2021.00032

Can network analysis of self-reported psychopathology shed light on the core phenomenology of bipolar disorders in adolescents and young adults?

Scott, Jan, Crouse, Jacob J., Ho, Nicholas, Carpenter, Joanne, Martin, Nicholas, Medland, Sarah, Parker, Richard, Byrne, Enda, Couvy-Duchesne, Baptiste, Mitchell, Brittany, Merikangas, Kathleen, Gillespie, Nathan A. and Hickie, Ian (2021). Can network analysis of self-reported psychopathology shed light on the core phenomenology of bipolar disorders in adolescents and young adults?. Bipolar Disorders, 23 (6), 584-594. doi: 10.1111/bdi.13067

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

Gharahkhani, Puya, NEIGHBORHOOD consortium, Jorgenson, Eric, Hysi, Pirro, Khawaja, Anthony P., Pendergrass, Sarah, Han, Xikun, Ong, Jue Sheng, Hewitt, Alex W., Segrè, Ayellet V., Rouhana, John M., Hamel, Andrew R., Igo, Robert P., Choquet, Helene, Qassim, Ayub, Josyula, Navya S., Cooke Bailey, Jessica N., Bonnemaijer, Pieter W. M., Iglesias, Adriana, Siggs, Owen M., Young, Terri L., Vitart, Veronique, Thiadens, Alberta A. H. J., Karjalainen, Juha, Uebe, Steffen, Melles, Ronald B., Nair, K. Saidas, Luben, Robert, Simcoe, Mark ... 23 and Me Research Team (2021). Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Nature Communications, 12 (1) 1258, 1-16. doi: 10.1038/s41467-020-20851-4

Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years

Frangou, Sophia, Modabbernia, Amirhossein, Williams, Steven C. R., Papachristou, Efstathios, Doucet, Gaelle E., Agartz, Ingrid, Aghajani, Moji, Akudjedu, Theophilus N., Albajes-Eizagirre, Anton, Alnaes, Dag, Alpert, Kathryn I, Andersson, Micael, Andreasen, Nancy C, Andreassen, Ole A, Asherson, Philip, Banaschewski, Tobias, Bargallo, Nuria, Baumeister, Sarah, Baur-Streubel, Ramona, Bertolino, Alessandro, Bonvino, Aurora, Boomsma, Dorret I, Borgwardt, Stefan, Bourque, Josiane, Brandeis, Daniel, Breier, Alan, Brodaty, Henry, Brouwer, Rachel M, Buitelaar, Jan K ... Dima, Danai (2021). Cortical thickness across the lifespan: Data from 17,075 healthy individuals aged 3-90 years. Human Brain Mapping, 43 (1) hbm.25364, 431-451. doi: 10.1002/hbm.25364

The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption

Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics, 51 (3), 223-236. doi: 10.1007/s10519-021-10044-0

Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years

Dima, Danai, Modabbernia, Amirhossein, Papachristou, Efstathios, Doucet, Gaelle E., Agartz, Ingrid, Aghajani, Moji, Akudjedu, Theophilus N., Albajes-Eizagirre, Anton, Alnaes, Dag, Alpert, Kathryn I., Andersson, Micael, Andreasen, Nancy C., Andreassen, Ole A., Asherson, Philip, Banaschewski, Tobias, Bargallo, Nuria, Baumeister, Sarah, Baur-Streubel, Ramona, Bertolino, Alessandro, Bonvino, Aurora, Boomsma, Dorret I., Borgwardt, Stefan, Bourque, Josiane, Brandeis, Daniel, Breier, Alan, Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Busatto, Geraldo F. ... Karolinska Schizophrenia Project (KaSP) (2021). Subcortical volumes across the lifespan: Data from 18,605 healthy individuals aged 3-90 years. Human Brain Mapping, 43 (1) hbm.25320, 452-469. doi: 10.1002/hbm.25320

16Up: Outline of a study investigating wellbeing and information and communication technology use in adolescent twins

Mitchell, Brittany L., Kirk, Katherine M., McAloney, Kerrie, Wright, Margaret J., Davenport, Tracey A., Hermens, Daniel F., Scott, James G., McGrath, John J., Gillespie, Nathan A., Carpenter, Joanne S., O’Callaghan, Victoria S., Medland, Sarah, Christensen, Helen, Martin, Nicholas G., Burns, Jane M. and Hickie, Ian B. (2021). 16Up: Outline of a study investigating wellbeing and information and communication technology use in adolescent twins. Twin Research and Human Genetics, 23 (6), 1-13. doi: 10.1017/thg.2020.83

Comparison of Familial, Polygenic and Biochemical Predictors of Mortality

Whitfield, John B., Colodro-Conde, Lucía, Timmers, Paul R. H. J., Joshi, Peter K., Montgomery, Grant W. and Martin, Nicholas G. (2021). Comparison of Familial, Polygenic and Biochemical Predictors of Mortality. Twin Research and Human Genetics, 23 (6), 307-315. doi: 10.1017/thg.2020.89

Are prescription misuse and illicit drug use etiologically distinct? A genetically-informed analysis of opioids and stimulants

Dash, Genevieve F., Martin, Nicholas G., Agrawal, Arpana, Lynskey, Michael T. and Slutske, Wendy S. (2021). Are prescription misuse and illicit drug use etiologically distinct? A genetically-informed analysis of opioids and stimulants. Psychological Medicine, 52 (14), 3176-3183. doi: 10.1017/S0033291720005267

Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning

Van Dongen, Jenny, Gordon, Scott D., Odintsova, Veronika V., McRae, Allan F., Robinson, Wendy P., Hall, Judith G., Boomsma, Dorret I. and Martin, Nicholas G. (2021). Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning. Twin Research and Human Genetics, 24 (3), 155-159. doi: 10.1017/thg.2021.25

Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data

García-Marín, Luis M., Campos, Adrián I., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Inference of causal relationships between sleep-related traits and 1,527 phenotypes using genetic data. Sleep, 44 (1) zsaa154. doi: 10.1093/sleep/zsaa154

A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

Guo, Yanjun, Rist, Pamela M., Daghlas, Iyas, Giulianini, Franco, Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H. ... Chasman, Daniel I. (2020). A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Nature Communications, 11 (1) 3368. doi: 10.1038/s41467-020-17002-0

A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: genes, brain and behaviour (PISA)

Lupton, Michelle K., Robinson, Gail A., Adam, Robert J, Rose, Stephen, Byrne, Gerard J., Salvado, Olivier, Pachana, Nancy A., Almeida, Osvaldo P., McAloney, Kerrie, Gordon, Scott D., Raniga, Parnesh, Fazlollahi, Amir, Xia, Ying, Ceslis, Amelia, Sonkusare, Saurabh, Zhang, Qing, Kholghi, Mahnoosh, Karunanithi, Mohan, Mosley, Philip E., Lv, Jinglei, Borne, Léonie, Adsett, Jessica, Garden, Natalie, Fripp, Jurgen, Martin, Nicholas G., Guo, Christine C. and Breakspear, Michael (2020). A prospective cohort study of prodromal Alzheimer’s disease: Prospective Imaging Study of Ageing: genes, brain and behaviour (PISA). NeuroImage: Clinical, 29 102527, 102527. doi: 10.1016/j.nicl.2020.102527

Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts

Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Latvala, Antti, Honda, Chika, Inui, Fujio, Tomizawa, Rie, Watanabe, Mikio, Sakai, Norio, Rebato, Esther, Busjahn, Andreas, Tyler, Jessica, Hopper, John L., Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Calais-Ferreira, Lucas, Oliveira, Vinicius C., Ferreira, Paulo H., Medda, Emanuela, Nisticò, Lorenza, Toccaceli, Virgilia, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling ... Kaprio, Jaakko (2020). Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts. Scientific Reports, 10 (1) 12681, 12681. doi: 10.1038/s41598-020-69526-6

Pessimism is associated with greater all-cause and cardiovascular mortality, but optimism is not protective

Whitfield, John B., Zhu, Gu, Landers, J. George and Martin, Nicholas G. (2020). Pessimism is associated with greater all-cause and cardiovascular mortality, but optimism is not protective. Scientific Reports, 10 (1) 12609, 1-7. doi: 10.1038/s41598-020-69388-y

The genetic architecture of sporadic and multiple consecutive miscarriage

Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y., Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S., Yang, Ling, Becker, Christian M., Børglum, Anders D., Gordon, Scott D., Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M., Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A., Metspalu, Andres ... Lindgren, Cecilia M. (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11 (1) 5980, 1-12. doi: 10.1038/s41467-020-19742-5

High-throughput phenotyping of soybean maturity using time series UAV imagery and convolutional neural networks

Trevisan, Rodrigo, Pérez, Osvaldo, Schmitz, Nathan, Diers, Brian and Martin, Nicolas (2020). High-throughput phenotyping of soybean maturity using time series UAV imagery and convolutional neural networks. Remote Sensing, 12 (21) 3617, 1-19. doi: 10.3390/rs12213617

The role of locus of control in adulthood outcomes: Evidence from Australian twins

Xue, Sen, Kidd, Michael P., Le, Anh.T., Kirk, Kathy and Martin, Nicholas G. (2020). The role of locus of control in adulthood outcomes: Evidence from Australian twins. Journal of Economic Behavior and Organization, 179, 566-588. doi: 10.1016/j.jebo.2020.09.018

Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature

Ho, Yvonne Y. W., Mina-Vargas, Angela, Zhu, Gu, Brims, Mark, Mcnevin, Dennis, Montgomery, Grant W., Martin, Nicholas G., Medland, Sarah E. and Painter, Jodie N. (2020). Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature. Twin Research and Human Genetics, 23 (5), 271-277. doi: 10.1017/thg.2020.78

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

Erzurumluoglu, A. Mesut, Liu, Mengzhen, Jackson, Victoria E., Barnes, Daniel R., Datta, Gargi, Melbourne, Carl A., Young, Robin, Batini, Chiara, Surendran, Praveen, Jiang, Tao, Adnan, Sheikh Daud, Afaq, Saima, Agrawal, Arpana, Altmaier, Elisabeth, Antoniou, Antonis C., Asselbergs, Folkert W., Baumbach, Clemens, Bierut, Laura, Bertelsen, Sarah, Boehnke, Michael, Bots, Michiel L., Brazel, David M, Chambers, John C., Chang-Claude, Jenny, Chen, Chu, Corley, Janie, Chou, Yi-Ling, David, Sean P., de Boer, Rudolf A. ... CHD Exome+ consortium (2020). Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Molecular Psychiatry, 25 (10), 2392-2409. doi: 10.1038/s41380-018-0313-0

Sex differences in the relative influence of marital status and parenthood on alcohol use disorder symptoms: a multilevel discordant twin design

Dash, Genevieve F., Martin, Nicholas G., Lynskey, Michael T. and Slutske, Wendy S. (2020). Sex differences in the relative influence of marital status and parenthood on alcohol use disorder symptoms: a multilevel discordant twin design. Journal of Abnormal Psychology, 129 (7), 737-747. doi: 10.1037/abn0000611

Genome-wide association study identifies 48 common genetic variants associated with handedness

Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y

The reliability and heritability of cortical folds and their genetic correlations across hemispheres

Pizzagalli, Fabrizio, Auzias, Guillaume, Yang, Qifan, Mathias, Samuel R., Faskowitz, Joshua, Boyd, Joshua D., Amini, Armand, Rivière, Denis, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Mangin, Jean-François, Glahn, David C., Blangero, John, Wright, Margaret J., Thompson, Paul M., Kochunov, Peter and Jahanshad, Neda (2020). The reliability and heritability of cortical folds and their genetic correlations across hemispheres. Communications Biology, 3 (1) 510, 510. doi: 10.1038/s42003-020-01163-1

Septic shock: a genomewide association study and polygenic risk score analysis

D'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4), 204-213. doi: 10.1017/thg.2020.60

Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression

Hagenaars, Saskia P., Coleman, Jonathan R. I., Choi, Shing Wan, Gaspar, Héléna, Adams, Mark J., Howard, David M., Hodgson, Karen, Traylor, Matthew, Air, Tracy M., Andlauer, Till F. M., Arolt, Volker, Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Campbell, Archie, Cearns, Micah, Czamara, Darina, Dannlowski, Udo, Domschke, Katharina, de Geus, Eco J. C., Hamilton, Steven P., Hayward, Caroline, Hickie, Ian B., Hottenga, Jouke Jan, Ising, Marcus, Jones, Ian, Jones, Lisa, Kutalik, Zoltan ... Lewis, Cathryn M. (2020). Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 183 (6) ajmg.b.32807, 309-330. doi: 10.1002/ajmg.b.32807

Genetic aetiology of self-harm ideation and behaviour

Campos, Adrian I., Verweij, Karin J. H., Statham, Dixie J., Madden, Pamela A. F., Maciejewski, Dominique F., Davis, Katrina A. S., John, Ann, Hotopf, Matthew, Heath, Andrew C., Martin, Nicholas G. and Rentería, Miguel E. (2020). Genetic aetiology of self-harm ideation and behaviour. Scientific Reports, 10 (1) 9713, 9713. doi: 10.1038/s41598-020-66737-9

Cohort profile: the Australian genetics of depression study

Byrne, Enda M., Kirk, Katherine M., Medland, Sarah E., McGrath, John J., Colodro-Conde, Lucia, Parker, Richard, Cross, Simone, Sullivan, Lenore, Statham, Dixie J., Levinson, Douglas F., Licinio, Julio, Wray, Naomi R, Hickie, Ian B. and Martin, Nicholas G. (2020). Cohort profile: the Australian genetics of depression study. BMJ Open, 10 (5) e032580, e032580. doi: 10.1136/bmjopen-2019-032580

Single cell transcriptomics reveals opioid usage evokes widespread suppression of antiviral gene program

Karagiannis, Tanya T., Cleary, John P., Gok, Busra, Henderson, Andrew J., Martin, Nicholas G., Yajima, Masanao, Nelson, Elliot C. and Cheng, Christine S. (2020). Single cell transcriptomics reveals opioid usage evokes widespread suppression of antiviral gene program. Nature Communications, 11 (1) 2611, 2611. doi: 10.1038/s41467-020-16159-y

Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory

Mitchell, Brittany L., Cuéllar-Partida, Gabriel, Grasby, Katrina L., Campos, Adrian I., Strike, Lachlan T., Hwang, Liang-Dar, Okbay, Aysu, Thompson, Paul M., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J. and Rentería, Miguel E. (2020). Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory. NeuroImage, 212 116691, 116691. doi: 10.1016/j.neuroimage.2020.116691

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

Landi, Maria Teresa, GenoMEL Consortium, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andreas, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M., Potrony, Miriam, Kypreou, Katerina P., Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew ... MelaNostrum Consortium (2020). Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5), 494-504. doi: 10.1038/s41588-020-0611-8

Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

Revez, Joana A., Lin, Tian, Qiao, Zhen, Xue, Angli, Holtz, Yan, Zhu, Zhihong, Zeng, Jian, Wang, Huanwei, Sidorenko, Julia, Kemper, Kathryn E., Vinkhuyzen, Anna A. E., Frater, Julanne, Eyles, Darryl, Burne, Thomas H. J., Mitchell, Brittany, Martin, Nicholas G., Zhu, Gu, Visscher, Peter M., Yang, Jian, Wray, Naomi R. and McGrath, John J. (2020). Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nature Communications, 11 (1) 1647, 1-12. doi: 10.1038/s41467-020-15421-7

Changes in thyroid function across adolescence: a longitudinal study

Campbell, Purdey J., Brown, Suzanne J., Kendrew, Phillip, Lewer, Michelle, Lim, Ee Mun, Joseph, John, Cross, Simone M., Wright, Margaret J., Martin, Nicholas G., Wilson, Scott G. and Walsh, John P. (2020). Changes in thyroid function across adolescence: a longitudinal study. The Journal of Clinical Endocrinology and Metabolism, 105 (4), e1162-e1170. doi: 10.1210/clinem/dgz331

Minimal phenotyping yields genome-wide association signals of low specificity for major depression

Cai, Na, Revez, Joana A., Adams, Mark J., Andlauer, Till F. M., Breen, Gerome, Byrne, Enda M., Clarke, Toni-Kim, Forstner, Andreas J., Grabe, Hans J., Hamilton, Steven P., Levinson, Douglas F., Lewis, Cathryn M., Lewis, Glyn, Martin, Nicholas G., Milaneschi, Yuri, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W. J. H., Perlis, Roy H., Pistis, Giorgio, Potash, James B., Preisig, Martin, Shi, Jianxin, Smoller, Jordan W., Streit, Fabien, Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Viktorin, Alexander ... Flint, Jonathan (2020). Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nature Genetics, 52 (4), 437-447. doi: 10.1038/s41588-020-0594-5

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Fan, Qiao, Pozarickij, Alfred, Tan, Nicholas Y. Q., Guo, Xiaobo, Verhoeven, Virginie J. M., Vitart, Veronique, Guggenheim, Jeremy A., Miyake, Masahiro, Tideman, J. Willem L., Khawaja, Anthony P., Zhang, Liang, MacGregor, Stuart, Höhn, René, Chen, Peng, Biino, Ginevra, Wedenoja, Juho, Saffari, Seyed Ehsan, Tedja, Milly S., Xie, Jing, Lanca, Carla, Wang, Ya Xing, Sahebjada, Srujana, Mazur, Johanna, Mirshahi, Alireza, Martin, Nicholas G., Yazar, Seyhan, Pennell, Craig E., Yap, Maurice, Haarman, Annechien E. G. ... Evans, David M. (2020). Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Communications Biology, 3 (1) 133, 133. doi: 10.1038/s42003-020-0802-y

Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization

Ong, Jue-Sheng, Hwang, Liang-Dar, Zhong, Victor W., An, Jiyuan, Gharahkhani, Puya, Breslin, Paul A. S., Wright, Margaret J., Lawlor, Deborah A., Whitfield, John, MacGregor, Stuart, Martin, Nicholas G. and Corneli, Marilyn C. (2020). Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization. Scientific Reports, 10 (1) 4778, 4778. doi: 10.1038/s41598-020-60488-3

Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent

Buchwald, Jadwiga, Chenoweth, Meghan J., Palviainen, Teemu, Zhu, Gu, Benner, Christian, Gordon, Scott, Korhonen, Tellervo, Ripatti, Samuli, Madden, Pamela A. F., Lehtimäki, Terho, Raitakari, Olli T., Salomaa, Veikko, Rose, Richard J., George, Tony P., Lerman, Caryn, Pirinen, Matti, Martin, Nicholas G., Kaprio, Jaakko, Loukola, Anu and Tyndale, Rachel F. (2020). Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Molecular Psychiatry, 26 (6), 2212-2223. doi: 10.1038/s41380-020-0702-z

Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length

Li, Chen, Stoma, Svetlana, Lotta, Luca A., Warner, Sophie, Albrecht, Eva, Allione, Alessandra, Arp, Pascal P., Broer, Linda, Buxton, Jessica L., Da Silva Couto Alves, Alexessander, Deelen, Joris, Fedko, Iryna O., Gordon, Scott D., Jiang, Tao, Karlsson, Robert, Kerrison, Nicola, Loe, Taylor K., Mangino, Massimo, Milaneschi, Yuri, Miraglio, Benjamin, Pervjakova, Natalia, Russo, Alessia, Surakka, Ida, van der Spek, Ashley, Verhoeven, Josine E., Amin, Najaf, Beekman, Marian, Blakemore, Alexandra I., Canzian, Federico ... Codd, Veryan (2020). Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length. American Journal of Human Genetics, 106 (3), 389-404. doi: 10.1016/j.ajhg.2020.02.006

Atomic spectrometry update: Review of advances in the analysis of clinical and biological materials, foods and beverages

Taylor, Andrew, Catchpole, Anthony, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2020). Atomic spectrometry update: Review of advances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 35 (3), 426-454. doi: 10.1039/d0ja90005b

Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium

Polimanti, Renato, Walters, Raymond K., Johnson, Emma C., McClintick, Jeanette N., Adkins, Amy E., Adkins, Daniel E., Bacanu, Silviu-Alin, Bierut, Laura J., Bigdeli, Tim B., Brown, Sandra, Bucholz, Kathleen K., Copeland, William E., Costello, E. Jane, Degenhardt, Louisa, Farrer, Lindsay A, Foroud, Tatiana M., Fox, Louis, Goate, Alison M., Grucza, Richard, Hack, Laura M., Hancock, Dana B., Hartz, Sarah M., Heath, Andrew C., Hewitt, John K., Hopfer, Christian J., Johnson, Eric O., Kendler, Kenneth S., Kranzler, Henry R., Krauter, Kenneth ... Gelernter, Joel (2020). Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Molecular Psychiatry, 25 (8), 1673-1687. doi: 10.1038/s41380-020-0677-9

Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank

Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2020). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Nature Communications, 11 (1) 817, 817. doi: 10.1038/s41467-020-14625-1

Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls

Duffy, David L., Jagirdar, Kasturee, Lee, Katie J., McWhirter, Seamus R., McMeniman, Erin K., De’Ambrosis, Brian, Pflugfelder, Annette, Rayner, Jenna E., Whiteman, David C., Brown, Matthew A., Martin, N.G., Smithers, B.M., Schaider, Helmut, Soyer, H. Peter and Sturm, Richard A. (2020). Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls. Journal of Investigative Dermatology, 140 (2), 498-501.e17. doi: 10.1016/j.jid.2019.05.032

High-intensity drinking in adult Australian twins

Dash, Genevieve F., Davis, Christal N., Martin, Nicholas G., Statham, Dixie J., Lynskey, Michael T. and Slutske, Wendy S. (2020). High-intensity drinking in adult Australian twins. Alcoholism: Clinical and Experimental Research, 44 (2), 522-531. doi: 10.1111/acer.14262

The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults

Doust, Catherine, Gordon, Scott D., Garden, Natalie, Fisher, Simon E., Martin, Nicholas G., Bates, Timothy C. and Luciano, Michelle (2020). The Association of Dyslexia and Developmental Speech and Language Disorder Candidate Genes with Reading and Language Abilities in Adults. Twin Research and Human Genetics, 23 (1), 23-32. doi: 10.1017/thg.2020.7

Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

Craig, Jamie E., Han, Xikun, Qassim, Ayub, Hassall, Mark, Cooke Bailey, Jessica N., Kinzy, Tyler G., Khawaja, Anthony P., An, Jiyuan, Marshall, Henry, Gharahkhani, Puya, Igo, Robert P., Graham, Stuart L., Healey, Paul R., Ong, Jue-Sheng, Zhou, Tiger, Siggs, Owen, Law, Matthew H., Souzeau, Emmanuelle, Ridge, Bronwyn, Hysi, Pirro G., Burdon, Kathryn P., Mills, Richard A., Landers, John, Ruddle, Jonathan B., Agar, Ashish, Galanopoulos, Anna, White, Andrew J. R., Willoughby, Colin E., Andrew, Nicholas H. ... MacGregor, Stuart (2020). Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Nature Genetics, 52 (2), 160-166. doi: 10.1038/s41588-019-0556-y

Genome-wide association study of opioid cessation

Cox, Jiayi W., Sherva, Richard M., Lunetta, Kathryn L., Johnson, Emma C., Martin, Nicholas G., Degenhardt, Louisa, Agrawal, Arpana, Nelson, Elliot C., Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2020). Genome-wide association study of opioid cessation. Journal of Clinical Medicine, 9 (1) 180, 180. doi: 10.3390/jcm9010180

Blood and plasma titanium levels associated with well-functioning hip implants

Swiatkowska, Ilona, Martin, Nicholas G., Henckel, Johann, Apthorp, Hugh, Hamshere, Jane and Hart, Alister J. (2020). Blood and plasma titanium levels associated with well-functioning hip implants. Journal of Trace Elements in Medicine and Biology, 57, 9-17. doi: 10.1016/j.jtemb.2019.09.005

Exploring the genetic relationship between hearing impairment and Alzheimer's disease

Mitchell, Brittany L., Thorp, Jackson G., Evans, David M., Nyholt, Dale R., Martin, Nicholas G. and Lupton, Michelle K. (2020). Exploring the genetic relationship between hearing impairment and Alzheimer's disease. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 12 (1) e12108, 1-10. doi: 10.1002/dad2.12108

Prevalence of self-reported subthreshold phenotypes of major mental disorders and their association with functional impairment, treatment and full-threshold syndromes in a community-residing cohort of young adults

Scott, Jan, Martin, Nicholas G., Parker, Richard, Couvy-Duchesne, Baptiste, Medland, Sarah E. and Hickie, Ian (2020). Prevalence of self-reported subthreshold phenotypes of major mental disorders and their association with functional impairment, treatment and full-threshold syndromes in a community-residing cohort of young adults. Early Intervention in Psychiatry, 15 (2) eip.12942, 306-313. doi: 10.1111/eip.12942

Shared genetic risk between eating disorder- and substance-use-related phenotypes: evidence from genome-wide association studies

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Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders

Lee, Phil H., Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A., Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M., Nivard, Michel G., Grotzinger, Andrew D., Posthuma, Danielle, Wang, Meg M.-J., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K., Anney, Richard J.L., Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H., Coppola, Giovanni, Derks, Eske M., Hoekstra, Pieter J., Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George, Kranzler, Henry R., Luykx, Jurjen J. ... Smoller, Jordan W. (2019). Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders. Cell, 179 (7), 1469-1482.e11. doi: 10.1016/j.cell.2019.11.020

Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group

Jia, Tianye, Chu, Congying, Liu, Yun, van Dongen, Jenny, Papastergios, Evangelos, Armstrong, Nicola J., Bastin, Mark E., Carrillo-Roa, Tania, den Braber, Anouk, Harris, Mathew, Jansen, Rick, Liu, Jingyu, Luciano, Michelle, Ori, Anil P. S., Roiz Santiañez, Roberto, Ruggeri, Barbara, Sarkisyan, Daniil, Shin, Jean, Sungeun, Kim, Tordesillas Gutiérrez, Diana, van’t Ent, Dennis, Ames, David, Artiges, Eric, Bakalkin, Georgy, Banaschewski, Tobias, Bokde, Arun L. W., Brodaty, Henry, Bromberg, Uli, Brouwer, Rachel ... Desrivières, Sylvane (2019). Epigenome-wide meta-analysis of blood DNA methylation and its association with subcortical volumes: findings from the ENIGMA Epigenetics Working Group. Molecular Psychiatry, 26 (8), 1-12. doi: 10.1038/s41380-019-0605-z

Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults

Chang, Lun-Hsien, Whitfield, John B., Liu, Mengzhen, Medland, Sarah E., Hickie, Ian B., Martin, Nicholas G., Verhulst, Brad, Heath, Andrew C., Madden, Pamela A., Statham, Dixie J., Gillespie, Nathan A. and GSCAN Consortium (2019). Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults. Drug and Alcohol Dependence, 205 107704, 107704. doi: 10.1016/j.drugalcdep.2019.107704

Identifying subtypes of cannabis users based on simultaneous polysubstance use

Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Identifying subtypes of cannabis users based on simultaneous polysubstance use. Drug and Alcohol Dependence, 205 107696, 1-7. doi: 10.1016/j.drugalcdep.2019.107696

Shared and specific genetic risk factors for lifetime major depression, depressive symptoms and neuroticism in three population-based twin samples

Kendler, Kenneth S., Gardner, Charles O., Neale, Michael C., Aggen, Steve, Heath, Andrew, Colodro-Conde, Lucía, Couvyduchesne, Baptiste, Byrne, Enda M., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Shared and specific genetic risk factors for lifetime major depression, depressive symptoms and neuroticism in three population-based twin samples. Psychological Medicine, 49 (16), 2745-2753. doi: 10.1017/S003329171800377X

The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in Twins

Silventoinen, K., Jelenkovic, A., Yokoyama, Y., Sund, R., Sugawara, M., Tanaka, M., Matsumoto, S., Bogl, L. H., Freitas, D. L., Maia, J. A., Hjelmborg, J. V.B., Aaltonen, S., Piirtola, M., Latvala, A., Calais-Ferreira, L., Oliveira, V. C., Ferreira, P. H., Ji, F., Ning, F., Pang, Z., Ordoñana, J. R., Sánchez-Romera, J. F., Colodro-Conde, L., Burt, S. A., Klump, K. L., Martin, N. G., Medland, S. E., Montgomery, G. W., Kandler, C. ... Kaprio, J. (2019). The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in Twins. Twin Research and Human Genetics, 22 (6), 1-9. doi: 10.1017/thg.2019.35

The Nigerian Twin and Sibling Registry: An Update

Hur, Yoon-Mi, Jeong, Hoe-Uk, Kang, Man Chull, Ajose, Frances, Kim, Jong Woo, Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Martin, Nicholas G., De Geus, Eco J., Boomsma, Dorret I., Davies, Gareth E. and Bates, Timothy (2019). The Nigerian Twin and Sibling Registry: An Update. Twin Research and Human Genetics, 22 (6), 637-640. doi: 10.1017/thg.2019.110

Novel genetic loci affecting facial shape variation in humans

Xiong, Ziyi, Dankova, Gabriela, Howe, Laurence J., Lee, Myoung Keun, Hysi, Pirro G., de Jong, Markus A., Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi, Pan, Bo, Feingold, Eleanor, Marazita, Mary L., Shaffer, John R., McAloney, Kerrie, Xu, Shu-Hua, Jin, Li, Wang, Sijia, de Vrij, Femke Ms, Lendemeijer, Bas, Richmond, Stephen, Zhurov, Alexei, Lewis, Sarah, Sharp, Gemma C., Paternoster, Lavinia, Thompson, Holly, Gonzalez-Jose, Rolando, Bortolini, Maria Catira, Canizales-Quinteros, Samuel ... Kayser, Manfred (2019). Novel genetic loci affecting facial shape variation in humans. eLife, 8 e49898. doi: 10.7554/eLife.49898

The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese

Ye, Lin, Zhu, Gu, Martin, Nick and Liu, Yangyang (2019). The Relationship Between Adolescents’ Personality and Neurasthenia: A Comparison of Australian and Chinese. Journal of Early Adolescence, 39 (9), 1337-1342. doi: 10.1177/0272431618824710

Associations of autozygosity with a broad range of human phenotypes

Clark, David W., Okada, Yukinori, Moore, Kristjan H. S., Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Mattsson, Hannele, Barnes, Catriona L. K., Lin, Kuang, Zhao, Jing Hua, Deelen, Patrick, Rohde, Rebecca, Schurmann, Claudia, Guo, Xiuqing, Giulianini, Franco, Zhang, Weihua, Medina-Gomez, Carolina, Karlsson, Robert, Bao, Yanchun, Bartz, Traci M., Baumbach, Clemens, Biino, Ginevra, Bixley, Matthew J., Brumat, Marco, Chai, Jin-Fang, Corre, Tanguy, Cousminer, Diana L., Dekker, Annelot M., Eccles, David A. ... Wilson, James F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10 (1) 4957, 4957. doi: 10.1038/s41467-019-12283-6

Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition

Van Der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, De Geus, Eco J. C. ... Andreassen, Ole A. (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77 (4), 1-11. doi: 10.1001/jamapsychiatry.2019.3779

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A. ... Morton, C. C. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4

Genetic architecture of subcortical brain structures in 38,851 individuals

Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y

International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci

Nievergelt, Caroline M., Maihofer, Adam X., Klengel, Torsten, Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Dalvie, Shareefa, Duncan, Laramie E., Gelernter, Joel, Levey, Daniel F., Logue, Mark W., Polimanti, Renato, Provost, Allison C., Ratanatharathorn, Andrew, Stein, Murray B., Torres, Katy, Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Søren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Babić, Dragan, Bækvad-Hansen, Marie, Baker, Dewleen G. ... Koenen, Karestan C. (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications, 10 (1) 4558, 4558. doi: 10.1038/s41467-019-12576-w

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Tin, Adrienne, Marten, Jonathan, Halperin Kuhns, Victoria L., Li, Yong, Wuttke, Matthias, Kirsten, Holger, Sieber, Karsten B., Qiu, Chengxiang, Gorski, Mathias, Yu, Zhi, Giri, Ayush, Sveinbjornsson, Gardar, Li, Man, Chu, Audrey Y., Hoppmann, Anselm, O’Connor, Luke J., Prins, Bram, Nutile, Teresa, Noce, Damia, Akiyama, Masato, Cocca, Massimiliano, Ghasemi, Sahar, van der Most, Peter J., Horn, Katrin, Xu, Yizhe, Fuchsberger, Christian, Sedaghat, Sanaz, Afaq, Saima, Amin, Najaf ... Köttgen, Anna (2019). Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nature Genetics, 51 (10), 1459-1474. doi: 10.1038/s41588-019-0504-x

White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group

van Velzen, Laura S., Kelly, Sinead, Isaev, Dmitry, Aleman, Andre, Aftanas, Lyubomir I., Bauer, Jochen, Baune, Bernhard T., Brak, Ivan V., Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Danilenko, Konstantin V., Dannlowski, Udo, Enneking, Verena, Filimonova, Elena, Förster, Katharina, Frodl, Thomas, Gotlib, Ian H., Groenewold, Nynke A., Grotegerd, Dominik, Harris, Mathew A., Hatton, Sean N., Hawkins, Emma L., Hickie, Ian B., Ho, Tiffany C., Jansen, Andreas, Kircher, Tilo, Klimes-Dougan, Bonnie ... Schmaal, Lianne (2019). White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group. Molecular Psychiatry, 25 (7), 1511-1525. doi: 10.1038/s41380-019-0477-2

Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

Van der Spek, Ashley, Broer, Linda, Draisma, Harmen H. M., Pool, René, Albrecht, Eva, Beekman, Marian, Mangino, Massimo, Raag, Mait, Nyholt, Dale R., Dharuri, Harish K., Codd, Veryan, Amin, Najaf, de Geus, Eco J. C., Deelen, Joris, Demirkan, Ayse, Yet, Idil, Fischer, Krista, Haller, Toomas, Henders, Anjali K., Isaacs, Aaron, Medland, Sarah E., Montgomery, Grant W., Mooijaart, Simon P., Strauch, Konstantin, Suchiman, H. Eka D., Vaarhorst, Anika A. M., van Heemst, Diana, Wang-Sattler, Rui, Whitfield, John B. ... Gieger, Christian (2019). Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium. Scientific Reports, 9 (1) 11623, 11623. doi: 10.1038/s41598-019-47282-6

Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression

Glanville, Kylie P., Coleman, Jonathan R. I., Hanscombe, Ken B., Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L., Breen, Gerome, Air, Tracy M., Andlauer, Till F. M., Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Buttenschøn, Henriette N., Colodro-Conde, Lucía, Dannlowski, Udo, Direk, Nese, Dunn, Erin C., Forstner, Andreas J., de Geus, Eco J. C., Grabe, Hans J., Hamilton, Steven P., Jones, Ian, Jones, Lisa A., Knowles, James A., Kutalik, Zoltán, Levinson, Douglas F., Lewis, Glyn, Lind, Penelope A. ... Børglum, Anders D. (2019). Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated With depression. Biological Psychiatry, 87 (5), 419-430. doi: 10.1016/j.biopsych.2019.06.031

Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array

Beck, Jeffrey J., Hottenga, Jouke-Jan, Mbarek, Hamdi, Finnicum, Casey T., Ehli, Erik A., Hur, Yoon-Mi, Martin, Nicholas G., De Geus, Eco J.C., Boomsma, Dorret I. and Davies, Gareth E. (2019). Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array. Twin Research and Human Genetics, 22 (4), 210-219. doi: 10.1017/thg.2019.41

New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

Evangelou, Evangelos, Gao, He, Chu, Congying, Ntritsos, Georgios, Blakeley, Paul, Butts, Andrew R., Pazoki, Raha, Suzuki, Hideaki, Koskeridis, Fotios, Yiorkas, Andrianos M., Karaman, Ibrahim, Elliott, Joshua, Luo, Qiang, Aeschbacher, Stefanie, Bartz, Traci M., Baumeister, Sebastian E., Braund, Peter S., Brown, Michael R., Brody, Jennifer A., Clarke, Toni-Kim, Dimou, Niki, Faul, Jessica D., Homuth, Georg, Jackson, Anne U., Kentistou, Katherine A., Joshi, Peter K., Lemaitre, Rozenn N., Lind, Penelope A., Lyytikäinen, Leo-Pekka ... Elliott, Paul (2019). New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Nature Human Behaviour, 3 (9), 950-961. doi: 10.1038/s41562-019-0653-z

Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins

Gillespie, Nathan A., Bates, Timothy C., Hickie, Ian B., Medland, Sarah E., Verhulst, Brad, Kirkpatrick, Robert M., Kendler, Kenneth S., Martin, Nicholas G. and Benotsch, Eric G. (2019). Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins. Addiction, 114 (12) add.14750, 2229-2240. doi: 10.1111/add.14750

Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

Watson, Hunna J., Yilmaz, Zeynep, Thornton, Laura M., Hübel, Christopher, Coleman, Jonathan R. I., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Purves, Kirstin L., Adan, Roger A. H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Baker, Jessica H., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Perica, Vesna Boraska, Buehren, Katharina, Burghardt, Roland, Cassina, Matteo, Cichon, Sven ... Bulik, Cynthia M. (2019). Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nature Genetics, 51 (8), 1207-1214. doi: 10.1038/s41588-019-0439-2

Genetic and environmental influences on gambling disorder liability: A replication and combined analysis of two twin studies

Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Genetic and environmental influences on gambling disorder liability: A replication and combined analysis of two twin studies. Psychological Medicine, 49 (10), 1705-1712. doi: 10.1017/S0033291718002325

Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans

Peng, Fuduan, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Chen, Yan, Li, Yi, Hamer, Merel A., Zeng, Changqing, Hopkins, Racquel L., Jacobus, Case L., Wallace, Paige L., Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Duffy, David L., Medland, Sarah E., Spector, Timothy D., Walsh, Susan, Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2019). Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans. Journal of Investigative Dermatology, 139 (7), 1601-1605. doi: 10.1016/j.jid.2018.12.029

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando ... Walters, James T. R. (2019). Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 51 (7), 1193-1193. doi: 10.1038/s41588-019-0450-7

Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability

Pasman, Joëlle A., Verweij, Karin J. H., Gerring, Zachary, Stringer, Sven, Sanchez-Roige, Sandra, Treur, Jorien L., Abdellaoui, Abdel, Nivard, Michel G., Baselmans, Bart M. L., Ong, Jue-Sheng, Ip, Hill F., van der Zee, Matthijs D., Bartels, Meike, Day, Felix R., Fontanillas, Pierre, Elson, Sarah L., de Wit, Harriet, Davis, Lea K., MacKillop, James, Derringer, Jaime L., Branje, Susan J. T., Hartman, Catharina A., Heath, Andrew C., van Lier, Pol A. C., Madden, Pamela A. F., Mägi, Reedik, Meeus, Wim, Montgomery, Grant W., Oldehinkel, A. J. ... Vink, Jacqueline M. (2019). Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability. Nature Neuroscience, 22 (7), 1196-1196. doi: 10.1038/s41593-019-0402-7

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

Brazel, David M., Jiang, Yu, Hughey, Jordan M., Turcot, Valérie, Zhan, Xiaowei, Gong, Jian, Batini, Chiara, Weissenkampen, J. Dylan, Liu, MengZhen, Surendran, Praveen, Young, Robin, Barnes, Daniel R., Nielsen, Sune Fallgaard, Rasheed, Asif, Samuel, Maria, Zhao, Wei, Kontto, Jukka, Perola, Markus, Caslake, Muriel, de Craen, Anton J.M., Trompet, Stella, Uria-Nickelsen, Maria, Malarstig, Anders, Reily, Dermot F., Hoek, Maarten, Vogt, Thomas, Jukema, J. Wouter, Sattar, Naveed, Ford, Ian ... Vrieze, Scott (2019). Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Biological Psychiatry, 85 (11), 946-955. doi: 10.1016/j.biopsych.2018.11.024

Genetic Epidemiology of Liability for Alcohol-Induced Blacking and Passing Out

Davis, Christal N., Slutske, Wendy S., Martin, Nicholas G., Agrawal, Arpana and Lynskey, Michael T. (2019). Genetic Epidemiology of Liability for Alcohol-Induced Blacking and Passing Out. Alcoholism: Clinical and Experimental Research, 43 (6) acer.14045, 1103-1112. doi: 10.1111/acer.14045

New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances

Hwang, Liang-Dar, Lin, Cailu, Gharahkhani, Puya, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, An, Jiyuan, Gordon, Scott D., Zhu, Gu, MacGregor, Stuart, Lawlor, Deborah A., Breslin, Paul A. S., Wright, Margaret J., Martin, Nicholas G. and Reed, Danielle R. (2019). New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. The American Journal of Clinical Nutrition, 109 (6), 1724-1737. doi: 10.1093/ajcn/nqz043

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B., Feitosa, Mary F., Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y., Hoppmann, Anselm, Kirsten, Holger, Giri, Ayush, Chai, Jin-Fang, Sveinbjornsson, Gardar, Tayo, Bamidele O., Nutile, Teresa, Fuchsberger, Christian, Marten, Jonathan, Cocca, Massimiliano, Ghasemi, Sahar, Xu, Yizhe, Horn, Katrin, Noce, Damia, van der Most, Peter J., Sedaghat, Sanaz, Yu, Zhi, Akiyama, Masato, Afaq, Saima, Ahluwalia, Tarunveer S. ... Pattaro, Cristian (2019). A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nature Genetics, 51 (6), 957-972. doi: 10.1038/s41588-019-0407-x

Multi-site meta-analysis of morphometry

Jahanshad, Neda, Faskowitz, Joshua I., Roshchupkin, Gennady, Hibar, Derrek, Gutman, Boris A, Tustison, Nicholas J., Adams, Hieab H. H., Niessen, Wiro, Vernooij, Meike W, Ikram, M Arfan, Zwiers, Marcel P., Vasquez, Alejandro Arias, Franke, Barbara, Kroll, Jennifer L., Mwangi, Benson, Soares, Jair C, Ing, Alex, Desrivieres, Sylvane, Schumann, Gunter, Hansell, Narelle K, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2019). Multi-site meta-analysis of morphometry. IEEE/ACM Transactions on Computational Biology and Bioinformatics, 16 (5) 3370702, 1-1. doi: 10.1109/TCBB.2019.2914905

Associations between brain structure and perceived intensity of sweet and bitter tastes

Hwang, Liang-Dar, Strike, Lachlan T, Couvy-Duchesne, Baptiste, de Zubicaray, Greig I, McMahon, Katie, Breslin, Paul A. S., Reed, Danielle R., Martin, Nicholas G. and Wright, Margaret J. (2019). Associations between brain structure and perceived intensity of sweet and bitter tastes. Behavioural Brain Research, 363, 103-108. doi: 10.1016/j.bbr.2019.01.046

Author correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

Davies, Gail, Lam, Max, Harris, Sarah E., Trampush, Joey W., Luciano, Michelle, Hill, W. David, Hagenaars, Saskia P., Ritchie, Stuart J., Marioni, Riccardo E., Fawns-Ritchie, Chloe, Liewald, David C. M., Okely, Judith A., Ahola-Olli, Ari V., Barnes, Catriona L. K., Bertram, Lars, Bis, Joshua C., Burdick, Katherine E., Christoforou, Andrea, DeRosse, Pamela, Djurovic, Srdjan, Espeseth, Thomas, Giakoumaki, Stella, Giddaluru, Sudheer, Gustavson, Daniel E., Hayward, Caroline, Hofer, Edith, Ikram, M. Arfan, Karlsson, Robert, Knowles, Emma ... Deary, Ian J. (2019). Author correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications, 10 (1) 2068, 2068. doi: 10.1038/s41467-019-10160-w

Blood titanium level as a biomarker of orthopaedic implant wear

Swiatkowska, Ilona, Martin, Nicholas and Hart, Alister J. (2019). Blood titanium level as a biomarker of orthopaedic implant wear. Journal of Trace Elements in Medicine and Biology, 53, 120-128. doi: 10.1016/j.jtemb.2019.02.013

Evidence of causal effect of major depression on alcohol dependence: Findings from the psychiatric genomics consortium

Polimanti, Renato, Peterson, Roseann E., Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C., Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A., Lind, Penelope A., Maes, Hermine H., Martin, Nicholas G., Mbarek, Hamdi, Medland, Sarah E., Streit, Fabian, Agrawal, Arpana, Edenberg, Howard J., Kendler, Kenneth S., Lewis, Cathryn M., Sullivan, Patrick F., Wray, Naomi R., Gelernter, Joel and Derks, Eske M. (2019). Evidence of causal effect of major depression on alcohol dependence: Findings from the psychiatric genomics consortium. Psychological Medicine, 49 (07), 1-9. doi: 10.1017/S0033291719000667

Genome-wide association study identifies 30 loci associated with bipolar disorder

Stahl, Eli A., Breen, Gerome, Forstner, Andreas J., McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan R. I., Gaspar, Héléna A., de Leeuw, Christiaan A., Steinberg, Stacy, Pavlides, Jennifer M. Whitehead, Trzaskowski, Maciej, Byrne, Enda M., Pers, Tune H., Holmans, Peter A., Richards, Alexander L., Abbott, Liam, Agerbo, Esben, Akil, Huda, Albani, Diego, Alliey-Rodriguez, Ney, Als, Thomas D., Anjorin, Adebayo, Antilla, Verneri, Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie ... Sklar, Pamela (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics, 51 (5), 793-803. doi: 10.1038/s41588-019-0397-8

Genetic structure of IQ, phonemic decoding skill, and academic achievement

Lazaroo, Nikita K., Bates, Timothy C., Hansell, Narelle K., Wright, Margaret J., Martin, Nicholas G. and Luciano, Michelle (2019). Genetic structure of IQ, phonemic decoding skill, and academic achievement. Frontiers in Genetics, 10 (MAR) 195, 195. doi: 10.3389/fgene.2019.00195

Homogenizing estimates of heritability among SOLAR-Eclipse, OpenMx, APACE, and FPHI software packages in neuroimaging data

Kochunov, Peter, Patel, Binish, Ganjgahi, Habib, Donohue, Brian, Ryan, Meghann, Hong, Elliot L., Chen, Xu, Adhikari, Bhim, Jahanshad, Neda, Thompson, Paul M., Van't Ent, Dennis, den Braber, Anouk, de Geus, Eco J. C., Brouwer, Rachel M., Boomsma, Dorret, Pol, Hilleke E. Hulshoff, de Zubicaray, Greig, McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Nichols, Thomas E. (2019). Homogenizing estimates of heritability among SOLAR-Eclipse, OpenMx, APACE, and FPHI software packages in neuroimaging data. Frontiers in Neuroinformatics, 13 16, 16. doi: 10.3389/fninf.2019.00016

Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci

Dudding, Tom, Haworth, Simon, Lind, Penelope A., Sathirapongsasuti, J. Fah, Tung, Joyce Y., Mitchell, Ruth, Colodro-Conde, Lucía, Medland, Sarah E., Gordon, Scott, Elsworth, Benjamin, Paternoster, Lavinia, Franks, Paul W., Thomas, Steven J., Martin, Nicholas G. and Timpson, Nicholas J. (2019). Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. Nature Communications, 10 (1) 1052, 1052. doi: 10.1038/s41467-019-08923-6

Atomic Spectrometry Update: Review of adVances in the analysis of clinical and biological materials, foods and beverages

Taylor, Andrew, Barlow, Nicola, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2019). Atomic Spectrometry Update: Review of adVances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 34 (3), 426-459. doi: 10.1039/c9ja90004g

Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers

Whitfield, John B., Zhu, Gu, Madden, Pamela A. F., Montgomery, Grant W., Heath, Andrew C. and Martin, Nicholas G. (2019). Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Alcoholism: Clinical and Experimental Research, 43 (3), 473-482. doi: 10.1111/acer.13949

Association between polygenic risk for tobacco or alcohol consumption and liability to licit and illicit substance use in young Australian adults

Chang, Lun-Hsien, Couvy-Duchesne, Baptiste, Liu, Mengzhen, Medland, Sarah E., Verhulst, Brad, Benotsch, Eric G., Hickie, Ian B., Martin, Nicholas G., Gillespie, Nathan A. and GSCAN Consortium (2019). Association between polygenic risk for tobacco or alcohol consumption and liability to licit and illicit substance use in young Australian adults. Drug and Alcohol Dependence, 197, 271-279. doi: 10.1016/j.drugalcdep.2019.01.015

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Liu, Mengzhen, Jiang, Yu, Wedow, Robbee, Li, Yue, Brazel, David M., Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, McGuire, Daniel, Tian, Chao, Zhan, Xiaowei, Choquet, Hélène, Docherty, Anna R., Faul, Jessica D., Foerster, Johanna R., Fritsche, Lars G., Gabrielsen, Maiken Elvestad, Gordon, Scott D., Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R., Ling, Yueh, Mägi, Reedik, Matoba, Nana, McMahon, George, Mulas, Antonella, Orrù, Valeria ... Vrieze, Scott (2019). Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Nature Genetics, 51 (2), 237-244. doi: 10.1038/s41588-018-0307-5

Common genetic contributions to high-risk trauma exposure and self-injurious thoughts and behaviors

Richmond-Rakerd, Leah S., Trull, Timothy J., Gizer, Ian R., McLaughlin, Kristin, Scheiderer, Emily M., Nelson, Elliot C., Agrawal, Arpana, Lynskey, Michael T., Madden, Pamela A.F., Heath, Andrew C., Statham, Dixie J. and Martin, Nicholas G. (2019). Common genetic contributions to high-risk trauma exposure and self-injurious thoughts and behaviors. Psychological Medicine, 49 (3), 421-430. doi: 10.1017/S0033291718001034

Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder

Trzaskowski, Maciej, Mehta, Divya, Peyrot, Wouter J., Hawkes, David, Davies, Daniel, Howard, David M., Kemper, Kathryn E., Sidorenko, Julia, Maier, Robert, Ripke, Stephan, Mattheisen, Manuel, Baune, Bernhard T., Grabe, Hans J., Heath, Andrew C., Jones, Lisa, Jones, Ian, Madden, Pamela A.F., McIntosh, Andrew M., Breen, Gerome, Lewis, Cathryn M., Børglum, Anders D., Sullivan, Patrick F., Martin, Nicholas G., Kendler, Kenneth S., Levinson, Douglas F. and Wray, Naomi R. (2019). Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 180 (6), 439-447. doi: 10.1002/ajmg.b.32713

Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA

Bates, Timothy C., Maher, Brion S., Colodro-Conde, Lucía, Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Okbay, Aysu, Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA. Twin Research and Human Genetics, 22 (01), 1-3. doi: 10.1017/thg.2018.75

Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Liu, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, M. Arfan, Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2019). Publisher correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 10 (1) 299, 299. doi: 10.1038/s41467-018-08078-w

Author correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A. ... MacGregor, Stuart (2019). Author correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Nature Communications, 10 (1) 155, 155. doi: 10.1038/s41467-018-07819-1

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

Morris, Andrew P., Le, Thu H., Wu, Haojia, Akbarov, Artur, van der Most, Peter J., Hemani, Gibran, Smith, George Davey, Mahajan, Anubha, Gaulton, Kyle J., Nadkarni, Girish N., Valladares-Salgado, Adan, Wacher-Rodarte, Niels, Mychaleckyj, Josyf C., Dueker, Nicole D., Guo, Xiuqing, Hai, Yang, Haessler, Jeffrey, Kamatani, Yoichiro, Stilp, Adrienne M., Zhu, Gu, Cook, James P., Ärnlöv, Johan, Blanton, Susan H., de Borst, Martin H., Bottinger, Erwin P., Buchanan, Thomas A., Cechova, Sylvia, Charchar, Fadi J., Chu, Pei-Lun ... Franceschini, Nora (2019). Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. Nature Communications, 10 (1) 29, 29. doi: 10.1038/s41467-018-07867-7

Big Five Personality Traits and Alcohol, Nicotine, Cannabis, and Gambling Disorder Comorbidity

Dash, Genevieve F., Slutske, Wendy S., Martin, Nicholas G., Statham, Dixie J., Agrawal, Arpana and Lynskey, Michael T. (2019). Big Five Personality Traits and Alcohol, Nicotine, Cannabis, and Gambling Disorder Comorbidity. Psychology of Addictive Behaviors, 33 (4), 420-429. doi: 10.1037/adb0000468

Comparing the Potential Causal Influence of Two Indicators of Early Alcohol Use on Later Alcohol Use Disorder Symptoms

Davis, Christal N., Slutske, Wendy S., Piasecki, Thomas M., Martin, Nicholas G. and Lynskey, Michael T. (2019). Comparing the Potential Causal Influence of Two Indicators of Early Alcohol Use on Later Alcohol Use Disorder Symptoms. Journal of Abnormal Psychology, 129 (3), 256-265. doi: 10.1037/abn0000474

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

Demontis, Ditte, Walters, Raymond K., Martin, Joanna, Mattheisen, Manuel, Als, Thomas D., Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline I., Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian B., Martin, Alicia R., Martin, Nicholas G., Moran, Jennifer ... Kemp, John P. (2019). Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nature Genetics, 51 (1), 63-75. doi: 10.1038/s41588-018-0269-7

Half the genetic variance in vitamin D concentration is shared with skin colour and sun exposure genes

Mitchell, Brittany L., Zhu, Gu, Medland, Sarah E., Renteria, Miguel. E., Eyles, Darryl W., Grasby, Katrina L., McGrath, John J. and Martin, Nicholas G. (2019). Half the genetic variance in vitamin D concentration is shared with skin colour and sun exposure genes. Behavior Genetics, 49 (4), 386-398. doi: 10.1007/s10519-019-09954-x

In vivo biocompatibility and immunogenicity of metal-phenolic gelation

Björnmalm, Mattias, Wong, Lok Man, Wojciechowski, Jonathan P., Penders, Jelle, Horgan, Conor C., Booth, Marsilea A., Martin, Nicholas G., Sattler, Susanne and Stevens, Molly M. (2019). In vivo biocompatibility and immunogenicity of metal-phenolic gelation. Chemical Science, 10 (43), 10179-10194. doi: 10.1039/c9sc03325d

Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study

Mitchell, Brittany L., Campos, Adrian I., Rentería, Miguel E., Parker, Richard, Sullivan, Lenore, McAloney, Kerrie, Couvy-Duchesne, Baptiste, Medland, Sarah E., Gillespie, Nathan A., Scott, Jan, Zietsch, Brendan P., Lind, Penelope A., Martin, Nicholas G. and Hickie, Ian B. (2019). Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study. Twin Research and Human Genetics, 22 (03), 154-163. doi: 10.1017/thg.2019.27

Antibody response to common human viruses is shaped by genetic factors

Hayward, Tanisha A., Zhu, Gu, Warrington, Nicole M., Wong, Yide, Ryan, Rachael Y.M., Murray, Abella M., Haigh, Oscar, Martin, Nicholas G., Miles, John J. and Evans, David M. (2018). Antibody response to common human viruses is shaped by genetic factors. Journal of Allergy and Clinical Immunology, 143 (4), 1640-1643. doi: 10.1016/j.jaci.2018.11.039

Identification of 55,000 replicated DNA methylation QTL

McRae, Allan F., Marioni, Riccardo E., Shah, Sonia, Yang, Jian, Powell, Joseph E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Bowdler, Lisa, Painter, Jodie N., Murphy, Lee, Martin, Nicholas G., Starr, John M., Wray, Naomi R., Deary, Ian J., Visscher, Peter M. and Montgomery, Grant W. (2018). Identification of 55,000 replicated DNA methylation QTL. Scientific Reports, 8 (1) 17605, 17605. doi: 10.1038/s41598-018-35871-w

Getting to the genetic and environmental roots of educational inequality

Martin, Nicholas (2018). Getting to the genetic and environmental roots of educational inequality. npj Science of Learning, 3 (1) 4. doi: 10.1038/s41539-018-0021-1

PPD ACT: an app-based genetic study of postpartum depression

Guintivano, Jerry, Krohn, Holly, Lewis, Carol, Byrne, Enda M., Henders, Anjali K., Ploner, Alexander, Kirk, Katherine, Martin, Nicholas G., Milgrom, Jeannette, Wray, Naomi R., Sullivan, Patrick F. and Meltzer-Brody, Samantha (2018). PPD ACT: an app-based genetic study of postpartum depression. Translational Psychiatry, 8 (1) 260, 260. doi: 10.1038/s41398-018-0305-5

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

Walters, Raymond K., Polimanti, Renato, Johnson, Emma C., McClintick, Jeanette N., Adams, Mark J., Adkins, Amy E., Aliev, Fazil, Bacanu, Silviu-Alin, Batzler, Anthony, Bertelsen, Sarah, Biernacka, Joanna M., Bigdeli, Tim B., Chen, Li-Shiun, Clarke, Toni-Kim, Chou, Yi-Ling, Degenhardt, Franziska, Docherty, Anna R., Edwards, Alexis C., Fontanillas, Pierre, Foo, Jerome C., Fox, Louis, Frank, Josef, Giegling, Ina, Gordon, Scott, Hack, Laura M., Hartmann, Annette M., Hartz, Sarah M., Heilmann-Heimbach, Stefanie, Herms, Stefan ... Agrawal, Arpana (2018). Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Nature Neuroscience, 21 (12), 1656-1669. doi: 10.1038/s41593-018-0275-1

A fast method for estimating statistical power of multivariate GWAS in real case scenarios: examples from the field of imaging genetics

Couvy-Duchesne, Baptiste, Strike, Lachlan T., McMahon, Katie L., de Zubicaray, Greig I., Thompson, Paul M., Martin, Nicholas G., Medland, Sarah E. and Wright, Margaret J. (2018). A fast method for estimating statistical power of multivariate GWAS in real case scenarios: examples from the field of imaging genetics. Behavior Genetics, 49 (1), 112-121. doi: 10.1007/s10519-018-9936-9

Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization

Ong, Jue-Sheng, Hwang, Liang-Dar, Zhong, Victor W., An, Jiyuan, Gharahkhani, Puya, Breslin, Paul A. S., Wright, Margaret J., Lawlor, Deborah A., Whitfield, John, MacGregor, Stuart, Martin, Nicholas G. and Cornelis, Marilyn C. (2018). Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization. Scientific Reports, 8 (1) 16414, 16414. doi: 10.1038/s41598-018-34713-z

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Duffy, David L., Zhu, Gu, Li, Xin, Sanna, Marianna, Iles, Mark M., Jacobs, Leonie C., Evans, David M., Yazar, Seyhan, Beesley, Jonathan, Law, Matthew H., Kraft, Peter, Visconti, Alessia, Taylor, John C., Lui, Fan, Wright, Margaret J., Henders, Anjali K., Bowdler, Lisa, Glass, Dan, Ikram, Arfan M., Uitterlinden, André G., Madden, Pamela A., Heath, Andrew C., Nelson, Elliot C., Green, Adele C., Chanock, Stephen, Barrett, Jennifer H., Brown, Matthew A., Hayward, Nicholas K., MacGregor, Stuart ... Martin, Nicholas G. (2018). Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nature Communications, 9 (1) 4774, 4774. doi: 10.1038/s41467-018-06649-5

Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders

Ligthart, Symen, Vaez, Ahmad, Võsa, Urmo, Stathopoulou, Maria G., de Vries, Paul S., Prins, Bram P., Van der Most, Peter J., Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M., Wu, Ying, Karlsson, Robert, Barbalic, Maja, Lin, Honghuang, Pool, René, Zhu, Gu, Macé, Aurélien, Sidore, Carlo, Trompet, Stella, Mangino, Massimo, Sabater-Lleal, Maria, Kemp, John P., Abbasi, Ali, Kacprowski, Tim, Verweij, Niek, Smith, Albert V., Huang, Tao, Marzi, Carola, Feitosa, Mary F. ... Alizadeh, Behrooz Z. (2018). Genome analyses of >200,000 individuals identify 58 loci for chronic inflammation and highlight pathways that link inflammation and complex disorders. American Journal of Human Genetics, 103 (5), 691-706. doi: 10.1016/j.ajhg.2018.09.009

Genome-wide association meta-analysis of age at first cannabis use

Minică, Camelia C., Verweij, Karin J. H., van der Most, Peter J., Mbarek, Hamdi, Bernard, Manon, van Eijk, Kristel R., Lind, Penelope A., Liu, Meng Zhen, Maciejewski, Dominique F., Palviainen, Teemu, Sánchez-Mora, Cristina, Sherva, Richard, Taylor, Michelle, Walters, Raymond K., Abdellaoui, Abdel, Bigdeli, Timothy B., Branje, Susan J. T., Brown, Sandra A., Casas, Miguel, Corley, Robin P., Smith, George Davey, Davies, Gareth E., Ehli, Erik A., Farrer, Lindsay, Fedko, Iryna O., Garcia-Martínez, Iris, Gordon, Scott D., Hartman, Catharina A., Heath, Andrew C. ... Derks, Eske M. (2018). Genome-wide association meta-analysis of age at first cannabis use. Addiction, 113 (11), 2073-2086. doi: 10.1111/add.14368

The Anorexia Nervosa Genetics Initiative (ANGI): overview and methods

Thornton, Laura M., Munn-Chernoff, Melissa A., Baker, Jessica H., Juréus, Anders, Parker, Richard, Henders, Anjali K., Larsen, Janne T., Petersen, Liselotte, Watson, Hunna J., Yilmaz, Zeynep, Kirk, Katherine M., Gordon, Scott, Leppä, Virpi M., Martin, Felicity C., Whiteman, David C., Olsen, Catherine M., Werge, Thomas M., Pedersen, Nancy L., Kaye, Walter, Bergen, Andrew W., Halmi, Katherine A., Strober, Michael, Kaplan, Allan S., Woodside, D. Blake, Mitchell, James, Johnson, Craig L., Brandt, Harry, Crawford, Steven, Horwood, L. John ... Bulik, Cynthia M. (2018). The Anorexia Nervosa Genetics Initiative (ANGI): overview and methods. Contemporary Clinical Trials, 74, 61-69. doi: 10.1016/j.cct.2018.09.015

Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA

Pośpiech, Ewelina, Chen, Yan, Kukla-Bartoszek, Magdalena, Breslin, Krystal, Aliferi, Anastasia, Andersen, Jeppe D., Ballard, David, Chaitanya, Lakshmi, Freire-Aradas, Ana, van der Gaag, Kristiaan J., Girón-Santamaría, Lorena, Gross, Theresa E., Gysi, Mario, Huber, Gabriela, Mosquera-Miguel, Ana, Muralidharan, Charanya, Skowron, Małgorzata, Carracedo, Ángel, Haas, Cordula, Morling, Niels, Parson, Walther, Phillips, Christopher, Schneider, Peter M., Sijen, Titia, Syndercombe-Court, Denise, Vennemann, Marielle, Wu, Sijie, Xu, Shuhua, Jin, Li ... EUROFORGEN NoE Consortium (2018). Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA. Forensic Science International: Genetics, 37, 241-251. doi: 10.1016/j.fsigen.2018.08.017

Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

Niemi, Mari E. K., Martin, Hilary C., Rice, Daniel L., Gallone, Giuseppe, Gordon, Scott, Kelemen, Martin, McAloney, Kerrie, McRae, Jeremy, Radford, Elizabeth J., Yu, Sui, Gecz, Jozef, Martin, Nicholas G., Wright, Caroline F., Fitzpatrick, David R., Firth, Helen V., Hurles, Matthew E. and Barrett, Jeffrey C. (2018). Common genetic variants contribute to risk of rare severe neurodevelopmental disorders. Nature, 562 (7726), 268-271. doi: 10.1038/s41586-018-0566-4

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L., Ota, Vanessa K., Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J., Patel, Hamel, Hall, Lynsey S., O'Reilly, Paul F., Belangero, Sintia, Bressan, Rodrigo A., Breen, Gerome, Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F. M., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B. ... Major Depressive Disorder and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium (2018). Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. Communications Biology, 1 (163) 163. doi: 10.1038/s42003-018-0155-y

Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste

Hwang, Liang-Dar, Gharahkhani, Puya, Breslin, Paul A. S., Gordon, Scott D., Zhu, Gu, Martin, Nicholas G., Reed, Danielle R. and Wright, Margaret J. (2018). Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste. BMC Genomics, 19 (678) 678, 678. doi: 10.1186/s12864-018-5058-2

Are there distinct cognitive types?

Loehlin, John C., Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2018). Are there distinct cognitive types?. Intelligence, 70, 7-11. doi: 10.1016/j.intell.2018.07.002

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

MacGregor, Stuart, Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Zhou, Tiger, Siggs, Owen M., Law, Matthew H., Souzeau, Emmanuelle, Sharma, Shiwani, Lynn, David J., Beesley, Jonathan, Sheldrick, Bronwyn, Mills, Richard A., Landers, John, Ruddle, Jonathan B., Graham, Stuart L., Healey, Paul R., White, Andrew J. R., Casson, Robert J., Best, Stephen, Grigg, John R., Goldberg, Ivan, Powell, Joseph E., Whiteman, David C., Radford-Smith, Graham L., Martin, Nicholas G., Montgomery, Grant W., Burdon, Kathryn P., Mackey, David A. ... Hewitt, Alex W. (2018). Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. Nature Genetics, 50 (8), 1067-1071. doi: 10.1038/s41588-018-0176-y

The genetic relationship between psychological distress, somatic distress, affective disorders, and substance use in young Australian adults: a multivariate twin study

Chang, Lun-Hsien, Couvy-Duchesne, Baptiste, Medland, Sarah E., Gillespie, Nathan A., Hickie, Ian B., Parker, Richard and Martin, Nicholas G. (2018). The genetic relationship between psychological distress, somatic distress, affective disorders, and substance use in young Australian adults: a multivariate twin study. Twin Research and Human Genetics, 21 (5), 347-360. doi: 10.1017/thg.2018.33

Association of current and former smoking with body mass index: a study of smoking discordant twin pairs from 21 twin cohorts

Piirtola, Maarit, Jelenkovic, Aline, Latvala, Antti, Sund, Reijo, Honda, Chika, Inui, Fujio, Watanabe, Mikio, Tomizawa, Rie, Iwatani, Yoshinori, Ordoñana, Juan R., Sánchez-Romera, Juan F., Colodro-Conde, Lucia, Tarnoki, Adam D., Tarnoki, David L., Martin, Nicholas G., Montgomery, Grant W., Medland, Sarah E., Rasmussen, Finn, Tynelius, Per, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Rebato, Esther, Stazi, Maria A., Fagnani, Corrado, Brescianini, Sonia, Busjahn, Andreas, Harris, Jennifer R., Brandt, Ingunn ... Silventoinen, Karri (2018). Association of current and former smoking with body mass index: a study of smoking discordant twin pairs from 21 twin cohorts. PLoS One, 13 (7) e0200140, e0200140. doi: 10.1371/journal.pone.0200140

A multivariate behavior genetic investigation of dual-systems models of alcohol involvement

Ellingson, Jarrod M., Slutske, Wendy S., Vergés, Alvaro, Littlefield, Andrew K., Statham, Dixie J. and Martin, Nicholas G. (2018). A multivariate behavior genetic investigation of dual-systems models of alcohol involvement. Journal of Studies on Alcohol and Drugs, 79 (4), 617-626. doi: 10.15288/JSAD.2018.79.617

The relationship between personality and somatic and psychological distress: a comparison of Chinese and Australian adolescents

Liu, Yangyang, Gillespie, Nathan A., Ye, Lin, Zhu, Gu, Duffy, David L. and Martin, Nicholas G. (2018). The relationship between personality and somatic and psychological distress: a comparison of Chinese and Australian adolescents. Behavior Genetics, 48 (4), 315-322. doi: 10.1007/s10519-018-9905-3

Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

Smit, Dirk J. A., Wright, Margaret J., Meyers, Jacquelyn L., Martin, Nicholas G., Ho, Yvonne Y. W., Malone, Stephen M., Zhang, Jian, Burwell, Scott J., Chorlian, David B., de Geus, Eco J. C., Denys, Damiaan, Hansell, Narelle K., Hottenga, Jouke-Jan, McGue, Matt, van Beijsterveldt, Catharina E. M., Jahanshad, Neda, Thompson, Paul M., Whelan, Christopher D., Medland, Sarah E., Porjesz, Bernice, Lacono, William G. and Boomsma, Dorret I. (2018). Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Human Brain Mapping, 39 (11), 4183-4195. doi: 10.1002/hbm.24238

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

Savage, Jeanne E., Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, Bryois, Julien, de Leeuw, Christiaan A., Nagel, Mats, Awasthi, Swapnil, Barr, Peter B., Coleman, Jonathan R. I., Grasby, Katrina L., Hammerschlag, Anke R., Kaminski, Jakob A., Karlsson, Robert, Krapohl, Eva, Lam, Max, Nygaard, Marianne, Reynolds, Chandra A., Trampush, Joey W., Young, Hannah, Zabaneh, Delilah, Hägg, Sara, Hansell, Narelle K., Karlsson, Ida K., Linnarsson, Sten, Montgomery, Grant W., Muñoz-Manchado, Ana B., Quinlan, Erin B., Schumann, Gunter ... Posthuma, Danielle (2018). Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics, 50 (7), 912-919. doi: 10.1038/s41588-018-0152-6

Cross-cultural comparison of genetic and cultural transmission of smoking initiation using an extended twin kinship model

Maes, Hermine H., Morley, Kate, Neale, Michael C., Kendler, Kenneth S., Heath, Andrew C., Eaves, Lindon J. and Martin, Nicholas G. (2018). Cross-cultural comparison of genetic and cultural transmission of smoking initiation using an extended twin kinship model. Twin Research and Human Genetics, 21 (3), 179-190. doi: 10.1017/thg.2018.22

Establishing a twin register: an invaluable resource for (behavior) genetic, epidemiological, biomarker, and ‘omics’ studies

Odintsova, Veronika V., Willemsen, Gonneke, Dolan, Conor V., Hottenga, Jouke-Jan, Martin, Nicholas G., Slagboom, P. Eline, Ordoñana, Juan R. and Boomsma, Dorret I. (2018). Establishing a twin register: an invaluable resource for (behavior) genetic, epidemiological, biomarker, and ‘omics’ studies. Twin Research and Human Genetics, 21 (3), 239-252. doi: 10.1017/thg.2018.23

Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans

Cuellar Partida, Gabriel, Laurin, Charles, Ring, Susan M., Gaunt, Tom R., McRae, Allan, Visscher, Peter M., Montgomery, Grant W., Martin, Nicholas G., Hemani, Gibran, Suderman, Matthew, Relton, Caroline L., Davey Smith, George and Evans, David M. (2018). Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans. Human Molecular Genetics, 27 (16), 2927-2939. doi: 10.1093/hmg/ddy206

Childhood aggression and the co-occurrence of behavioural and emotional problems: results across ages 3-16 years from multiple raters in six cohorts in the EU-ACTION project

Bartels, Meike, Hendriks, Anne, Mauri, Matteo, Krapohl, Eva, Whipp, Alyce, Bolhuis, Koen, Conde, Lucia Colodro, Luningham, Justin, Fung Ip, Hill, Hagenbeek, Fiona, Roetman, Peter, Gatej, Raluca, Lamers, Audri, Nivard, Michel, van Dongen, Jenny, Lu, Yi, Middeldorp, Christel, van Beijsterveldt, Toos, Vermeiren, Robert, Hankemeijer, Thomas, Kluft, Cees, Medland, Sarah, Lundström, Sebastian, Rose, Richard, Pulkkinen, Lea, Vuoksimaa, Eero, Korhonen, Tellervo, Martin, Nicholas G., Lubke, Gitta ... Boomsma, Dorret I. (2018). Childhood aggression and the co-occurrence of behavioural and emotional problems: results across ages 3-16 years from multiple raters in six cohorts in the EU-ACTION project. European Child & Adolescent Psychiatry, 27 (9), 1-17. doi: 10.1007/s00787-018-1169-1

Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure

Visconti, Alessia, Duffy, David L., Liu, Fan, Zhu, Gu, Wu, Wenting, Chen, Yan, Hysi, Pirro G., Zeng, Changqing, Sanna, Marianna, Iles, Mark M., Kanetsky, Peter A., Demenais, Florence, Hamer, Merel A., Uitterlinden, Andre G., Ikram, M. Arfan, Nijsten, Tamar, Martin, Nicholas G., Kayser, Manfred, Spector, Tim D., Han, Jiali, Bataille, Veronique and Falchi, Mario (2018). Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. Nature Communications, 9 (1) 1684. doi: 10.1038/s41467-018-04086-y

Testing associations between cannabis use and subcortical volumes in two large population-based samples

Gillespie, Nathan A., Neale, Michael C., Bates, Timothy C., Eyler, Lisa T., Fennema-Notestine, Christine, Vassileva, Jasmin, Lyons, Michael J., Prom-Wormley, Elizabeth C., McMahon, Katie L., Thompson, Paul M., de Zubicaray, Greig., Hickie, Ian B., McGrath, John J., Strike, Lachlan T., Rentería, Miguel E., Panizzon, Matthew S., Martin, Nicholas G., Franz, Carol E., Kremen, William S. and Wright, Margaret J. (2018). Testing associations between cannabis use and subcortical volumes in two large population-based samples. Addiction, 113 (9), 1661-1672. doi: 10.1111/add.14252

Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

Hysi, Pirro G., Valdes, Ana M., Liu, Fan, Furlotte, Nicholas A., Evans, David M., Bataille, Veronique, Visconti, Alessia, Hemani, Gibran, McMahon, George, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Lin, Bochao D., Willemsen, Gonneke, Jan Hottenga, Jouke, Vuckovic, Dragana, Girotto, Giorgia, Gandin, Ilaria, Sala, Cinzia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan ... Spector, Timothy D. (2018). Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nature Genetics, 50 (5), 652-656. doi: 10.1038/s41588-018-0100-5

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero

Warrington, Nicole M., Shevroja, Enisa, Hemani, Gibran, Hysi, Pirro G., Jiang, Yunxuan, Auton, Adam, Boer, Cindy G., Mangino, Massimo, Wang, Carol A., Kemp, John P., McMahon, George, Medina-Gomez, Carolina, Hickey, Martha, Trajanoska, Katerina, Wolke, Dieter, Ikram, Arfan M., 23 and Me Research Team, Montgomery, Grant W., Felix, Janine F., Wright, Margaret J., Mackey, David A., Jaddoe, Vincent W., Martin, Nicholas G., Tung, Joyce Y., Davey Smith, George, Pennell, Craig E., Spector, Tim D., van Meurs, Joyce, Rivadeneira, Fernando ... Evans, David M. (2018). Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Human Molecular Genetics, 27 (11), 2025-2038. doi: 10.1093/hmg/ddy121

Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses

Painter, Jodie N., O'Mara, Tracy A., Morris, Andrew P., Cheng, Timothy H. T., Gorman, Maggie, Martin, Lynn, Hodson, Shirley, Jones, Angela, Martin, Nicholas G., Gordon, Scott, Henders, Anjali K, Attia, John, McEvoy, Mark, Holliday, Elizabeth G., Scott, Rodney J, Webb, Penelope M., Fasching, Peter A.., Beckmann, Matthias W, Ekici, Arif B, Hein, Alexander, Rübner, Matthias, Hall, Per, Czene, Kamila, Dörk, Thilo, Dürst, Matthias, Hillemanns, Peter, Runnebaum, Ingo, Lambrechts, Diether, Amant, Frederic ... Spurdle, Amanda B (2018). Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Cancer Medicine, 7 (5), 1978-1987. doi: 10.1002/cam4.1445

Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins

Couvy-Duchesne, Baptiste, O'Callaghan, Victoria, Parker, Richard, Mills, Natalie, Kirk, Katherine M., Scott, Jan, Vinkhuyzen, Anna., Hermens, Daniel F., Lind, Penelope A., Davenport, Tracey A., Burns, Jane M., Connell, Melissa, Zietsch, Brendan P., Scott, James, Wright, Margaret J., Medland, Sarah E., McGrath, John, Martin, Nicholas G., Hickie, Ian B. and Gillespie, Nathan A. (2018). Nineteen and Up study (19Up): Understanding pathways to mental health disorders in young Australian twins. BMJ Open, 8 (3) e018959, 1-13. doi: 10.1136/bmjopen-2017-018959

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

Bates, Timothy C., Maher, Brion S., Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2018). The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics, 21 (2), 73-83. doi: 10.1017/thg.2018.11

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

Wu, Yang, Zeng, Jian, Zhang, Futao, Zhu, Zhihong, Qi, Ting, Zheng, Zhili, Lloyd-Jones, Luke R., Marioni, Riccardo E., Martin, Nicholas G., Montgomery, Grant W., Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F. and Yang, Jian (2018). Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits. Nature Communications, 9 (918) 918, 918. doi: 10.1038/s41467-018-03371-0

Atomic spectrometry update: review of advances in the analysis of clinical and biological materials, foods and beverages

Taylor, Andrew, Barlow, Nicola, Day, Martin P., Hill, Sarah, Martin, Nicholas and Patriarca, Marina (2018). Atomic spectrometry update: review of advances in the analysis of clinical and biological materials, foods and beverages. Journal of Analytical Atomic Spectrometry, 33 (3), 338-382. doi: 10.1039/c8ja90005a

Endogenous cortisol in keratinized matrices: systematic determination of baseline cortisol levels in hair and the influence of sex, age and hair color

Binz, T. M., Rietschel, L., Streit, F., Hofmann, M., Gehrke, J., Herdener, M., Quednow, B. B., Martin, N. G., Rietschel, M., Kraemer, T. and Baumgartner, M. R. (2018). Endogenous cortisol in keratinized matrices: systematic determination of baseline cortisol levels in hair and the influence of sex, age and hair color. Forensic Science International, 284, 33-38. doi: 10.1016/j.forsciint.2017.12.032

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

Mühleisen, Thomas W., Reinbold, Céline S., Forstner, Andreas J., Abramova, Lilia I., Alda, Martin, Babadjanova, Gulja, Bauer, Michael, Brennan, Paul, Chuchalin, Alexander, Cruceanu, Cristiana, Czerski, Piotr M., Degenhardt, Franziska, Fischer, Sascha B., Fullerton, Janice M., Gordon, Scott D., Grigoroiu-Serbanescu, Maria, Grof, Paul, Hauser, Joanna, Hautzinger, Martin, Herms, Stefan, Hoffmann, Per, Kammerer-Ciernioch, Jutta, Khusnutdinova, Elza, Kogevinas, Manolis, Krasnov, Valery, Lacour, André, Laprise, Catherine, Leber, Markus, Lissowska, Jolanta ... Cichon, Sven (2018). Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. Journal of Affective Disorders, 228, 20-25. doi: 10.1016/j.jad.2017.11.068

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Pardiñas, Antonio F, Holmans, Peter, Pocklington, Andrew J, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E, Bishop, Sophie, Cameron, Darren, Hamshere, Marian L, Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H, McCarroll, Steven A, Baune, Bernhard T, Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C, Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M, Plomin, Robert, Porteous, David J, Wray, Naomi R, Caballero, Armando ... CRESTAR Consortium (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 50 (3), 381-389. doi: 10.1038/s41588-018-0059-2

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

Gharahkhani, Puya, Burdon, Kathryn P., Cooke Bailey, Jessica N, Hewitt, Alex W., Law, Matthew H., Pasquale, Louis R., Kang, Jae H., Haines, Jonathan L., Souzeau, Emmanuelle, Zhou, Tiger, Siggs, Owen M., Landers, John, Awadalla, Mona, Sharma, Shiwani, Mills, Richard A., Ridge, Bronwyn, Lynn, David, Casson, Robert, Graham, Stuart L., Goldberg, Ivan, White, Andrew, Healey, Paul R., Grigg, John, Lawlor, Mitchell, Mitchell, Paul, Ruddle, Jonathan, Coote, Michael, Walland, Mark, Best, Stephen ... NEIGHBORHOOD consortium (2018). Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Scientific reports, 8 (1) 3124, 3124. doi: 10.1038/s41598-018-20435-9

Personality types: a twin study

Loehlin, John C. and Martin, Nicholas G. (2018). Personality types: a twin study. Personality and Individual Differences, 122, 99-103. doi: 10.1016/j.paid.2017.10.012

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

Chang, H., Hoshina, N., Zhang, C., Ma, Y., Cao, H., Wang, Y., Wu, D. D., Bergen, S. E., Landén, M., Hultman, C. M., Preisig, M., Kutalik, Z., Castelao, E., Grigoroiu-Serbanescu, M., Forstner, A. J., Strohmaier, J., Hecker, J., Schulze, T. G., Müller-Myhsok, B., Reif, A., Mitchell, P. B., Martin, N. G., Schofield, P. R., Cichon, S., Nöthen, M. M., Walter, H., Erk, S., Heinz, A., Amin, N. ... MooDS Bipolar Consortium (2018). The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders. Molecular Psychiatry, 23 (2), 400-412. doi: 10.1038/mp.2016.231

A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence

Crist, R. C., Doyle, G. A., Nelson, E. C., Degenhardt, L., Martin, N. G., Montgomery, G. W., Saxon, A. J., Ling, W. and Berrettini, W. H. (2018). A polymorphism in the OPRM1 3'-untranslated region is associated with methadone efficacy in treating opioid dependence. The Pharmacogenomics Journal, 18 (1), 173-179. doi: 10.1038/tpj.2016.89

Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels

Lupton, Michelle K., Medland, Sarah E., Gordon, Scott D., Goncalves, Tabatha, MacGregor, Stuart, Mackey, David A., Young, Terri L., Duffy, David L., Visscher, Peter M., Wray, Naomi R., Nyholt, Dale R., Bain, Lisa, Ferreira, Manuel A., Henders, Anjali K., Wallace, Leanne, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2018). Accuracy of inferred APOE genotypes for a range of genotyping arrays and imputation reference panels. Journal of Alzheimer's Disease, 64 (1), 49-54. doi: 10.3233/JAD-171104

Effects of high alcohol intake, alcohol-related symptoms and smoking on mortality

Whitfield, John B., Heath, Andrew C., Madden, Pamela A. F., Landers, J. George and Martin, Nicholas G. (2018). Effects of high alcohol intake, alcohol-related symptoms and smoking on mortality. Addiction, 113 (1), 158-166. doi: 10.1111/add.14008

Lingual Gyrus Surface Area Is Associated with Anxiety-Depression Severity in Young Adults: A Genetic Clustering Approach

Couvy-Duchesne, Baptiste, Strike, Lachlan T., de Zubicaray, Greig I., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G. and Wright, Margaret J. (2018). Lingual Gyrus Surface Area Is Associated with Anxiety-Depression Severity in Young Adults: A Genetic Clustering Approach. eNeuro, 5 (1) e0153-17.2017, 1-14. doi: 10.1523/ENEURO.0153-17.2017

Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence

Scott, Jan, Davenport, Tracey A., Parker, Richard, Hermens, Daniel F., Lind, Penelope A., Medland, Sarah E., Wright, Margaret J., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2017). Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. Journal of Affective Disorders, 230, 1-6. doi: 10.1016/j.jad.2017.12.007

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders

Xiao, Xiao, Wang, Lu, Wang, Chuang, Yuan, Ti-Fei, Zhou, Dongsheng, Zheng, Fanfan, Li, Lingyi, Grigoroiu-Serbanescu, Maria, Ikeda, Masashi, Iwata, Nakao, Takahashi, Atsushi, Kamatani, Yoichiro, Kubo, Michiaki, Preisig, Martin, Kutalik, Zoltán, Castelao, Enrique, Pistis, Giorgio, Amin, Najaf, Van Duijn, Cornelia M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Schofield, Peter R., Cichon, Sven ... MooDS Bipolar Consortium (2017). Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. Translational Psychiatry, 7 (12) 1273. doi: 10.1038/s41398-017-0019-0

Genome-wide association studies of a broad spectrum of antisocial behavior

Tielbeek, Jorim J., Johansson, Ada, Polderman, Tinca J.C., Rautiainen, Marja-Riitta, Jansen, Philip, Taylor, Michelle, Tong, Xiaoran, Lu, Qing, Burt, Alexandra S., Tiemeier, Henning, Viding, Essi, Plomin, Robert, Martin, Nicholas G., Heath, Andrew C., Madden, Pamela A.F., Montgomery, Grant, Beaver, Kevin M., Waldman, Irwin, Gelernter, Joel, Kranzler, Henry R., Farrer, Lindsay A., Perry, John R.B., Munafò, Marcus, LoParo, Devon, Paunio, Tiina, Tiihonen, Jari, Mous, Sabine E., Pappa, Irene, De Leeuw, Christiaan ... Broad Antisocial Behavior Consortium (2017). Genome-wide association studies of a broad spectrum of antisocial behavior. JAMA Psychiatry, 74 (12), 1242-1250. doi: 10.1001/jamapsychiatry.2017.3069

Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

Joshi, Peter K., Pirastu, Nicola, Kentistou, Katherine A., Fischer, Krista, Hofer, Edith, Schraut, Katharina E., Clark, David W., Nutile, Teresa, Barnes, Catriona L. K., Timmers, Paul R. H. J., Shen, Xia, Gandin, Ilaria, McDaid, Aaron F., Hansen, Thomas Folkmann, Gordon, Scott D., Giulianini, Franco, Boutin, Thibaud S., Abdellaoui, Abdel, Zhao, Wei, Medina-Gomez, Carolina, Bartz, Traci M., Trompet, Stella, Lange, Leslie A., Raffield, Laura, Van Der Spek, Ashley, Galesloot, Tessel E., Proitsi, Petroula, Yanek, Lisa R., Bielak, Lawrence F. ... Wilson, James F. (2017). Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Nature Communications, 8 (1) 910, 910. doi: 10.1038/s41467-017-00934-5

Heritability and GWAS analyses of acne in australian adolescent twins

Mina-Vargas, Angela, Colodro-Conde, Lucía, Grasby, Katrina, Zhu, Gu, Gordon, Scott, Medland, Sarah E. and Martin, Nicholas G. (2017). Heritability and GWAS analyses of acne in australian adolescent twins. Twin Research and Human Genetics, 20 (6), 541-549. doi: 10.1017/thg.2017.58

Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study

Ong, Jue-Sheng, Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Martin, Nicholas G., Chenevix-Trench, Georgia, Quinn, Michael C. J., Cornelis, Marilyn C., Gharahkhani, Puya, Webb, Penelope M., MacGregor, Stuart and Ovarian Cancer Association Consortium (2017). Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study. International Journal of Epidemiology, 47 (2), 450-459. doi: 10.1093/ije/dyx236

Genome-wide association study identifies a novel locus for cannabis dependence

Agrawal, A., Chou, Y.- L., Carey, C. E., Baranger, D. A. A., Zhang, B., Sherva, R., Wetherill, L., Kapoor, M., Wang, J.-.C., Bertelsen, S., Anokhin, A. P., Hesselbrock, V., Kramer, J., Lynskey, M. T., Meyers, J. L., Nurnberger, J. I., Rice, J. P., Tischfield, J., Bierut, L. J., Degenhardt, L., Farrer, L. A., Gelernter, J., Hariri, A. R., Heath, A. C., Kranzler, H. R., Madden, P. A. F., Martin, N. G., Montgomery, G. W., Porjesz, B. ... Nelson, E. C. (2017). Genome-wide association study identifies a novel locus for cannabis dependence. Molecular Psychiatry, 23 (5), 1293-1302. doi: 10.1038/mp.2017.200

Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans

Zhong, Kaiyin, Zhu, Gu, Jing, Xiaoxi, Hendriks, A. Emile J., Drop, Sten L. S., Ikram, M. Arfan, Gordon, Scott, Zeng, Changqing, Uitterlinden, Andre G., Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2017). Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans. Human Genetics, 136 (11-12), 1407-1417. doi: 10.1007/s00439-017-1842-3

Investigating the relationship between iron and depression

Mills, Natalie T., Maier, Robert, Whitfield, John B., Wright, Margaret J., Colodro-Conde, Lucia, Byrne, Enda M., Scott, James G., Byrne, Gerard J., Hansell, Narelle K., Vinkhuyzen, Anna A. E., CouvyDuchesne, Baptiste, Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Wray, Naomi R. and Benyamin, Beben (2017). Investigating the relationship between iron and depression. Journal of Psychiatric Research, 94, 148-155. doi: 10.1016/j.jpsychires.2017.07.006

Education in twins and their parents across birth cohorts over 100 years: an individual-level pooled analysis of 42-twin cohorts

Silventoinen, Karri, Jelenkovic, Aline, Latvala, Antti, Sund, Reijo, Yokoyama, Yoshie, Ullemar, Vilhelmina, Almqvist, Catarina, Derom, Catherine A., Vlietinck, Robert F., Loos, Ruth J. F., Kandler, Christian, Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Rebato, Esther, Stazi, Maria A., Fagnani, Corrado, Brescianini, Sonia, Hur, Yoon-Mi, Jeong, Hoe-Uk, Cutler, Tessa L., Hopper, John L., Busjahn, Andreas, Saudino, Kimberly J., Ji, Fuling, Ning, Feng, Pang, Zengchang, Rose, Richard J. ... Kaprio, Jaakko (2017). Education in twins and their parents across birth cohorts over 100 years: an individual-level pooled analysis of 42-twin cohorts. Twin Research and Human Genetics, 20 (5), 395-405. doi: 10.1017/thg.2017.49

Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex

Guadalupe, Tulio, Mathias, Samuel R., vanErp, Theo G. M., Whelan, Christopher D., Zwiers, Marcel P., Abe, Yoshinari, Abramovic, Lucija, Agartz, Ingrid, Andreassen, Ole A., Arias-Vásquez, Alejandro, Aribisala, Benjamin S., Armstrong, Nicola J., Arolt, Volker, Artiges, Eric, Ayesa-Arriola, Rosa, Baboyan, Vatche G., Banaschewski, Tobias, Barker, Gareth, Bastin, Mark E., Baune, Bernhard T., Blangero, John, Bokde, Arun L.W., Boedhoe, Premika S.W., Bose, Anushree, Brem, Silvia, Brodaty, Henry, Bromberg, Uli, Brooks, Samantha, Büchel, Christian ... Francks, Clyde (2017). Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex. Brain Imaging and Behavior, 11 (5), 1497-1514. doi: 10.1007/s11682-016-9629-z

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Macé, Aurélien, Tuke, Marcus A., Deelen, Patrick, Kristiansson, Kati, Mattsson, Hannele, Nõukas, Margit, Sapkota, Yadav, Schick, Ursula, Porcu, Eleonora, Rüeger, Sina, McDaid, Aaron F., Porteous, David, Winkler, Thomas W., Salvi, Erika, Shrine, Nick, Liu, Xueping, Ang, Wei Q., Zhang, Weihua, Feitosa, Mary F., Venturini, Cristina, Van Der Most, Peter J., Rosengren, Anders, Wood, Andrew R., Beaumont, Robin N., Jones, Samuel E., Ruth, Katherine S., Yaghootkar, Hanieh, Tyrrell, Jessica, Havulinna, Aki S. ... Kutalik, Zoltán (2017). CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nature Communications, 8 (1) 744, 744. doi: 10.1038/s41467-017-00556-x

Hidden heritability due to heterogeneity across seven populations

Tropf, Felix C., Lee, S Hong, Verweij, Renske M., Stulp, Gert, van der Most, Peter J., de Vlaming, Ronald, Bakshi, Andrew, Briley, Daniel A., Rahal, Charles, Hellpap, Robert, Nyman, Anastasia, Esko, Tõnu, Metspalu, Andres, Medland, Sarah E., Martin, Nicholas G., Barban, Nicola, Snieder, Harold, Robinson, Matthew R. and Mills, Melinda C. (2017). Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour, 1 (10), 757-765. doi: 10.1038/s41562-017-0195-1

Assessing the accuracy of perceptions of intelligence based on heritable facial features

Lee, Anthony J., Hibbs, Courtney, Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2017). Assessing the accuracy of perceptions of intelligence based on heritable facial features. Intelligence, 64, 1-8. doi: 10.1016/j.intell.2017.06.002

Genome-Wide Association shows that pigmentation genes play a role in skin aging

Law, Matthew H., Medland, Sarah E., Zhu, Gu, Yazar, Seyhan, Vinuela, Ana, Wallace, Leanne, Shekar, Sri Niranjan, Duffy, David L., Bataille, Veronique, Glass, Dan, Spector, Tim D., Wood, Diane, MuTHER Consortium, Gordon, Scott D., Barbour, Julie M., Henders, Anjali K., Hewitt, Alex W., Montgomery, Grant W., Sturm, Richard A., Mackey, David A., Green, Adele C., Martin, Nicholas G. and MacGregor, Stuart (2017). Genome-Wide Association shows that pigmentation genes play a role in skin aging. Journal of Investigative Dermatology, 137 (9), 1887-1894. doi: 10.1016/j.jid.2017.04.026

Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1

Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban ... MooDS Consortium (2017). Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1. Molecular Neurobiology, 54 (7), 5166-5176. doi: 10.1007/s12035-016-0041-x

Major depressive disorder, suicidal thoughts and behaviours, and cannabis involvement in discordant twins: a retrospective cohort study

Agrawal, Arpana, Nelson, Elliot C., Bucholz, Kathleen K., Tillman, Rebecca, Grucza, Richard A., Statham, Dixie J., Madden, Pamela A. F., Martin, Nicholas G., Heath, Andrew C. and Lynskey, Michael T. (2017). Major depressive disorder, suicidal thoughts and behaviours, and cannabis involvement in discordant twins: a retrospective cohort study. The Lancet Psychiatry, 4 (9), 706-714. doi: 10.1016/S2215-0366(17)30280-8

Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts

Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Yokoyama, Yoshie, Hur, Yoon-Mi, Cozen, Wendy, Hwang, Amie E., Mack, Thomas M., Honda, Chika, Inui, Fujio, Iwatani, Yoshinori, Watanabe, Mikio, Tomizawa, Rie, Pietilainen, Kirsi H., Rissanen, Aila, Siribaddana, Sisira H., Hotopf, Matthew, Sumathipala, Athula, Rijsdijk, Fruhling, Tan, Qihua, Zhang, Dongfeng, Pang, Zengchang, Piirtola, Maarit, Aaltonen, Sari, Oncel, Sevgi Y., Aliev, Fazil, Rebato, Esther, Hjelmborg, Jacob B., Christensen, Kaare ... Kaprio, Jaakko (2017). Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts. American Journal of Clinical Nutrition, 106 (2), 457-466. doi: 10.3945/ajcn.117.153643

From alcohol initiation to tolerance to problems: Discordant twin modeling of a developmental process

Deutsch, Arielle R., Slutske, Wendy S., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C. and Martin, Nicholas G. (2017). From alcohol initiation to tolerance to problems: Discordant twin modeling of a developmental process. Development and Psychopathology, 29 (3), 845-861. doi: 10.1017/S0954579416000523

Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins

Park, Shin-Ho, Guastella, Adam J., Lynskey, Michael, Agrawal, Arpana, Constantino, John N., Medland, Sarah E., Song, Yun Ju C., Martin, Nicholas G. and Colodro-Conde, Lucía (2017). Neuroticism and the Overlap between Autistic and ADHD Traits: Findings from a Population Sample of Young Adult Australian Twins. Twin Research and Human Genetics, 20 (4), 319-329. doi: 10.1017/thg.2017.38

Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric item response theory

Couvy-Duchesne, Baptiste, Davenport, Tracey A., Martin, Nicholas G., Wright, Margaret J. and Hickie, Ian B. (2017). Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric item response theory. BMC Psychiatry, 17 (1) 279, 279. doi: 10.1186/s12888-017-1420-1

Facial trustworthiness is associated with heritable aspects of face shape

Lee, Anthony J., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2017). Facial trustworthiness is associated with heritable aspects of face shape. Adaptive Human Behavior and Physiology, 3 (4), 351-364. doi: 10.1007/s40750-017-0073-0

No genetic overlap between circulating iron levels and Alzheimer's disease

Lupton, Michelle K., Benyamin, Beben, Proitsi, Petroula, Nyholt, Dale R., Ferreira, Manuel A., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A., Medland, Sarah E., Gordon, Scott D., Lovestone, Simon, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Vellas, Bruno, Powell, John F., Bush, Ashley I., Wright, Margaret J., Martin, Nicholas G. and Whitfield, John B. (2017). No genetic overlap between circulating iron levels and Alzheimer's disease. Journal of Alzheimers Disease, 59 (1), 85-99. doi: 10.3233/JAD-170027

Cannabis and Depression: A Twin Model Approach to Co-morbidity

Smolkina, M., Morley, K. I., Rijsdijk, F., Agrawal, A., Bergin, J. E., Nelson, E. C., Statham, D., Martin, N. G. and Lynskey, M. T. (2017). Cannabis and Depression: A Twin Model Approach to Co-morbidity. Behavior Genetics, 47 (4), 394-404. doi: 10.1007/s10519-017-9848-0

Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes

Luciano, Michelle, Hagenaars, Saskia P. , Cox, Simon R. , Hill, William David , Davies, Gail , Harris, Sarah E. , Deary, Ian J. , Evans, David M. , Martin, Nicholas G. , Wright, Margaret J.  and Bates, Timothy C.  (2017). Single Nucleotide Polymorphisms Associated with Reading Ability Show Connection to Socio-Economic Outcomes. Behavior Genetics, 47 (5), 469-479. doi: 10.1007/s10519-017-9859-x

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.

Witt, S. H., Streit, F., Jungkunz, M., Frank, J., Awasthi, S., Reinbold, C. S., Treutlein, J., Degenhardt, F., Forstner, A. J., Heilmann-Heimbach, S., Dietl, L., Schwarze, C. E., Schendel, D., Strohmaier, J., Abdellaoui, A., Adolfsson, R., Air, T. M., Akil, H., Alda, M., Alliey-Rodriguez, N., Andreassen, O. A., Babadjanova, G., Bass, N. J., Bauer, M., Baune, B. T., Bellivier, F., Bergen, S., Bethell, A., Biernacka, J. M. ... Rietschel, M. (2017). Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia.. Translational psychiatry, 7 (6), e1155-e1155. doi: 10.1038/tp.2017.115

Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group

Brouwer, Rachel M., Panizzon, Matthew S., Glahn, David C., Hibar, David P., Hua, Xue, Jahanshad, Neda, Abramovic, Lucija, de Zubicaray, Greig I., Franz, Carol E., Hansell, Narelle K., Hickie, Ian B., Koenis, Marinka M. G., Martin, Nicholas G., Mather, Karen A., McMahon, Katie L., Schnack, Hugo G., Strike, Lachlan T., Swagerman, Suzanne C., Thalamuthu, Anbupalam, Wen, Wei, Gilmore, John H., Gogtay, Nitin, Kahn, Rene S., Sachdev, Perminder S., Wright, Margaret J., Boomsma, Dorret I., Kremen, William S., Thompson, Paul M. and Hulshoff Pol, Hilleke E. (2017). Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group. Human Brain Mapping, 8 (9), 4444-4458. doi: 10.1002/hbm.23672

Familiality and heritability of fatigue in an Australian twin sample

Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2017). Familiality and heritability of fatigue in an Australian twin sample. Twin Research and Human Genetics, 20 (3), 208-215. doi: 10.1017/thg.2017.22

The Anorexia Nervosa Genetics Initiative: study description and sample characteristics of the Australian and New Zealand arm

Kirk, Katherine M., Martin, Felicity C., Mao, Amy, Parker, Richard, Maguire, Sarah, Thornton, Laura M., Zhu, Gu, McAloney, Kerrie, Freeman, Jeremy L., Hay, Phillipa, Madden, Sloane, Morgan, Christine, Russell, Janice, Sawyer, Susan M., Hughes, Elizabeth K., Fairweather-Schmidt, A. Kate, Fursland, Anthea, McCormack, Julie, Wagg, Fiona, Jordan, Jennifer, Kennedy, Martin A., Ward, Warren, Wade, Tracey D., Bulik, Cynthia M. and Martin, Nicholas G. (2017). The Anorexia Nervosa Genetics Initiative: study description and sample characteristics of the Australian and New Zealand arm. Australian and New Zealand Journal of Psychiatry, 51 (6), 583-594. doi: 10.1177/0004867417700731

Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism

Sapkota, Yadav, Steinthorsdottir, Valgerdur, Morris, Andrew P., Fassbender, Amelie, Rahmioglu, Nilufer, De Vivo, Immaculata, Buring, Julie E., Zhang, Futao, Edwards, Todd L., Jones, Sarah, Dorien, O., Peterse, Danielle, Rexrode, Kathryn M., Ridker, Paul M., Schork, Andrew J., MacGregor, Stuart, Martin, Nicholas G., Becker, Christian M., Adachi, Sosuke, Yoshihara, Kosuke, Enomoto, Takayuki, Takahashi, Atsushi, Kamatani, Yoichiro, Matsuda, Koichi, Kubo, Michiaki, Thorleifsson, Gudmar, Geirsson, Reynir T., Thorsteinsdottir, Unnur, Wallace, Leanne M. ... Nyholt, Dale R. (2017). Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Nature Communications, 8 (1) 15539, 15539. doi: 10.1038/ncomms15539

Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa

Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Helena, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Thornton, Laura, Hinney, Anke, Daly, Mark, Sullivan, Patrick F., Zeggini, Eleftheria, Breen, Gerome, Bulik, Cynthia M., Duncan, Laramie, Yilmaz, Zeynep, Gaspar, Héléna, Walters, Raymond, Goldstein, Jackie, Anttila, Verneri, Bulik-Sullivan, Brendan, Ripke, Stephan, Adan, Roger, Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole, Aschauer, Harald, Baker, Jessica ... Eating Disorders Working Group of the Psychiatric Genomics Consortium (2017). Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa. American Journal of Psychiatry, 174 (9), 850-858. doi: 10.1176/appi.ajp.2017.16121402

Association between telomere length and risk of cancer and non-neoplastic diseases a Mendelian randomization study

Haycock, Philip C., Burgess, Stephen, Nounu, Aayah, Zheng, Jie, Okoli, George N., Bowden, Jack, Wade, Kaitlin Hazel, Timpson, Nicholas J., Evans, David M., Willeit, Peter, Aviv, Abraham, Gaunt, Tomr., Hemani, Gibran, Mangino, Massimo, Ellis, Hayley Patricia, Kurian, Kathreena M., Pooley, Karen A., Eeles, Rosalind A., Lee, Jeffrey E., Fang, Shenying, Chen, Wei V., Law, Matthew H., Bowdler, Lisa M., Iles, Mark M., Yang, Qiong, Worrall, Bradford B., Markus, Hugh Stephen, Hung, Rayjean J., Amos, Chris I. ... Smith, George Davey (2017). Association between telomere length and risk of cancer and non-neoplastic diseases a Mendelian randomization study. JAMA Oncology, 3 (5), 636-651. doi: 10.1001/jamaoncol.2016.5945

Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group

Renteria, M. E., Schmaal, L., Hibar, D. P., Couvy-Duchesne, B., Strike, L. T., Mills, N. T., de Zubicaray, G. I., McMahon, K. L., Medland, S. E., Gillespie, N. A., Hatton, S. N., Lagopoulos, J., Veltman, D. J., van der Wee, N., van Erp, T. G. M., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Voelzke, H., Veer, I. M., Walter, H., Schnell, K., Schramm, E., Normann, C., Schoepf, D., Konrad, C., Zurowski, B., Godlewska, B. R. ... Hickie, I. B. (2017). Subcortical brain structure and suicidal behaviour in major depressive disorder: a meta-analysis from the ENIGMA-MDD working group. Translational Psychiatry, 7 (5) e1116, e1116-e1116. doi: 10.1038/tp.2017.84

Genome-wide physical activity interactions in adiposity ― a meta-analysis of 200,452 adults

Graff, Mariaelisa, Scott, Robert A., Justice, Anne E., Young, Kristin L., Feitosa, Mary F., Barata, Llilda, Winkler, Thomas W., Chu, Audrey Y., Mahajan, Anubha, Hadley, David, Xue, Luting, Workalemahu, Tsegaselassie, Heard-Costa, Nancy L., den Hoed, Marcel, Ahluwalia, Tarunveer S., Qi, Qibin, Ngwa, Julius S., Renström, Frida, Quaye, Lydia, Eicher, John D., Hayes, James E., Cornelis, Marilyn, Kutalik, Zoltan, Lim, Elise, Luan, Jian’an, Huffman, Jennifer E., Zhang, Weihua, Zhao, Wei, Griffin, Paula J. ... Kilpeläinen, Tuomas O. (2017). Genome-wide physical activity interactions in adiposity ― a meta-analysis of 200,452 adults. PLoS Genetics, 13 (4) e1006528, e1006528. doi: 10.1371/journal.pgen.1006528

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts

Hagg, S., Zhan, Y., Karlsson, R., Gerritsen, L., Ploner, A., van der Lee, S. J., Broer, L., Deelen, J., Marioni, R. E., Wong, A., Lundquist, A., Zhu, G., Hansell, N. K., Sillanpaa, E., Fedko, I. O., Amin, N. A., Beekman, M., de Craen, A. J. M., Degerman, S., Harris, S. E., Kan, K-J, Martin-Ruiz, C. M., Montgomery, G. W., Adolfsson, A. N., Reynolds, C. A., Samani, N. J., Suchiman, H. E. D., Viljanen, A., von Zglinicki, T. ... Pedersen, N. L. (2017). Short telomere length is associated with impaired cognitive performance in European ancestry cohorts. Translational Psychiatry, 7 (4) e1100, 983-992. doi: 10.1038/tp.2017.73

Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression

Culverhouse, R. C., Saccone, N. L., Horton, A. C., Ma, Y., Anstey, K. J., Banaschewski, T., Burmeister, M., Cohen-Woods, S., Etain, B., Fisher, H. L., Goldman, N., Guillaume, S., Horwood, J., Juhasz, G., Lester, K. J., Mandelli, L., Middeldorp, C. M., Olie, E., Villafuerte, S., Air, T. M., Araya, R., Bowes, L., Burns, R., Byrne, E. M., Coffey, C., Coventry, W. L., Gawronski, K. A. B., Glei, D., Hatzimanolis, A. ... Bierut, L. J. (2017). Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression. Molecular Psychiatry, 23 (1), 133-142. doi: 10.1038/mp.2017.44

Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling

Ferreira, Manuel A. R., Jansen, Rick, Willemsen, Gonneke, Penninx, Brenda, Bain, Lisa M., Vicente, Cristina T., Revez, Joana A., Matheson, Melanie C., Hui, Jennie, Tung, Joyce Y., Baltic, Svetlana, Le Souef, Peter, Montgomery, Grant W., Martin, Nicholas G., Robertson, Colin F., James, Alan, Thompson, Philip J., Boomsma, Dorret I., Hopper, John L., Hinds, David A., Werder, Rhiannon B., Phipps, Simon and and the Australian Asthma Genetics Consortium Collaborators (2017). Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling. Journal of Allergy and Clinical Immunology, 139 (4), 1148-1157. doi: 10.1016/j.jaci.2016.07.017

Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

Day, Felix R., Thompson, Deborah J., Helgason, Hannes, Chasman, Daniel I., Finucane, Hilary, Sulem, Patrick, Ruth, Katherine S., Whalen, Sean, Sarkar, Abhishek K., Albrecht, Eva, Altmaier, Elisabeth, Amini, Marzyeh, Barbieri, Caterina M., Boutin, Thibaud, Campbell, Archie, Demerath, Ellen, Giri, Ayush, He, Chunyan, Hottenga, Jouke J., Karlsson, Robert, Kolcic, Ivana, Loh, Po-Ru, Lunetta, Kathryn L., Mangino, Massimo, Marco, Brumat, McMahon, George, Medland, Sarah E., Nolte, Ilja M., Noordam, Raymond ... Perry, John R. B. (2017). Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. Nature Genetics, 49 (6), 834-841. doi: 10.1038/ng.3841

Intuitive ethics and political orientations: testing moral foundations as a theory of political ideology

Smith, Kevin B., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Hatemi, Peter K. (2017). Intuitive ethics and political orientations: testing moral foundations as a theory of political ideology. American Journal of Political Science, 61 (2), 424-437. doi: 10.1111/ajps.12255

Genetic effects influencing risk for major depressive disorder in China and Europe

Bigdeli, T. B., Ripke, S., Peterson, R. E., Trzaskowski, M., Bacanu, S-A, Abdellaoui, A., Andlauer, T. F. M., Beekman, A. T. F., Berger, K., Blackwood, D. H. R., Boomsma, D. I., Breen, G., Buttenschon, H. N., Byrne, E. M., Cichon, S., Clarke, T-K, Couvy-Duchesne, B., Craddock, N., de Geus, E. J. C., Degenhardt, F., Dunn, E. C., Edwards, A. C., Fanous, A. H., Forstner, A. J., Frank, J., Gill, M., Gordon, S. D., Grabe, H. J., Hamilton, S. P. ... Kendler, K. S. (2017). Genetic effects influencing risk for major depressive disorder in China and Europe. Translational Psychiatry, 7 (3) e1074, e1074-e1074. doi: 10.1038/tp.2016.292

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

Heilmann-Heimbach, Stefanie, Herold, Christine, Hochfeld, Lara M., Hillmer, Axel M., Nyholt, Dale R., Hecker, Julian, Javed, Asif, Chew, Elaine G. Y., Pechlivanis, Sonali, Drichel, Dmitriy, Heng, Xiu Ting, Del Rosario, Ricardo C.-H., Fier, Heide L., Paus, Ralf, Rueedi, Rico, Galesloot, Tessel E., Moebus, Susanne, Anhalt, Thomas, Prabhakar, Shyam, Li, Rui, Kanoni, Stavroula, Papanikolaou, George, Kutalik, Zoltán, Deloukas, Panos, Philpott, Michael P., Waeber, Gérard, Spector, Tim D., Vollenweider, Peter, Kiemeney, Lambertus A. L. M. ... Nöthen, Markus M. (2017). Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Nature Communications, 8 (1) 14694, 14694. doi: 10.1038/ncomms14694

GSTP1 does not modify MC1R effects on melanoma risk

Daley, G. M., Duffy, D. L., Pflugfelder, A., Jagirdar, K., Lee, K. J., Yong, X. L., Eigentler, T. K., Weide, B., Smithers, B. M., Martin, N. G., Garbe, C., Soyer, H. P. and Sturm, R. A. (2017). GSTP1 does not modify MC1R effects on melanoma risk. Experimental Dermatology, 26 (8), 730-733. doi: 10.1111/exd.13114

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

Forstner, Andreas J., Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Céline S., Mühleisen, Thomas W., Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Schumacher, Johannes, Streit, Fabian, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne ... Nöthen, Markus M. (2017). Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS ONE, 12 (2) e0171595, e0171595. doi: 10.1371/journal.pone.0171595

Novel genetic loci associated with hippocampal volume

Hibar, Derrek P., Adams, Hieab H. H., Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L., Hofer, Edith, Renteria, Miguel E., Bis, Joshua C., Arias-Vasquez, Alejandro, Ikram, M. Kamran, Desrivieres, Sylvane, Vernooij, Meike W., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beecham, Ashley H., Beiser, Alexa, Bernard, Manon, Blanton, Susan H., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M. ... Ikram, M. Arfan (2017). Novel genetic loci associated with hippocampal volume. Nature Communications, 8 (1) 13624, 13624. doi: 10.1038/ncomms13624

Sensation seeking and impulsive traits as personality endophenotypes for antisocial behavior: evidence from two independent samples

Mann, Frank D., Engelhardt, Laura, Briley, Daniel A., Grotzinger, Andrew D., Patterson, Megan W., Tackett, Jennifer L., Strathan, Dixie B., Heath, Andrew, Lynskey, Michael, Slutske, Wendy, Martin, Nicholas G., Tucker-Drob, Elliot M. and Harden, K. Paige (2017). Sensation seeking and impulsive traits as personality endophenotypes for antisocial behavior: evidence from two independent samples. Personality and Individual Differences, 105, 30-39. doi: 10.1016/j.paid.2016.09.018

Genetic analysis of hyperemesis gravidarum reveals association with intracellular calcium release channel (RYR2)

Fejzo, Marlena Schoenberg, Myhre, Ronny, Colodro-Conde, Lucía, MacGibbon, Kimber W, Sinsheimer, Janet S., Reddy, M. V. Prasad Linga, Pajukanta, Paivi, Nyholt, Dale R., Wright, Margaret J., Martin, Nicholas G., Engel, Stephanie M., Medland, Sarah E., Magnus, Per and Mullin, Patrick M. (2017). Genetic analysis of hyperemesis gravidarum reveals association with intracellular calcium release channel (RYR2). Molecular and Cellular Endocrinology, 439 (C), 308-316. doi: 10.1016/j.mce.2016.09.017

Identification of novel loci affecting circulating chromogranins and related peptides

Benyamin, Beben, Maihofer, Adam X., Schork, Andrew J., Hamilton, Bruce A., Rao, Fangwen, Schmid-Schonbein, Geert W., Zhang, Kuixing, Mahata, Manjula, Stridsberg, Mats, Schork, Nicholas J., Biswas, Nilima, Hook, Vivian Y., Wei, Zhiyun, Montgomery, Grant W., Martin, Nicholas G., Nievergelt, Caroline M., Whitfield, John B. and O'Connor, Daniel T. (2017). Identification of novel loci affecting circulating chromogranins and related peptides. Human Molecular Genetics, 26 (1), 233-242. doi: 10.1093/hmg/ddw380

Genome-wide regional heritability mapping identifies a locus within the TOX2 gene associated with major depressive disorder

Zeng, Yanni, Navarro, Pau, Shirali, Masoud, Howard, David M., Adams, Mark J., Hall, Lynsey S., Clarke, Toni-Kim, Thomson, Pippa A., Smith, Blair H., Murray, Alison, Padmanabhan, Sandosh, Hayward, Caroline, Boutin, Thibaud, MacIntyre, Donald J., Lewis, Cathryn M., Wray, Naomi R., Mehta, Divya, Penninx, Brenda W. J. H., Milaneschi, Yuri, Baune, Bernhard T., Air, Tracy, Hottenga, Jouke-Jan, Mbarek, Hamdi, Castelao, Enrique, Pistis, Giorgio, Schulze, Thomas G., Streit, Fabian, Forstner, Andreas J., Byrne, Enda M. ... McIntosh, Andrew M. (2016). Genome-wide regional heritability mapping identifies a locus within the TOX2 gene associated with major depressive disorder. Biological Psychiatry, 82 (5), 312-321. doi: 10.1016/j.biopsych.2016.12.012

Heritability of the shape of subcortical brain structures in the general population

Roshchupkin, Gennady V., Gutman, Boris A., Vernooij, Meike W., Jahanshad, Neda, Martin, Nicholas G., Hofman, Albert, McMahon, Katie L., van der Lee, Sven J., Van Duijn, Cornelia M., de Zubicaray, Greig I., Uitterlinden, Andre´ G., Wright, Margaret J., Niessen, Wiro J., Thompson, Paul M., Ikram, M. Arfan and Adams, Hieab H.H. (2016). Heritability of the shape of subcortical brain structures in the general population. Nature Communications, 7 (1) 13738, 1-8. doi: 10.1038/ncomms13738

Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis

Li, Ming, Huang, Liang, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Alkelai, Anna, Lerer, Bernard, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, MooDS Consortium, and The Swedish Bipolar Study Group, (2016). Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis. Molecular Neurobiology, 53 (10), 6608-6619. doi: 10.1007/s12035-015-9559-6

Hans J. Eysenck and Raymond B. Cattell on intelligence and personality

Boyle, Gregory J., Stankov, Lazar, Martin, Nicholas G., Petrides, K. V., Eysenck, Michael W. and Ortet, Generos (2016). Hans J. Eysenck and Raymond B. Cattell on intelligence and personality. Personality and Individual Differences, 103, 40-47. doi: 10.1016/j.paid.2016.04.029

Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia

Lee, P. H., Baker, J. T., Holmes, A. J., Jahanshad, N., Ge, T., Jung, J. -Y., Cruz, Y., Manoach, D. S., Hibar, D. P., Faskowitz, J., McMahon, K. L., De Zubicaray, G. I., Martin, N. H., Wright, M. J., Ongur, D., Buckner, R., Roffman, J., Thompson, P. M. and Smoller, J. W. (2016). Partitioning heritability analysis reveals a shared genetic basis of brain anatomy and schizophrenia. Molecular Psychiatry, 21 (12), 1680-1689. doi: 10.1038/mp.2016.164

Shared genetic factors in the co-occurrence of depression and fatigue

Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Shared genetic factors in the co-occurrence of depression and fatigue. Twin Research and Human Genetics, 19 (6), 610-618. doi: 10.1017/thg.2016.79

Cannabis involvement and nonsuicidal self-injury: A discordant twin approach

Few, Lauren R., Grant, Julia D., Nelson, Elliot C., Trull, Timothy J., Grucza, Richard A., Bucholz, Kathleen K., Verweij, Karin J. H., Martin, Nicholas G., Statham, Dixie J., Madden, Pamela A. F., Heath, Andrew C., Lynskey, Michael T. and Agrawal, Arpana (2016). Cannabis involvement and nonsuicidal self-injury: A discordant twin approach. Journal of Studies on Alcohol and Drugs, 77 (6), 873-880. doi: 10.15288/jsad.2016.77.873

Co-occurrence and symptomatology of fatigue and depression

Corfield, Elizabeth C., Martin, Nicholas G. and Nyholt, Dale R. (2016). Co-occurrence and symptomatology of fatigue and depression. Comprehensive Psychiatry, 71, 1-10. doi: 10.1016/j.comppsych.2016.08.004

Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal

Loehlin, John C., Hansell, Narelle K., Wright, Margaret J. and Martin, Nicholas G. (2016). Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal. Intelligence, 59, 24-31. doi: 10.1016/j.intell.2016.05.007

Is the association between sweet and bitter perception due to genetic variation?

Hwang, Liang-Dar, Breslin, Paul A. S., Reed, Danielle R., Zhu, Gu, Martin, Nicholas G. and Wright, Margaret J. (2016). Is the association between sweet and bitter perception due to genetic variation?. Chemical Senses, 41 (9), 737-744. doi: 10.1093/chemse/bjw083

Evidence for mitochondrial genetic control of autosomal gene expression

Kassam, Irfahan, Qi, Tuan, Lloyd-Jones, Luke, Holloway, Alexander, Bonder, Marc Jan, Henders, Anjali K., Martin, Nicholas G., Powell, Joseph E., Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and McRae, Allan F. (2016). Evidence for mitochondrial genetic control of autosomal gene expression. Human Molecular Genetics, 25 (24), 5332-5338. doi: 10.1093/hmg/ddw347

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M. ... Thompson, Paul M. (2016). Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 (12), 1569-1582. doi: 10.1038/nn.4398

Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis

Richmond-Rakerd, Leah S., Slutske, Wendy S., Lynskey, Michael T., Agrawal, Arpana, Madden, Pamela A. F., Bucholz, Kathleen K., Heath, Andrew C., Statham, Dixie J. and Martin, Nicholas G. (2016). Age at first use and later substance use disorder: shared genetic and environmental pathways for nicotine, alcohol, and cannabis. Journal of Abnormal Psychology, 125 (7), 946-959. doi: 10.1037/abn0000191

Genetic variants in RBFOX3 are associated with sleep latency

Amin, Najaf, Allebrandt, Karla V., van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G., Mbarek, Hamdi, Watson, Nathaniel F., Melville, Scott A., Del Greco, Fabiola M., Byrne, Enda M., Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S., Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A., Zgaga, Lina, Mihailov, Evelin, Stone, Katie L., Campbell, Harry, Brouwer, Rutger W. W., Demirkan, Ayse ... van Duijn, Cornelia M. (2016). Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics, 24 (10), 1488-1495. doi: 10.1038/ejhg.2016.31

Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins

Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Frank, Josef, Hansell, Narelle K., Wright, Margaret J., McGrath, John J., Witt, Stephanie H., Rietschel, Marcella and Martin, Nicholas G. (2016). Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins. Twin Research and Human Genetics, 19 (5), 438-446. doi: 10.1017/thg.2016.50

Meta-analysis of genome-wide association studies of anxiety disorders

Otowa, T., Hek, K., Lee, M., Byrne, E. M., Mirza, S. S., Nivard, M. G., Bigdeli, T., Aggen, S. H., Adkins, D., Wolen, A., Fanous, A., Keller, M. C., Castelao, E., Kutalik, Z., Der Auwera, S. V., Homuth, G., Nauck, M., Teumer, A., Milaneschi, Y., Hottenga, J. -J., Direk, N., Hofman, A., Uitterlinden, A., Mulder, C. L., Henders, A. K., Medland, S. E., Gordon, S., Heath, A. C., Madden, P. A. F. ... Hettema, J. M. (2016). Meta-analysis of genome-wide association studies of anxiety disorders. Molecular Psychiatry, 21 (10), 1391-1399. doi: 10.1038/mp.2015.197

Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control

Ellingson, J. M., Richmond-Rakerd, L. S., Statham, D. J., Martin, N. G. and Slutske, W. S. (2016). Most of the genetic covariation between major depressive and alcohol use disorders is explained by trait measures of negative emotionality and behavioral control. Psychological Medicine, 46 (14), 2919-2930. doi: 10.1017/S0033291716001525

Sweet taste perception is associated with body mass index at the phenotypic and genotypic level

Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, Breslin, Paul A. S., Reed, Danielle R., Macgregor, Stuart, Gharahkhani, Puya, Martin, Nicholas G. and Renteria, Miguel E. (2016). Sweet taste perception is associated with body mass index at the phenotypic and genotypic level. Twin Research and Human Genetics, 19 (5), 465-471. doi: 10.1017/thg.2016.60

Genome-wide association study of working memory brain activation

Blokland, Gabriella A. M., Wallace, Angus K., Hansell, Narelle K., Thompson, Paul M., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G., McMahon, Katie L., de Zubicaray, Greig I. and Wright, Margaret J. (2016). Genome-wide association study of working memory brain activation. International Journal of Psychophysiology, 115, 98-111. doi: 10.1016/j.ijpsycho.2016.09.010

The association of genetic predisposition to depressive symptoms with non-suicidal and suicidal self-injuries

Maciejewski, Dominique F., Renteria, Miguel E., Abdellaoui, Abdel, Medland, Sarah E., Few, Lauren R., Gordon, Scott D., Madden, Pamela A. F., Montgomery, Grant, Trull, Timothy J., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G., Zietsch, Brendan P. and Verweij, Karin J. H. (2016). The association of genetic predisposition to depressive symptoms with non-suicidal and suicidal self-injuries. Behavior Genetics, 47 (1), 1-8. doi: 10.1007/s10519-016-9809-z

The role of genes and environment in degree of partner self-similarity

Sherlock, James M., Verweij, Karin J. H., Murphy, Sean C., Heath, Andrew C., Martin, Nicholas G. and Zietsch, Brendan P. (2016). The role of genes and environment in degree of partner self-similarity. Behavior Genetics, 47 (1), 1-11. doi: 10.1007/s10519-016-9808-0

Trans-ethnic fine mapping highlights kidney-function genes linked to salt sensitivity

Mahajan, Anubha, Rodan, Aylin R., Le, Thu H., Gaulton, Kyle J., Haessler, Jeffrey, Stilp, Adrienne M., Kamatani, Yoichiro, Zhu, Gu, Sofer, Tamar, Puri, Sanjana, Schellinger, Jeffrey N., Chu, Pei-Lun, Cechova, Sylvia, van Zuydam, Natalie, Arnlov, Johan, Flessner, Michael F., Giedraitis, Vilmantas, Heath, Andrew C., Kubo, Michiaki, Larsson, Anders, Lindgren, Cecilia M., Madden, Pamela A.F., Montgomery, Grant W., Papanicolaou, George J., Reiner, Alex P., Sundström, Johan, Thornton, Timothy A., Lind, Lars, Ingelsson, Erik ... Franceschini, Nora (2016). Trans-ethnic fine mapping highlights kidney-function genes linked to salt sensitivity. American Journal of Human Genetics, 99 (3), 636-646. doi: 10.1016/j.ajhg.2016.07.012

An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype

Direk, Nese, Williams, Stephanie, Smith, Jennifer A., Ripke, Stephan, Air, Tracy, Amare, Azmeraw T., Amin, Najaf, Baune, Bernhard T., Bennett, David A., Blackwood, Douglas H. R., Boomsma, Dorret, Breen, Gerome, Buttenschon, Henriette N., Byrne, Enda M., Borglum, Anders D., Castelao, Enrique, Cichon, Sven, Clarke, Toni-Kim, Cornelis, Marilyn C., Dannlowski, Udo, De Jager, Philip L., Demirkan, Ayse, Domenici, Enrico, van Duijn, Cornelia M., Dunn, Erin C., Eriksson, Johan G., Esko, Tonu, Faul, Jessica D., Ferrucci, Luigi ... Sullivan, Patrick F. (2016). An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biological Psychiatry, 82 (5), 322-329. doi: 10.1016/j.biopsych.2016.11.013

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Gormley, Padhraig, Anttila, Verneri, Winsvold, Bendik S., Palta, Priit, Esko, Tonu, Pers, Tune H., Farh, Kai-How, Cuenca-Leon, Ester, Muona, Mikko, Furlotte, Nicholas A., Kurth, Tobias, Ingason, Andres, McMahon, George, Ligthart, Lannie, Terwindt, Gisela M., Kallela, Mikko, Freilinger, Tobias M., Ran, Caroline, Gordon, Scott G., Stam, Anine H., Steinberg, Stacy, Borck, Guntram, Koiranen, Markku, Quaye, Lydia, Adams, Hieab H. H., Lehtimäki, Terho, Sarin, Antti-Pekka, Wedenoja, Juho, Hinds, David A. ... Palotie, Aarno (2016). Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics, 48 (8), 856-866. doi: 10.1038/ng.3598

Variation and heritability in hair diameter and curvature in an Australian twin sample

Ho, Yvonne Y. W., Brims, Mark, McNevin, Dennis, Spector, Timothy D., Martin, Nicholas G. and Medland, Sarah E. (2016). Variation and heritability in hair diameter and curvature in an Australian twin sample. Twin Research and Human Genetics, 19 (4), 351-358. doi: 10.1017/thg.2016.45

Identification of STOML2 as a putative novel asthma risk gene associated with IL6R

Revez, J. A., Matheson, M. C., Hui, J., Baltic, S., James, A., Upham, J. W., Dharmage, S., Thompson, P. J., Martin, N. G., Hopper, J. L. and Ferreira, M. A. R. (2016). Identification of STOML2 as a putative novel asthma risk gene associated with IL6R. Allergy, 71 (7), 1020-1030. doi: 10.1111/all.12869

Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci

Smith, D. J., Escott-Price, V., Davies, G., Bailey, M. E. S., Colodro-Conde, L., Ward, J., Vedernikov, A., Marioni, R., Cullen, B., Lyall, D., Hagenaars, S. P., Liewald, D. C. M., Luciano, M., Gale, C. R., Ritchie, S. J., Hayward, C., Nicholl, B., Bulik-Sullivan, B., Adams, M., Couvy-Duchesne, B., Graham, N., Mackay, D., Evans, J., Smith, B. H., Porteous, D. J., Medland, S. E., Martin, N. G., Holmans, P., McIntosh, A. M. ... O'Donovan, M. C. (2016). Genome-wide analysis of over 106000 individuals identifies 9 neuroticism-associated loci. Molecular Psychiatry, 21 (6), 749-757. doi: 10.1038/mp.2016.49

Heritability and genetic correlation between the cerebral cortex and associated white matter connections

Shen, Kai-Kai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2016). Heritability and genetic correlation between the cerebral cortex and associated white matter connections. Human Brain Mapping, 37 (6), 2331-2347. doi: 10.1002/hbm.23177

Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility

Mbarek, Hamdi, Steinberg, Stacy, Nyholt, Dale R., Gordon, Scott D., Miller, Michael B., McRae, Allan F, Hottenga, Jouke Jan, Day, Felix R., Willemsen, Gonneke, de Geus, Eco J., Davies, Gareth E, Martin, Hilary C, Penninx, Brenda W, Jansen, Rick, McAloney, Kerrie, Vink, Jacqueline M., Kaprio, Jaakko, Plomin, Robert, Spector, Tim D., Magnusson, Patrik K., Reversade, Bruno, Harris, R. Alan, Aagaard, Kjersti, Kristjansson, Ragnar P., Olafsson, Isleifur, Eyjolfsson, Gudmundur Ingi, Sigurdardottir, Olof, Iacono, William G., Lambalk, Cornelis B ... Boomsman, Dorret I. (2016). Identification of common genetic variants influencing spontaneous dizygotic twinning and female fertility. American Journal of Human Genetics, 98 (5), 898-908. doi: 10.1016/j.ajhg.2016.03.008

Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits

van Beijsterveldt, C. E.M., Overbeek, L. I.H., Rozendaal, L., McMaster, M. T.B., Glasner, T. J., Bartels, M., Vink, J. M., Martin, N. G., Dolan, C. V. and Boomsma, D. I. (2016). Chorionicity and heritability estimates from twin studies: the prenatal environment of twins and their resemblance across a large number of traits. Behavior Genetics, 46 (3), 304-314. doi: 10.1007/s10519-015-9745-3

Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families

Read, Jazlyn, Symmons, Judith, Palmer, Jane M., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2016). Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families. Familial Cancer, 15 (4), 651-663. doi: 10.1007/s10689-016-9907-3

Shared genetic control of expression and methylation in peripheral blood

Shakhbazov, Konstantin, Powell, Joseph E., Hemani, Gibran, Henders, Anjali K., Martin, Nicholas G., Visscher, Peter M., Montgomery, Grant W. and McRae, Allan F. (2016). Shared genetic control of expression and methylation in peripheral blood. BMC Genomics, 17 (1) 278, 278. doi: 10.1186/s12864-016-2498-4

Common genetic variants influence whorls in fingerprint patterns

Ho, Yvonne Y. W., Evans, David M., Montgomery, Grant W., Henders, Anjali K., Kemp, John P., Timpson, Nicholas J., Pourcain, Beate St., Heath, Andrew C., Madden, Pamela A. F., Loesch, Danuta Z., McNevin, Dennis, Daniel, Runa, Davey-Smith, George, Martin, Nicholas G. and Medland, Sarah E. (2016). Common genetic variants influence whorls in fingerprint patterns. Journal of Investigative Dermatology, 136 (4), 859-862. doi: 10.1016/j.jid.2015.10.062

Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group

Schmaal, L., Hibar, D. P., Samann, P. G., Hall, G. B., Baune, B. T., Jahanshad, N., Cheung, J. W., van Erp, T. G. M., Bos, D., Ikram, M. A., Vernooij, M. W., Niessen, W. J., Tiemeier, H., Hofman, A., Wittfeld, K., Grabe, H. J., Janowitz, D., Bulow, R., Selonke, M., Volzke, H., Grotegerd, D., Dannlowski, U., Arolt, V., Opel, N., Heindel, W., Kugel, H., Hoehn, D., Czisch, M., Couvy-Duchesne, B. ... Veltman, D. J. (2016). Cortical abnormalities in adults and adolescents with major depression based on brain scans from 20 cohorts worldwide in the ENIGMA Major Depressive Disorder Working Group. Molecular Psychiatry, 22 (6), 900-909. doi: 10.1038/mp.2016.60

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Schwantes-An, Tae-Hwi, Zhang, Juan, Chen, Li-Shiun, Hartz, Sarah M., Culverhouse, Robert C., Chen, Xiangning, Coon, Hilary, Frank, Josef, Kamens, Helen M., Konte, Bettina, Kovanen, Leena, Latvala, Antti, Legrand, Lisa N., Maher, Brion S., Melroy, Whitney E., Nelson, Elliot C., Reid, Mark W., Robinson, Jason D., Shen, Pei-Hong, Yang, Bao-Zhu, Andrews, Judy A., Aveyard, Paul, Beltcheva, Olga, Brown, Sandra A., Cannon, Dale S., Cichon, Sven, Corley, Robin P., Dahmen, Norbert, Degenhardt, Louisa ... Saccone, Nancy L. (2016). Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2), 151-169. doi: 10.1007/s10519-015-9737-3

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population

Clarke, T-K, Lupton, M. K., Fernandez-Pujals, A. M., Starr, J., Davies, G., Cox, S., Pattie, A., Liewald, D. C., Hall, L. S., MacIntyre, D. J., Smith, B. H., Hocking, L. J., Padmanabhan, S., Thomson, P. A., Hayward, C., Hansell, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Porteous, D. J., Deary, I. J. and McIntosh, A. M. (2016). Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population. Molecular Psychiatry, 21 (3), 419-425. doi: 10.1038/mp.2015.12

Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium

Stringer, S., Minică, C. C., Verweij, K. J. H., Mbarek, H., Bernard, M., Derringer, J., van Eijk, K. R., Isen, J. D., Loukola, A., Maciejewsk, D. F., Mihailov, E., van der Most, P. J., Sánchez-Mora, C., Roos, L., Sherva, R., Walters, R., Ware, J. J., Abdellaoui, A., Bigdeli, T. B., Branje, S. J. T., Brown, S. A., Bruinenberg, M., Casas, M., Esko, T., Garcia-Martinez, I., Gordon, S. D., Harris, J. M., Hartman, C. A., Henders, A. K. ... Vink, J. M. (2016). Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry, 6 (3) e769, e769-e769. doi: 10.1038/tp.2016.36

Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?

Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2016). Onset of opportunity to use cannabis and progression from opportunity to dependence: are influences consistent across transitions?. Drug and Alcohol Dependence, 160, 57-64. doi: 10.1016/j.drugalcdep.2015.12.032

CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer

Thompson, Deborah J., O'Mara, Tracy A., Glubb, Dylan M., Painter, Jodie N., Cheng, Timothy, Folkerd, Elizabeth, Doody, Deborah, Dennis, Joe, Webb, Penelope M., Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Michailidou, Kyriaki, Tyrer, Jonathan P., Maranian, Mel J., Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Fasching, Peter A., Hein, Alexander, Beckmann, Matthias W., Ekici, Arif B., Doerk, Thilo, Hillemanns, Peter, Duerst, Matthias, Runnebaum, Ingo, Zhao, Hui, Depreeuw, Jeroen ... Spurdle, Amanda B. (2016). CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer. Endocrine-Related Cancer, 23 (2), 77-91. doi: 10.1530/ERC-15-0386

Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: A cross-sectional study

Lee, S., Duffy, D.L., Mcclenahan, P., Lee, K. J., McEniery, E., Burke, B., Jagirdar, K., Martin, N.G., Sturm, R.A., Soyer, H.P. and Schaider, H. (2016). Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: A cross-sectional study. British Journal of Dermatology, 174 (2), 356-363. doi: 10.1111/bjd.14291

Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

Li, Ming, Luo, Xiong-Jian, Landén, Mikael, Bergen, Sarah E., Hultman, Christina M., Li, Xiao, Zhang, Wen, Yao, Yong-Gang, Zhang, Chen, Liu, Jiewei, Mattheisen, Manuel, Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Nöthen, Markus M., Schulze, Thomas G., Grigoroiu-Serbanescu, Maria, Li, Hao, Fuller, Chris K., Chen, Chunhui, Dong, Qi, Chen, Chuansheng, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Preisig, Martin ... The Swedish Bipolar Study Group (2016). Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. British Journal of Psychiatry, 208 (2), 128-137. doi: 10.1192/bjp.bp.114.156976

The Genetic and Environmental Contributions to Internet Use and Associations with Psychopathology: A Twin Study

Long, Elizabeth C., Verhulst, Brad, Neale, Michael C., Lind, Penelope A., Hickie, Ian B., Martin, Nicholas G. and Gillespie, Nathan A. (2016). The Genetic and Environmental Contributions to Internet Use and Associations with Psychopathology: A Twin Study. Twin Research and Human Genetics, 19 (1), 1-9. doi: 10.1017/thg.2015.91

A metabolic study of Huntington's disease

Nambron, Rajasree, Silajdžić, Edina, Kalliolia, Eirini, Ottolenghi, Chris, Hindmarsh, Peter, Hill, Nathan R., Costelloe, Seán J., Martin, Nicholas G., Positano, Vincenzo, Watt, Hilary C., Frost, Chris, Björkqvist, Maria and Warner, Thomas T. (2016). A metabolic study of Huntington's disease. PLoS ONE, 11 (1) e0146480, e0146480. doi: 10.1371/journal.pone.0146480

Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHD

Couvy-Duchesne, Baptiste, Ebejer, Jane L., Gillespie, Nathan A., Duffy, David L., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E. and Wright, Margaret J. (2016). Head motion and inattention/hyperactivity share common genetic influences: Implications for fMRI studies of ADHD. PLoS One, 11 (1) e0146271, 1-19. doi: 10.1371/journal.pone.0146271

Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences

Hill, W. D., Davies, G., Liewald, D. C., Payton, A., McNeil, C. J., Whalley, L. J., Horan, M., Ollier, W., Starr, J. M., Pendleton, N., Hansel, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Bates, T. C. and Deary, I. J. (2016). Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. Intelligence, 54, 80-89. doi: 10.1016/j.intell.2015.11.005

Facial averageness and genetic quality: Testing heritability, genetic correlation with attractiveness, and the paternal age effect

Lee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2016). Facial averageness and genetic quality: Testing heritability, genetic correlation with attractiveness, and the paternal age effect. Evolution and Human Behavior, 37 (1), 61-66. doi: 10.1016/j.evolhumbehav.2015.08.003

Genes influence the amplitude and timing of brain hemodynamic responses

Shan, Zuyao Y., Vinkhuyzen, Anna A. E., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella A.M., de Zubicaray, Greig I., Calhoun, Vince, Martin, Nicholas G., Visscher, Peter M., Wright, Margaret J. and Reutens, David C. (2016). Genes influence the amplitude and timing of brain hemodynamic responses. NeuroImage, 124 (Part A), 663-671. doi: 10.1016/j.neuroimage.2015.09.016

Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group

Schmaal, L., Veltman, D. J., van Erp, T. G. M., Sämann, P. G., Frodl, T., Jahanshad, N., Loehrer, E., Tiemeier, H., Hofman, A., Niessen, W. J., Vernooij, M. W., Ikram, M. A., Wittfeld, K., Grabe, H. J., Block, A., Hegenscheid, K., Völzke, H., Hoehn, D., Czisch, M., Lagopoulos, J., Hatton, S. N., Hickie, I. B., Goya-Maldonado, R., Krämer, B., Gruber, O., Couvy-Duchesne, B., Rentería, M. E., Strike, L. T., Mills, N. T. ... Hibar, D. P. (2016). Subcortical brain alterations in major depressive disorder: findings from the ENIGMA Major Depressive Disorder working group. Molecular Psychiatry, 21 (6), 806-812. doi: 10.1038/mp.2015.69

Trait-based assessment of borderline personality disorder using the NEO five-factor inventory: phenotypic and genetic support

Few, Lauren R., Miller, Joshua D., Grant, Julia D., Maples, Jessica, Trull, Timothy J., Nelson, Elliot C., Oltmanns, Thomas F., Martin, Nicholas G., Lynskey, Michael T. and Agrawal, Arpana (2016). Trait-based assessment of borderline personality disorder using the NEO five-factor inventory: phenotypic and genetic support. Psychological Assessment, 28 (1), 39-50. doi: 10.1037/pas0000142

Sharing a placenta is associated with a greater similarity in DNA methylation in monochorionic versus dichorionic twin pars in blood at age 14

Bui, Masato, Benyamin, Beben, Shah, Sonia, Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W. and McRae, Allan F. (2015). Sharing a placenta is associated with a greater similarity in DNA methylation in monochorionic versus dichorionic twin pars in blood at age 14. Twin Research and Human Genetics, 18 (6), 680-685. doi: 10.1017/thg.2015.87

Meta-analysis identifies seven susceptibility loci involved in the atopic March

Marenholz, Ingo, Esparza-Gordillo, Jorge, Ruschendorf, Franz, Bauerfeind, Anja, Strachan, David P., Spycher, Ben D., Baurecht, Hansjorg, Margaritte-Jeannin, Patricia, Saaf, Annika, Kerkhof, Marjan, Ege, Markus, Baltic, Svetlana, Matheson, Melanie C., Li, Jin, Michel, Sven, Ang, Wei Q., McArdle, Wendy, Arnold, Andreas, Homuth, Georg, Demenais, Florence, Bouzigon, Emmanuelle, Soderhall, Cilla, Pershagen, Goran, De Jongste, Johan C., Postma, Dirkje S., Braun-Fahrlander, Charlotte, Horak, Elisabeth, Ogorodova, Ludmila M., Puzyrev, Valery P. ... Lee, Young Ae (2015). Meta-analysis identifies seven susceptibility loci involved in the atopic March. Nature Communications, 6 (1) 8804, 8804.1-8804.8. doi: 10.1038/ncomms9804

Heritability of the network architecture of intrinsic brain functional connectivity

Sinclair, Benjamin, Hansell, Narelle K., Blokland, Gabriella A. M., Martin, Nicholas G., Thompson, Paul M., Breakspear, Michael, de Zubicaray, Greig I., Wright, Margret J. and McMahon, Katie L. (2015). Heritability of the network architecture of intrinsic brain functional connectivity. NeuroImage, 121, 243-252. doi: 10.1016/j.neuroimage.2015.07.048

Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis

Carey, Caitlin E., Agrawal, Arpana, Zhang, Bo, Conley, Emily D., Degenhardt, Louisa, Heath, Andrew C., Li, Daofeng, Lynskey, Michael T., Martin, Nicholas G., Montgomery, Grant W., Wang, Ting, Bierut, Laura J., Hariri, Ahmad R., Nelson, Elliot C. and Bogdan, Ryan (2015). Monoacylglycerol lipase (MGLL) polymorphism rs604300 interacts with childhood adversity to predict cannabis dependence symptoms and amygdala habituation: Evidence from an endocannabinoid system-level analysis. Journal of Abnormal Psychology, 124 (4), 860-877. doi: 10.1037/abn0000079

Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait

Franic, Sanja, Groen-Blokhuis, Maria M., Dolan, Conor V., Kattenberg, Mathijs V., Pool, Rene, Xiao, Xiangjun, Scheet, Paul A., Ehli, Erik A., Davies, Gareth E., van der Sluis, Sophie, Abdellaoui, Abdel, Hansell, Narelle K., Martin, Nicholas G., Hudziak, James J., van Beijsterveldt, Catherina E. M., Swagerman, Suzanne C., Pol, Hilleke E. Hulshoff, de Geus, Eco J. C., Bartels, Meike, Ropers, H. Hilger, Hottenga, Jouke-Jan and Boomsma, Dorret I. (2015). Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait. European Journal of Human Genetics, 23 (10), 1378-1383. doi: 10.1038/ejhg.2015.3

A 24-hour study of the Hypothalamo-pituitary axes in Huntington's disease

Kalliolia, Eirini, Silajdžic, Edina, Nambron, Rajasree, Costelloe, Seán J., Martin, Nicholas G., Hill, Nathan R., Frost, Chris, Watt, Hilary C., Hindmarsh, Peter, Björkqvist, Maria and Warner, Thomas T. (2015). A 24-hour study of the Hypothalamo-pituitary axes in Huntington's disease. PLoS ONE, 10 (10) e0138848, e0138848. doi: 10.1371/journal.pone.0138848

Cis-expression quantitative trait loci mapping reveals replicable associations with heroin addiction in OPRM1

Hancock, Dana B., Levy, Joshua L., Gaddis, Nathan C., Glasheen, Cristie, Saccone, Nancy L., Page, Grier P., Hulse, Gary K., Wildenauer, Dieter, Kelty, Erin A., Schwab, Sibylle G., Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Bierut, Laura J., Nelson, Elliot C., Kral, Alex H. and Johnson, Eric O. (2015). Cis-expression quantitative trait loci mapping reveals replicable associations with heroin addiction in OPRM1. Biological Psychiatry, 78 (7), 474-484. doi: 10.1016/j.biopsych.2015.01.003

Genome-wide autozygosity is associated with lower general cognitive ability

Howrigan, D.P., Simonson, M.A., Davies, G., Harris, S.E., Tenesa, A., Starr, J.M., Liewald, D.C., Deary, I.J., McRae, A., Wright, M.J., Montgomery, G.W., Hansell, N., Martin, N.G., Payton, A., Horan, M., Ollier, W.E., Abdellaoui, A., Boomsma, D.I., DeRosse, P., Knowles, E.E.M., Glahn, D.C., Djurovic, S., Melle, I., Andreassen, O.A., Christoforou, A., Steen, V.M., Hellard, S.L., Sundet, K., Reinvang, I. ... Keller, M.C. (2015). Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry, 21 (6), 837-843. doi: 10.1038/mp.2015.120

Population genetic differentiation of height and body mass index across Europe

Robinson, Matthew R., Hemani, Gibran, Medina-Gomez, Carolina, Mezzavilla, Massimo, Esko, Tonu, Shakhbazov, Konstantin, Powell, Joseph E., Vinkhuyzen, Anna, Berndt, Sonja I., Gustafsson, Stefan, Justice, Anne E., Kahali, Bratati, Locke, Adam E., Pers, Tune H., Vedantam, Sailaja, Wood, Andrew R., van Rheenen, Wouter, Andreassen, Ole A., Gasparini, Paolo, Metspalu, Andres, van den Berg, Leonard H., Veldink, Jan H., Rivadeneira, Fernando, Werge, Thomas M., Abecasis, Goncalo R., Boomsma, Dorret I., Chasman, Daniel I., de Geus, Eco J. C., Frayling, Timothy M. ... Visscher, Peter M. (2015). Population genetic differentiation of height and body mass index across Europe. Nature Genetics, 47 (11), 1357-1361. doi: 10.1038/ng.3401

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

van Den Berg, Stephanie M., de Moor, Marleen H.M., Verweij, Karin J.H., Krueger, Robert F., Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K., Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppala, Ilkka, Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Juri ... Boomsma, Dorret I. (2015). Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics, 46 (2), 170-182. doi: 10.1007/s10519-015-9735-5

A test of the facultative calibration/reactive heritability model of extraversion

Haysom, Hannah J., Mitchem, Dorian G., Lee, Anthony J., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2015). A test of the facultative calibration/reactive heritability model of extraversion. Evolution and Human Behavior, 36 (5), 414-419. doi: 10.1016/j.evolhumbehav.2015.03.002

Does shared genetic risk contribute to the co-occurrence of eating disorders and suicidality?

Wade, Tracey D., Fairweather-Schmidt, A. Kate, Zhu, Gu and Martin, Nicholas G. (2015). Does shared genetic risk contribute to the co-occurrence of eating disorders and suicidality?. International Journal of Eating Disorders, 48 (6), 684-691. doi: 10.1002/eat.22421

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

Law, Matthew H., Bishop, D. Timothy, Lee, Jeffrey E., Brossard, Myriam, Martin, Nicholas G., Moses, Eric K., Song, Fengju, Barrett, Jennifer H., Kumar, Rajiv, Easton, Douglas F., Pharoah, Paul D. P., Swerdlow, Anthony J., Kypreou, Katerina P., Taylor, John C., Harland, Mark, Randerson-Moor, Juliette, Akslen, Lars A., Andresen, Per A., Avril, Marie-Franoise, Azizi, Esther, Scarra, Giovanna Bianchi, Brown, Kevin M., Debniak, Tadeusz, Duffy, David L., Elder, David E., Fang, Shenying, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola ... Iles, Mark M. (2015). Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47 (9), 987-995. doi: 10.1038/ng.3373

Evidence of CNIH3 involvement in opioid dependence

Nelson, E. C., Agrawal, A., Heath, A. C., Bogdan, R., Sherva, R., Zhang, B., Al-Hasani, R., Bruchas, M. R., Chou, Y.-L., Demers, C. H., Carey, C. E., Conley, E. D., Fakira, A. K., Farrer, L. A., Goate, A., Gordon, S., Henders, A. K., Hesselbrock, V., Kapoor, M., Lynskey, M. T., Madden, P. A. F., Moron, J. A., Rice, J. P., Saccone, N. L., Schwab, S. G., Shand, F. L., Todorov, A. A., Wallace, L., Wang, T. ... Montgomery, G. W. (2015). Evidence of CNIH3 involvement in opioid dependence. Molecular Psychiatry, 21 (5), 608-614. doi: 10.1038/mp.2015.102

The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traits

Silventoinen, Karri, Jelenkovic, Aline, Sund, Reijo, Honda, Chika, Aaltonen, Sari, Yokoyama, Yoshie, Tarnoki, Adam D., Tarnoki, David L., Ning, Feng, Ji, Fuling, Pang, Zengchang, Ordonana, Juan R., Sanchez-Romera, Juan F., Colodro-Conde, Lucia, Burt, S. Alexandra, Klump, Kelly L., Medland, Sarah E., Montgomery, Grant W., Kandler, Christian, McAdams, Tom A., Eley, Thalia C., Gregory, Alice M., Saudino, Kimberly J., Dubois, Lise, Boivin, Michel, Haworth, Claire M. A., Plomin, Robert, Oncel, Sevgi Y., Aliev, Fazil ... Kaprio, Jaakko (2015). The CODATwins project: the cohort description of collaborative project of development of anthropometrical measures in twins to study macro-environmental variation in genetic and environmental effects on anthropometric traits. Twin Research and Human Genetics, 18 (4), 348-360. doi: 10.1017/thg.2015.29

A common genetic influence on human intensity ratings of sugars and high-potency sweeteners

Hwang, Liang-Dar, Zhu, Gu, Breslin, Paul A. S., Reed, Danielle R., Martin, Nicholas G. and Wright, Margaret J. (2015). A common genetic influence on human intensity ratings of sugars and high-potency sweeteners. Twin Research and Human Genetics, 18 (4), 361-367. doi: 10.1017/thg.2015.42

Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up

Liu, Fan, Visser, Mijke, Duffy, David L., Hysi, Pirro G., Jacobs, Leonie C., Lao, Oscar, Zhong, Kaiyin, Walsh, Susan, Chaitanya, Lakshmi, Wollstein, Andreas, Zhu, Gu, Montgomery, Grant W., Henders, Anjali K., Mangino, Massimo, Glass, Daniel, Bataille, Veronique, Sturm, Richard A., Rivadeneira, Fernando, Hofman, Albert, van IJcken, Wilfred F. J., Uitterlinden, André G., Palstra, Robert-Jan T. S., Spector, Timothy D., Martin, Nicholas G., Nijsten, Tamar E. C. and Kayser, Manfred (2015). Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Human Genetics, 134 (8), 823-835. doi: 10.1007/s00439-015-1559-0

Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder

De Moor, Marleen H.M, Van Den Berg, Stephanie M, Verweij, Karin J.H, Krueger, Robert F, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K, Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D, Hansell, Narelle K, Hart, Amy B, Seppala, Ilkka, Huffman, Jennifer E, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abecasis, Goncalo R, Adkins, Daniel E, Agrawal, Arpana, Allik, Juri, Appel, Katja ... Boomsma, Dorret I (2015). Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder. JAMA Psychiatry, 72 (7), 642-650. doi: 10.1001/jamapsychiatry.2015.0554

WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness

Cuellar-Partida, Gabriel, Springelkamp, Henriet, Lucas, Sionne E. M., Yazar, Seyhan, Hewitt, Alex W., Iglesias, Adriana I., Montgomery, Grant W., Martin, Nicholas G., Pennell, Craig E., van Leeuwen, Elisabeth M., Verhoeven, Virginie J. M., Hofman, Albert, Uitterlinden, Andre G., Ramdas, Wishal D., Wolfs, Roger. C. W., Vingerling, Johannes R., Brown, Matthew A., Mills, Richard A., Craig, Jamie E., Klaver, Caroline C. W., van Duijn, Cornelia M., Burdon, Kathryn P., MacGregor, Stuart and Mackey, David A. (2015). WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness. Human Molecular Genetics, 24 (17), 5060-5068. doi: 10.1093/hmg/ddv211

Is there a genetic correlation between general factors of intelligence and personality?

Loehlin, John C., Bartels, Meike, Boomsma, Dorret I., Bratko, Denis, Martin, Nicholas G., Nichols, Robert C. and Wright, Margaret J. (2015). Is there a genetic correlation between general factors of intelligence and personality?. Twin Research and Human Genetics, 18 (3), 234-242. doi: 10.1017/thg.2015.28

The effect of education on smoking behavior: new evidence from smoking durations of a sample of twins

Koning, Pierre, Webbink, Dinand and Martin, Nicholas G. (2015). The effect of education on smoking behavior: new evidence from smoking durations of a sample of twins. Empirical Economics, 48 (4), 1479-1497. doi: 10.1007/s00181-014-0842-6

The genetic and environmental foundations of political, psychological, social, and economic behaviors: a panel study of twins and families

Hatemi, Peter K., Smith, Kevin, Alford, John R., Martin, Nicholas G. and Hibbing, John R. (2015). The genetic and environmental foundations of political, psychological, social, and economic behaviors: a panel study of twins and families. Twin Research and Human Genetics, 18 (3), 243-255. doi: 10.1017/thg.2015.13

ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure

Springelkamp, Henriet, Iglesias, Adriana I., Cuellar-Partida, Gabriel, Amin, Najaf, Burdon, Kathryn P., van Leeuwen, Elisabeth M., Gharahkhani, Puya, Mishra, Aniket, van der Lee, Sven J., Hewitt, Alex W., Rivadeneira, Fernando, Viswanathan, Ananth C., Wolfs, Roger C. W., Martin, Nicholas G., Ramdas, Wishal D., van Koolwijk, Leonieke M., Pennell, Craig E., Vingerling, Johannes R., Mountain, Jenny E., Uitterlinden, Andre G., Hofman, Albert, Mitchell, Paul, Lemij, Hans G., Wang, Jie Jin, Klaver, Caroline C. W., Mackey, David A., Craig, Jamie E., van Duijn, Cornelia M. and MacGregor, Stuart (2015). ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure. Human Molecular Genetics, 24 (9), 2689-2699. doi: 10.1093/hmg/ddv027

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

Fall, Tove, Hagg, Sara, Ploner, Alexander, Maegi, Reedik, Fischer, Krista, Draisma, Harmen H. M., Sarin, Antti-Pekka, Benyamin, Beben, Ladenvall, Claes, Akerlund, Mikael, Kals, Mart, Esko, Tonu, Nelson, Christopher P., Kaakinen, Marika, Huikari, Ville, Mangino, Massimo, Meirhaeghe, Aline, Kristiansson, Kati, Nuotio, Marja-Liisa, Kobl, Michael, Grallert, Harald, Dehghan, Abbas, Kuningas, Maris, de Vries, Paul S., de Bruijn, Renee F. A. G., Willems, Sara M., Heikkila, Kauko, Silventoinen, Karri, Pietilainen, Kirsi H. ... Ingelsson, Erik (2015). Age- and sex-specific causal effects of adiposity on cardiovascular risk factors. Diabetes, 64 (5), 1841-1852. doi: 10.2337/db14-0988

Development of a global network of induced pluripotent stem cell haplobanks

Wilmut, Ian, Leslie, Stephen, Martin, Nicholas G., Peschanski, Marc, Rao, Mahendra, Trounson, Alan, Turner, David, Turner, Marc L., Yamanaka, Shinya and Taylor, Craig J. (2015). Development of a global network of induced pluripotent stem cell haplobanks. Regenerative Medicine, 10 (3), 235-238. doi: 10.2217/RME.15.1

Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data

Kochunov, Peter, Jahanshad, Neda, Marcus, Daniel, Winkler, Anderson, Sprooten, Emma, Nichols, Thomas E, Wright, Susan N, Hong, L. Elliot, Patel, Binish, Behrens, Timothy, Jbabdi, Saad, Andersson, Jesper, Lenglet, Christophe, Yacoub, Essa, Moeller, Steen, Auerbach, Eddie, Ugurbil, Kamil, Sotiropoulos, Stamatios N, Brouwer, Rachel M, Landman, Bennett, Lemaitre, Herve, den Braber, Anouk, Zwiers, Marcel P, Ritchie, Stuart, van Hulzen, Kimm, Almasy, Laura, Curran, Joanne, deZubicaray, Greig I, Duggirala, Ravi ... Van Essen, David C (2015). Heritability of fractional anisotropy in human white matter: A comparison of Human Connectome Project and ENIGMA-DTI data. NeuroImage, 111, 300-311. doi: 10.1016/j.neuroimage.2015.02.050

No relationship between intelligence and facial attractiveness in a large, genetically informative sample

Mitchem, Dorian G., Zietsch, Brendan P., Wright, Margaret J., Martin, Nicholas G., Hewitt, John K. and Keller, Matthew C. (2015). No relationship between intelligence and facial attractiveness in a large, genetically informative sample. Evolution and Human Behavior, 36 (3), 240-247. doi: 10.1016/j.evolhumbehav.2014.11.009

Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls

Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, McGrath, John, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2015). Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls. Schizophrenia Research, 164 (1-3), 47-52. doi: 10.1016/j.schres.2015.01.045

The relationship between cannabis involvement and suicidal thoughts and behaviors

Delforterie, M. J., Lynskey, M. T., Huizink, A. C., Creemers, H. E., Grant, J. D., Few, L. R., Glowinski, A. L., Statham, D. J., Trull, T. J., Bucholz, K. K., Madden, P. A. F., Martin, N. G., Heath, A. C. and Agrawal, A. (2015). The relationship between cannabis involvement and suicidal thoughts and behaviors. Drug and Alcohol Dependence, 150, 98-104. doi: 10.1016/j.drugalcdep.2015.02.019

Common genetic variants influence human subcortical brain structures

Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivieres, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Mallar Chakravarty M., Chen, Qiang, Ching, Christopher R.K., Cuellar-Partida, Gabriel, Den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J ... Medland, Sarah E (2015). Common genetic variants influence human subcortical brain structures. Nature, 520 (7546), 224-229. doi: 10.1038/nature14101

Genetic basis of a cognitive complexity metric

Hansell, Narelle K., Halford, Graeme S., Andrews, Glenda, Shum, David H. K., Harris, Sarah E., Davies, Gail, Franic, Sanja, Christoforou, Andrea, Zietsch, Brendan, Painter, Jodie, Medland, Sarah E., Ehli, Erik A., Davies, Gareth E., Steen, Vidar M., Lundervold, Astri J., Reinvang, Ivar, Montgomery, Grant W., Espeseth, Thomas, Pol, Hilleke E. Hulshoff, Starr, John M., Martin, Nicholas G., Le Hellard, Stephanie, Boomsma, Dorret I., Deary, Ian J. and Wright, Margaret J. (2015). Genetic basis of a cognitive complexity metric. PLoS One, 10 (4) e0123886, 1-19. doi: 10.1371/journal.pone.0123886

Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults

Zimmermann, E., Angquist, L. H., Mirza, S. S., Zhao, J. H., Chasman, D. I., Fischer, K., Qi, Q., Smith, A. V., Thinggaard, M., Jarczok, M. N., Nalls, M. A., Trompet, S., Timpson, N. J., Schmidt, B., Jackson, A. U., Lyytikainen, L. P., Verweij, N., Mueller-Nurasyid, M., Vikstrom, M., Marques-Vidal, P., Wong, A., Meidtner, K., Middelberg, R. P., Strawbridge, R. J., Christiansen, L., Kyvik, K. O., Hamsten, A., Jaaskelainen, T., Tjonneland, A. ... Montgomery, G. W. (2015). Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults. Obesity Reviews, 16 (4), 327-340. doi: 10.1111/obr.12263

Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life

Strohmaier, Jana, van Dongen, Jenny, Willemsen, Gonneke, Nyholt, Dale R., Zhu, Gu, Codd, Veryan, Novakovic, Boris, Hansell, Narelle, Wright, Margaret J., Rietschel, Liz, Streit, Fabian, Henders, Anjali K., Montgomery, Grant W., Samani, Nilesh J., Gillespie, Nathan A., Hickie, Ian B., Craig, Jeffrey M., Saffery, Richard, Boomsma, Dorret I., Rietschel, Marcella and Martin, Nicholas G. (2015). Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life. Twin Research and Human Genetics, 18 (2), 198-209. doi: 10.1017/thg.2015.3

Prevalence of germline BAP1, CDKN2A, and CDK4 mutations in an australian population-based sample of cutaneous melanoma cases

Aoude, Lauren G., Gartside, Michael, Johansson, Peter, Palmer, Jane M., Symmons, Judith, Martin, Nicholas G., Montgomery, Grant W. and Hayward, Nicholas K. (2015). Prevalence of germline BAP1, CDKN2A, and CDK4 mutations in an australian population-based sample of cutaneous melanoma cases. Twin Research and Human Genetics, 18 (2), 126-133. doi: 10.1017/thg.2015.12

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014)

Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jianan, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haelldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2015). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis (vol 5, 4926, 2014). Nature Communications, 6 (1) 6542, 1-1. doi: 10.1038/ncomms7542

Genome-wide association study of blood lead shows multiple associations near ALAD

Warrington, Nicole M., Zhu, Gu, Dy, Veronica, Heath, Andrew C., Madden, Pamela A. F., Hemani, Gibran, Kemp, John P., Mcmahon, George, St Pourcain, Beate, Timpson, Nicholas J., Taylor, Caroline M., Golding, Jean, Lawlor, Debbie A., Steer, Colin, Montgomery, Grant W., Martin, Nicholas G., Smith, George Davey, Evans, David M. and Whitfield, John B. (2015). Genome-wide association study of blood lead shows multiple associations near ALAD. Human Molecular Genetics, 24 (13) ddv112, 3871-3879. doi: 10.1093/hmg/ddv112

DCAF4, a novel gene associated with leucocyte telomere length

Mangino, Massimo, Christiansen, Lene, Stone, Rivka, Hunt, Steven C., Horvath, Kent, Eisenberg, Dan T. A., Kimura, Masayuki, Petersen, Inge, Kark, Jeremy D., Herbig, Utz, Reiner, Alex P., Benetos, Athanase, Codd, Veryan, Nyholt, Dale R., Sinnreich, Ronit, Christensen, Kaare, Nassar, Hisham, Hwang, Shih-Jen, Levy, Daniel, Bataille, Veronique, Fitzpatrick, Annette L., Chen, Wei, Berenson, Gerald S., Samani, Nilesh J., Martin, Nicholas G., Tishkoff, Sarah, Schork, Nicholas J., Kyvik, Kirsten Ohm, Dalgard, Christine ... Aviv, Abraham (2015). DCAF4, a novel gene associated with leucocyte telomere length. Journal of Medical Genetics, 52 (3), 157-162. doi: 10.1136/jmedgenet-2014-102681

Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins

Sanfilippo, Paul G., Wilkinson, Colleen H., Ruddle, Jonathan B., Zhu, Gu, Martin, Nicholas G., Hewitt, Alex W. and Mackey, David A. (2015). Don't it make your brown eyes blue? A comparison of iris colour across latitude in Australian twins. Clinical and Experimental Optometry, 98 (2), 172-176. doi: 10.1111/cxo.12209

Hepascore and hyaluronic acid as markers of fibrosis in liver disease of mixed aetiology

Costelloe, Seán J., Theocharidou, Eleni, Tsochatzis, Emmanuel, Thalassinos, Evangelos, Martin, Nicholas, Fede, Guiseppe, Thomas, Michael and Burroughs, Anthony K. (2015). Hepascore and hyaluronic acid as markers of fibrosis in liver disease of mixed aetiology. European Journal of Gastroenterology and Hepatology, 27 (3), 313-320. doi: 10.1097/MEG.0000000000000267

Introduction to the statistical concepts symposium section: Selected review topics to improve our understanding and use of statistics

Glaz, Barry, Wiersma, Jochum, Hernandez, Jose A., Martin, Nicolas F. and Yeater, Kathleen M. (2015). Introduction to the statistical concepts symposium section: Selected review topics to improve our understanding and use of statistics. Agronomy Journal, 107 (2), 691-691. doi: 10.2134/agronj14.0888

A twin study of breastfeeding with a preliminary genome-wide association scan

Colodro-Conde, Lucia, Zhu, Gu, Power, Robert A., Henders, Anjali, Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Medland, Sarah, Ordonana, Juan R. and Martin, Nicholas G. (2015). A twin study of breastfeeding with a preliminary genome-wide association scan. Twin Research and Human Genetics, 18 (1), 61-72. doi: 10.1017/thg.2014.74

Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins

Mills, Natalie T., Wright, Margaret J., Henders, Anjali K., Eyles, Darryl W., Baune, Bernhard T., McGrath, John J., Byrne, Edna M., Hansell, Narelle K., Birosova, Eva, Scott, James G., Martin, Nicholas G., Montgomery, Grant W., Wray, Naomi R. and Vinkhuyzen, Anna A. E. (2015). Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins. Twin Research and Human Genetics, 18 (1), 28-35. doi: 10.1017/thg.2014.70

Large autosomal copy-number differences within unselected monozygotic twin pairs are rare

Mcrae, Allan F., Visscher, Peter M., Montgomery, Grant W. and Martin, Nicholas G. (2015). Large autosomal copy-number differences within unselected monozygotic twin pairs are rare. Twin Research and Human Genetics, 18 (1), 13-18. doi: 10.1017/thg.2014.85

Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma

Aoude, Lauren G., Pritchard, Antonia L., Robles-Espinoza, Carla Daniela, Wadt, Karin, Harland, Mark, Choi, Jiyeon, Gartside, Michael, Quesada, Victor, Johansson, Peter, Palmer, Jane M., Ramsay, Andrew J., Zhang, Xijun, Jones, Kristine, Symmons, Judith, Holland, Elizabeth A., Schmid, Helen, Bonazzi, Vanessa, Woods, Susan, Dutton-Regester, Ken, Stark, Mitchell S., Snowden, Helen, van Doom, Remco, Montgomery, Grant W., Martin, Nicholas G., Keane, Thomas M., Lopez-Otin, Carlos, Gerdes, Anne-Marie, Olsson, Hakan, Ingvar, Christian ... Hayward, Nicholas K. (2015). Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. Journal of the National Cancer Institute, 107 (2) dju408, 1-7. doi: 10.1093/jnci/dju408

DNA methylation age of blood predicts all-cause mortality in later life

Marioni, Riccardo E., Shah, Sonia, McRae, Allan F., Chen, Brian H., Colicino, Elena, Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Feinberg, Andrew P., Fallin, M. Daniele, Multhaup, Michael L., Jaffe, Andrew E., Joehanes, Roby, Schwartz, Joel, Just, Allan C., Lunetta, Kathryn L., Murabito, Joanne M., Starr, John M., Horvath, Steve, Baccarelli, Andrea A., Levy, Daniel, Visscher, Peter M. ... Deary, Ian J. (2015). DNA methylation age of blood predicts all-cause mortality in later life. Genome Biology, 16 (1) 25, 25.1-25.12. doi: 10.1186/s13059-015-0584-6

Association between endometriosis and the interleukin 1A (IL1A) locus

Sapkota, Yadav, Low, Siew-Kee, Attia, John, Gordon, Scott D., Henders, Anjali K., Holliday, Elizabeth G., MacGregor, Stuart, Martin, Nicholas G., McEvoy, Mark, Morris, Andrew P., Takahashi, Atsushi, Scott, Rodney J., Kubo, Michiaki, Zondervan, Krina T., Montgomery, Grant W. and Nyholt, Dale R. (2015). Association between endometriosis and the interleukin 1A (IL1A) locus. Human Reproduction, 30 (1), 239-248. doi: 10.1093/humrep/deu267

Contrast Effects and Sex Influence Maternal and Self-Report Dimensional Measures of Attention-Deficit Hyperactivity Disorder

Ebejer, J. L., Medland, S. E., van der Werf, J., Wright, M. J., Henders, A. K., Gillespie, N. A., Hickie, I. B., Martin, N. G. and Duffy, D. L. (2015). Contrast Effects and Sex Influence Maternal and Self-Report Dimensional Measures of Attention-Deficit Hyperactivity Disorder. Behavior Genetics, 45 (1), 35-50. doi: 10.1007/s10519-014-9670-x

Telescoping and gender differences in the time course of disordered gambling: evidence from a general population sample

Slutske, Wendy S., Piasecki, Thomas M., Deutsch, Arielle R., Statham, Dixie J. and Martin, Nicholas G. (2015). Telescoping and gender differences in the time course of disordered gambling: evidence from a general population sample. Addiction, 110 (1), 144-151. doi: 10.1111/add.12717

The association between speed of transition from initiation to subsequent use of cannabis and later problematic cannabis use, abuse and dependence

Hines, Lindsey A., Morley, Katherine I., Strang, John, Agrawal, Arpana, Nelson, Elliot C., Statham, Dixie, Martin, Nicholas G. and Lynskey, Michael T. (2015). The association between speed of transition from initiation to subsequent use of cannabis and later problematic cannabis use, abuse and dependence. Addiction, 110 (8), 1311-1320. doi: 10.1111/add.12963

Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study

Gottlieb, D. J., Hek, K., Chen, T. H., Watson, N. F., Eiriksdottir, G., Byrne, E. M., Cornelis, M., Warby, S. C., Bandinelli, S., Cherkas, L., Evans, D. S., Grabe, H. J., Lahti, J., Li, M., Lehtimaki, T., Lumley, T., Marciante, K. D., Perusse, L., Psaty, B. M., Robbins, J., Tranah, G. J., Vink, J. M., Wilk, J. B., Stafford, J. M., Bellis, C., Biffar, R., Bouchard, C., Cade, B., Curhan, G. C. ... Tiemeier, H. (2014). Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Molecular Psychiatry, 20 (10), 1232-1239. doi: 10.1038/mp.2014.133

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

Evangelou, Evangelos, Kerkhos, Hanneke J., Styrkarsdottir, Unnur, Ntzani, Evangelia E., Bos, Steffan D., Esko, Tonu, Evans, Daniel S., Metrustry, Sarah, Panoutsopoulou, Kalliope, Ramos, Yolande F. M., Thorleifsson, Gudmar, Tsilides, Konstantinos K., arcOGEN Consortium, Arden, Nigel, Aslam, Nadim, Bellamy, Nicholas, Birrell, Fraser, Blanco, Francisco J., Carr, Andrew, Chapman, Kay, Day-Williams, Aaron G., Deloukas, Panos, Doherty, Michael, Engstrom, Gunnar, Helgadottir, Hafdis T., Hoffman, Albert, Ingvarsson, Thorvaldur, Jonsson, Helgi, Keis, Aime ... Valdes, Anna M. (2014). A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Annals of the Rheumatic Diseases, 73 (12), 2130-2136. doi: 10.1136/annrheumdis-2012-203114

Challenges and opportunities in mass spectrometric analysis of proteins from dried blood spots

Martin, Nicholas J. and Cooper, Helen J. (2014). Challenges and opportunities in mass spectrometric analysis of proteins from dried blood spots. Expert Review of Proteomics, 11 (6), 685-695. doi: 10.1586/14789450.2014.965158

Genetic influences on alcohol-related hangover

Slutske, Wendy S., Piasecki, Thomas M., Nathanson, Lisa, Statham, Dixie J. and Martin, Nicholas G. (2014). Genetic influences on alcohol-related hangover. Addiction, 109 (12), 2027-2034. doi: 10.1111/add.12699

Genetic variation in personality traits explains genetic overlap between borderline personality features and substance use disorders

Few, Lauren R., Grant, Julia D., Trull, Timothy J., Statham, Dixie J., Martin, Nicholas G., Lynskey, Michael T. and Agrawal, Arpana (2014). Genetic variation in personality traits explains genetic overlap between borderline personality features and substance use disorders. Addiction, 109 (12), 2118-2127. doi: 10.1111/add.12690

Personality and gambling involvement: a person-centered approach

Savage, Jeanne E., Slutske, Wendy S. and Martin, Nicholas G. (2014). Personality and gambling involvement: a person-centered approach. Psychology of Addictive Behaviors, 28 (4), 1198-1211. doi: 10.1037/a0037413

Test of a potential causal influence of earlier age of gambling initiation on gambling involvement and disorder: a multilevel discordant twin design

Slutske, Wendy S., Deutsch, Arielle R., Richmond-Rakerd, Leah S., Chernyavskiy, Pavel, Statham, Dixie J. and Martin, Nicholas G. (2014). Test of a potential causal influence of earlier age of gambling initiation on gambling involvement and disorder: a multilevel discordant twin design. Psychology of Addictive Behaviors, 28 (4), 1177-1189. doi: 10.1037/a0035356

The genetic correlation between procrastination and impulsivity

Loehlin, John C. and Martin, Nicholas G. (2014). The genetic correlation between procrastination and impulsivity. Twin Research and Human Genetics, 17 (6), 512-515. doi: 10.1017/thg.2014.60

Obesity gene NEGR1 associated with white matter integrity in healthy young adults

Dennis, Emily L., Jahanshad, Neda, Braskie, Meredith N., Warstadt, Nicholus M., Hibar, Derrek P., Kohannim, Omid, Nir, Talia M., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2014). Obesity gene NEGR1 associated with white matter integrity in healthy young adults. Neuroimage, 102 (Part 2), 548-557. doi: 10.1016/j.neuroimage.2014.07.041

Defining the role of common variation in the genomic and biological architecture of adult human height

Wood, Andrew R., Esko, Tonu, Yang, Jian, Vedantam, Sailaja, Pers, Tune H., Gustafsson, Stefan, Chu, Audrey Y., Estrada, Karol, Luan, Jian'an, Kutalik, Zoltan, Amin, Najaf, Buchkovich, Martin L., Croteau-Chonka, Damien C., Day, Felix R., Duan, Yanan, Fall, Tove, Fehrmann, Rudolf, Ferreira, Teresa, Jackson, Anne U., Karjalainen, Juha, Lo, Ken Sin, Locke, Adam E., Magi, Reedik, Mihailov, Evelin, Porcu, Evelin, Randall, Joshua C., Scherag, Andre, Vinkhuyzen, Anne A. E., Westra, Harm-Jan ... Frayling, Timothy M. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46 (11), 1173-1186. doi: 10.1038/ng.3097

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Li, Qing, Wojciechowski, Robert, Simpson, Claire L., Hysi, Pirro G., Verhoeven, Virginie J. M., Ikram, Mohammad Kamran, Hohn, Rene, Vitart, Veronique, Hewitt, Alex W., Oexle, Konrad, Makela, Kari-Matti, MacGregor, Stuart, Pirastu, Mario, Fan, Qiao, Cheng, Ching-Yu, St Pourcain, Beate, McMahon, George, Kemp, John P., Northstone, Kate, Rahi, Jugnoo S., Cumberland, Phillippa M., Martin, Nicholas G., Sanfilippo, Paul G., Lu, Yi, Wang, Ya Xing, Hayward, Caroline, Polasek, Ozren, Campbell, Harry, Bencic, Goran ... Guggenheim, Jeremy A. (2014). Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Human Genetics, 134 (2), 131-146. doi: 10.1007/s00439-014-1500-y

Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults

Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2014). Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults. Psychosomatic Medicine, 76 (9), 732-738. doi: 10.1097/PSY.0000000000000117

Genetic and environmental exposures constrain epigenetic drift over the human life course

Shah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J. and Visscher, Peter M. (2014). Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Research, 24 (11), 1725-1733. doi: 10.1101/gr.176933.114

Genetic architecture of subcortical brain regions: common and region-specific genetic contributions

Rentería, M. E., Hansell, N. K., Strike, L. T., McMahon, K. L., de Zubicaray, G. I., Hickie, Ian B., Thompson, Paul M., Martin, N. G., Medland, S. E. and Wright, M. J. (2014). Genetic architecture of subcortical brain regions: common and region-specific genetic contributions. Genes, Brain and Behavior, 13 (8), 821-830. doi: 10.1111/gbb.12177

Perceived stress has genetic influences distinct from neuroticism and depression

Rietschel, Liz, Zhu, Gu, Kirschbaum, Clemens, Strohmaier, Jana, Wuest, Stefan, Rietschel, Marcella and Martin, Nicholas G. (2014). Perceived stress has genetic influences distinct from neuroticism and depression. Behavior Genetics, 44 (6), 639-645. doi: 10.1007/s10519-013-9636-4

Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure

Warstadt, Nicholus M., Dennis, Emily L., Jahanshad, Neda, Kohannim, Omid, Nir, Talia M., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Jack, Clifford R. Jr., Bernstein, Matt A., Weiner, Michael W., Toga, Arthur W., Wright, Margaret J., Thompson, Paul M. and for the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (2014). Serum cholesterol and variant in cholesterol-related gene CETP predict white matter microstructure. Neurobiology of Aging, 35 (11), 2504-2513. doi: 10.1016/j.neurobiolaging.2014.05.024

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian'an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haeldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2014). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 5 (1) 5926, 4926.1-4926.10. doi: 10.1038/ncomms5926

Investigating brain connectivity heritability in a twin study using diffusion imaging data

Shen, Kai-Kai, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2014). Investigating brain connectivity heritability in a twin study using diffusion imaging data. Neuroimage, 100, 628-641. doi: 10.1016/j.neuroimage.2014.06.041

Another explanation for apparent epistasis: reply

Hemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014). Another explanation for apparent epistasis: reply. Nature, 514 (7520), E5-E6. doi: 10.1038/nature13692

Attitudes toward economic risk and occupational choice

Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2014). Attitudes toward economic risk and occupational choice. Industrial Relations, 53 (4), 568-592. doi: 10.1111/irel.12054

Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

Hysi, Pirro G., Cheng, Ching-Yu, Springelkamp, Henriet, Macgregor, Stuart, Bailey, Jessica N. Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W., Hohn, Rene, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D., Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B., Liao, Jiemin, Haines, Jonathan L., Amin, Najaf, Wang, Ya Xing, Wild, Philipp S., Ozel, Ayse B., Li, Jun Z., Fleck, Brian W., Zeller, Tanja, Staffieri, Sandra E., Teo, Yik-Ying, Cuellar-Partida, Gabriel ... Aung, Tin (2014). Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Nature Genetics, 46 (10), 1126-1130. doi: 10.1038/ng.3087

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., De Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, Van Der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, Van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111 (38), 13790-13794. doi: 10.1073/pnas.1404623111

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014)

Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014). Proceedings of the National Academy of Sciences of the United States of America, 112 (4), E380-E380. doi: 10.1073/pnas.1424631112

Human mate selection and addiction: A conceptual critique

Heath, Andrew C., Waldron, Mary C., Martin, Nicholas G., Nelson, Elliot C., Bucholz, Kathleen K. and Madden, Pamela A. F. (2014). Human mate selection and addiction: A conceptual critique. Behavior Genetics, 44 (5), 419-426. doi: 10.1007/s10519-014-9669-3

Identification of a melanoma susceptibility locus and somatic mutation in TET2

Song, Fengju, Amos, Christopher I., Lee, Jeffrey E., Lian, Christine G., Fang, Shenying, Liu, Hongliang, MacGregor, Stuart, Iles, Mark M., Law, Matthew H., Lindeman, Neal I., Montgomery, Grant W., Duffy, David L., Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Bishop, Julia A. Newton, Kraft, Peter, Qureshi, Abrar A., Kanetsky, Peter A., Hayward, Nicholas K. ... Han, Jiali (2014). Identification of a melanoma susceptibility locus and somatic mutation in TET2. Carcinogenesis, 35 (9) bgu140, 2097-2101. doi: 10.1093/carcin/bgu140

Genome-wide interaction analysis reveals replicated epistatic effects on brain structure

Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Hua, Xue, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Alzheimer’s Disease Neuroimaging Initiative, Weiner, Michael W. and Thompson, Paul M. (2014). Genome-wide interaction analysis reveals replicated epistatic effects on brain structure. Neurobiology of Aging, 36 (S1), S151-S158. doi: 10.1016/j.neurobiolaging.2014.02.033

Variants close to NTRK2 gene are associated with birth weight in female twins

Metrustry, Sarah J., Edwards, Mark H., Medland, Sarah E., Holloway, John W., Montgomery, Grant W., Martin, Nicholas G., Spector, Tim D., Cooper, Cyrus and Valdes, Ana M. (2014). Variants close to NTRK2 gene are associated with birth weight in female twins. Twin Research and Human Genetics, 17 (4), 254-261. doi: 10.1017/thg.2014.34

Applying polygenic risk scores to postpartum depression

Byrne, Edna M., Carrillo-Roa, Tania, Penninx, Brenda W. J. H., Sallis, Hannah M., Viktorin, Alexander, Chapman, Brett, Henders, Anjali K., Pergadia, Michele L., Heath, Andrew C., Madden, Pamela A. F., Sullivan, Patrick F., Boschloo, Lynn, van Grootheest, Gerard, McMahon, George, Lawlor, Debbie A., Landen, Mikael, Lichtenstein, Paul, Magnusson, Patrik K. E., Evans, David M., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G., Meltzer-Brody, Samantha and Wray, Naomi R. (2014). Applying polygenic risk scores to postpartum depression. Archives of Women's Mental Health, 17 (6), 519-528. doi: 10.1007/s00737-014-0428-5

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and megaanalytical approaches for data pooling

Kochunov, Peter, Jahanshad, Neda, Sprooten, Emma, Nichols, Thomas E., Mandl, René C., Almasy, Laura, Booth, Tom, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Dimitrova, Rali, Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Lemaitre, Hervé, Lopez, Lorna M., Martin, Nicholas G., McMahon, Katie L., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Wright, Susan N., Bastin, Mark E. ... Glahn, David C. (2014). Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: comparing meta and megaanalytical approaches for data pooling. Neuroimage, 95, 136-150. doi: 10.1016/j.neuroimage.2014.03.033

Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory

van den Berg, Stephanie M., de Moor, Marleen H. M., McGue, Matt, Pettersson, Erik, Terracciano, Antonio, Verweij, Karin J. H., Amin, Najaf, Derringer, Jaime, Esko, Tonu, van Grootheest, Gerard, Hansell, Narelle K., Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Luciano, Michelle, Matteson, Lindsay K., Viktorin, Alexander, Wouda, Jasper, Agrawal, Arpana, Allik, Jueri, Bierut, Laura, Broms, Ulla, Campbell, Harry, Smith, George Davey, Eriksson, Johan G., Ferrucci, Luigi, Franke, Barbera, Fox, Jean-Paul, de Geus, Eco J. C. ... Boomsma, Dorret I. (2014). Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory. Behavior Genetics, 44 (4), 295-313. doi: 10.1007/s10519-014-9654-x

PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals

Nelson, Elliot C., Heath, Andrew C., Lynskey, Michael T., Agrawal, Arpana, Henders, Anjali K., Bowdler, Lisa M., Todorov, Alexandre A., Madden, Pamela A. F., Moore, Elizabeth, Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). PTSD risk associated with a functional DRD2 polymorphism in heroin-dependent cases and controls is limited to amphetamine-dependent individuals. Addiction Biology, 19 (4), 700-707. doi: 10.1111/adb.12062

Assessment of PALB2 as a candidate melanoma susceptibility gene

Aoude, Lauren G., Xu, Mai, Zhao, Zhen Zhen, Kovacs, Michael, Palmer, Jane M., Johansson, Peter, Symmons, Judith, Trent, Jeffrey M., Martin, Nicholas G., Montgomery, Grant W., Brown, Kevin M. and Hayward, Nicholas K. (2014). Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One, 9 (6) e100683, e100683.1-e100683.7. doi: 10.1371/journal.pone.0100683

Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

Jagirdar, Kasturee, Smit, Darren J., Ainger, Stephen A., Lee, Katie J., Brown, Darren L., Chapman, Brett, Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Stow, Jennifer L., Duffy, David L. and Sturm, Richard A. (2014). Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits. Pigment Cell and Melanoma Research, 27 (4), 552-564. doi: 10.1111/pcmr.12253

Overlapping genetic and environmental influences on nonsuicidal self-injury and suicidal ideation different outcomes, same etiology?

Maciejewski, Dominique F., Creemers, Hanneke E., Lynskey, Michael T., Madden, Pamela A. F., Heath, Andrew C., Statham, Dixie J., Martin, Nicholas G. and Verweij, Karin J. H. (2014). Overlapping genetic and environmental influences on nonsuicidal self-injury and suicidal ideation different outcomes, same etiology?. Jama Psychiatry, 71 (6), 699-705. doi: 10.1001/jamapsychiatry.2014.89

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Thompson, Paul M., Stein, Jason L., Medland, Sarah E., Hibar, Derrek P., Arias Vasquez, Alejandro, Renteria, Miguel E., Toro, Roberto, Jahanshad, Neda, Schumann, Gunter, Franke, Barbara, Wright, Margaret J., Martin, Nicholas G., Agartz, Ingrid, Alda, Martin, Alhusaini, Saud, Almasy, Laura, Almeida, Jorge, Alpert, Kathryn, Andreasen, Nancy C., Andreassen, Ole A., Apostolova, Liana G., Appel, Katja, Armstrong, Nicola J., Aribisala, Benjamin, Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Bergmann, Ørjan, Binder, Elisabeth B. ... Saguenay Youth Study (SYS) Group (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8 (2), 153-182. doi: 10.1007/s11682-013-9269-5

Contribution of genetic variation to transgenerational inheritance of DNA methylation

McRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5), 1-10. doi: 10.1186/gb-2014-15-5-r73

Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations

Hatemi, Peter K., Medland, Sarah E., Klemmensen, Robert, Oskarsson, Sven, Littvay, Levente, Dawes, Christopher T., Verhulst, Brad, McDermott, Rose, Norgaard, Asbjorn Sonne, Klofstad, Casey A., Christensen, Kaare, Johannesson, Magnus, Magnusson, Patrik K. E., Eaves, Lindon J. and Martin, Nicholas G. (2014). Genetic influences on political ideologies: Twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations. Behavior Genetics, 44 (3), 282-294. doi: 10.1007/s10519-014-9648-8

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

Purrington, Kristen S., Slager, Susan, Eccles, Diana, Yannoukakos, Drakoulis, Fasching, Peter A., Miron, Penelope, Carpenter, Jane, Chang-Claude, Jenny, Martin, Nicholas G., Montgomery, Grant W., Kristensen, Vessela, Anton-Culver, Hoda, Goodfellow, Paul, Tapper, William J., Rafiq, Sajjad, Gerty, Susan M., Durcan, Lorraine, Konstantopoulou, Irene, Fostira, Florentia, Vratimos, Athanassios, Apostolou, Paraskevi, Konstanta, Irene, Kotoula, Vassiliki, Lakis, Sotiris, Dimopoulos, Meletios A., Skarlos, Dimosthenis, Pectasides, Dimitrios, Fountzilas, George, Beckmann, Matthias W. ... Couch, Fergus J. (2014). Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. Carcinogenesis, 35 (5), 1012-1019. doi: 10.1093/carcin/bgt404

Lindon eaves: The astonishing decade

Martin, Nick (2014). Lindon eaves: The astonishing decade. Behavior Genetics, 44 (3), 193-197. doi: 10.1007/s10519-013-9613-y

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

Davies, Matthew N., Krause, Lutz, Bell, Jordana T., Gao, Fei, Ward, Kirsten J., Wu, Honglong, Lu, Hanlin, Liu, Yuan, Tsai, Pei-Chein, Collier, David A., Murphy, Therese, Dempster, Emma, Mill, Jonathan, UK Brain Expression Consortium, Battle, Alexis, Mostafavi, Sara, Zhu, Xiaowei, Henders, Anjali, Byrne, Enda, Wray, Naomi R., Martin, Nicholas G., Spector, Tim D. and Wang, Jun (2014). Hypermethylation in the ZBTB20 gene is associated with major depressive disorder. Genome Biology, 15 (4) R56, R56.1-R56.12. doi: 10.1186/gb-2014-15-4-r56

A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations

Roussotte, Florence F., Jahanshad, Neda, Hibar, Derrek P., Sowell, Elizabeth R., Kohannim, Omid, Barysheva, Marina, Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Jack Jr, Clifford R., Weiner, Michael W., Thompson, Paul M. and ADNI (2014). A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations. Human Brain Mapping, 35 (4), 1226-1236. doi: 10.1002/hbm.22247

Comparing factor, class, and mixture models of cannabis initiation and DSM cannabis use disorder criteria, including craving, in the Brisbane longitudinal twin study

Kubarych, Thomas S., Kendler, Kenneth S., Aggen, Steven H., Estabrook, Ryne, Edwards, Alexis C., Clark, Shaunna L., Martin, Nicholas G., Hickie, Ian B., Neale, Michael C. and Gillespie, Nathan A. (2014). Comparing factor, class, and mixture models of cannabis initiation and DSM cannabis use disorder criteria, including craving, in the Brisbane longitudinal twin study. Twin Research and Human Genetics, 17 (2), 89-98. doi: 10.1017/thg.2014.9

Development of insula connectivity between ages 12 and 30 revealed by high angular resolution diffusion imaging

Dennis, Emily L., Jahanshad, Neda, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2014). Development of insula connectivity between ages 12 and 30 revealed by high angular resolution diffusion imaging. Human Brain Mapping, 35 (4), 1790-1800. doi: 10.1002/hbm.22292

Hepatitis C testing and status among opioid substitution treatment clients in New South Wales

Shand, Fiona L., Day, Carolyn, Rawlinson, William, Degenhardt, Louisa, Martin, Nicholas G. and Nelson, Elliot C. (2014). Hepatitis C testing and status among opioid substitution treatment clients in New South Wales. Australian and New Zealand Journal of Public Health, 38 (2), 160-164. doi: 10.1111/1753-6405.12173

Sex differences in magical ideation: A community-based twin study

Karcher, Nicole R., Slutske, Wendy S., Kerns, John G., Piasecki, Thomas M. and Martin, Nicholas G. (2014). Sex differences in magical ideation: A community-based twin study. Personality Disorders-Theory Research and Treatment, 5 (2), 212-219. doi: 10.1037/per0000040

Sleep spindles and rapid eye movement sleep as predictors of next morning cognitive performance in healthy middle-aged and older participants

Lafortune, Marjolaine, Gagnon, Jean-Francois, Martin, Nicolas, Latreille, Veronique, Dube, Jonathan, Bouchard, Maude, Bastien, Celyne and Carrier, Julie (2014). Sleep spindles and rapid eye movement sleep as predictors of next morning cognitive performance in healthy middle-aged and older participants. Journal of Sleep Research, 23 (2), 159-167. doi: 10.1111/jsr.12108

Telomere length in circulating leukocytes is associated with lung function and disease

Albrecht, Eva, Sillanpaa, Elina, Karrasch, Stefan, Alves, Alexessander Couto, Codd, Veryan, Hovatta, Iiris, Buxton, Jessica L., Nelson, Christopher P., Broer, Linda, Hagg, Sara, Mangino, Massimo, Willemsen, Gonneke, Surakka, Ida, Ferreira, Manuel A. R., Amin, Najaf, Oostra, Ben A., Backmand, Hell M., Peltonen, Markku, Sarna, Seppo, Rantanen, Taina, Sipila, Sarianna, Korhonen, Tellervo, Madden, Pamela A. F., Gieger, Christian, Jorres, Rudolf A., Heinrich, Joachim, Behr, Juergen, Huber, Rudolf M., Peters, Annette ... Schulz, Holger (2014). Telomere length in circulating leukocytes is associated with lung function and disease. European Respiratory Journal, 43 (4), 983-992. doi: 10.1183/09031936.00046213

Genome-wide association study reveals two new risk loci for bipolar disorder

Muehleisen, Thomas W., Leber, Markus, Schulze, Thomas G., Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Forstner, Andreas J., Schumacher, Johannes, Breuer, Rene, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, Andre, Witt, Stephanie H., Reif, Andreas, Mueller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Priebe, Lutz, Czerski, Piotr M., Hauser, Joanna ... Cichon, Sven (2014). Genome-wide association study reveals two new risk loci for bipolar disorder. Nature Communications, 5 (3339) 3339, 1-8. doi: 10.1038/ncomms4339

ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins

De Alwis, Duneesha, Agrawal, Arpana, Reiersen, Angela M., Constantino, John N., Henders, Anjali, Martin, Nicholas G. and Lynskey, Michael T. (2014). ADHD symptoms, autistic traits, and substance use and misuse in adult Australian twins. Journal of Studies On Alcohol and Drugs, 75 (2), 211-221. doi: 10.15288/jsad.2014.75.211

Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis

Fede, Giuseppe, Spadaro, Luisa, Tomaselli, Tania, Privitera, Graziella, Scicali, Roberto, Vasianopoulou, Panayota, Thalassinos, Evangelos, Martin, Nicholas, Thomas, Michael, Purrello, Francesco and Burroughs, Andrew Kenneth (2014). Comparison of total cortisol, free cortisol, and surrogate markers of free cortisol in diagnosis of adrenal insufficiency in patients with stable cirrhosis. Clinical Gastroenterology and Hepatology, 12 (3), 504-512. doi: 10.1016/j.cgh.2013.08.028

Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences

Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2014). Genetic and environmental influences on the ages of drinking and gambling initiation: evidence for distinct aetiologies and sex differences. Addiction, 109 (2), 323-331. doi: 10.1111/add.12310

Genetic effects on the cerebellar role in working memory: same brain, different genes?

Blokland, Gabriëlla A. M., McMahon, Katie L., Thompson, Paul M., Hickie, Ian B., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2014). Genetic effects on the cerebellar role in working memory: same brain, different genes?. NeuroImage, 86, 392-403. doi: 10.1016/j.neuroimage.2013.10.006

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

Ligthart, Lannie, Hottenga, Jouke-Jan, Lewis, Cathryn M., Farmer, Anne E., Craig, Ian W., Breen, Gerome, Willemsen, Gonneke, Vink, Jacqueline M., Middeldorp, Christel M., Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W., Martin, Nicholas G., Penninx, Brenda W. J. H., McGuffin, Peter, Boomsma, Dorret I. and Nyholt, Dale R. (2014). Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders. Human Genetics, 133 (2), 173-186. doi: 10.1007/s00439-013-1370-8

Modeling of the hemodynamic responses in block design fMRI studies

Shan, Zuyao Y., Wright, Margaret J., Thompson, Paul M., McMahon, Katie L., Blokland, Gabriella G. A. M., de Zubicaray, Greig I., Martin, Nicholas G., Vinkhuyzen, Anna A. E. and Reutens, David C. (2014). Modeling of the hemodynamic responses in block design fMRI studies. Journal of Cerebral Blood Flow and Metabolism, 34 (2), 316-324. doi: 10.1038/jcbfm.2013.200

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013)

Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, Rene C., Nichols, Thomas E., Almasy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Pol, Hilleke E. Hulshoff, Bastin, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2014). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA-DTI working group (vol 81, pg 455, 2013). Neuroimage, 90, 470-471. doi: 10.1016/j.neuroimage.2013.12.053

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins

Hill, W. D., Davies, G., Van De Lagemaat, L. N., Christoforou, A., Marioni, R. E., Fernandes, C. P. D., Liewald, D. C., Croning, M. D. R., Payton, A., Craig, L. C. A., Whalley, L. J., Horan, M., Ollier, W., Hansell, N. K., Wright, M. J., Martin, N. G., Montgomery, G. W., Steen, V. M., Le Hellard, S., Espeseth, T., Lundervold, A. J., Reinvang, I., Starr, J. M., Pendleton, N., Grant, S. G. N., Bates, T. C. and Deary, I. J. (2014). Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. Translational Psychiatry, 4 (1) e341, 1-8. doi: 10.1038/tp.2013.114

DNA modification study of major depressive disorder: beyond locus-by-locus comparisons

Oh, Gabriel, Wang, Sun-Chong, Pal, Mrinal, Chen, Zheng Fei, Khare, Tarang, Tochigi, Mamoru, Ng, Catherine, Yang, Yeqing A., Kwan, Andrew, Kaminsky, Zachary A., Mill, Jonathan, Gunasinghe, Cerisse, Tackett, Jennifer L., Gottesman, Irving I., Willemsen, Gonneke, de Geus, Eco J. C., Vink, Jacqueline M., Slagboom, P. Eline, Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Turecki, Gustavo, Martin, Nicholas G., Boomsma, Dorret I., McGuffin, Peter, Kustra, Rafal and Petronis, Art (2014). DNA modification study of major depressive disorder: beyond locus-by-locus comparisons. Biological Psychiatry, 77 (3), 246-255. doi: 10.1016/j.biopsych.2014.06.016

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

Li, M., Luo, X-j, Rietschel, M., Lewis, C. M., Mattheisen, M., Mueller-Myhsok, B., Jamain, S., Leboyer, M., Landen, M., Thompson, P. M., Cichon, S., Noethen, M. M., Schulze, T. G., Sullivan, P. F., Bergen, S. E., Donohoe, G., Morris, D. W., Hargreaves, A., Gill, M., Corvin, A., Hultman, C., Toga, A. W., Shi, L., Lin, Q., Shi, H., Gan, L., Meyer-Lindenberg, A., Czamara, D., Henry, C. ... Su, B. (2014). Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4), 452-461. doi: 10.1038/mp.2013.37

Association of OPRD1 polymorphisms with heroin dependence in a large case-control series

Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2014). Association of OPRD1 polymorphisms with heroin dependence in a large case-control series. Addiction Biology, 19 (1), 111-121. doi: 10.1111/j.1369-1600.2012.00445.x

Automatic clustering and population analysis of white matter tracts using maximum density paths

Prasad, Gautam, Joshi, Shantanu H., Jahanshad, Neda, Villalon-Reina, Julio, Aganj, Iman, Lenglet, Christophe, Guillermo Sapiro, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2014). Automatic clustering and population analysis of white matter tracts using maximum density paths. NeuroImage, 97, 284-295. doi: 10.1016/j.neuroimage.2014.04.033

Common variant at 16p11.2 conferring risk of psychosis

Steinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., Pietilainen, O. P. H., Lin, K., Papiol, S., Huttenlocher, J., Sigurdsson, E., Vassos, E., Giegling, I., Breuer, R., Fraser, G., Walker, N., Melle, I., Djurovic, S., Agartz, I., Tuulio-Henriksson, A., Suvisaari, J., Lonnqvist, J., Paunio, T., Olsen, L., Hansen, T., Ingason, A., Pirinen, M., Strengman, E., Hougaard, D. M. ... Stefansson, K. (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1), 108-114. doi: 10.1038/mp.2012.157

Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis

Painter, Jodie N., Nyholt, Dale R, Krause, Lutz, Zhao, Zhen Z., Chapman, Brett, Zhang, Christine, Medland, Sarah, Martin, Nicholas G., Kennedy, Stephen, Treloar, Susan, Zondervan, Krina and Montgomery, Grant W. (2014). Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertility and Sterility, 102 (2), 496-502.e5. doi: 10.1016/j.fertnstert.2014.04.015

Genetic factors that increase male facial masculinity decrease facial attractiveness of female relatives

Lee, Anthony J., Mitchem, Dorian G., Wright, Margaret J., Martin, Nicholas G., Keller, Matthew C. and Zietsch, Brendan P. (2014). Genetic factors that increase male facial masculinity decrease facial attractiveness of female relatives. Psychological Science, 25 (2), 476-484. doi: 10.1177/0956797613510724

Genetic predisposition to schizophrenia associated with increased use of cannabis

Power, R. A., Verweij, K. J. H., Zuhair, M., Montgomery, G. W., Henders, A. K., Heath, A. C., Madden, P. A. F., Medland, S. E., Wray, N. R. and Martin, N. G. (2014). Genetic predisposition to schizophrenia associated with increased use of cannabis. Molecular Psychiatry, 19 (11), 1201-1204. doi: 10.1038/mp.2014.51

Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample

Loukola, A., Wedenoja, J., Keskitalo-Vuokko, K., Broms, U., Korhonen, T., Ripatti, S., Sarin, A-P, Pitkaniemi, J., He, L., Happola, A., Heikkila, K., Chou, Y-L, Pergadia, M. L., Heath, A. C., Montgomery, G. W., Martin, N. G., Madden, P. A. F. and Kaprio, J. (2014). Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample. Molecular Psychiatry, 19 (5), 615-624. doi: 10.1038/mp.2013.72

Heritability of head motion during resting state functional MRI in 462 healthy twins

Couvy-Duchesne, Baptiste, Blokland, Gabriëlla A.M., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2014). Heritability of head motion during resting state functional MRI in 462 healthy twins. Neuroimage, 102 (2), 424-434. doi: 10.1016/j.neuroimage.2014.08.010

Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index

Hoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J.H., Teumer, A., Winkler, T. W., Tsernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Mace, A., Rueger, S., Bochud, P.-Y., Barcella, M., Dauvilliers, Y., Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S. ... Kutalik Z. (2014). Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index. PLoS Genetics, 10 (7) e1004508, 1-12. doi: 10.1371/journal.pgen.1004508

POT1 loss-of-function variants predispose to familial melanoma

Robles-Espinoza, Carla Daniela, Harland, Mark, Ramsay, Andrew J, Aoude, Lauren G, Quesada, Víctor, Ding, Zhihao, Pooley, Karen A, Pritchard, Antonia L, Tiffen, Jessamy C, Petljak, Mia, Palmer, Jane M, Symmons, Judith, Johansson, Peter, Stark, Mitchell S., Gartside, Michael G, Snowden, Helen, Montgomery, Grant W, Martin, Nicholas G, Liu, Jimmy Z, Choi, Jiyeon, Makowski, Matthew, Brown, Kevin M, Dunning, Alison M, Keane, Thomas M, Lopez-Otin, Carlos, Gruis, Nelleke A, Hayward, Nicholas K, Bishop, D Timothy, Newton-Bishop, Julia A and Adams, David J (2014). POT1 loss-of-function variants predispose to familial melanoma. Nature Genetics, 46 (5), 478-481. doi: 10.1038/ng.2947

Parental separation and early substance involvement: results from children of alcoholic and cannabis dependent twins

Waldron, Mary, Grant, Julia D., Bucholz, Kathleen K., Lynskey, Michael T., Slutske, Wendy S., Glowinski, Anne L., Henders, Anjali, Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2014). Parental separation and early substance involvement: results from children of alcoholic and cannabis dependent twins. Drug and Alcohol Dependence, 134 (1), 78-84. doi: 10.1016/j.drugalcdep.2013.09.010

Sexual orientation, prejudice, and segregation

Plug, Erik, Webbink, Dinand and Martin, Nick (2014). Sexual orientation, prejudice, and segregation. Journal of Labor Economics, 32 (1), 123-159. doi: 10.1086/673315

Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin design

Deutsch, Arielle R., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2014). Substance use and sexual intercourse onsets in adolescence: A genetically informative discordant twin design. Journal of Adolescent Health, 54 (1), 114-116. doi: 10.1016/j.jadohealth.2013.07.013

Testing the role of circadian genes in conferring risk for psychiatric disorders

Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G. and Wray, Naomi R. (2014). Testing the role of circadian genes in conferring risk for psychiatric disorders. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 165 (3), 254-260. doi: 10.1002/ajmg.b.32230

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

Ferreira, Manuel A. R., Matheson, Melanie C., Tang, Clara S., Granell, Raquel, Ang, Wei., Hui, Jennie, Kiefer, Amy K., Duffy, David L., Baltic, Svetlana, Danoy, Patrick, Bui, Minh, Price, Loren, Sly, Peter D., Eriksson, Nicholas, Madden, Pamela A., Abraham, Michael J. A., Holt, Patrick G., Heath, p Andrew C., Hunter, Michael, Musk, Bill, Robertson, Colin F., Le Souef, Peter, Montgomery, Grant W., Henderson, A. John, Tung, Joyce Y., Dharmage, Shyamali C., Brown, Matthew A., James, Alan, Thompson, Philip J. ... Australian Asthma Genetics Consortium Collaborators (2013). Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. Journal of Allergy And Clinical Immunology, 133 (6), 1564-1571. doi: 10.1016/j.jaci.2013.10.030

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

Stephens, Sarah H., Hartz, Sarah M., Hoft, Nicole R., Saccone, Nancy L., Corley, Robin C., Hewitt, John K., Hopfer, Christian J., Breslau, Naomi, Coon, Hilary, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Han, Younghun, Hansel, Nadia N., Jiang, Chenhui, Korhonen, Tellervo, Lind, Penelope A., Liu, Jason, Lyytikaeinen, Leo-Pekka, Michel, Martha, Shaffer, John R., Short, Susan E., Sun, Juzhong, Teumer, Alexander, Thompson, John R., Vogelzangs, Nicole, Vink, Jacqueline M. ... Ehringer, Marissa A. (2013). Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. Genetic Epidemiology, 37 (8), 846-859. doi: 10.1002/gepi.21760

Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study

Wang, Jiping, Carvajal-Carmona, Luis G., Chu, Jen-Hwa, Zauber, Ann G., Kubo, Michikai, Matsuda, Koichi, Dunlop, Malcolm, Houlston, Richard S., Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Ratain, Mark J., Nakamura, Yusuke, Weiss, Scott T., Tomlinson, Ian and Bertagnolli, Monica M. (2013). Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study. Clinical Cancer Research, 19 (23), 6430-6437. doi: 10.1158/1078-0432.CCR-13-0550

Is the relationship between early-onset cannabis use and educational attainment causal or due to common liability?

Verweij, Karin J. H., Huizink, Anja C., Agrawal, Arpana, Martin, Nicholas G. and Lynskey, Michael T. (2013). Is the relationship between early-onset cannabis use and educational attainment causal or due to common liability?. Drug and Alcohol Dependence, 133 (2), 580-586. doi: 10.1016/j.drugalcdep.2013.07.034

Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults

Braskie, Meredith N., Kohannim, Omid, Jahanshad, Neda, Chiang, Ming-Chang, Barysheva, Marina, Toga, Arthur W., Ringman, John M., Montgomery, Grant W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Relation between variants in the neurotrophin receptor gene, NTRK3, and white matter integrity in healthy young adults. Neuroimage, 82, 146-153. doi: 10.1016/j.neuroimage.2013.05.095

Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism

Mitchem, Dorian G., Purkey, Alicia M., Grebe, Nicholas M., Carey, Gregory, Garver-Apgar, Christine E., Bates, Timothy C., Arden, Rosalind, Hewitt, John K., Medland, Sarah E., Martin, Nicholas G., Zietsch, Brendan P. and Keller, Matthew C. (2013). Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism. Behavior Genetics, 44 (3), 270-281. doi: 10.1007/s10519-013-9627-5

A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53

Wang, J-C, Foroud, T., Hinrichs, A. L., Le, N. X. H., Bertelsen, S., Budde, J. P., Harari, O., Koller, D. L., Wetherill, L., Agrawal, A., Almasy, L., Brooks, A. I., Bucholz, K., Dick, D., Hesselbrock, V., Johnson, E. O., Kang, S., Kapoor, M., Kramer, J., Kuperman, S., Madden, P. A. F., Manz, N., Martin, N. G., McClintick, J. N., Montgomery, G. W., Nurnberger, J. I., Rangaswamy, M., Rice, J., Schuckit, M. ... Goate, A. M. (2013). A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry, 18 (11), 1218-1224. doi: 10.1038/mp.2012.143

Are bottom-up and top-down traits in dual-systems models of risky behavior genetically distinct?

Ellingson, Jarrod M., Verges, Alvaro, Littlefield, Andrew K., Martin, Nicholas G. and Slutske, Wendy S. (2013). Are bottom-up and top-down traits in dual-systems models of risky behavior genetically distinct?. Behavior Genetics, 43 (6), 480-490. doi: 10.1007/s10519-013-9615-9

Common variants associated with plasma triglycerides and risk for coronary artery disease

Do, Ron, Willer, Cristen J., Schmidt, Ellen M., Sengupta, Sebanti, Gao, Chi, Peloso, Gina M., Gustafsson, Stefan, Kanoni, Stavroula, Ganna, Andrea, Chen, Jin, Buchkovich, Martin L., Mora, Samia, Beckmann, Jacques S., Bragg-Gresham, Jennifer L., Chang, Hsing-Yi, Demirkan, Ayse, Den Hertog, Heleen M., Donnelly, Louise A., Ehret, Georg B., Esko, Tonu, Feitosa, Mary F., Ferreira, Teresa, Fischer, Krista, Fontanillas, Pierre, Fraser, Ross M., Freitag, Daniel F., Gurdasani, Deepti, Heikkila, Kauko, Hyppoenen, Elina ... Kathiresan, Sekar (2013). Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics, 45 (11), 1345-1352. doi: 10.1038/ng.2795

Discovery and refinement of loci associated with lipid levels

Willer C.J., Schmidt E.M., Sengupta S., Peloso G.M., Gustafsson S., Kanoni S., Ganna A., Chen J., Buchkovich M.L., Mora S., Beckmann J.S., Bragg-Gresham J.L., Chang H.-Y., Demirkan A., Den Hertog H.M., Do R., Donnelly L.A., Ehret G.B., Esko T., Feitosa M.F., Ferreira T., Fischer K., Fontanillas P., Fraser R.M., Freitag D.F., Gurdasani D., Heikkila K., Hypponen E., Isaacs A. ... Abecasis G.R. (2013). Discovery and refinement of loci associated with lipid levels. Nature Genetics, 45 (11), 1274-1285. doi: 10.1038/ng.2797

Genetic and environmental contributions to sleep-wake behavior in 12-year-old twins

Sletten, Tracey L., Rajaratnam, Shantha M. W., Wright, Margaret J., Zhu, Gu, Naismith, Sharon, Martin, Nicholas G. and Hickie, Ian (2013). Genetic and environmental contributions to sleep-wake behavior in 12-year-old twins. Sleep, 36 (11), 1715-1722. doi: 10.5665/sleep.3136

Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs

Hemani, Gibran, Yang, Jian, Vinkhuyzen, Anna, Powell, Joseph E., Willemsen, Gonneke, Hottenga, Jouke-Jan, Abdellaoui, Abdel, Mangino, Massimo, Valdes, Ana M., Medland, Sarah E., Madden, Pamela A., Heath, Andrew C., Henders, Anjali K., Nyholt, Dale R., de Geus, Eco J. C., Magnusson, Patrik K. E., Ingelsson, Erik, Montgomery, Grant W., Spector, Timothy D., Boomsma, Dorret I., Pedersen, Nancy L., Martin, Nicholas G. and Visscher, Peter M. (2013). Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics, 93 (5), 865-875. doi: 10.1016/j.ajhg.2013.10.005

Personality and occupational markers of 'solid citizenship' are associated with having fewer children

Perkins, Adam M., Cserjesi, Renata, Ettinger, Ulrich, Kumari, Veena, Martin, Nicholas G. and Arden, Rosalind (2013). Personality and occupational markers of 'solid citizenship' are associated with having fewer children. Personality and Individual Differences, 55 (8), 871-876. doi: 10.1016/j.paid.2013.07.011

Toward the development of a global induced pluripotent stem cell library

Turner, Marc, Leslie, Stephen, Martin, Nicholas G., Peschanski, Marc, Rao, Mahendra, Taylor, Craig J., Trounson, Alan, Turner, David, Yamanaka, Shinya and Wilmut, Ian (2013). Toward the development of a global induced pluripotent stem cell library. Cell Stem Cell, 13 (4), 382-384. doi: 10.1016/j.stem.2013.08.003

A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk

Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013). A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 (7), 441-446. doi: 10.1038/gene.2013.38

A twin study of alcohol dependence, binge eating, and compensatory behaviors

Munn-Chernoff, Melissa A., Duncan, Alexis E., Grant, Julia D., Wade, Tracey D., Agrawal, Arpana, Bucholz, Kathleen K., Madden, Pamela A. F., Martin, Nicholas G. and Heath, Andrew C. (2013). A twin study of alcohol dependence, binge eating, and compensatory behaviors. Journal of Studies On Alcohol and Drugs, 74 (5), 664-673. doi: 10.15288/jsad.2013.74.664

Causal influence of age at first drink on alcohol involvement in adulthood and its moderation by familial context

Deutsch, Arielle R., Slutske, Wendy S., Richmond-Rakerd, Leah S., Chernyavskiy, Pavel, Heath, Andrew C. and Martin, Nicholas G. (2013). Causal influence of age at first drink on alcohol involvement in adulthood and its moderation by familial context. Journal of Studies On Alcohol and Drugs, 74 (5), 703-713. doi: 10.15288/jsad.2013.74.703

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. Hong, Ripke, Stephan, Neale, Benjamin M., Faraone, Stephen V., Purcell, Shaun M., Perlis, Roy H., Mowry, Bryan J., Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas ... Wray, Naomi R. (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45 (9), 984-995. doi: 10.1038/ng.2711

Genetic variants associated with disordered eating

Wade, Tracey D., Gordon, Scott, Medland, Sarah, Bulik, Cynthia M., Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2013). Genetic variants associated with disordered eating. International Journal of Eating Disorders, 46 (6), 594-608. doi: 10.1002/eat.22133

A genetic perspective on the proposed inclusion of cannabis withdrawal in DSM-5

Verweij, K. J. H., Agrawal, A., Nat, N. O., Creemers, H. E., Huizink, A. C., Martin, N. G. and Lynskey, M. T. (2013). A genetic perspective on the proposed inclusion of cannabis withdrawal in DSM-5. Psychological Medicine, 43 (8), 1713-1722. doi: 10.1017/S0033291712002735

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

Fernández-Rhodes, Lindsay, Demerath, Ellen W., Cousminer, Diana L., Tao, Ran, Dreyfus, Jill G., Esko, Tõnu, Smith, Albert V., Gudnason, Vilmundur, Harris, Tamara B., Launer, Lenore, McArdle, Patrick F., Yerges-Armstrong, Laura M., Elks, Cathy E., Strachan, David P., Kutalik, Zoltán, Vollenweider, Peter, Feenstra, Bjarke, Boyd, Heather A., Metspalu, Andres, Mihailov, Evelin, Broer, Linda, Zillikens, M. Carola, Oostra, Ben, van Duijn, Cornelia M., Lunetta, Kathryn L., Perry, John R. B., Murray, Anna, Koller, Daniel L., Lai, Dongbing ... Franceschini, Nora (2013). Association of adiposity genetic variants with menarche timing in 92,105 women of European descent. American Journal of Epidemiology, 178 (3), 451-460. doi: 10.1093/aje/kws473

GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association

Rentería, Miguel E., Coolen, Marcel W., Statham, Aaron L., Choi, R. Seong Min, Qu, Wenjia, Campbell, Megan J., Smith, Sara, Henders, Anjali K., Montgomery, Grant W., Clark, Susan J., Martin, Nicholas G. and Medland, Sarah E. (2013). GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. Twin Research and Human Genetics, 16 (4), 767-781. doi: 10.1017/thg.2013.30

Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization

Bønnelykke, Klaus, Matheson, Melanie C., Pers, Tune H., Granell, Raquel, Strachan, David P., Alves, Alexessander Couto, Linneberg, Allan, Curtin, John A., Warrington, Nicole M., Standl, Marie, Kerkhof, Marjan, Jonsdottir, Ingileif, Bukvic, Blazenka K., Kaakinen, Marika, Sleimann, Patrick, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Schramm, Katharina, Baltic, Svetlana, Kreiner-Møller, Eskil, Simpson, Angela, St Pourcain, Beate, Coin, Lachlan, Hui, Jennie, Walters, Eugene H., Tiesler, Carla M. T., Duffy, David L., Jones, Graham, Ring, Susan M. ... Brown, Matthew A. (2013). Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Nature Genetics, 45 (8), 902-906. doi: 10.1038/ng.2694

The nature and nurture of high IQ: an extended sensitive period for intellectual development

Brant, Angela M., Munakata, Yuko, Boomsma, Dorret I., DeFries, John C., Haworth, Claire M. A., Keller, Matthew C., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J., Wright, Margaret J. and Hewitt, John K. (2013). The nature and nurture of high IQ: an extended sensitive period for intellectual development. Psychological Science, 24 (8), 1487-1495. doi: 10.1177/0956797612473119

No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia

Heilmann, S., Nyholt, D. R., Brockschmidt, F. F., Hillmer, A. M., Herold, C., Becker, T., Martin, N. G. and Noethen, M. M. (2013). No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia. British Journal of Dermatology, 169 (1), 222-224. doi: 10.1111/bjd.12292

Scrutiny of the CHRNA5-CHRNA3-CHRNB4 smoking behavior locus reveals a novel association with alcohol use in a Finnish population based study

Haefors, Jenni, Loukola, Anu, Pitkaeemi, Janne, Broms, Ulla, Maennistoe, Satu, Salomaa, Veikko, Helioevaara, Markku, Lehtimaeki, Terho, Raitakari, Olli, Madden, Pamela A. F., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Korhonen, Tellervo and Kaprio, Jaakko (2013). Scrutiny of the CHRNA5-CHRNA3-CHRNB4 smoking behavior locus reveals a novel association with alcohol use in a Finnish population based study. International Journal of Molecular Epidemiology and Genetics, 4 (2), 109-119.

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

Fall, Tove, Hägg, Sara, Maegi, Reedik, Ploner, Alexander, Fischer, Krista, Horikoshi, Momoko, Sarin, Antti-Pekka, Thorleifsson, Gudmar, Ladenvall, Claes, Kals, Mart, Kuningas, Maris, Draisma, Harmen H. M., Ried, Janina S., van Zuydam, Natalie R., Huikari, Ville, Mangino, Massimo, Sonestedt, Emily, Benyamin, Beben, Nelson, Christopher P., Rivera, Natalia V., Kristiansson, Kati, Shen, Huei-yi, Havulinna, Aki S., Dehghan, Abbas, Donnelly, Louise A., Kaakinen, Marika, Nuotio, Marja-Liisa, Robertson, Neil, de Bruijn, Renee F. A. G. ... Prokopenko, Inga (2013). The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis. PLoS Medicine, 10 (6) e1001474, e1001474.1-e1001474.15. doi: 10.1371/journal.pmed.1001474

Genetic Loci for Retinal Arteriolar Microcirculation

Sim X., Jensen R.A., Ikram M.K., Cotch M.F., Li X., MacGregor S., Xie J., Smith A.V., Boerwinkle E., Mitchell P., Klein R., Klein B.E.K., Glazer N.L., Lumley T., McKnight B., Psaty B.M., de Jong P.T.V.M., Hofman A., Rivadeneira F., Uitterlinden A.G., van Duijn C.M., Aspelund T., Eiriksdottir G., Harris T.B., Jonasson F., Launer L.J., Attia J., Baird P.N., Harrap S. ... Wong T.Y. (2013). Genetic Loci for Retinal Arteriolar Microcirculation. PLoS ONE, 8 (6) e65804, e65804.1-e65804.12. doi: 10.1371/journal.pone.0065804

Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology

Heilmann, Stefanie, Kiefer, Amy K., Fricker, Nadine, Drichel, Dmitriy, Hillmer, Axel M., Herold, Christine, Tung, Joyce Y., Eriksson, Nicholas, Redler, Silke, Betz, Regina C., Li, Rui, Karason, Ari, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Dedoussis, George, Martin, Nicholas G., Kiemeney, Lambertus A., Mooser, Vincent, Stefansson, Kari, Richards, J. Brent, Becker, Tim, Brockschmidt, Felix F., Hinds, David A. and Noethen, Markus M. (2013). Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology. Journal of Investigative Dermatology, 133 (6), 1489-1496. doi: 10.1038/jid.2013.43

Effects of sibship size and composition on younger brothers' and sisters' alcohol use initiation: findings from an Australian twin sample

Richmond-Rakerd, Leah S., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2013). Effects of sibship size and composition on younger brothers' and sisters' alcohol use initiation: findings from an Australian twin sample. Alcoholism-Clinical and Experimental Research, 37 (6), 1016-1024. doi: 10.1111/acer.12052

GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

Rietveld, Cornelius A., Medland, Sarah E., Derringer, Jaime, Yang, Jian, Esko, Tonu, Martin, Nicolas W., Westra, Harm-Jan, Shakhbazov, Konstantin, Abdellaoui, Abdel, Agrawal, Arpana, Albrecht, Eva, Alizadeh, Behrooz Z., Amin, Najaf, Bamard, John, Baumeister, Sebastian E., Benke, Kelly S., Bielak, Lawrence F., Boatman, Jeffrey A., Boyle, Patricia A., Davies, Gail, De Leeuw, Christiaan, Eklund, Niina, Evans, Daniel S., Ferhmann, Rudolf, Fischer, Krista, Gieger, Christian, Gjessing, Hakon K., Haegg, Sara, Harris, Jennifer R. ... Koellinger, Philipp D. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340 (6139), 1467-1471. doi: 10.1126/science.1235488

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

den Hoed, Marcel, Eijgelsheim, Mark, Esko, Tonu, Brundel, Bianca J. J. M., Peal, David S., Evans, David M., Nolte, Ilja M., Segre, Ayellet V., Holm, Hilma, Handsaker, Robert E., Westra, Harm-Jan, Johnson, Toby, Isaacs, Aaron, Yang, Jian, Lundby, Alicia, Zhao, Jing Hua, Kim, Young Jin, Go, Min Jin, Almgren, Peter, Bochud, Murielle, Boucher, Gabrielle, Cornelis, Marilyn C., Gudbjartsson, Daniel, Hadley, David, van der Harst, Pim, Hayward, Caroline, den Heijer, Martin, Igl, Wilmar, Jackson, Anne U. ... Loos, Ruth J. F. (2013). Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics, 45 (6), 621-634. doi: 10.1038/ng.2610

Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin

Byrne, E. M., Carrillo-Roa, T., Henders, A. K., Bowdler, L., McRae, A. F., Heath, A. C., Martin, N. G., Montgomery, G. W., Krause, L. and Wray, N. R. (2013). Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin. Translational Psychiatry, 3 (6) e269, e269.1-e269.6. doi: 10.1038/tp.2013.45

Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

Randall, Joshua C., Winkler, Thomas W., Kutalik, Zoltan, Berndt, Sonja I., Jackson, Anne U., Monda, Keri L., Kilpelaeinen, Tuomas O., Esko, Tonu, Maegi, Reedik, Li, Shengxu, Workalemahu, Tsegaselassie, Feitosa, Mary F., Croteau-Chonka, Damien C., Day, Felix R., Fall, Tove, Ferreira, Teresa, Gustafsson, Stefan, Locke, Adam E., Mathieson, Iain, Scherag, Andre, Vedantam, Sailaja, Wood, Andrew R., Liang, Liming, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Dermitzakis, Emmanouil T., Dimas, Antigone S., Karpe, Fredrik, Min, Josine L. ... MAGIC Investigators (2013). Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. Plos Genetics, 9 (6) e1003500, e1003500.1-e1003500.19. doi: 10.1371/journal.pgen.1003500

The general factor of personality and humor styles

Schermer, Julie Aitken, Martin, Rod A., Martin, Nicholas G., Lynskey, Michael and Vernon, Philip A. (2013). The general factor of personality and humor styles. Personality and Individual Differences, 54 (8), 890-893. doi: 10.1016/j.paid.2012.12.026

A genome-wide association study of sleep habits and insomnia

Byrne, Enda M., Gehrman, Philip R., Medland, Sarah E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Hickie, Ian B., Van Duijn, Cornelia M., Henders, Anjali K., Montgomery, Grant W., Martin, Nicholas G., Wray, Naomi R. and The Chronogen Consortium (2013). A genome-wide association study of sleep habits and insomnia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162 (5), 439-451. doi: 10.1002/ajmg.b.32168

Genome-wide association study identifies loci affecting blood copper, selenium and zinc.

Evans, David M., Zhu, Gu, Dy, Veronica, Heath, Andrew C., Madden, Pamela A. F., Kemp, John P., McMahon, George, St Pourcain, Beate, Timpson, Nicholas J., Golding, Jean, Lawlor, Debbie A., Steer, Colin, Montgomery, Grant W., Martin, Nicholas G, Smith, George Davey and Whitfield, John B. (2013). Genome-wide association study identifies loci affecting blood copper, selenium and zinc.. Human Molecular Genetics, 22 (19), 3998-4006. doi: 10.1093/hmg/ddt239

Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data

Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W. and Visscher, Peter M. (2013). Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9 (5) e1003502, e1003502.1-e1003502.10. doi: 10.1371/journal.pgen.1003502

Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012)

Verweij, K. J. H., Yang, J., Lahti, J., Veijola, J., Hintsanen, M., Pulkki-Raback, L., Heinonen, K., Pouta, A., Pesonen, A. -K., Widen, E., Taanila, A., Isohanni, M., Miettunen, J., Palotie, A., Penke, L., Service, S. K., Heath, A. C., Montgomery, G. W., Raitakari, O., Kaehoenen, M., Viikari, J., Raeikkoenen, K., Eriksson, J. G., Keltikangas-Jaervinen, L., Lehtimaeki, T., Martin, N. G., Jaervelin, M. -R., Visscher, P. M., Keller, M. C. and Zietsch, B. P. (2013). Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012). Evolution, 67 (5), 1537-1537. doi: 10.1111/evo.12095

First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip

Keating, Brendan, Bansal, Aruna T., Walsh, Susan, Millman, Jonathan, Newman, Jonathan, Kidd, Kenneth, Budowle, Bruce, Eisenberg, Arthur, Donfack, Joseph, Gasparini, Paolo, Budimlija, Zoran, Henders, Anjali K., Chandrupatla, Hareesh, Duffy, David L., Gordon, Scott D., Hysi, Pirro, Liu, Fan, Medland, Sarah E., Rubin, Laurence, Martin, Nicholas G., Spector, Timothy D. and Kayser, Manfred (2013). First all-in-one diagnostic tool for DNA intelligence: genome-wide inference of biogeographic ancestry, appearance, relatedness, and sex with the Identitas v1 Forensic Chip. International Journal of Legal Medicine, 127 (3), 559-572. doi: 10.1007/s00414-012-0788-1

Genome-wide association study of a quantitative disordered gambling trait

Lind, Penelope A., Zhu, Gu, Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2013). Genome-wide association study of a quantitative disordered gambling trait. Addiction Biology, 18 (3), 511-522. doi: 10.1111/j.1369-1600.2012.00463.x

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Berndt, Sonja I., Gustafsson, Stefan, Maegi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, Tonu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian'an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W., Wood, Andrew R., Workalemahu, Tsegaselassie, Hu, Yi-Juan, Lee, Sang Hong, Liang, Liming, Lin, Dan-Yu, Min, Josine L., Neale, Benjamin M., Thorleifsson, Gudmar ... Ingelsson, Erik (2013). Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45 (5), 501-U69. doi: 10.1038/ng.2606

Genotype by environment interactions in cognitive ability: a survey of 14 studies from four countries covering four age groups

Molenaar, Dylan, van der Sluis, Sophie, Boomsma, Dorret I., Haworth, Claire M. A., Hewitt, John K., Martin, Nicholas G., Plomin, Robert, Wright, Margaret J. and Dolan, Conor V. (2013). Genotype by environment interactions in cognitive ability: a survey of 14 studies from four countries covering four age groups. Behavior Genetics, 43 (3), 208-219. doi: 10.1007/s10519-012-9581-7

Investigating the influence of prenatal androgen exposure and sibling effects on alcohol use and alcohol use disorder in females from opposite-sex twin pairs

Ellingson, Jarrod M., Slutske, Wendy S., Richmond-Rakerd, Leah S. and Martin, Nicholas G. (2013). Investigating the influence of prenatal androgen exposure and sibling effects on alcohol use and alcohol use disorder in females from opposite-sex twin pairs. Alcoholism-Clinical and Experimental Research, 37 (5), 868-876. doi: 10.1111/acer.12035

No association between general cognitive ability and rare copy number variation

McRae, Allan F., Wright, Margaret J., Hansell, Narelle K., Montgomery, Grant W. and Martin, Nicholas G. (2013). No association between general cognitive ability and rare copy number variation. Behavior Genetics, 43 (3), 202-207. doi: 10.1007/s10519-013-9587-9

A mega-analysis of genome-wide association studies for major depressive disorder

Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Wray, Naomi, Byrne, Enda M., Martin, Nicholas G., Gordon, Scott D., Henders, Anjali K., Montgomery, Grant M., Nyholt, Dale R. and Middeldorp, Christel M. (2013). A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18 (4), 497-511. doi: 10.1038/mp.2012.21

General and supplementary factors of personality in genetic and environmental correlation matrices

Loehlin, John C. and Martin, Nicholas G. (2013). General and supplementary factors of personality in genetic and environmental correlation matrices. Personality and Individual Differences, 54 (6), 761-766. doi: 10.1016/j.paid.2012.12.014

Metabolic and biochemical effects of low-to-moderate alcohol consumption

Whitfield, John B., Heath, Andrew C., Madden, Pamela A. F., Pergadia, Michele L., Montgomery, Grant W. and Martin, Nicholas G. (2013). Metabolic and biochemical effects of low-to-moderate alcohol consumption. Alcoholism: Clinical and Experimental Research, 37 (4), 575-586. doi: 10.1111/acer.12015

Shared genetic vulnerability for disordered gambling and alcohol use disorder in men and women: evidence from a national community-based Australian twin study

Slutske, Wendy S., Ellingson, Jarrod M., Richmond-Rakerd, Leah S., Zhu, Gu and Martin, Nicholas G. (2013). Shared genetic vulnerability for disordered gambling and alcohol use disorder in men and women: evidence from a national community-based Australian twin study. Twin Research and Human Genetics, 16 (2), 525-534. doi: 10.1017/thg.2013.11

The effect of schooling on problem drinking: evidence from Australian twins

Zubanov, N., Webbink, H. D. and Martin, N. G. (2013). The effect of schooling on problem drinking: evidence from Australian twins. Applied Economics, 45 (12), 1583-1599. doi: 10.1080/00036846.2011.631897

The genetic correlation between height and IQ: shared genes or assortative mating?

Keller, Matthew C., Garver-Apgar, Christine E., Wright, Margaret J., Martin, Nicholas G., Corley, Robin P., Stallings, Michael C., Hewitt, John K. and Zietsch, Brendan P. (2013). The genetic correlation between height and IQ: shared genes or assortative mating?. PLoS Genetics, 9 (4) e1003451, e1003451.1-e1003451.10. doi: 10.1371/journal.pgen.1003451

Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

Jahanshad, Neda, Rajagopalan, Priya, Hua, Xue, Hibar, Derrek P., Nir, Talia M., Toga, Arthur W., Jack, Jr, Clifford R., Saykin, Andrew J., Green, Robert C., Weiner, Michael W., Medland, Sarah E., Montgomery, Grant W., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2013). Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. Proceedings of the National Academy of Sciences of the United States of America, 110 (12), 4768-4773. doi: 10.1073/pnas.1216206110

Correction: Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA (PLoS ONE)

Ramasamy, Adaikalavan, Kuokkanen, Mikko, Vedantam, Sailaja, Gajdos, Zofia K., Alves, Alexessander Couto, Lyon, Helen N., Ferreira, Manuel A. R., Strachan, David P., Zhao, Jing Hua, Abramson, Michael J., Brown, Matthew A., Coin, Lachlan, Dharmage, Shyamali C., Duffy, David L., Haahtela, Tari, Heath, Andrew C., Janson, Christer, Kähönen, Mika, Khaw, Kay-Tee, Laitinen, Jaana, Souef, Peter Le, Lehtimäki, Terho, Madden, Pamela A. F., Marks, Guy B., Martin, Nicholas G., Matheson, Melanie C., Palmer, Cameron D., Palotie, Aarno, Pouta, Anneli ... Hirschhorn, Joel N. (2013). Correction: Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA (PLoS ONE). PLoS ONE, 8 (3), 1-1. doi: 10.1371/annotation/9630862b-4676-4b82-9869-8d8fbb2a2e65

ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure

Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Saccone, Nancy L., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2013). ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. JAMA Psychiatry, 70 (3), 325-333. doi: 10.1001/jamapsychiatry.2013.282

Do early experiences with cannabis vary in cigarette smokers?

Agrawal, Arpana, Madden, Pamela A. F., Martin, Nicholas G. and Lynskey, Michael T. (2013). Do early experiences with cannabis vary in cigarette smokers?. Drug and Alcohol Dependence, 128 (3), 255-259. doi: 10.1016/j.drugalcdep.2012.09.002

Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls

Panagopoulos, Vassilis N., Trull, Timothy J., Glowinski, Anne L., Lynskey, Michael T., Heath, Andrew C., Agrawal, Arpana, Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Madden, Pamela A. F., Moore, Elizabeth, Degenhardt, Louisa, Martin, Nicholas G., Montgomery, Grant W. and Nelson, Elliot C. (2013). Examining the association of NRXN3 SNPs with borderline personality disorder phenotypes in heroin dependent cases and socio-economically disadvantaged controls. Drug and Alcohol Dependence, 128 (3), 187-193. doi: 10.1016/j.drugalcdep.2012.11.011

A study of changes in genetic and environmental influences on weight and shape concern across adolescence

Wade, Tracey D., Hansell, Narelle K., Crosby, Ross D., Bryant-Waugh, Rachel, Treasure, Janet, Nixon, Reginald, Byrne, Susan and Martin, Nicholas G. (2013). A study of changes in genetic and environmental influences on weight and shape concern across adolescence. Journal of Abnormal Psychology, 122 (1), 119-130. doi: 10.1037/a0030290

Genetic overlap between personality and risk for disordered gambling: evidence from a national community-based Australian twin study

Slutske, Wendy S., Cho, Seung Bin, Piasecki, Thomas M. and Martin, Nicholas G. (2013). Genetic overlap between personality and risk for disordered gambling: evidence from a national community-based Australian twin study. Journal of Abnormal Psychology, 122 (1), 250-255. doi: 10.1037/a0029999

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Koettgen, Anna, Albrecht, Eva, Teumer, Alexander, Vitart, Veronique, Krumsiek, Jan, Hundertmark, Claudia, Pistis, Giorgio, Ruggiero, Daniela, O'Seaghdha, Conall M., Haller, Toomas, Yang, Qiong, Tanaka, Toshiko, Johnson, Andrew D., Kutalik, Zoltan, Smith, Albert V., Shi, Julia, Struchalin, Maksim, Middelberg, Rita P. S., Brown, Morris J., Gaffo, Angelo L., Pirastu, Nicola, Li, Guo, Hayward, Caroline, Zemunik, Tatijana, Huffman, Jennifer, Yengo, Loic, Zhao, Jing Hua, Demirkan, Ayse, Feitosa, Mary F. ... Gieger, Christian (2013). Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature Genetics, 45 (2), 145-154. doi: 10.1038/ng.2500

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Lu, Yi, Vitart, Veronique, Burdon, Kathryn P., Khor, Chiea Chuen, Bykhovskaya, Yelena, Mirshahi, Alireza, Hewitt, Alex W., Koehn, Demelza, Hysi, Pirro G., Ramdas, Wishal D., Zeller, Tanja, Vithana, Eranga N., Cornes, Belinda K., Tay, Wan-Ting, Tai, E. Shyong, Cheng, Ching-Yu, Liu, Jianjun, Foo, Jia-Nee, Saw, Seang Mei, Thorleifsson, Gudmar, Stefansson, Kari, Dimasi, David P., Mills, Richard A., Mountain, Jenny, Ang, Wei, Hoehn, Rene, Verhoeven, Virginie J. M., Grus, Franz, Wolfs, Roger ... Wong, Tien Y. (2013). Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics, 45 (2), 155-163. doi: 10.1038/ng.2506

Topography of age-related changes in sleep spindles

Martin, Nicolas, Lafortune, Marjolaine, Godbout, Jonathan, Barakat, Marc, Robillard, Rebecca, Poirier, Gaetan, Bastien, Celyne and Carrier, Julie (2013). Topography of age-related changes in sleep spindles. Neurobiology of Aging, 34 (2), 468-476. doi: 10.1016/j.neurobiolaging.2012.05.020

Why are criminals less educated than non-criminals? Evidence from a cohort of young Australian twins

Webbink, Dinand, Koning, Pierre, Vujić, Sunčica and Martin, Nicholas G. (2013). Why are criminals less educated than non-criminals? Evidence from a cohort of young Australian twins. Journal of Law Economics & Organization, 29 (1), 115-144. doi: 10.1093/jleo/ews014

A genome-wide association study for reading and language abilities in two population cohorts

Luciano, M., Evans, D. M., Hansell, N. K., Medland, S. E., Montgomery, G. W., Martin, N. G., Wright, M. J. and Bates, T. C. (2013). A genome-wide association study for reading and language abilities in two population cohorts. Genes, Brain and Behavior, 12 (6), 645-652. doi: 10.1111/gbb.12053

A variant in FTO shows association with melanoma risk not due to BMI

Iles M.M., Law M.H., Stacey S.N., Han J., Fang S., Pfeiffer R., Harland M., MacGregor S., Taylor J.C., Aben K.K., Akslen L.A., Avril M.-F., Azizi E., Bakker B., Benediktsdottir K.R., Bergman W., Scarra G.B., Brown K.M., Calista D., Chaudru V., Fargnoli M.C., Cust A.E., Demenais F., De Waal A.C., Debniak T., Elder D.E., Friedman E., Galan P., Ghiorzo P. ... Barrett J.H. (2013). A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics, 45 (4), 428-432. doi: 10.1038/ng.2571

Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy

Porter, J. B., Elalfy, M. S., Taher, A. T., Aydinok, Y., Chan, L. L., Lee, S. H., Sutcharitchan, P., Habr, D., Martin, N. and El-Beshlawy, A. (2013). Efficacy and safety of deferasirox at low and high iron burdens: results from the EPIC magnetic resonance imaging substudy. Annals of Hematology, 92 (2), 211-219. doi: 10.1007/s00277-012-1588-x

Genetic and nongenetic variation revealed for the principal components of human gene expression

Goldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013). Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 (3), 1117-1128. doi: 10.1534/genetics.113.153221

Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects

Hibar, Derrek P., Stein, Jason L., Ryles, April B., Kohannim, Omid, Jahanshad, Neda, Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Saykin, Andrew J., Jack, lifford R., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013). Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. Brain Imaging and Behavior, 7 (2), 102-115. doi: 10.1007/s11682-012-9199-7

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Garcia-Closas M., Couch F.J., Lindstrom S., Michailidou K., Schmidt M.K., Brook M.N., Orr N., Rhie S.K., Riboli E., Feigelson H.S., Le Marchand L., Buring J.E., Eccles D., Miron P., Fasching P.A., Brauch H., Chang-Claude J., Carpenter J., Godwin A.K., Nevanlinna H., Giles G.G., Cox A., Hopper J.L., Bolla M.K., Wang Q., Dennis J., Dicks E., Howat W.J., Schoof N. ... Kraft P. (2013). Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Nature Genetics, 45 (4), 392-398. doi: 10.1038/ng.2561

Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits

Ebejer, Jane L., Duffy, David L., van der Werf, Julius, Wright, Margaret J., Montgomery, Grant, Gillespie, Nathan A., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2013). Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. Twin Research and Human Genetics, 16 (2), 560-574. doi: 10.1017/thg.2013.12

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Anttila, Verneri, Winsvold, Bendik S., Gormley, Padhraig, Kurth, tobias, Bettella, Francesco, McMahon, george, Kallela, mikko, Malik, Rainer, De Vries, Boukje, Terwindt, Gisela, Medland, Sarah E., Todt, Unda, McArdle, Wendy L., Quaye, Lydia, Koiranen, Markku, Ikram, M. Arfan, Lehtimaki, Terho, Stam, Anine H., Ligthart, Lannie, Wedenoja, Juho, Dunham, Ian, Neale, Benjamin M., Palta, Priit, Hamalainen, Eija, Schurks, Markus, Rose, Lynda M., Buring, Julie E., Ridker, Paul M., Steinberg, Stacy ... Palotie, Aarno (2013). Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nature Genetics, 45 (8), 912-917. doi: 10.1038/ng.2676

Identification of seven loci affecting mean telomere length and their association with disease

Codd, Veryan, Nelson, Christopher P., Albrecht, Eva, Mangino, Massimo, Deelen, Joris, Buxton, Jessica L., Hottenga, Jouke Jan, Fischer, Krista, Esko, Tonu, Surakka, Ida, Broer, Linda, Nyholt, Dale R., Leach, Irene Mateo, Salo, Perttu, Hagg, Sara, Matthews, Mary K., Palmen, Jutta, Norata, Giuseppe D., O'Reilly, Paul F., Saleheen, Danish, Amin, Najaf, Balmforth, Anthony J., Beekman, Marian, de Boer, Rudolf A., Bohringer, Stefan, Braund, Peter S., Burton, Paul R., de Craen, Anton J. M., Denniff, Matthew ... Samani, Nilesh J. (2013). Identification of seven loci affecting mean telomere length and their association with disease. Nature Genetics, 45 (4), 422-427. doi: 10.1038/ng.2528

Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect

Broer, Linda, Codd, Veryan, Nyholt, Dale R., Deelen, Joris, Mangino, Massimo, Willemsen, Gonneke, Albrecht, Eva, Amin, Najaf, Beekman, Marian, de Geus, Eco J. C., Henders, Anjali, Nelson, Christopher P., Steves, Claire J., Wright, Margie J., de Craen, Anton J. M., Isaacs, Aaron, Matthews, Mary, Moayyeri, Alireza, Montgomery, Grant W., Oostra, Ben A., Vink, Jacqueline M., Spector, Tim D., Slagboom, P. Eline, Martin, Nicholas G., Samani, Nilesh J., van Duijn, Cornelia M. and Boomsma, Dorret I. (2013). Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect. European Journal of Human Genetics, 21 (10), 1163-1168. doi: 10.1038/ejhg.2012.303

Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates

Evans, David M., Brion, Marie Jo A., Paternoster, Lavinia, Kemp, John P., McMahon, George, Munafo, Marcus, Whitfield, John B., Medland, Sarah E., Montgomery, Grant W., The GIANT consortium, The CRP consortium, The TAG Consortium, Timpson, Nicholas J., St. Pourcain, Beate, Lawlor, Debbie A., Martin, Nicholas G., Dehghan, Abbas, Hirschhorn, Joel and Davey Smith, George (2013). Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates. PLoS Genetics, 9 (10) e1003919, e1003919.1-e1003919.15. doi: 10.1371/journal.pgen.1003919

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA–DTI working group

Jahanshad, Neda, Kochunov, Peter V., Sprooten, Emma, Mandl, René C., Nichols, Thomas E., Almassy, Laura, Blangero, John, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Duggirala, Ravi, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Martin, Nicholas G., McMahon, Katie L., Medland, Sarah E., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Starr, John M., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Hulshoff Pol, Hilleke E., Bastind, Mark E., McIntosh, Andrew M., Deary, Ian J. ... Glahn, David C. (2013). Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: a pilot project of the ENIGMA–DTI working group. NeuroImage, 81, 455-469. doi: 10.1016/j.neuroimage.2013.04.061

Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions

Amin, Najaf, Hottenga, Jouke-Jan, Hansell, Narelle K., Janssens, A. Cecile J. W., de Moor, Marleen H. M., Madden, Pamela A. F., Zorkoltseva, Irina V., Penninx, Brenda W., Terracciano, Antonio, Uda, Manuela, Tanaka, Toshiko, Esko, Tonu, Realo, Anu, Ferrucci, Luigi, Luciano, Michelle, Davies, Gail, Metspalu, Andres, Abecasis, Goncalo R., Deary, Ian J., Raikkonen, Katri, Bierut, Laura J., Costa, Paul T., Saviouk, Viatcheslav, Zhu, Gu, Kirichenko, Anatoly V., Isaacs, Aaron, Aulchenko, Yurii S., Willemsen, Gonneke, Heath, Andrew C. ... van Duijn, Cornelia M. (2013). Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, 21 (8), 876-882. doi: 10.1038/ejhg.2012.263

The Brisbane Longitudinal Twin Study: pathways to cannabis use, abuse, and dependence project - current status, preliminary results, and future directions

Gillespie, Nathan A., Henders, Anjali K., Davenport, Tracy A., Hermens, Daniel F., Wright, Margie J., Martin, Nicholas G. and Hickie, Ian B. (2013). The Brisbane Longitudinal Twin Study: pathways to cannabis use, abuse, and dependence project - current status, preliminary results, and future directions. Twin Research and Human Genetics, 16 (1), 21-33. doi: 10.1017/thg.2012.111

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11

Siddiq, Afshan, Couch, Fergus J., Chen, Gary K., Lindstrom, Sara, Eccles, Diana, Millikan, Robert C., Michailidou, Kyriaki, Stram, Daniel O., Beckmann, Lars, Rhie, Suhn Kyong, Ambrosone, Christine B., Aittomaki, Kristiina, Amiano, Pilar, Apicella, Carmel, Baglietto, Laura, Bandera, Elisa V., Beckmann, Matthias W., Berg, Christine D., Bernstein, Leslie, Blomqvist, Carl, Brauch, Hiltrud, Brinton, Louise, Bui, Quang M., Buring, Julie E., Buys, Saundra S., Campa, Daniele, Carpenter, Jane E., Chasman, Daniel I., Chang-Claude, Jenny ... Vachon, Celine M. (2012). A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Human Molecular Genetics, 21 (24), 5373-5384. doi: 10.1093/hmg/dds381

Pathway analysis of smoking quantity in multiple GWAS identifies cholinergic and sensory pathways

Harari, Oscar, Wang, Jen-Chyong, Bucholz, Kathleen, Edenberg, Howard J., Heath, Andrew, Martin, Nicholas G., Pergadia, Michele L., Montgomery, Grant, Schrage, Andrew, Bierut, Laura J., Madden, Pamela F. and Goate, Alison M. (2012). Pathway analysis of smoking quantity in multiple GWAS identifies cholinergic and sensory pathways. Plos One, 7 (12) e50913, e50913. doi: 10.1371/journal.pone.0050913

Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the Alcohol Challenge Twin Study

Lind, Penelope A., Macgregor, Stuart, Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Association between in vivo alcohol metabolism and genetic variation in pathways that metabolize the carbon skeleton of ethanol and NADH reoxidation in the Alcohol Challenge Twin Study. Alcoholism: Clinical and Experimental Research, 36 (12), 2074-2085. doi: 10.1111/j.1530-0277.2012.01829.x

Genome-wide association meta-analysis identifies new endometriosis risk loci

Nyholt, Dale R., Low, Siew-Kee, Anderson, Carl A., Painter, Jodie N., Uno, Satoko, Morris, Andrew P., MacGregor, Stuart, Gordon, Scott D., Henders, Anjali K., Martin, Nicholas G., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Kennedy, Stephen H., Treloar, Susan A., Missmer, Stacey A., Adachi, Sosuke, Tanaka, Kenichi, Nakamura, Yusuke, Zondervan, Krina T., Zembutsu, Hitoshi and Montgomery, Grant W. (2012). Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics, 44 (12), 1355-1359. doi: 10.1038/ng.2445

Liberal neutrality and charitable purposes

Martin, Nick (2012). Liberal neutrality and charitable purposes. Political Studies, 60 (4), 936-952. doi: 10.1111/j.1467-9248.2011.00942.x

Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility

Li, Ming, Wang, Yi, Zheng, Xue-bin, Ikeda, Masashi, Iwata, Nakao, Luo, Xiong-jian, Chong, Siow-Ann, Lee, Jimmy, Rietschel, Marcella, Zhang, Fengyu, Mueller-Myhsok, Bertram, Cichon, Sven, Weinberger, Daniel R., Mattheisen, Manuel, Schulze, Thomas G., Martin, Nicholas G., Mitchell, Philip B., Schofield, Peter R., Liu, Jian-jun and Su, Bing (2012). Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. Schizophrenia Research, 142 (1-3), 200-205. doi: 10.1016/j.schres.2012.10.008

Modeling the direction of causation between cross-sectional measures of disrupted sleep, anxiety and depression in a sample of male and female Australian twins

Gillespie, Nathan A., Gehrman, Philip, Byrne, Enda M., Kendler, Kenneth S., Heath, Andrew C. and Martin, Nicholas G. (2012). Modeling the direction of causation between cross-sectional measures of disrupted sleep, anxiety and depression in a sample of male and female Australian twins. Journal of Sleep Research, 21 (6), 675-683. doi: 10.1111/j.1365-2869.2012.01026.x

Offspring ADHD as a risk factor for parental marital problems: controls for genetic and environmental confounds

Schermerhorn, Alice C., D'Onofrio, Brian M., Slutske, Wendy S., Emery, Robert E., Turkheimer, Eric, Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2012). Offspring ADHD as a risk factor for parental marital problems: controls for genetic and environmental confounds. Twin Research and Human Genetics, 15 (6), 700-713. doi: 10.1017/thg.2012.55

Seventy-five genetic loci influencing the human red blood cell

van der Harst, Pim, Zhang, Weihua, Leach, Irene Mateo, Rendon, Augusto, Verweij, Niek, Sehmi, Joban, Paul, Dirk S., Elling, Ulrich, Allayee, Hooman, Li, Xinzhong, Radhakrishnan, Aparna, Tan, Sian-Tsung, Voss, Katrin, Weichenberger, Christian X., Albers, Cornelis A., Al-Hussani, Abtehale, Asselbergs, Folkert W., Ciullo, Marina, Danjou, Fabrice, Dina, Christian, Esko, Tonu, Evans, David M., Franke, Lude, Goegele, Martin, Hartiala, Jaana, Hersch, Micha, Holm, Hilma, Hottenga, Jouke-Jan, Kanoni, Stavroula ... Chambers, John C. (2012). Seventy-five genetic loci influencing the human red blood cell. Nature, 492 (7429), 369-375. doi: 10.1038/nature11677

Neuropeptide Y (NPY): Genetic Variation in the Human Promoter Alters Glucocorticoid Signaling, Yielding Increased NPY Secretion and Stress Responses (vol 60, pg 1678, 2012)

Zhang, K., Rao, F., Miramontes-Gonzalez, J. P., Hightower, C. M., Vaught, B., Chen, Y., Greenwood, T. A., Schork, A. J., Wang, L., Mahata, M., Stridsberg, M., Khandrika, S., Biswas, N., Fung, M. M., Waalen, J., Middelberg, R. P., Heath, A. C., Montgomery, G. W., Martin, N. G., Whitfield, J. B., Baker, D. G., Schork, N. J., Nievergelt, C. M. and O'Connor, D. T. (2012). Neuropeptide Y (NPY): Genetic Variation in the Human Promoter Alters Glucocorticoid Signaling, Yielding Increased NPY Secretion and Stress Responses (vol 60, pg 1678, 2012). Journal of the American College of Cardiology, 60 (21), 2261-2261. doi: 10.1016/j.jacc.2012.10.002

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

Asselbergs, Folkert W., Guo, Yiran, van Iperen, Erik P. A., Sivapalaratnam, Suthesh, Tragante, Vinicius, Lanktree, Matthew B., Lange, Leslie A., Almoguera, Berta, Appelman, Yolande E., Barnard, John, Baumert, Jens, Beitelshees, Amber L., Bhangale, Tushar R., Chen, Yii-Der Ida, Gaunt, Tom R., Gong, Yan, Hopewell, Jemma C., Johnson, Toby, Kleber, Marcus E., Langaee, Taimour Y., Li, Mingyao, Li, Yun R., Liu, Kiang, McDonough, Caitrin W., Meijs, Matthijs El., Middelberg, Rita P. S., Musunuru, Kiran, Nelson, Christopher P., O'Connell, Jeffery R. ... Drenos, Fotios (2012). Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics, 91 (5), 823-838. doi: 10.1016/j.ajhg.2012.08.032

Environmental influences predominate in remission from alcohol use disorder in young adult twins

McCutcheon, V. V., Grant, J. D., Heath, A. C., Bucholz, K. K., Sartor, C. E., Nelson, E. C., Madden, P. A. F. and Martin, N. G. (2012). Environmental influences predominate in remission from alcohol use disorder in young adult twins. Psychological Medicine, 42 (11), 2421-2431. doi: 10.1017/S003329171200044X

Erratum: The genetics of addiction - a translational perspective (Translational Psychiatry (2012) 2 (e140) DOI: 10.1038/tp.2012.54)

Agrawal, A., Verweij, K. J. H., Gillespie, N. A., Heath, A. C., Lessov-Schlaggar, C. N., Martin, N. G., Nelson, E. C., Slutske, W. S., Whitfield, J. B. and Lynskey, M. T. (2012). Erratum: The genetics of addiction - a translational perspective (Translational Psychiatry (2012) 2 (e140) DOI: 10.1038/tp.2012.54). Translational Psychiatry, 2 (11) e193, e193-e193. doi: 10.1038/tp.2012.129

Genetic and environmental transmission of body mass index fluctuation

Bergin, Jocilyn E., Neale, Michael C., Eaves, Lindon J., Martin, Nicholas G., Heath, Andrew C. and Maes, Hermine H. (2012). Genetic and environmental transmission of body mass index fluctuation. Behavior Genetics, 42 (6), 867-874. doi: 10.1007/s10519-012-9567-5

Genome-wide meta-analysis of common variant differences between men and women

Boraska, Vesna, Jeroncic, Ana, Colonna, Vincenza, Southam, Lorraine, Nyholt, Dale R., Rayner, Nigel William, Perry, John R. B., Toniolo, Daniela, Albrecht, Eva, Ang, Wei, Bandinelli, Stefania, Barbalic, Maja, Barroso, Ines, Beckmann, Jacques S., Biffar, Reiner, Boomsma, Dorret, Campbell, Harry, Corre, Tanguy, Erdmann, Jeanette, Esko, Tonu, Fischer, Krista, Franceschini, Nora, Frayling, Timothy M., Girotto, Giorgia, Gonzalez, Juan R., Harris, Tamara B., Heath, Andrew C., Heid, Iris M., Hoffmann, Wolfgang ... Zeggini, Eleftheria (2012). Genome-wide meta-analysis of common variant differences between men and women. Human Molecular Genetics, 21 (21) dds304, 4805-4815. doi: 10.1093/hmg/dds304

Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder

Lee, P. H., Perlis, R. H., Jung, J-Y, Byrne, E. M., Rueckert, E., Siburian, R., Haddad, S., Mayerfeld, C. E., Heath, A. C., Pergadia, M. L., Madden, P. A. F., Boomsma, D. I., Penninx, B. W., Sklar, P., Martin, N. G., Wray, N. R., Purcell, S. M. and Smoller, J. W. (2012). Multi-locus genome-wide association analysis supports the role of glutamatergic synaptic transmission in the etiology of major depressive disorder. Translational Psychiatry, 2 (11) e184, e184.1-e184.9. doi: 10.1038/tp.2012.95

The genetics of addiction - a translational perspective

Agrawal, A., Verweij, K. J. H., Gillespie, N. A., Heath, A. C., Lessov-Schlaggar, C. N., Martin, N. G., Nelson, E. C., Slutske, W. S., Whitfield, J. B. and Lynskey, M. T. (2012). The genetics of addiction - a translational perspective. Translational Psychiatry, 2 e140. doi: 10.1038/tp.2012.54

Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses

Zhang, Kuixing, Rao, Fangwen, Miramontes-Gonzalez, Jose Pablo, Hightower, C. Makena, Vaught, Brian, Chen, Yuhong, Greenwood, Tiffany A., Schork, Andrew J., Wang, Lei, Mahata, Manjula, Stridsberg, Mats, Khandrika, Srikrishna, Biswas, Nilima, Fung, Maple M., Waalen, Jill, Middelberg, Rita P., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Whitfield, John B., Baker, Dewleen G., Schork, Nicholas J., Nievergelt, Caroline M. and O'Connor, Daniel T. (2012). Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. Journal of the American College of Cardiology, 60 (17), 1678-1689. doi: 10.1016/j.jacc.2012.06.042

Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage

Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Gondro, Cedric, Henders, Anjali K., Lynskey, Michael, Martin, Nicholas G. and Duffy, David L. (2012). Attention deficit hyperactivity disorder in Australian adults: prevalence, persistence, conduct problems and disadvantage. Plos One, 7 (10) e47404, e47404. doi: 10.1371/journal.pone.0047404

Genome-wide linkage and association analyses implicate FASN in predisposition to uterine leiomyomata

Eggert, Stacey L., Huyck, Karen L., Somasundaram, Priya, Kavalla, Raghava, Stewart, Elizabeth A., Lu, Ake T., Painter, Jodie N., Montgomery, Grant W., Medland, Sarah E., Nyholt, Dale R., Treloar, Susan A., Zondervan, Krina T., Heath, Andrew C., Madden, Pamela A. F., Rose, Lynda, Buring, Julie E., Ridker, Paul M., Chasman, Daniel I., Martin, Nicholas G., Cantor, Rita M. and Morton, Cynthia C. (2012). Genome-wide linkage and association analyses implicate FASN in predisposition to uterine leiomyomata. American Journal of Human Genetics, 91 (4), 621-628. doi: 10.1016/j.ajhg.2012.08.009

A behavioral genetic study of humor styles in an Australian sample

Baughman, H. M., Giammarco, E. A., Veselka, Livia, Schermer, Julie A., Martin, Nicholas G., Lynskey, Michael and Vernon, Phillip A. (2012). A behavioral genetic study of humor styles in an Australian sample. win Research and Human Genetics, 15 (5), 663-667. doi: 10.1017/thg.2012.23

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol

Surakka, Ida, Whitfield, John B., Perola, Markus, Visscher, Peter M., Montgomery, Grant W., Falchi, Mario, Willemsen, Gonneke, de Geus, Eco J. C., Magnusson, Patrik K. E., Christensen, Kaare, Sorensen, Thorild I. A., Pietilainen, Kirsi H., Rantanen, Taina, Silander, Kaisa, Widen, Elisabeth, Muilu, Juhu, Rahman, Iffat, Liljedahl, Ulrika, Syvanen, Ann-Christine, Palotie, Aarno, Kaprio, Jaakko, Kyvik, Kirsten O., Pedersen, Nancy L., Boomsma, Dorret I., Spector, Tim, Martin, Nicolas G., Ripatti, Samuli and Peltonen, Leena (2012). A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Research and Human Genetics, 15 (6), 691-699. doi: 10.1017/thg.2012.63

An Australian twin study of cannabis and other illicit drug use and misuse, and other psychopathology

Lynskey, Michael T., Agrawal, Arpana, Henders, Anjali, Nelson, Elliot C., Madden, Pamela A. F. and Martin, Nicholas G. (2012). An Australian twin study of cannabis and other illicit drug use and misuse, and other psychopathology. Twin Research and Human Genetics, 15 (5), 631-641. doi: 10.1017/thg.2012.41

Genetic variants near PDGFRA are associated with corneal curvature in Australians

Mishra, Aniket, Yazar, Seyhan, Hewitt, Alex W., Mountain, Jenny A., Ang, Wei, Pennell, Craig E., Martin, Nicholas G., Montgomery, Grant W., Hammond, Christopher J., Young, Terri L., Macgregor, Stuart and Mackey, David A. (2012). Genetic variants near PDGFRA are associated with corneal curvature in Australians. Investigative Ophthalmology and Visual Science, 53 (11), 7131-7136. doi: 10.1167/iovs.12-10489

Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error

Sanfilippo, Paul G., Hammond, Christopher J., Staffieri, Sandra E., Kearns, Lisa S., Liew, S. H. Melissa, Barbour, Julie M., Hewitt, Alex W., Ge, Dongliang, Snieder, Harold, MacKinnon, Jane R., Brown, Shayne A., Lorenz, Birgit, Spector, Tim D., Martin, Nicholas G., Wilmer, Jeremy B. and Mackeymo, David A. (2012). Heritability of strabismus: genetic influence is specific to eso-deviation and independent of refractive error. Twin Research and Human Genetics, 15 (5), 624-630. doi: 10.1017/thg.2012.22

Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding

Verweij, Karin J. H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Raback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kahonen, Mika, Viikari, Jorma, Raikkonen, Katri, Eriksson, Johan G., Keltikangas-Jarvinen, Liisa, Lehtimaki, Terho, Martin, Nicholas G., Jarvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C. and Zietsch, Brendan P. (2012). Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding. Evolution, 66 (10), 3238-3251. doi: 10.1111/j.1558-5646.2012.01679.x

Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study

Tielbeek, Jorim J., Medland, Sarah E., Benyamin, Beben, Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Wray, Naomi R. and Verweij, Karin J. H. (2012). Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. PLoS One, 7 (10) e45086, e1005378-e1005378. doi: 10.1371/journal.pone.0045086

FTO genotype is associated with phenotypic variability of body mass index

Yang, Jian, Loos, Ruth J., Powell, Joseph E., Medland, Sarah E, Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Magi, Reedik, Waite, Lindsay, Vernon Smith, Albert, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, To˜nu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayse, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an ... Visscher, Peter (2012). FTO genotype is associated with phenotypic variability of body mass index. Nature, 490 (7419), 267-272. doi: 10.1038/nature11401

A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans

Liu, Fan, van der Lijn, Fedde, Schurmann, Claudia, Zhu, Gu, Chakravarty, M. Mallar, Hysi, Pirro G., Wollstein, Andreas, Lao, Oscar, de Bruijne, Marleen, Ikram, M. Arfan, van der Lugt, Aad, Rivadeneira, Fernando, Uitterlinden, Andre G., Hofman, Albert, Niessen, Wiro J., Homuth, Georg, de Zubicaray, Greig, McMahon, Katie L., Thompson, Paul M., Daboul, Amro, Puls, Ralf, Hegenscheid, Katrin, Bevan, Liisa, Pausova, Zdenka, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J., Wicking, Carol A., Boehringer, Stefan ... Kayser, Manfred for the International Visible Trait Genetics (VisiGen) Consortium (2012). A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans. PLoS Genetics, 8 (9) e1002932, e1002932.1-e1002932.13. doi: 10.1371/journal.pgen.1002932

Genetic and environmental influences on analogical and categorical verbal and spatial reasoning in 12-year old twins

Mosing, Miriam A., Mellanby, Jane, Martin, Nicholas G. and Wright, Margaret J. (2012). Genetic and environmental influences on analogical and categorical verbal and spatial reasoning in 12-year old twins. Behavior Genetics, 42 (5), 722-731. doi: 10.1007/s10519-012-9540-3

Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA

Ramasamy, Adaikalavan, Kuokkanen, Mikko, Vedantam, Sailaja, Gajdos, Zofia K., Alves, Alexessander Couto, Lyon, Helen N., Ferreira, Manuel A. R., Strachan, David P., Zhao, Jing Hua, Abramson, Michael J., Brown, Matthew A., Coin, Lachlan, Dharmage, Shyamali C., Duffy, David L., Haahtela, Tari, Heath, Andrew C., Janson, Christer, Kahonen, Mika, Khaw, Kay-Tee, Laitinen, Jaana, Le Souef, Peter, Lehtimaki, Terho, Madden, Pamela A. F., Marks, Guy B., Martin, Nicholas G., Matheson, Melanie C., Palmer, Cameron D., Palotie, Aarno, Pouta, Anneli ... Hirschhorn, Joel N. (2012). Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA. PLoS One, 7 (9 Article No. e44008) e44008, e44008-1-e44008-10. doi: 10.1371/journal.pone.0044008

Genome-wide association uncovers shared genetic effects among personality traits and mood states

Luciano, Michelle, Huffman, Jennifer E., Arias-Vasquez, Alejandro, Vinkhuyzen, Anna A. E., Middeldorp, Christel M., Giegling, Ina, Payton, Antony, Davies, Gail, Zgaga, Lina, Janzing, Joost, Ke, Xiayi, Galesloot, Tessel, Hartmann, Annette M., Ollier, William, Tenesa, Albert, Hayward, Caroline, Verhagen, Maaike, Montgomery, Grant W., Hottenga, Jouke-Jan, Konte, Bettina, Starr, John M., Vitart, Veronique, Vos, Pieter E., Madden, Pamela A. F., Willemsen, Gonneke, Konnerth, Heike, Horan, Michael A., Porteous, David J., Campbell, Harry ... Deary, Ian J. (2012). Genome-wide association uncovers shared genetic effects among personality traits and mood states. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B (6), 684-695. doi: 10.1002/ajmg.b.32072

How a common variant in the growth factor receptor gene, NTRK1, affects white matter

Braskie, Meredith N., Jahanshad, Neda, Toga, Arthur W., McMahon, Katie L, de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). How a common variant in the growth factor receptor gene, NTRK1, affects white matter. BioArchitecture, 2 (5), 1-4. doi: 10.4161/bioa.22190

Substantial genetic overlap between schizotypy and neuroticism: a twin study

Macare, Christine, Bates, Timothy C., Heath, Andrew C., Martin, Nicholas G. and Ettinger, Ulrich (2012). Substantial genetic overlap between schizotypy and neuroticism: a twin study. Behavior Genetics, 42 (5), 732-742. doi: 10.1007/s10519-012-9558-6

The continuing value of twin studies in the omics era

van Dongen, Jenny, Slagboom, P. Eline, Draisma, Harmen H. M., Martin, Nicholas G. and Boomsma, Dorret I. (2012). The continuing value of twin studies in the omics era. Nature Reviews Genetics, 13 (9), 640-653. doi: 10.1038/nrg3243

Commentary: discussion of 'The history of twins, as a criterion of the relative powers of nature And nurture' by Francis Galton (1875)

Martin, Nicholas G. (2012). Commentary: discussion of 'The history of twins, as a criterion of the relative powers of nature And nurture' by Francis Galton (1875). International Journal of Epidemiology, 41 (4) dys110, 917-919. doi: 10.1093/ije/dys110

Reduced slow-wave rebound during daytime recovery sleep in middle-aged subjects

Lafortune, Marjolaine, Gagnon, Jean-Francois, Latreille, Veronique, Vandewalle, Gilles, Martin, Nicolas, Filipini, Daniel, Doyon, Julien and Carrier, Julie (2012). Reduced slow-wave rebound during daytime recovery sleep in middle-aged subjects. Plos One, 7 (8) e43224, e43224. doi: 10.1371/journal.pone.0043224

Discovery and replication of gene influences on brain structure using LASSO regression

Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Hua, Xue, Rajagopalan, Priya, Toga, Arthur W., Jack Jr., Clifford R., Weiner, Michael W., de Zubicaray, Greig I., McMahon, Katie L., Hansell, Narelle K., Martin, Nicholas G., Margaret J. Wright, Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2012). Discovery and replication of gene influences on brain structure using LASSO regression. Frontiers in Neuroscience, 6 (AUG) Article 115, 115.1-115.13. doi: 10.3389/fnins.2012.00115

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Hartz, Sarah M., Short, Susan E., Saccone, Nancy L., Culverhouse, Robert, Chen, LiShiun, Schwantes-An, Tae-Hwi, Coon, Hilary, Han, Younghun, Stephens, Sarah H., Sun, Juzhong, Chen, Xiangning, Ducci, Francesca, Dueker, Nicole, Franceschini, Nora, Frank, Josef, Geller, Frank, Guobjartsson, Daniel, Hansel, Nadia N., Jiang, Chenhui, Keskitalo-Vuokko, Kaisu, Liu, Zhen, Lyytikainen, Leo-Pekka, Michel, Martha, Rawal, Rajesh, Hum, Sc, Rosenberger, Albert, Scheet, Paul, Shaffer, John R., Teumer, Alexander ... Bierut, Laura J. (2012). Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Archives of General Psychiatry, 69 (8), 854-861. doi: 10.1001/archgenpsychiatry.2012.124

The effect of childhood conduct disorder on human capital

Webbink, Dinand, Vujić, Sunčica, Koning, Pierre and Martin, Nicholas G. (2012). The effect of childhood conduct disorder on human capital. Health Economics, 21 (8), 928-945. doi: 10.1002/hec.1767

The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation

Verweij, Karin J. H., Vinkhuyzen, Anna A. E., Benyamin, Beben, Lynskey, Michael T., Quaye, Lydia, Agrawal, Arpana, Gordon, Scott D., Montgomery, Grant W., Madden, Pamela A. F., Heath, Andrew C., Spector, Andrew C., Martin, Nicholas G. and Medland, Sarah E. (2012). The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Addiction Biology, 18 (5), 846-850. doi: 10.1111/j.1369-1600.2012.00478.x

A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor

Byrne, Enda M., Johnson, Julie, McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Gehrman, Philip R., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Chenevix-Trench, Georgia and Martin, Nicholas G. (2012). A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Sleep, 35 (7), 967-975. doi: 10.5665/sleep.1962

Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression

Agrawal, Arpana, Nelson, Elliot C., Littlefield, Andrew K., Bucholz, Kathleen K., Degenhardt, Louisa, Henders, Anjali K., Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Pergadia, Michele L., Sher, Kenneth J., Heath, Andrew C. and Lynskey, Michael T. (2012). Cannabinoid receptor genotype moderation of the effects of childhood physical abuse on anhedonia and depression. Archives of General Psychiatry, 69 (7), 732-740. doi: 10.1001/archgenpsychiatry.2011.2273

Evidence of inbreeding depression on human height

McQuillan, Ruth, Eklund, Niina, Pirastu, Nicola, Kuningas, Maris, McEvoy, Brian P., Esko, Tonu, Corre, Tanguy, Davies, Gail, Kaakinen, Marika, Lyytikainen, Leo-Pekka, Kristiansson, Kati, Havulinna, Aki S., Gogele, Martin, Vitart, Veronique, Tenesa, Albert, Aulchenko, Yurii, Hayward, Caroline, Johansson, Asa, Boban, Mladen, Ulivi, Sheila, Robino, Antonietta, Boraska, Vesna, Igl, Wilmar, Wild, Sarah H., Zgaga, Lina, Amin, Najaf, Theodoratou, Evropi, Polasek, Ozren, Girotto, Giorgia ... Wilson, James F. (2012). Evidence of inbreeding depression on human height. Plos Genetics, 8 (7) e1002655, e1002655. doi: 10.1371/journal.pgen.1002655

Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study

Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Ames, David, Martin, Nicholas G., Wright, Margaret J., Sachdev, Perminder S. and OATS Research Team (2012). Genetic influences on four measures of executive functions and their covariation with general cognitive ability: The Older Australian Twins Study. Behavior Genetics, 42 (4), 528-538. doi: 10.1007/s10519-012-9526-1

Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6

Bloom, A. Joseph, Harari, Oscar, Martinez, Maribel, Madden, Pamela A. F., Martin, Nicholas G., Montgomery, Grant W., Rice, John P., Murphy, Sharon E., Bierut, Laura J. and Goate, Alison (2012). Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6. Human Molecular Genetics, 21 (13) dds114, 3050-3062. doi: 10.1093/hmg/dds114

Gene network effects on brain microstructure and intellectual performance identified in 472 twins

Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Montgomery, Grant W., Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J., Shapshak, Paul and Thompson, Paul M. (2012). Gene network effects on brain microstructure and intellectual performance identified in 472 twins. Journal of Neuroscience, 32 (25), 8732-8745. doi: 10.1523/JNEUROSCI.5993-11.2012

Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins

Hibar, Derrek P., Jahanshad, Neda, Stein, Jason L., Kohannim, Omid, Toga, Arthur W., Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Twin Research and Human Genetics, 15 (3), 286-295. doi: 10.1017/thg.2012.15

Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases

Li, Rui, Brockschmidt, Felix F., Kiefer, Amy K., Stefansson, Hreinn, Nyholt, Dale R., Song, Kijoung, Vermeulen, Sita H., Kanoni, Stavroula, Glass, Daniel, Medland, Sarah E., Dimitriou, Maria, Waterworth, Dawn, Tung, Joyce Y., Geller, Frank, Heilmann, Stefanie, Hillmer, Axel M., Bataille, Veronique, Eigelshoven, Sibylle, Hanneken, Sandra, Moebus, Susanne, Herold, Christine, den Heijer, Martin, Montgomery, Grant W., Deloukas, Panos, Eriksson, Nicholas, Heath, Andrew C., Becker, Tim, Sulem, Patrick, Mangino, Massimo ... Richards, J. Brent (2012). Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genetics, 8 (5) e1002746, 222-224. doi: 10.1371/journal.pgen.1002746

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012)

Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012). Translational Psychiatry, 2 (5) e125, e125-e125. doi: 10.1038/tp.2012.49

A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales

Service, S. K., Verweij, K. J. H., Lahti, J., Congdon, E., Ekelund, J., Hintsanen, M., Raikkonen, K., Lehtimaki, T., Kahonen, M., Widen, E., Taanila, A., Veijola, J., Heath, A. C., Madden, P. A. F., Montgomery, G. W., Sabatti, C., Jarvelin, M-R, Palotie, A., Raitakari, O., Viikari, J., Martin, N. G., Eriksson, J. G., Keltikangas-Jarvinen, L., Wray, N. R. and Freimer, N. B. (2012). A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales. Translational Psychiatry, 2 (5) e116, e116-e116. doi: 10.1038/tp.2012.37

Common variants at 12q14 and 12q24 are associated with hippocampal volume

Bis, Joshua C., DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M., Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F. J., DeStefano, Anita L., Lambert, Jean-Charles, Jack, Clifford R., Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A., Fleischman, Debta, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H., Enzinger, Christian, Danoy, Patrick, Amin, Najaf ... Cohorts Heart Aging Res Genomic Ep (2012). Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics, 44 (5), 545-551. doi: 10.1038/ng.2237

No association of candidate genes with cannabis use in a large sample of Australian twin families

Verweij, Karin J. H., Zietsch, Brendan P., Liu, Jimmy Z., Medland, Sarah E., Lynskey, Michael T., Madden, Pamela A. F., Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C. and Martin, Nicholas G. (2012). No association of candidate genes with cannabis use in a large sample of Australian twin families. Addiction Biology, 17 (3), 687-690. doi: 10.1111/j.1369-1600.2011.00320.x

Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults

Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2012). Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults. The Journal of Neuroscience, 32 (17), 5964-5972. doi: 10.1523/JNEUROSCI.5561-11.2012

Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein

Middelberg, Rita P. S., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Evidence of differential allelic effects between adolescents and adults for plasma high-density lipoprotein. PLoS ONE, 7 (4) e35605, e35605. doi: 10.1371/journal.pone.0035605

Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes

Webb, Bradley T., Guo, An-Yuan, Maher, Brion S., Zhao, Zhongming, van den Oord, Edwin J., Kendler, Kenneth S., Riley, Brien P., Gillespie, Nathan A., Prescott, Carol A., Middeldorp, Christel M., Willemsen, Gonneke, de Geus, Eco J. C., Hottenga, Jouke-Jan, Boomsma, Dorret I., Slagboom, Eline P., Wray, Naomi R., Montgomery, Grant W., Martin, Nicholas G., Wright, Margie J., Heath, Andrew C., Madden, Pamela A., Gelernter, Joel, Knowles, James A., Hamilton, Steven P., Weissman, Myrna M., Fyer, Abby J., Huezo-Diaz, Patricia, McGuffin, Peter, Farmer, Anne ... Hettema, John M. (2012). Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. European Journal of Human Genetics, 20 (10), 1078-1084. doi: 10.1038/ejhg.2012.47

Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene

Jahanshad, Neda, Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Whitfield, John B., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2012). Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Proceedings of the National Academy of Sciences of USA, 109 (14), E851-E859. doi: 10.1073/pnas.1105543109

Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2

Dennis, Emily L., Jahanshad, Neda, Rudie, Jeffrey D., Brown, Jesse A., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant, Martin, Nicholas G., Wright, Margaret J., Bookheimer, Susan Y., Dapretto, Mirella, Toga, Arthur W. and Thompson, Paul M. (2012). Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2. Brain Connectivity, 1 (6), 447-460. doi: 10.1089/brain.2011.0064

Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion

Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2 (e102) 201227, e102-e102. doi: 10.1038/tp.2012.27

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012). Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 (4), 369-375. doi: 10.1038/ng.2213

The Brisbane systems genetics study: genetical genomics meets complex trait genetics

Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Caracella, Anthony, Smith, Sara, Wright, Margaret J., Whitfield, John B., Dermitzakis, Emmanouil T., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2012). The Brisbane systems genetics study: genetical genomics meets complex trait genetics. PLoS One, 7 (4) e35430, e35430.1-e35430.9. doi: 10.1371/journal.pone.0035430

Genetic Influences on Four Measures of Executive Functions and Their Covariation with General Cognitive Ability: The Older Australian Twins Study (vol 42, pg 528, 2012)

Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Ames, David, Martin, Nicholas G., Wright, Margaret J. and Sachdev, Perminder S. (2012). Genetic Influences on Four Measures of Executive Functions and Their Covariation with General Cognitive Ability: The Older Australian Twins Study (vol 42, pg 528, 2012). Behavior Genetics, 42 (4), 539-540. doi: 10.1007/s10519-012-9536-z

Common heritable contributions to low-risk trauma, high-risk trauma, posttraumatic stress disorder, and major depression

Sartor, Carolyn E., Grant, Julia D., Lynskey, Michael T., McCutcheon, Vivia V., Waldron, Mary, Statham, Dixie J., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Nelson, Elliot C. (2012). Common heritable contributions to low-risk trauma, high-risk trauma, posttraumatic stress disorder, and major depression. Archives of General Psychiatry, 69 (3), 293-299. doi: 10.1001/archgenpsychiatry.2011.1385

Do shared etiological factors contribute to the relationship between sexual orientation and depression?

Zietsch, B. P., Verweij, K. J. H., Heath, A. C., Madden, P. A. F., Martin, N. G., Nelson, E. C. and Lynskey, M. T. (2012). Do shared etiological factors contribute to the relationship between sexual orientation and depression?. Psychological Medicine, 42 (3), 521-532. doi: 10.1017/S0033291711001577

Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent

Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111

Longevity candidate genes and their association with personality traits in the elderly

Luciano, Michelle, Lopez, Lorna M., de Moor, Marleen H. M., Harris, Sarah E., Davies, Gail, Nutile, Teresa, Krueger, Robert F., Esko, Tonu, Schlessinger, David, Toshiko, Tanaka, Derringer, Jaime L., Realo, Anu, Hansell, Narelle K., Pergadia, Michele L., Pesonen, Anu-Katriina, Sanna, Serena, Terracciano, Antonio, Madden, Pamela A. F., Penninx, Brenda, Spinhoven, Philip, Hartman, Catherina A., Oostra, Ben A., Janssens, A. Cecile J. W., Eriksson, Johan G., Starr, John M., Cannas, Alessandra, Ferrucci, Luigi, Metspalu, Andres, Wright, Margeret J. ... Deary, Ian J. (2012). Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159 B (2), 192-200. doi: 10.1002/ajmg.b.32013

The different effects of gender and sex on vote choice

Hatemi, Peter K., McDermott, Rose, Bailey, J. Michael and Martin, Nicholas G. (2012). The different effects of gender and sex on vote choice. Political Research Quarterly, 65 (1), 76-92. doi: 10.1177/1065912910391475

Hierarchical topological network analysis of anatomical human brain connectivity and differences related to sex and kinship

Duarte-Carvajalino, Julio M., Jahanshad, Neda, Lenglet, Christophe, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and Sapiro, Guillermo (2012). Hierarchical topological network analysis of anatomical human brain connectivity and differences related to sex and kinship. NeuroImage, 59 (4), 3784-3804. doi: 10.1016/j.neuroimage.2011.10.096

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

Spain, Sarah L., Carvajal-Carmona, Luis G., Howarth, Kimberley M., Jones, Angela M., Su, Zhan, Cazier, Jean-Baptiste, Williams, Jennet, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Cheadle, Jeremy, Li, Li, Casey, Graham, Vodicka, Pavel, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Morreau, Hans, van Wezel, Tom, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellvi-Bel, Sergi, Dunlop, Malcolm ... Tomlinson, Ian P. M. (2012). Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Human Molecular Genetics, 21 (4) ddr523, 934-946. doi: 10.1093/hmg/ddr523

Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: An international study of over 12,000 twin pairs

Dubois, Lise, Kyvik, Kirsten Ohm, Girard, Manon, Tatone-Tokuda, Fabiola, Perusse, Daniel, Hjelmborg, Jacob, Skytthe, Axel, Rasmussen, Finn, Wright, Margaret J., Lichtenstein, Paul and Martin, Nicholas G. (2012). Genetic and environmental contributions to weight, height, and BMI from birth to 19 years of age: An international study of over 12,000 twin pairs. PLoS ONE, 7 (2) e30153, e30153. doi: 10.1371/journal.pone.0030153

Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk

Law, Matthew H., Montgomery, Grant W., Brown, Kevin M., Martin, Nicholas G., Mann, Graham J., Hayward, Nicholas K., MacGregor, Stuart and Q-MEGA and AMFS Investigators (2012). Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. Journal of Investigative Dermatology, 132 (2), 485-487. doi: 10.1038/jid.2011.322

The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin

Martin, Nicholas G., Li, Ka Wah, Murray, Heather, Putt, Wendy, Packard, Chris J. and Humphries, Steve E. (2012). The effects of a single nucleotide polymorphism in SLCO1B1 on the pharmacodynamics of pravastatin. British Journal of Clinical Pharmacology, 73 (2), 303-306. doi: 10.1111/j.1365-2125.2011.04090.x

A genome-wide study on the perception of the odorants androstenone and galaxolide

Knaapila, Antti, Zhu, Gu, Medland, Sarah E., Wysocki, Charles J., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Reed, Danielle R. (2012). A genome-wide study on the perception of the odorants androstenone and galaxolide. Chemical Senses, 37 (6), 541-552. doi: 10.1093/chemse/bjs008

Development of brain structural connectivity between ages 12 and 30: a 4-tesla diffusion imaging study in 439 adolescents and adults

Dennis, Emily L., Jahanshad, Neda, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2012). Development of brain structural connectivity between ages 12 and 30: a 4-tesla diffusion imaging study in 439 adolescents and adults. NeuroImage, 64 (1), 671-684. doi: 10.1016/j.neuroimage.2012.09.004

Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins

Hansell, N. K., Wright, M. J., Medland, S. E., Davenprot, T. A., Wray, N. R., Martin, N. G. and Hickie, I. B. (2012). Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins. Psychological Medicine, 42 (6), 1249-1260. doi: 10.1017/S0033291711002431

Genetic influences on five measures of processing speed and their covariation with general cognitive ability in the elderly: The older Australian twins study

Lee, Teresa, Mosing, Miriam A., Henry, Julie D., Trollor, Julian N., Lammel, Andrea, Ames, David, Martin, Nicholas G., Wright, Margaret J. and Sachdev, Perminder S. (2012). Genetic influences on five measures of processing speed and their covariation with general cognitive ability in the elderly: The older Australian twins study. Behavior Genetics, 42 (1), 96-106. doi: 10.1007/s10519-011-9474-1

Genetic influences on life span and its relationship to personality: A 16-year follow-up study of a sample of aging twins

Mosing, Miriam A., Medland, Sarah E., McRae, Allan, Landers, Joseph George, Wright, Margaret J. and Martin, Nicholas G. (2012). Genetic influences on life span and its relationship to personality: A 16-year follow-up study of a sample of aging twins. Psychosomatic Medicine, 74 (1), 16-22. doi: 10.1097/PSY.0b013e3182385784

Genetic variation within a metabolic motif in the chromogranin A promoter: Pleiotropic influence on cardiometabolic risk traits in twins

Rao, Fangwen, Chiron, Stephane, Wei, Zhiyun, Fung, Maple M., Chen, Yuqing, Wen, Gen, Khandrika, Srikrishna, Ziegler, Michael G., Benyamin, Beben, Montgomery, Grant, Whitfield, John B., Martin, Nicholas G., Waalen, Jill, Hamiltoni, Bruce A., Mahata, Sushil K. and O'Connor, Daniel T. (2012). Genetic variation within a metabolic motif in the chromogranin A promoter: Pleiotropic influence on cardiometabolic risk traits in twins. American Journal of Hypertension, 25 (1), 29-40. doi: 10.1038/ajh.2011.163

Genome-wide association study of major depressive disorder: New results, meta-analysis, and lessons learned

Wray, N. R., Pergadia, M. L., Blackwood, D. H. R., Penninx, B. W. J. H., Gordon, S. D., Nyholt, D. R., Ripke, S., MacIntyre, D. J., McGhee, K. A., MacLean, A. W., Smit, J. H., Hottenga, J. J., Willemsen, G., Middeldorp, C. M., De Geus, E. J. C., Lewis, C. M., McGuffin, P., Hickie, I. B., Van Den Oord, E. J. C. G., Liu, J. Z., MacGregor, S., McEvoy, B. P., Byrne, E. M., Medland, S. E., Statham, D. J., Henders, A. K., Heath, A. C., Montgomery, G. W., Martin, N. G. ... Sullivan, P. F. (2012). Genome-wide association study of major depressive disorder: New results, meta-analysis, and lessons learned. Molecular Psychiatry, 17 (1), 36-48. doi: 10.1038/mp.2010.109

Health-related quality of life, treatment satisfaction, adherence and persistence in beta-thalassemia and myelodysplastic syndrome patients with iron overload receiving deferasirox: Results from the EPIC clinical trial

Porter, John, Bowden, Donald K., Economou, Marina, Troncy, Jacques, Ganser, Arnold, Habr, Dany, Martin, Nicolas, Gater, Adam, Rofail, Diana, Abetz-Webb, Linda, Lau, Helen and Cappellini, Maria Domenica (2012). Health-related quality of life, treatment satisfaction, adherence and persistence in beta-thalassemia and myelodysplastic syndrome patients with iron overload receiving deferasirox: Results from the EPIC clinical trial. Anemia, 2012 297641, 1-10. doi: 10.1155/2012/297641

Is CAG sequence length in the androgen receptor gene correlated with finger-length ratio?

Loehlin, John C., Medland, Sarah E. and Martin, Nicholas G. (2012). Is CAG sequence length in the androgen receptor gene correlated with finger-length ratio?. Personality and Individual Differences, 52 (2), 224-227. doi: 10.1016/j.paid.2011.09.009

Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations

Middelberg, Rita P., Benyamin, Beben, de Moor, Marleen H. M., Warrington, Nicole M., Gordon, Scott, Henders, Anjali K., Medland, Sarah E., Nyholt, Dale R., de Geus, Eco J. C., Hottenga, Jouke J., Willemsen, Gonneke, Beilin, Lawrence J., Mori, Trevor A., Wright, Margaret J., Heath, Andrew C., Madden, Pamela A. F., Boomsma, Dorret I., Pennell, Craig E., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2012). Loci affecting gamma-glutamyl transferase in adults and adolescents show age x SNP interaction and cardiometabolic disease associations. Human Molecular Genetics, 21 (2) ddr478, 446-455. doi: 10.1093/hmg/ddr478

Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M. ... Lunetta K.L. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051

Meta-analysis of genome-wide association studies for personality

de Moor, M. H. M., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Toshiko, T., Penninx, B. W. J. H., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J.-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A., Sullivan, P., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A., Lin, P., Grucza, R., Nutile, T., Ciullo, M., Rujescu, D. ... Boomsma, D. I. (2012). Meta-analysis of genome-wide association studies for personality. Molecular Psychiatry, 17 (3), 337-349. doi: 10.1038/mp.2010.128

Predicting white matter integrity from multiple common genetic variants

Kohannim, Omid, Jahanshad, Neda, Braskie, Meredith N., Stein, Jason L., Chiang, Ming-Chang, Reese. April H., Hibar, Derrek P., Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Medland, Sarah E., Montgomery, Grant W., Martin, Nicholas G., Wright. Margaret J. and Thompson, Paul M. (2012). Predicting white matter integrity from multiple common genetic variants. Neuropsychopharmacology, 37 (9), 2012-2019. doi: 10.1038/npp.2012.49

The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior

Miller, Geoffrey, Zhu, Gu, Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2012). The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior. Twin Research and Human Genetics, 15 (1), 97-106. doi: 10.1375/twin.15.1.97

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F. ... Brown, Kevin M. (2011). A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 (7375), 99-103. doi: 10.1038/nature10630

Genome-wide association study identifies novel loci predisposing to cutaneous melanoma

Amos, Christopher I., Wang, Li-E, Lee, Jeffrey E., Gershenwald, Jeffrey E., Chen, Wei V., Fang, Shenying, Kosoy, Roman, Zhang, Mingfeng, Qureshi, Abrar A., Vattathil, Selina, Schacherer, Christopher W., Gardner, Julie M., Wang, Yuling, Bishop, D. Tim, Barrett, Jennifer H., MacGregor, Stuart, Hayward, Nicholas K., Martin, Nicholas G., Duffy, David L., Mann, Graham J., Cust, Anne, Hopper, John, Brown, Kevin M., Grimm, Elizabeth A., Xu, Yaji, Han, Younghun, Jing, Kaiyan, McHugh, Caitlin, Laurie, Cathy C. ... Wei, Qingyi (2011). Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human Molecular Genetics, 20 (24) ddr415, 5012-5023. doi: 10.1093/hmg/ddr415

New gene functions in megakaryopoiesis and platelet formation

Gieger, Christian, Radhakrishnan, Aparna, Cvejic, Ana, Tang, Weihong, Porcu, Eleonora, Pistis, Giorgio, Serbanovic-Canic, Jovana, Elling, Ulrich, Goodall, Alison H., Labrune, Yann, Lopez, Lorna M., Magi, Reedik, Meacham, Stuart, Okada, Yukinori, Pirastu, Nicola, Sorice, Rossella, Teumer, Alexander, Voss, Katrin, Zhang, Weihua, Ramirez-Solis, Ramiro, Bis, Joshua C., Ellinghaus, David, Gogele, Martin, Hottenga, Jouke-Jan, Langenberg, Claudia, Kovacs, Peter, O'Reilly, Paul F., Shin, So-Youn, Esko, Tonu ... Soranzo, Nicole (2011). New gene functions in megakaryopoiesis and platelet formation. Nature, 480 (7376), 201-208. doi: 10.1038/nature10659

The value of twin studies: a response to Slate magazine

Segal, Nancy L., Turkheimer, Eric, Gottesman, Irving I., Gatz, Margaret and Martin, Nicholas G. (2011). The value of twin studies: a response to Slate magazine. Twin Research and Human Genetics, 14 (6), 593-597. doi: 10.1375/twin.14.6.593

GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors

Benyamin, Beben, Middelberg, Rita P., Lind, Penelope A., Valle, Anne M., Gordon, Scott, Nyholt, Dale R., Medland, Sarah E., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Visscher, Peter M., O'Connor, Daniel T., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human Molecular Genetics, 20 (22) ddr375, 4504-4514. doi: 10.1093/hmg/ddr375

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

MacGregor, Stuart, Montgomery, Grant W., Liu, Jimmy Z., Zhao, Zhen Zhen, Henders, Anjali K., Stark, Mitchell, Schmid, Helen, Holland, Elizabeth A., Duffy, David L., Zhang, Mingfeng, Painter, Jodie N., Nyholt, Dale R., Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Cust, Anne E., Jenkins, Mark A., Whiteman, David C., Olsson, Hakan, Puig, Susana, Bianchi-Scarra, Giovanna, Hansson, Johan, Demenais, Florence, Landi, Maria Teresa, Debniak, Tadeusz, Mackie, Rona, Azizi, Esther, Bressac-de Paillerets, Brigitte, Goldstein, Alisa M. ... Hayward, Nicholas K. (2011). Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics, 43 (11), 1114-1118. doi: 10.1038/ng.958

What does a general factor of personality look like in unshared environmental variance?

Loehlin, John C. and Martin, Nicholas G. (2011). What does a general factor of personality look like in unshared environmental variance?. Personality and Individual Differences, 51 (7), 862-865. doi: 10.1016/j.paid.2011.07.021

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking

Terracciano, A., Esko, T., Sutin, A. R., de Moor, M. H. M., Meirelles, O., Zhu, G., Tanaka, T., Giegling, I., Nutile, T., Realo, A., Allik, J., Hansell, N. K., Wright, M. J., Montgomery, G. W., Willemsen, G., Hottenga, J-J, Friedl, M., Ruggiero, D., Sorice, R., Sanna, S., Cannas, A., Raikkonen, K., Widen, E., Palotie, A., Eriksson, J. G., Cucca, F., Krueger, R. F., Lahti, J., Luciano, M. ... Uda, M. (2011). Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Translational Psychiatry, 1 (10) e49, e49-e49. doi: 10.1038/tp.2011.42

Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins

Coolen, Marcel W., Statham, Aaron L., Qu, Wenjia, Campbell, Megan J., Henders, Anjali K., Montgomery, Grant W., Martin, Nick G. and Clark, Susan J. (2011). Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins. PLoS ONE, 6 (10) e25590, 1-12. doi: 10.1371/journal.pone.0025590

A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol

Surakka, Ida, Isaacs, Aaron, Karssen, Lennart C., Laurila, Pirkka-Pekka P., Middelberg, Rita P. S., Tikkanen, Emmi, Ried, Janina S., Lamina, Claudia, Mangino, Massimo, Igl, Wilmar, Hottenga, Jouke-Jan, Lagou, Vasiliki, van der Harst, Pim, Leach, Irene Mateo, Esko, Tonu, Kutalik, Zoltan, Wainwright, Nicholas W., Struchalin, Maksim V., Sarin, Antti-Pekka, Kangas, Antti J., Viikari, Jorma S., Perola, Markus, Rantanen, Taina, Petersen, Ann-Kristin, Soininen, Pasi, Johansson, Asa, Soranzo, Nicole, Heath, Andrew C., Papamarkou, Theodore ... Ripatti, Samuli (2011). A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. PLoS Genetics, 7 (10) e1002333, e1002333. doi: 10.1371/journal.pgen.1002333

Cognitive functioning in older twins: The older Australian twins study

Sachdev, Perminder S., Lee, Teresa, Lammel, Andrea, Crawford, John, Trollor, Julian N., Wright, Margaret J., Brodaty, Henry, Ames, David, Martin, Nicholas G. and OATS Research Team (2011). Cognitive functioning in older twins: The older Australian twins study. Australasian Journal on Ageing, 30 (Supp. 2), 17-23. doi: 10.1111/j.1741-6612.2011.00534.x

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

Stevens, Kristen N., Vachon, Celine M., Lee, Adam M., Slager, Susan, Lesnick, Timothy, Olswold, Curtis, Fasching, Peter A., Miron, Penelope, Eccles, Diana, Carpenter, Jane E., Godwin, Andrew K., Ambrosone, Christine, Winqvist, Robert, Brauch, Hiltrud, Schmidt, Marjanka K., Cox, Angela, Cross, Simon S., Sawyer, Elinor, Hartmann, Arndt, Beckmann, Matthias W., Schulz-Wendtland, Ruediger, Ekici, Arif B., Tapper, William J., Gerty, Susan M., Durcan, Lorraine, Graham, Nikki, Hein, Rebecca, Nickels, Stephan, Flesch-Janys, Dieter ... Couch, Fergus J. (2011). Common breast cancer susceptibility loci are associated with triple-negative breast cancer. Cancer Research, 71 (19), 6240-6249. doi: 10.1158/0008-5472.CAN-11-1266

Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma

Kvaskoff, Marina, Whiteman, David C., Zhao, Zhen Z., Montgomery, Grant W., Martin, Nicholas G., Hayward, Nicholas K. and Duffy, David L. (2011). Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma. Twin Research and Human Genetics, 14 (5), 422-432. doi: 10.1375/twin.14.5.422

Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning

Luong, Hein T. T., Chaplin, Justin, McRae, Allan F., Medland, Sarah E., Willemsen, Gonneke, Nyholt, Dale R., Henders, Anjali K., Hoekstra, Chantal, Duffy, David L., Martin, Nicholas G., Boomsma, Dorret I., Montgomery, Grant W. and Painter, Jodie N. (2011). Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning. Twin Research and Human Genetics, 14 (5), 408-416. doi: 10.1375/twin.14.5.408

Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits

Middelberg, Rita P. S., Ferreira, Manuel A. R., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. BMC Medical Genetics, 12 (123) 123, 1-9. doi: 10.1186/1471-2350-12-123

A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications

Heath, Andrew C., Whitfield, John B., Martin, Nicholas G., Pergadia, Michele L., Goate, Alison M., Lind, Penelope A., McEvoy, Brian P., Schrage, Andrew J., Grant, Julia D., Chou, Yi-Ling, Zhu, Rachel, Henders, Anjali K., Medland, Sarah E., Gordon, Scott D., Nelson, Elliot C., Agrawal, Arpana, Nyholt, Dale R., Bucholz, Kathleen K., Madden, Pamela A. F. and Montgomery, Grant W. (2011). A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Biological Psychiatry, 70 (6), 513-518. doi: 10.1016/j.biopsych.2011.02.028

Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search

Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M, McMahon, K. L., de Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack Jr, C. R., Weiner. M. W., Toga. A. W., Thompson, P. M. and The Alzheimer’s Disease Neuroimaging Initiative (2011). Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Molecular Psychiatry, 16 (9), 927-937. doi: 10.1038/mp.2011.32

Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

Kutalik, Zoltan, Benyamin, Beben, Bergmann, Sven, Mooser, Vincent, Waeber, Gerard, Montgomery, Grant W., Martin, Nicholas G., Madden, Pamela A. F., Heath, Andrew C., Beckmann, Jacques S., Vollenweider, Peter, Marques-Vidal, Pedro and Whitfield, John B. (2011). Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. Human Molecular Genetics, 20 (18) ddr272, 3710-3717. doi: 10.1093/hmg/ddr272

Identification of IL6R and chromosome 11q13.5 as risk loci for asthma

Ferreira, Manuel A. R., Matheson, Melanie C., Duffy, David L., Marks, Guy B., Hui, Jennie, Le Souef, Peter, Danoy, Patrick, Baltic, Svetlana, Nyholt, Dale R., Jenkins, Mark, Hayden, Catherine, Willemsen, Gonneke, Ang, Wei, Kuokkanen, Mikko, Beilby, John, Cheah, Faang, de Geus, Eco J.C., Ramasamy, Adaikalavan, Vedantam, Sailaka, Salomaa, Veikko, Madden, Pamela A., Heath, Andrew C., Hopper, John L., Visscher, Peter M., Musk, Bill, Leeder, Stephen R., Jarvelin, Marjo-Riitta, Pennell, Craig, Boomsma, Dorret I. ... Wright, Margaret J. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378 (9795), 1006-1014. doi: 10.1016/S0140-6736(11)60874-X

Genome-wide association reveals dopamine-related genetic effects on caudate volume

Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M., McMahon, K. L., De Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack, C. R., Weiner, M. W., Toga, A. W. and Thompson, P. M. (2011). Genome-wide association reveals dopamine-related genetic effects on caudate volume. Molecular Psychiatry, 16 (9), 881-881. doi: 10.1038/mp.2011.98

Attitudes towards economic risk and the gender pay gap

Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Attitudes towards economic risk and the gender pay gap. Labour Economics, 18 (4), 555-561. doi: 10.1016/j.labeco.2010.12.007

Disordered gambling as defined by the diagnostic and statistical manual of mental disorders and the South Oaks Gambling Screen: evidence for a common etiologic structure

Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2011). Disordered gambling as defined by the diagnostic and statistical manual of mental disorders and the South Oaks Gambling Screen: evidence for a common etiologic structure. Journal of Abnormal Psychology, 120 (3), 743-751. doi: 10.1037/a0022879

Female orgasm rates are largely independent of other traits: Implications for "female orgasmic disorder" and evolutionary theories of orgasm

Zietsch, Brendan P., Miller, Geoffrey F., Bailey, J. Michael and Martin, Nicholas G. (2011). Female orgasm rates are largely independent of other traits: Implications for "female orgasmic disorder" and evolutionary theories of orgasm. Journal of Sexual Medicine, 8 (8), 2305-2316. doi: 10.1111/j.1743-6109.2011.02300.x

GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development

Larsson, Mats, Duffy, David L., Zhu, Gu, Liu, Jimmy Z., Macgregor, Stuart, McRae, Allan F., Wright, Margaret J., Sturm, Richard A., Mackey, David A., Montgomery, Grant W., Martin, Nicholas G. and Medland, Sarah E. (2011). GWAS findings for human iris patterns: Associations with variants in genes that influence normal neuronal pattern development. American Journal of Human Genetics, 89 (2), 334-343. doi: 10.1016/j.ajhg.2011.07.011

Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

Amin, N., Byrne, E., Johnson, J., Chenevix-Trench, G., Walter, S., Nolte, I. M., kConFab Investigators, Vink, J.M., Rawal, R., Mangino, M., Teumer, A., Keers, J. C., Verwoert, G., Baumeister, S., Biffar, R., Petersmann, A., Dahmen, N., Doering, A., Isaacs, A., Broer, L., Wray, N. R., Montgomery, G. W., Levy, D., Psaty, B. M., Gudnason, V., Chakravarti, A., Sulem, P., Gudbjartsson, D. F., Kiemeney, L. A. ... van Duijn, C. M. (2011). Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry, 17 (11), 1116-1129. doi: 10.1038/mp.2011.101

LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts

Maugeri, Narelle, Powell, Joseph E., 't Hoen, Peter A. C., de Geus, Eco J. C., Willemsen, Gonneke, Kattenberg, Mathijs, Henders, Anjali K., Wallace, Leanne, Penninx, Brenda, Hottenga, Jouke-Jan, Medland, Sarah E., Saviouk, Viatcheslav, Martin, Nicholas G., Visscher, Peter M., van Ommen, Gert-Jan B., Frazer, Ian H., Boomsma, Dorret I., Montgomery, Grant W. and Ferreira, Manuel A. R (2011). LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, 32 (8), 873-876. doi: 10.1002/humu.21536

Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men

Bedi, Saaniya, Nelson, Elliot C., Lynskey, Michael T., McCutcheon, Vivia V., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men. Suicide and Life-Threatening Behavior, 41 (4), 406-415. doi: 10.1111/j.1943-278X.2011.00040.x

Heritability of working memory brain activation

Blokland, Gabriella A. M., McMahon, Katie L., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2011). Heritability of working memory brain activation. Journal of Neuroscience, 31 (30), 10882-10890. doi: 10.1523/JNEUROSCI.5334-10.2011

Genetic architecture of circulating lipid levels

Demirkan, Ayse, Amin, Najaf, Isaacs, Aaron, Jarvelin, Marjo-Riitta, Whitfield, John B., Wichmann, Heinz-Erich, Kyvik, Kirsten Ohm, Rudan, Igor, Gieger, Christian, Hicks, Andrew A., Johansson, Asa, Hottenga, Jouke-Jan, Smith, Johannes J., Wild, Sarah H., Pedersen, Nancy L., Willemsen, Gonneke, Mangino, Massimo, Hayward, Caroline, Uitterlinden, Andre G., Hofman, Albert, Witteman, Jacqueline, Montgomery, Grant W., Pietilainen, Kirsi H., Rantanen, Taina, Kaprio, Jaakko, Doering, Angela, Pramstaller, Peter P., Gyllensten, Ulf, de Geus, Eco J. C. ... van Duijn, Cornelia M. (2011). Genetic architecture of circulating lipid levels. European Journal of Human Genetics, 19 (7), 813-819. doi: 10.1038/ejhg.2011.21

Genomic inflation factors under polygenic inheritance

Yang, Jian, Weedon, Michael N., Purcell, Shaun, Lettre, Guillaume, Estrada, Karol, Willer, Cristen J., Smith, Albert V., Ingelsson, Erik, O'Connell, Jeffrey R., Mangino, Massimo, Maegi, Reedik, Madden, Pamela A., Heath, Andrew C., Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Frayling, Timothy M., Hirschhorn, Joel N., McCarthy, Mark I., Goddard, Michael E. and Visscher, Peter M. (2011). Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics, 19 (7), 807-812. doi: 10.1038/ejhg.2011.39

Ophthalmic phenotypes and the representativeness of twin data for the general population

Sanfilippo, Paul G., Medland, Sarah E., Hewitt, Alex W., Kearns, Lisa S., Ruddle, Jonathan B., Sun, Cong, Hammond, Christopher J., Young, Terri L., Martin, Nicholas G. and Mackey, David A. (2011). Ophthalmic phenotypes and the representativeness of twin data for the general population. Investigative Ophthalmology & Visual Science, 52 (8), 5565-5572. doi: 10.1167/iovs.11-7258

Parental depression and offspring psychopathology: a Children of Twins study

Singh, A. L., D'Onofrio, B. M., Slutske, W. S., Turkheimer, E., Emery, R. E., Harden, K. P., Heath, A. C., Madden, P. A. F., Statham, D. J. and Martin, N. G. (2011). Parental depression and offspring psychopathology: a Children of Twins study. Psychological Medicine, 41 (7), 1385-1395. doi: 10.1017/S0033291710002059

Performance of a third-generation TSH-receptor antibody in a UK clinic

Theodoraki, A., Jones, G., Parker, J., Woolman, E., Martin, N., Perera, S., Thomas, M., Bunn, C., Khoo, B., Bouloux, P. M. and Vanderpump, M. P. J. (2011). Performance of a third-generation TSH-receptor antibody in a UK clinic. Clinical Endocrinology, 75 (1), 127-133. doi: 10.1111/j.1365-2265.2011.04022.x

Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?

Slutske, Wendy S., Bascom, Elise N., Meier, Madeline H., Medland, Sarah E. and Martin, Nicholas G. (2011). Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?. Behavior Genetics, 41 (4), 533-542. doi: 10.1007/s10519-010-9416-3

Educational Attainment: A Genome Wide Association Study in 9538 Australians

Martin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Educational Attainment: A Genome Wide Association Study in 9538 Australians. PLoS One, 6 (6) e20128, e20128.1-e20128.8. doi: 10.1371/journal.pone.0020128

Genetics of insomnia

Gehrman, Philip R., Byrne, Enda, Gillespie, Nathan and Martin, Nicholas G. (2011). Genetics of insomnia. Sleep Medicine Clinics, 6 (2), 191-202. doi: 10.1016/j.jsmc.2011.03.003

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

Burdon, Kathryn P., Macgregor, Stuart, Hewitt, Alex W., Sharma, Shiwani, Chidlow, Glyn, Mills, Richard A., Danoy, Patrick, Casson, Robert, Viswanathan, Ananth C., Liu, Jimmy Z., Landers, John, Henders, Anjali K., Wood, John, Souzeau, Emmanuelle, Crawford, April, Leo, Paul, Wang, Jie Jin, Rochtchina, Elena, Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Mitchell, Paul, Brown, Matthew A., Mackey, David A. and Craig, Jamie E. (2011). Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nature Genetics, 43 (6), 574-578. doi: 10.1038/ng.824

High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19

Painter, Jodie N., Nyholt, Dale R., Morris, Andrew, Zhao, Zhen Z., Henders, Anjali K., Lambert, Ann, Wallace, Leanne, Martin, Nicholas G., Kennedy, Stephen H., Treloar, Susan A., Zondervan, Krina T. and Montgomery, Grant W. (2011). High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertility and Sterility, 95 (7), 2236-2240. doi: 10.1016/j.fertnstert.2011.03.062

Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study

Beam, Christopher R., Horn, Erin E., Hunt, Stacy Karagis, Emery, Robert E., Turkheimer, Eric and Martin, Nick (2011). Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study. Journal of Family Psychology, 25 (3), 336-344. doi: 10.1037/a0023758

SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample

Luciano, Michelle, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample. Twin Research and Human Genetics, 14 (3), 228-232. doi: 10.1375/twin.14.3.228

Transferrin saturation and mortality

Benyamin, Beben, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Transferrin saturation and mortality. Clinical Chemistry, 57 (6), 921-923. doi: 10.1373/clinchem.2011.162784

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011)

Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stephane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011). Proceedings of the National Academy of Sciences of the United States of America, 108 (22), 9316-9316. doi: 10.1073/pnas.1106917108

Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults

Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2011). Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. The Journal of Neuroscience, 31 (18), 6764-6770. doi: 10.1523/JNEUROSCI.5794-10.2011

Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior

Meier, Madeline H., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2011). Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior. Journal of Abnormal Psychology, 120 (2), 377-388. doi: 10.1037/a0022303

Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating

Zietsch, Brendan P., Verweij, Karin J. H., Heath, Andrew C. and Martin, Nicholas G. (2011). Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating. The American Naturalist, 177 (5), 605-616. doi: 10.1086/659629

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stéphane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America, 108 (17), 7119-7124. doi: 10.1073/pnas.1017288108

Alcoholic marriage: later start, sooner end

Waldron, Mary, Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Alcoholic marriage: later start, sooner end. Alcoholism: Clinical and Experimental Research, 35 (4), 632-642. doi: 10.1111/j.1530-0277.2010.01381.x

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia

Ferreira, Manuel A. R., McRae, Allan F., Medland, Sarah E., Nyholt, Dale R., Gordon, Scott D., Wright, Margaret J., Henders, Anjali K., Madden, Pamela A., Visscher, Peter M., Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Duffy, David L. and Martin, Nicholas G. (2011). Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. European Journal of Human Genetics, 19 (4), 458-464. doi: 10.1038/ejhg.2010.191

Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]

Loehlin, John C. and Martin, Nicholas G. (2011). Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]. Journal of Research in Personality, 45 (2), 258-258. doi: 10.1016/j.jrp.2011.02.010

Does teenage childbearing reduce investment in human capital?

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2011). Does teenage childbearing reduce investment in human capital?. Journal of Population Economics, 24 (2), 701-730. doi: 10.1007/s00148-009-0270-7

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Obstetrical and Gynecological Survey, 66 (4), 214-216. doi: 10.1097/OGX.0b013e318210cea1

The politics of mate choice

Alford, John R., Hatemi, Peter K., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2011). The politics of mate choice. The Journal of Politics, 73 (2), 362-379. doi: 10.1017/S0022381611000016

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Aexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics, 88 (3), 372-381. doi: 10.1016/j.ajhg.2011.01.017

Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

Speliotes, Elizabeth K., Yerges-Armstrong, Laura M., Wu, Jun, Hernaez, Ruben, Kim, Lauren J., Palmer, Cameron D., Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E., Launer, Lenore J., Nalls, Michael A., Clark, Jeanne M., Mitchell, Braxton D., Shuldiner, Alan R., Butler, Johannah L., Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M., O'Donnell, Christopher J., Sahani, Dushyant V., Salomaa, Veikko, Schadt, Eric E., Schwartz, Stephen M., Siscovick, David S., NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F. ... Coin, Lachlan (2011). Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genetics, 7 (3) e1001324, e1001324.1-e1001324.14. doi: 10.1371/journal.pgen.1001324

BDNF gene effects on brain circuitry replicated in 455 twins

Chiang, M. C., Barysheva, M., Toga, A. W., Medland, S. E., Hansel, N. K., James, M. R., McMahon, K. L., de Zubicaray, G. I., Martin, N. G., Wright, M. J. and Thompson, P. M. (2011). BDNF gene effects on brain circuitry replicated in 455 twins. NeuroImage, 55 (2), 448-454. doi: 10.1016/j.neuroimage.2010.12.053

Whole genome association scan for genetic polymorphisms influencing information processing speed

Luciano, Michelle, Hansell, Narelle K., Lahti, Jari, Davies, Gail, Medland, Sarah E., Raikkonen, Katri, Tenesa, Albert, Widen, Elisabeth, McGhee, Kevin A., Palotie, Aarno, Liewald, David, Porteous, David J., Starr, John M., Montgomery, Grant W., Martin, Nicholas G., Eriksson, Johan G., Wright, Margaret J. and Deary, Ian J. (2011). Whole genome association scan for genetic polymorphisms influencing information processing speed. Biological Psychology, 86 (3), 193-202. doi: 10.1016/j.biopsycho.2010.11.008

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)

Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011). American Journal of Human Genetics, 88 (3), 396-396. doi: 10.1016/j.ajhg.2011.03.001

The contribution of genes to cortical thickness and volume

Joshi, A.A., Lepore, N., Joshi, S.H., Lee, A.D., Barysheva, M., Stein, J.L., McMahon, K.L., Johnson, K., de Zubicaray, G.I., Martin, N.G., Wright, M.J., Toga, A.W. and Thompson, P.M. (2011). The contribution of genes to cortical thickness and volume. NeuroReport, 22 (3), 101-105. doi: 10.1097/WNR.0b013e3283424c84

Fast and slow spindle involvement in the consolidation of a new motor sequence

Barakat, M., Doyon, J., Debas, K., Vandewalle, G., Morin, A., Poirier, G., Martin, N., Lafortune, M., Karni, A., Ungerleider, L. G., Benali, H. and Carrier, J. (2011). Fast and slow spindle involvement in the consolidation of a new motor sequence. Behavioural Brain Research, 217 (1), 117-121. doi: 10.1016/j.bbr.2010.10.019

Genetics of white matter development: A DTI study of 705 twins and their siblings aged 12 to 29

Chiang, MC, McMahon, KL, de Zubicaray, GI, Martin, NG, Hickie, I, Toga, AW, Wright, MJ and Thompson, PM (2011). Genetics of white matter development: A DTI study of 705 twins and their siblings aged 12 to 29. NeuroImage, 54 (3), 2308-2317. doi: 10.1016/j.neuroimage.2010.10.015

Nevi, family history, and fair skin increase the risk of second primary melanoma

Siskind, Victor, Hughes, Maria Celia B., Palmer, Jane M., Symmons, Judith M., Aitken, Joanne F., Martin, Nicholas G., Hayward, Nicholas K. and Whiteman, David C. (2011). Nevi, family history, and fair skin increase the risk of second primary melanoma. The Journal of Investigative Dermatology, 131 (2), 461-467. doi: 10.1038/jid.2010.298

Psychiatric and genetic studies of binocular rivalry: an endophenotype for bipolar disorder?

Ngo, Trung T., Mitchell, Philip B., Martin, Nicholas G. and Miller, Steven M. (2011). Psychiatric and genetic studies of binocular rivalry: an endophenotype for bipolar disorder?. Acta Neuropsychiatrica, 23 (1), 37-42. doi: 10.1111/j.1601-5215.2010.00510.x

Sexual orientation and psychiatric vulnerability: A twin study of neuroticism and psychoticism

Zietsch, Brendan P., Verweij, Karin J. H., Bailey, J. Michael, Wright, Margaret J. and Martin, Nicholas G. (2011). Sexual orientation and psychiatric vulnerability: A twin study of neuroticism and psychoticism. Archives of Sexual Behavior, 40 (1), 133-142. doi: 10.1007/s10508-009-9508-4

Sleep slow wave changes during the middle years of life

Carrier, Julie, Viens, Isabelle, Poirier, Gaétan , Robillard, Rébecca , Lafortune, Marjolaine, Vandewalle, Gilles, Martin, Nicolas, Barakat, Marc, Paquet, Jean and Filipini, Daniel (2011). Sleep slow wave changes during the middle years of life. European Journal of Neuroscience, 33 (4), 758-766. doi: 10.1111/j.1460-9568.2010.07543.x

The general factor of personality: questions and elaborations

Loehlin, John C. and Martin, Nicholas G. (2011). The general factor of personality: questions and elaborations. Journal of Research in Personality, 45 (1), 44-49. doi: 10.1016/j.jrp.2010.11.008

The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease

Fahy, Samantha J., Sun, Cong, Zhu, Gu, Healey, Paul R., Spector, Tim D., Martin, Nicolas G., Mitchell, Paul, Wong, Tien Y., Mackey, David A., Hammond, Christopher J. and Andrew, Toby (2011). The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease. Investigative Ophthalmology & Visual Science, 52 (2), 975-981. doi: 10.1167/iovs.10-5927

Variance components models for physical activity with age as modifier: a comparative twin study in seven countries

Vink, Jacqueline M., Boomsma, Dorret I., Medland, Sarah E., de Moor, Marleen H. M., Stubbe, Janine H., Cornes, Belinda K., Martin, Nicholas G., Skytthea, Axel, Kyvik, Kirsten O., Rose, Richard J., Kujala, Urho M., Kaprio, Jaakko, Harris, Jennifer R., Pedersen, Nancy L., Cherkas, Lynn, Spector, Tim D. and de Geus, Eco J. C. (2011). Variance components models for physical activity with age as modifier: a comparative twin study in seven countries. Twin Research and Human Genetics, 14 (1), 25-34. doi: 10.1375/twin.14.1.25

A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families

Pergadia, Michele L., Glowinski, Anne L., Wray, Naomi, Agrawal, Arpana, Saccone, Scott F., Loukola, Anu, Broms, Ulla, Koronen, Tellervo, Penninx, Brenda W. J. H., Grant, Julia D., Nelson, Elliot C., Henders, Anjali K., Schrage, Andrew J., Chou, Yi-Ling, Keskitalo-Vuokko, Kaisu, Zhu, Qin, Gordon, Scott D., Vink, Jacqueline M., de Geus, Eco J. C., MacGregor, Stuart, Liu, Jimmy Z., Willemsen, Gonneke, Medland, Sarah E., Boomsma, Dorret I., Montgomery, Grant W., Rice, John P., Goate, Alison M., Heath, Andrew, C, Martin, Nicholas G. and Madden, Pamela A. F. (2011). A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families. American Journal Psychiatry, 168 (8), 848-852. doi: 10.1176/appi.ajp.2011.10091319

A genome-wide analysis of liberal and conservative political attitudes

Hatemi, Peter K., Gillespie, Nathan A., Eaves, Lindon J., Maher, Brion S., Webb, Bradley T., Heath, Andrew C., Medland, Sarah E., Smyth, David C., Beeby, Harry N., Gordon, Scott D., Montgomery, Grant W., Zhu, Ghu, Byrne, Enda M. and Martin, Nicholas G. (2011). A genome-wide analysis of liberal and conservative political attitudes. Journal of Politics, 73 (1), 271-285. doi: 10.1017/S0022381610001015

Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms

Martin, Nicolas W., Benyamin, Beben, Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50 (1), 55-62.e4. doi: 10.1016/j.jaac.2010.10.010

Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits

Bates, Timothy C., Luciano, Michelle, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics, 41 (1), 50-57. doi: 10.1007/s10519-010-9402-9

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis

Painter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731

Genome-wide association study identifies three new melanoma susceptibility loci

Barrett, Jennifer H., Iles, Mark M., Harland, Mark, Taylor, John C., Aitken, Joanne F., Andresen, Per Arne, Akslen, Lars A., Armstrong, Bruce K., Avril, Marie-Francoise, Azizi, Esther, Bakker, Bert, Bergman, Wilma, Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Calista, Donato, Cannon-Albright, Lisa A., Corda, Eve, Cust, Anne E., Dębniak, Tadeusz, Duffy, David, Dunning, Alison M., Easton, Douglas F., Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Giles, Graham G., Hansson, Johan, Hocevar, Marko, Höiom, Veronica ... Bishop, D. Timothy (2011). Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics, 43 (11), 1108-1113. doi: 10.1038/ng.959

Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms

Vinkhuyzen, A. A. E., Dumenil, T., Ryan, L., Gordon, S. D., Henders, A. K., Madden, P. A. F., Heath, A. C., Montgomery, G. W., Martin, N. G. and Wray, N. R. (2011). Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms. Molecular Psychiatry, 16 (11), 1073-1075. doi: 10.1038/mp.2011.68

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J. ... Posthuma, Danielle (2011). The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 156 (2), 145-157. doi: 10.1002/ajmg.b.31149

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

Middeldorp, C. M., de Moor, M. H. M., McGrath, L. M., Gordon, S. D., Blackwood, D. H., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Nyholt, D. R., Tanaka, T., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A, Ripke, S., Sullivan, P. F., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A. ... Boomsma, D. I. (2011). The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data. Translational Psychiatry, 1 (10) e50, e50.1-e50.8. doi: 10.1038/tp.2011.45

Undue influence of weight and shape: Is it distinct from body dissatisfaction and concern about weight and shape?

Wade, T. D., Zhu, G. and Martin, N. G. (2011). Undue influence of weight and shape: Is it distinct from body dissatisfaction and concern about weight and shape?. Psychological Medicine, 41 (4), 819-828. doi: 10.1017/S0033291710001066

Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: The Australian twins eye study

Sun, Cong, Ponsonby, Anne-Louise, Brown, Shayne A., Kearns, Lisa S., Mackinnon, Jane R., Barbour, Julie M., Ruddle, Jonathan B., Wright, Margaret J., Martin, Nicholas G., Dwyer, Terence and Mackey, David A. (2010). Associations of birth weight with ocular biometry, refraction, and glaucomatous endophenotypes: The Australian twins eye study. American Journal of Ophthalmology, 150 (6), 909-916. doi: 10.1016/j.ajo.2010.06.028

Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation

Bates, T. C., Lind, P. A., Luciano, M., Montgomery, G. W., Martin, N. G. and Wright, M. J. (2010). Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation. Molecular Psychiatry, 15 (12), 1190-1196. doi: 10.1038/mp.2009.120

Pathological gambling recovery in the absence of abstinence

Slutske, Wendy S., Piasecki, Thomas M., Blaszczynski, Alex and Martin, Nicholas G. (2010). Pathological gambling recovery in the absence of abstinence. Addiction, 105 (12), 2169-2175. doi: 10.1111/j.1360-0443.2010.03080.x

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C. Y., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J. J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F., Smith, A. V., Stolk, L., Van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K. E. ... GIANT Consortium (2010). Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics, 42 (12), 1077-1085. doi: 10.1038/ng.714

Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states

Sprangers, Mirjam A. G., Bartels, Meike, Veenhoven, Ruut, Baas, Frank, Martin, Nicholas G., Mosing, Miriam, Movsas, Benjamin, Ropka, Mary E., Shinozaki, Gen, Swaab, Dick and The GENEQOL Consortium (2010). Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states. Quality of Life Research, 19 (10), 1429-1437. doi: 10.1007/s11136-010-9652-2

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Elizabeth K Speliotes, Cristen J Willer, Sonja I Berndt, Keri L Monda, Gudmar Thorleifsson, Anne U Jackson, Hana Lango Allen, Cecilia M Lindgren, Jian'an Luan, Reedik Magi, Joshua C Randall, Sailaja Vedantam, Thomas W Winkler, Lu Qi, Tsegaselassie Workalemahu, Iris M Heid, Valgerdur Steinthorsdottir, Heather M Stringham, Michael N Weedon, Eleanor Wheeler, Andrew R Wood, Teresa Ferreira, Robert J Weyant, Ayellet V Segre, Karol Estrada, Liming Liang, James Nemesh, Ju-Hyun Park, Stefan Gustafsson ... Ruth J F Loos (2010). Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics, 42 (11), 937-948. doi: 10.1038/ng.686

The heritability of general cognitive ability increases linearly from childhood to young adulthood

Haworth, Cma, Wright, MJ, Luciano, M, Martin, NG, de Geus, EJC, van Beijsterveldt, CEM, Bartels, M, Posthuma, D, Boomsma, DI, Davis, OSP, Kovas, Y, Corley, RP, DeFries, JC, Hewitt, JK, Olson, RK, Rhea, SA, Wadsworth, SJ, Iacono, WG, McGue, M, Thompson, LA, Hart, SA, Petrill, SA, Lubinski, D and Plomin, R (2010). The heritability of general cognitive ability increases linearly from childhood to young adulthood. Molecular Psychiatry, 15 (11), 1112-1120. doi: 10.1038/mp.2009.55

The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

Reed, Danielle R., Zhu, Gu, Breslin, Paul A. S., Duke, Fujiko F., Henders, Anjali K., Campbell, Megan J., Montgomery, Grant W., Medland, Sarah E., Martin, Nicholas G. and Wright, Margaret J. (2010). The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. Human Molecular Genetics, 19 (21) ddq324, 4278-4285. doi: 10.1093/hmg/ddq324

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Allen, Hana Lango, Estrada, Karol, Lettre, Guillaume, Berndt, Sonja I., Weedon, Michael N., Rivadeneira, Fernando, Willer, Cristen J., Jackson, Anne U., Vedantam, Sailaja, Raychaudhuri, Soumya, Nyholt, Dale, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2010). Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature, 467 (7317), 832-838. doi: 10.1038/nature09410

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25

Hysi, Pirro G., Young, Terri L., Mackey, David A., Andrew, Toby, Fernandez-Medarde, Alberto, Solouki, Abbas M., Hewitt, Alex W., Macgregor, Stuart, Vingerling, Johannes R., Li, Yi-Ju, Ikram, M. Kamran, Fai, Lee Yiu, Sham, Pak C., Manyes, Lara, Porteros, Angel, Lopes, Margarida C., Carbonaro, Francis, Fahy, Samantha J., Martin, Nicholas G., van Diujn, Cornelia M., Spector, Timothy D., Rahi, Jugnoo S., Santos, Eugenio, Klaver, Caroline C. W. and Hammond, Christopher J. (2010). A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Nature Genetics, 42 (10), 902-905. doi: 10.1038/ng.664

A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personality

Verweij, Kjh, Zietsch, BP, Medland, SE, Gordon, SD, Benyamin, B, Nyholt, DR, McEvoy, BP, Sullivan, PF, Heath, AC, Madden, PAF, Henders, AK, Montgomery, GW, Martin, NG and Wray, NR (2010). A genome-wide association study of Cloninger’s temperament scales: Implications for the evolutionary genetics of personality. Biological Psychology, 85 (2), 306-317. doi: 10.1016/j.biopsycho.2010.07.018

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Antoniou, Antonis C., Wang, Xianshu, Fredericksen, Zachary S., McGuffog, Lesley, Tarrell, Robert, Sinilnikova, Olga M., Healey, Sue, Morrison, Jonathan, Kartsonaki,Christiana, Lesnick, Timothy, Ghoussaini, Maya, Barrowdale, Daniel, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Eccles, Diana, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Chu, Carol, Douglas, Fiona, Paterson, Joan, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Mazoyer, Sylvie, Giraud, Sophie, Lasset, Christine, Remenieras, Audrey ... Lakhani, Sunil (2010). A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population. Nature Genetics, 42 (10), 885-892. doi: 10.1038/ng.669

Body mass index and breast size in women: Same or different genes?

Wade, Tracey D., Zhu, Gu and Martin, Nicholas G. (2010). Body mass index and breast size in women: Same or different genes?. Twin Research and Human Genetics, 13 (5), 450-454. doi: 10.1375/twin.13.5.450

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

Thorleifsson, Gudmar, Walters, G. Bragi, Hewitt, Alex W., Masson, Gisli, Helgason, Agnar, DeWan, Andrew, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Gudjonsson, Sigurjon A., Magnusson, Kristinn P., Stefansson, Hreinn, Lam, Dennis S. C., Tam, Pancy O. S., Gudmundsdottir, Gudrun J., Southgate, Laura, Burdon, Kathryn P., Gottfredsdottir, Maria Soffia, Aldred, Micheala A., Mitchell, Paul, St Clair, David, Collier, David A., Tang, Nelson, Sveinsson, Orn, Macgregor, Stuart, Martin, Nicholas G., Cree, Angela J., Gibson, Jane, MacLeod, Alex, Jacob, Aby ... Stefansson, Kari (2010). Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics, 42 (10), 906-910. doi: 10.1038/ng.661

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

Ikram, M. Kamran, Sim, Xueling, Jensen, Richard A., Cotch, Mary Frances, Hewitt, Alex W., Ikram, M. Arfan, Wang, Jie Jin, Klein, Ronald, Klein, Barbara E. K., Breteler, Monique M. B., Cheung, Ning, Liew, Gerald, Mitchell, Paul, Uitterlinden, Andrew G., Rivadeneira, Fernando, Hofman, Albert, de Jong, Paulus T. V. M., van Kuijn, Cornelia M., Kao, Linda, Cheng, Ching-Yu, Smith, Albert Vernon, Glazer, Nicole L., Lumley, Thomas, McKnight, Barbara, Psaty, Bruce M., Jonasson, Fridbert, Eiriksdottir, Gudny, Aspelund, Thor, Global BPgen Consortium ... Wong, Tien Y. (2010). Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genetics, 6 (10) e1001184, 1-12. doi: 10.1371/journal.pgen.1001184

Stringent programming of DNA methylation in humans

Aung, Hnin T., Harrison, Dion K., Findlay, Ian, Mattick, John S., Martin, Nicholas G. and Carroll, Bernard J. (2010). Stringent programming of DNA methylation in humans. Twin Research and Human Genetics, 13 (5), 405-411. doi: 10.1375/twin.13.5.405

The nature of the relationship between personality traits and political attitudes

Verhulst, Brad, Hatemi, Peter K. and Martin, Nicholas G. (2010). The nature of the relationship between personality traits and political attitudes. Personality and Individual Differences, 49 (4), 306-316. doi: 10.1016/j.paid.2009.11.013

Biological, clinical and population relevance of 95 loci for blood lipids

Teslovich, Tanya M., Musunuru, Kiran, Smith, Albert V., Edmondson, Andrew C., Stylianou, Ioannis M., Koseki, Masahiro, Pirruccello, James P., Ripatti, Samuli, Chasman, Daniel I., Willer, Cristen J., Johansen, Christopher T., Fouchier, Sigrid W., Isaacs, Aaron, Peloso, Gina M., Barbalic, Maja, Ricketts, Sally L., Bis, Joshua C., Aulchenko, Yurii S., Thorleifsson, Gudmar, Feitosa, Mary F., Chambers, John, Orho-Melander, Marju, Melander, Olle, Johnson, Toby, Li, Xiaohui, Guo, Xiuqing, Li, Mingyao, Cho, Yoon Shin, Go, Min Jin ... Kathiresan, Sekar (2010). Biological, clinical and population relevance of 95 loci for blood lipids. Nature, 466 (7307), 707-713. doi: 10.1038/nature09270

A genome-wide association study of self-rated health

Mosing, Miriam A., Verweij, Karin J. H., Medland, Sarah E., Painter, Jodie, Gordon, Scott D., Heath, Andrew C., Madden, Pamela A., Montgomery, Grant W. and Martin, Nicholas G. (2010). A genome-wide association study of self-rated health. Twin Research and Human Genetics, 13 (4), 398-403. doi: 10.1375/twin.13.4.398

Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling

Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2010). Are attitudes towards economic risk heritable? Analyses using the Australian twin study of gambling. Twin Research And Human Genetics, 13 (4), 330-339. doi: 10.1375/twin.13.4.330

Genetic covariance structure of the four main features of borderline personality disorder

Distel, Marijn A., Willemsen, Gonneke, Ligthart, Lannie, Derom, Catherine A., Martin, Nicholas G., Neale, Michael C., Trull, Timothy J. and Boomsma, Dorret I. (2010). Genetic covariance structure of the four main features of borderline personality disorder. Journal of Personality Disorders, 24 (4), 427-444. doi: 10.1521/pedi.2010.24.4.427

Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings

Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2010). Genetic influences on brain asymmetry: A DTI study of 374 twins and siblings. NeuroImage, 52 (2), 455-469. doi: 10.1016/j.neuroimage.2010.04.236

Heritability of head size in Dutch and Australian twin families at ages 0-50 years

Smit, Dirk J. A., Luciano, Michelle, Bartels, Meike, van Beijsterveldt, Catharine E. M., Wright, Margaret J., Hansell, Narelle K., Brunner, Han G., Estourgie-van Burk, G. Frederiek, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2010). Heritability of head size in Dutch and Australian twin families at ages 0-50 years. Twin Research And Human Genetics, 13 (4), 370-380. doi: 10.1375/twin.13.4.370

Imaging genomics

Thompson, Paul M., Martin, Nicholas G. and Wright, Margaret J. (2010). Imaging genomics. Current Opinion in Neurology, 23 (4), 368-373. doi: 10.1097/WCO.0b013e32833b764c

Major depression and the metabolic syndrome

Foley, Debra L., Morley, Katherine I., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2010). Major depression and the metabolic syndrome. Twin Research and Human Genetics, 13 (4), 347-358. doi: 10.1375/twin.13.4.347

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD

Saccone, Nancy L., Culverhouse, Robert C., Schwantes-An, Tae-Hwi, Cannon, Dale S., Chen, Xiangning, Cichon, Sven, Giegling, Ina, Han, Shizhong, Han, Younghun, Keskitalo-Vuokko, Kaisu, Kong, Xiangyang, Landi, Maria Teresa, Ma, Jennie Z., Short, Susan E., Stephens, Sarah H., Stevens, Victoria L., Sun, Lingwei, Wang, Yufei, Wenzlaff, Angela S., Aggen, Steven H., Breslau, Naomi, Broderick, Peter, Chatterjee, Nilanjan, Chen, Jingchun, Heath, Andrew C., Heliovaara, Markku, Hoft, Nicole R., Hunter, David J., Jensen, Majken K. ... Bierut, Laura J. (2010). Multiple independent loci at chromosome 15q25.1 affect smoking quantity: A meta-analysis and comparison with lung cancer and COPD. PLoS Genetics, 6 (8), 1-16. doi: 10.1371/journal.pgen.1001053

Nicotine withdrawal symptoms in adolescent and adult twins

Pergadia, Michele L., Agrawal, Arpana, Heath, Andrew C., Martin, Nicholas G., Bucholz, Kathleen K. and Madden, Pamela A. F. (2010). Nicotine withdrawal symptoms in adolescent and adult twins. Twin Research And Human Genetics, 13 (4), 359-369. doi: 10.1375/twin.13.4.359

Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins

Mosing, Miriam A., Pedersen, Nancy L., Martin, Nicholas G. and Wright, Margaret J. (2010). Sex differences in the genetic architecture of optimism and health and their interrelation: A study of Australian and Swedish twins. Twin Research And Human Genetics, 13 (4), 322-329. doi: 10.1375/twin.13.4.322

The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs

Slutske, Wendy S., Piasecki, Thomas M., Ellingson, Jarrod M. and Martin, Nicholas G. (2010). The family history method in disordered gambling research: A comparison of reports obtained from discordant twin pairs. Twin Research and Human Genetics, 13 (4), 340-346. doi: 10.1375/twin.13.4.340

A versatile gene-based test for genome-wide association studies

Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010). A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 (1), 139-145. doi: 10.1016/j.ajhg.2010.06.009

Common SNPs explain a large proportion of the heritability for human height

Yang, Jian, Benyamin, Beben, McEvoy, Brian P., Gordon, Scott, Henders, Anjali K., Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Goddard, Michael E. and Visscher, Peter M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42 (7), 565-569. doi: 10.1038/ng.608

Genome-wide association identifies ATOH7 as a major gene determining human optic disc size

Macgregor, Stuart, Hewitt, Alex W., Hysi, Pirro G., Ruddle, Jonathan B., Medland, Sarah E., Henders, Anjali K., Gordon, Scott D., Andrew, Toby, McEvoy, Brian, Sanfilippo, Paul G., Carbonaro, Francis, Tah, Vikas, Li, Yi Ju, Bennett, Sonya L., Craig, Jamie E., Montgomery, Grant W., Tran-Viet, Khanh-Nhat, Brown, Nadean L., Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond, Christopher J. and Mackey, David A. (2010). Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Human Molecular Genetics, 19 (13) ddq144, 2716-2724. doi: 10.1093/hmg/ddq144

IRF4 variants have age-specific effects on nevus count and predispose to melanoma

Duffy, David L., Iles, Mark M., Glass, Dan, Zhu, Gu, Barrett, Jennifer H., Hoiom, Veronica, Zhao, Zhen Z., Sturm, Richard A., Soranzo, Nicole, Hammond, Chris, Kvaskoff, Marina, Whiteman, David C., Mangino, Massimo, Hansson, Johan, Newton-Bishop, Julia A., Bataille, Veronique, Hayward, Nicholas K., Martin, Nicholas G., Bishop, D. Timothy, Spector, Timothy D. and Montgomery, Grant W. (2010). IRF4 variants have age-specific effects on nevus count and predispose to melanoma. American Journal of Human Genetics, 87 (1), 6-16. doi: 10.1016/j.ajhg.2010.05.017

Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs

Hatemi, Peter K., Hibbing, John R., Medland, Sarah E., Keller, Matthew C., Alford, John R., Smith, Kevin B., Martin, Nicholas G. and Eaves, Lindon J. (2010). Not by twins alone: Using the extended family design to investigate genetic influence on political beliefs. American Journal of Political Science, 54 (3), 798-814. doi: 10.1111/j.1540-5907.2010.00461.x

A genetic basis for social trust?

Sturgis, Patrick, Read, Sanna, Hatemi, Peter K., Zhu, Gu, Trull, Tim, Wright, Margaret J. and Martin, Nicholas G. (2010). A genetic basis for social trust?. Political Behavior, 32 (2), 205-230. doi: 10.1007/s11109-009-9101-5

A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins

Painter, Jodie N., Willemsen, Gonneke, Nyholt, Dale, Hoekstra, Chantal, Duffy, David L., Henders, Anjali K., Wallace, Leanne, Healey, Sue, Cannon-Albright, Lisa A., Skolnick, Mark, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2010). A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction, 25 (6), 1569-1580. doi: 10.1093/humrep/deq084

Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample

Lind, Penelope A., Luciano, Michelle, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2010). Dyslexia and DCDC2: Normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample. European Journal of Human Genetics, 18 (6), 668-673. doi: 10.1038/ejhg.2009.237

Genetic and environmental influences on disordered gambling in men and women

Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2010). Genetic and environmental influences on disordered gambling in men and women. Archives of General Psychiatry, 67 (6), 624-630. doi: 10.1001/archgenpsychiatry.2010.51

Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes

Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2010). Genetic effects on toxic and essential elements in humans: Arsenic, cadmium, copper, lead, mercury, selenium, and zinc in erythrocytes. Environmental Health Perspectives, 118 (6), 776-782. doi: 10.1289/ehp.0901541

The reliability and validity of the family history method for assessing pathological gambling and gambling involvement

Ellingson, Jarrod M., Slutske, Wendy S. and Martin, Nicholas G. (2010). The reliability and validity of the family history method for assessing pathological gambling and gambling involvement. Psychology of Addictive Behaviors, 24 (2), 292-299. doi: 10.1037/a0018126

Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010). Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 (5), e1000947.1-e1000947.10. doi: 10.1371/journal.pgen.1000947

Digital quantification of human eye color highlights genetic association of three new loci

Liu, Fan, Wollstein, Andreas, Hysi, Pirro G., Ankra-Badu, Georgina A., Spector, Timothy D., Park, Daniel, Zhu, Gu, Larsson, Mats, Duffy, David L., Montgomery, Grant W., Mackey, David A., Walsh, Susan, Lao, Oscar, Hofman, Albert, Rivadeneira, Fernando, Vingerling, Johannes R., Uitterlinden, Andrew G., Martin, Nicholas G., Hammond, Christopher J. and Kayser, Manfred (2010). Digital quantification of human eye color highlights genetic association of three new loci. PLoS Genetics, 6 (5), e1000934-1-e1000934-15. doi: 10.1371/journal.pgen.1000934

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

Thorgeirsson, Thorgeir E., Gudbjartsson, Daniel F., Surakka, Ida, Vink, Jacqueline M., Amin, Najaf, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Esko, Tōnu, Walter, Stefan, Gieger, Christian, Rawal, Rajesh, Mangino, Massimo, Prokopenko, Inga, Mägi, Reedik, Keskitalo, Kaisu, Gudjonsdottir, Iris H., Gretarsdottir, Solveig, Stefansson, Hreinn, Thompson, John R., Aulchenko, Yurii S., Nelis, Mari, Aben, Katja K., den Heijer, Martin, Dirksen, Asger, Ashraf, Haseem, Soranzo, Nicole, Valdes, Ana M., Steves, Claire ... Stefansson, Kari (2010). Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, 42 (5), 448-454. doi: 10.1038/ng.573

A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure

Medland, Sarah E., Zayats,Tetyana, Glaser, Beate, Nyholt, Dale R., Gordon,Scott D., Wright, Margaret J., Montgomery, Grant W., Campbell, Megan J., Henders, Anjali K., Timpson, Nicholas J., Peltonen, Leena, Wolke, Dieter, Ring, Susan M., Deloukas, Panos, Martin, Nicholas G., Smith, George Davey and Evans, David M. (2010). A variant in LIN28B is Associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. American Journal of Human Genetics, 86 (4), 519-525. doi: 10.1016/j.ajhg.2010.02.017

A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures

Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2010). A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures. Twin Research and Human Genetics, 13 (2), 121-130. doi: 10.1375/twin.13.2.121

Genome-wide association study of height and body mass index in Australian twin families

Liu, Jimmy Z., Medland, Sarah E., Wright, Margaret J., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Duncan, Alexis, Montgomery, Grant W., Martin, Nicholas G. and McRae, Allan F. (2010). Genome-wide association study of height and body mass index in Australian twin families. Twin Research And Human Genetics, 13 (2), 179-193. doi: 10.1375/twin.13.2.179

Characterization of the methylation patterns of MS4A2 in atopic cases and controls

M. A. R. Ferreira, N. A. Oates, J. van Vliet, Z. Z. Zhao, M. Ehrich, N. G. Martin, G. W. Montgomery, E. Whitelaw and D. L. Duffy (2010). Characterization of the methylation patterns of MS4A2 in atopic cases and controls. ALLERGY, 65 (3), 333-337. doi: 10.1111/j.1398-9995.2009.02135.x

Common genetic contributions to alcohol and cannabis use and dependence symptomatology

Sartor, Carolyn E., Grant, Julia D., Bucholz, Kathleen K., Madden, Pamela A. F., Heath, Andrew C., Agrawal, Arpana, Whitfield, John B., Statham, Dixie J., Martin, Nicholas G. and Lynkey, Michael T. (2010). Common genetic contributions to alcohol and cannabis use and dependence symptomatology. Alcoholism: Clinical and Experimental Research, 34 (3), 545-554. doi: 10.1111/j.1530-0277.2009.01120.x

Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies

Verweij, Karin J. H., Zietsch, Brendan P., Lynskey, Michael T., Medland, Sarah E., Neale, Michael C., Martin, Nicholas G., Boomsma, Dorret I. and Vink, Jacqueline M. (2010). Genetic and environmental influences on cannabis use initiation and problematic use: A meta-analysis of twin studies. Addiction, 105 (3), 417-430. doi: 10.1111/j.1360-0443.2009.02831.x

A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations

Lind, Penelope A., Macgregor, Stuart, Vink, Jacqueline M., Pergadia, Michele L., Hansell, Narelle K., de Moor, Marleen H. M., Smit, August B., Hottenga, Jouke-Jan, Richter, Melinda M., Heath, Andrew C., Martin, Nicholas G., Willemsen, Gonneke, de Geus, Eco J. C., Vogelzangs,Nicole, Penninx, Brenda W., Whitfield, John B., Montgomery, Grant W., Boomsma, Dorret I. and Madden, Pamela A. F. (2010). A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Research And Human Genetics, 13 (1), 10-29. doi: 10.1375/twin.13.1.10

Clustering of trauma and associations with single and co-occurring depression and panic attack over twenty years

McCutcheon, Vivia V., Heath, Andrew C., Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2010). Clustering of trauma and associations with single and co-occurring depression and panic attack over twenty years. Twin Research And Human Genetics, 13 (1), 57-65. doi: 10.1375/twin.13.1.57

Genetic contribution to individual variation in binocular rivalry rate

Miller, Steven M., Hansell, Narelle K., Ngo, Trung T., Liu, Guang B., Pettigrew, John D., Martin, Nicholas G. and Wright, Margaret J. (2010). Genetic contribution to individual variation in binocular rivalry rate. Proceedings of the National Academy of Sciences of the United States of America, 107 (6), 2664-2668. doi: 10.1073/pnas.0912149107

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma

Duffy, David L., Zhao, Zhen Z., Sturm, Richard A., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2010). Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma. Journal of Investigative Dermatology, 130 (2), 520-528. doi: 10.1038/jid.2009.258

Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control

Ferreira, Mar, Mangino, M, Brumme, CJ, Zhao, ZZ, Medland, SE, Wright, MJ, Nyholt, DR, Gordon, S, Campbell, M, McEvoy, BP, Henders, A, Evans, DM, Lanchbury, JS, Pereyra, F, Walker, BD, Haas, DW, Soranzo, N, Spector, TD, de Bakker, PIW, Frazer, IH, Montgomery, GW, Martin, NG and Int HIV Controllers Study (2010). Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. American Journal of Human Genetics, 86 (1), 88-92. doi: 10.1016/j.ajhg.2009.12.008

Does education reduce the probability of being overweight?

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2010). Does education reduce the probability of being overweight?. Journal of Health Economics, 29 (1), 29-38. doi: 10.1016/j.jhealeco.2009.11.013

Genetic and Environmental Influences on Sexual Orientation

Dawood, Khytam, Bailey, J. Michael and Martin, Nicholas G. (2010). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics, 269-279. doi: 10.1007/978-0-387-76727-7_19

Genetic and environmental influences on risky sexual behaviour and its relationship with personality

Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Genetic and environmental influences on risky sexual behaviour and its relationship with personality. Behavior Genetics, 40 (1), 12-21. doi: 10.1007/s10519-009-9300-1

H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence

Nelson, Elliot C., Agrawal, Arpana, Pergadia, Michele L., Wang, Jen C., Whitfield, John B., Saccone, F. Scott, Kern, Jason, Grant, Julia D., Schrage, Andrew J., Rice, John P., Montgomery, Grant W., Heath, Andrew C, Goate, Alison M., Martin, Nicholas G. and Madden, Pamela A. F. (2010). H2 haplotype at chromosome 17q21.31 protects against childhood sexual abuse-associated risk for alcohol consumption and dependence. Addiction Biology, 15 (1), 1-11. doi: 10.1111/j.1369-1600.2009.00181.x

Linkage analysis of alcohol dependence symptoms in the community

Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Gordon, Scott D., Lind, Penelope A., Pergadia, Michele L., Montgomery, Grant W., Madden, Pamela A. F., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2010). Linkage analysis of alcohol dependence symptoms in the community. Alcoholism: Clinical and Experimental Research, 34 (1), 158-163. doi: 10.1111/j.1530-0277.2009.01077.x

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

Bouzigon, Emmanuelle, Forabosco, Paola, Koppelman, Gerard H., Cookson, William O. C. M., Dizier, Marie-Helene, Duffy, David L., Evans, David M., Ferreira, Manuel A. R., Kere, Juha, Laitinen, Tarja, Malerba, Giovanni, Meyers, Deborah A., Moffatt, Miriam, Martin, Nicholas G, Ng, Mandy Y., Pignatti, Pier Franco, Wjst, Mathias, Kauffmann, Francine, Demenais, Florence and Lewis, Cathryn M. (2010). Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy. European Journal of Human Genetics, 18 (6), 700-706. doi: 10.1038/ejhg.2009.224

The Five-Factor Model of Personality and Borderline Personality Disorder: A Genetic Analysis of Comorbidity

Marijn A. Distel, Timothy J. Trull, Gonneke Willemsen, Jacqueline M. Vink, Catherine A. Derom, Michael Lynskey, Nicholas G. Martin and Dorret I. Boomsm (2009). The Five-Factor Model of Personality and Borderline Personality Disorder: A Genetic Analysis of Comorbidity. BIOLOGICAL PSYCHIATRY, 66 (12), 1131-1138. doi: 10.1016/j.biopsych.2009.07.017

A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study

Sachdev, Perminder S., Lammel, Andrea, Trollor, Julian N., Lee, Teresa, Wright, Margaret J., Ames, David, Wen, Wei, Martin, Nicholas G., Brodaty, Henry, Schofield, Peter R. and OATS Research Team (2009). A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study. Twin Research and Human Genetics, 12 (6), 573-582. doi: 10.1375/twin.12.6.573

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009). Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 (5), 750-755. doi: 10.1016/j.ajhg.2009.10.009

Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample

William L. Coventry, Michael R. James, Lindon J. Eaves, Scott D. Gordon, Nathan A. Gillespie, Leanne Ryan, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin and Naomi R. Wray (2009). Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sample. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 153b (3), 757-765. doi: 10.1002/ajmg.b.31044

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

Benyamin, B, Ferreira, MAR, Willemsen, G, Gordon, S, Middelberg, RPS, McEvoy, BP, Hottenga, JJ, Henders, AK, Campbell, MJ, Wallace, L, Frazer, IH, Heath, AC, de Geus, EJC, Nyholt, DR, Visscher, PM, Penninx, BW, Boomsma, DI, Martin, NG, Montgomery, GW and Whitfield, JB (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics, 41 (11), 1173-1175. doi: 10.1038/ng.456

Genetic and environmental influences on optimism and its relationship to mental and self-rated health: A study of aging twins

Mosing, Miriam A., Zietsch, Brendan P., Shekar, Sri N., Wright, Margaret J. and Martin, Nicholas G. (2009). Genetic and environmental influences on optimism and its relationship to mental and self-rated health: A study of aging twins. Behavior Genetics, 39 (6), 597-604. doi: 10.1007/s10519-009-9287-7

Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume

Ferreira, MAR, Hottenga, JJ, Warrington, NM, Medland, SE, Willemsen, G, Lawrence, RW, Gordon, S, de Geus, EJC, Henders, AK, Smit, JH, Campbell, MJ, Wallace, L, Evans, DM, Wright, MJ, Nyholt, DR, James, AL, Beilby, JP, Penninx, BW, Palmer, LJ, Frazer, IH, Montgomery, GW, Martin, NG and Boomsma, DI (2009). Sequence Variants in Three Loci Influence Monocyte Counts and Erythrocyte Volume. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (5), 745-749. doi: 10.1016/j.ajhg.2009.10.005

Alcohol consumption indices of genetic risk for alcohol dependence

Julia D. Grant, Arpana Agrawal, Kathleen K. Bucholz, Pamela A.F. Madden, Michele L. Pergadia, Elliot C. Nelson, Michael T. Lynskey, Richard D. Todd, Alexandre A. Todorov, Narelle K. Hansell, John B. Whitfield, Nicholas G. Martin and Andrew C. Heath (2009). Alcohol consumption indices of genetic risk for alcohol dependence. Biological Psychiatry, 66 (8), 795-800. doi: 10.1016/j.biopsych.2009.05.018

Association and interaction analyses of eight genes under asthma linkage peaks

Ferreira, M. A. R., Zhao, Z. Z., Thomsen, S. F., James, M., Evans, D. M., Postmus, P. E., Kyvik, K. O., Backer, V., Boomsma, D. I., Martin, N. G., Montgomery, G. W. and Duffy, D. L. (2009). Association and interaction analyses of eight genes under asthma linkage peaks. Allergy, 64 (11), 1623-1628. doi: 10.1111/j.1398-9995.2009.02091.x

Estimating the Heritability of Hair Curliness in Twins of European Ancestry

Sarah E. Medland, Gu Zhu and Nicholas G. Martin (2009). Estimating the Heritability of Hair Curliness in Twins of European Ancestry. Twin Research and Human Genetics, 12 (5), 514-518. doi: 10.1375/twin.12.5.514

Parental Alcoholism and Offspring Behavior Problems: Findings in Australian Children of Twins

Mary Waldron, Nicholas G. Martin and Andrew C. Heath (2009). Parental Alcoholism and Offspring Behavior Problems: Findings in Australian Children of Twins. Twin Research and Human Genetics, 12 (5), 433-440. doi: 10.1375/twin.12.5.433

Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study

Sun, Cong, Zhu, Gu, Wong, Tien Y, Hewitt, Alex W, Ruddle, Jonathan B, Hodgson, Lauren, Montgomery, Grant W, Young, Terri L, Hammond, Christopher J, Craig, Jamie E, Martin, Nicholas G, He, Mingguang and Mackey, David A. (2009). Quantitative Genetic Analysis of the Retinal Vascular Caliber: The Australian Twins Eye Study. Hypertension, 54 (4), 788-795. doi: 10.1161/HYPERTENSIONAHA.109.132902

Sex Differences in the Rates of Recovery, Treatment-Seeking, and Natural Recovery in Pathological Gambling: Results From an Australian Community-Based Twin Survey

Wendy S. Slutske, Alex Blaszczynski and Nicholas G. Martin (2009). Sex Differences in the Rates of Recovery, Treatment-Seeking, and Natural Recovery in Pathological Gambling: Results From an Australian Community-Based Twin Survey. Twin Research and Human Genetics, 12 (5), 425-432. doi: 10.1375/twin.12.5.425

Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins

David A. Mackey, Jane R. MacKinnon, Shayne A. Brown, Lisa S. Kearns, Jonathan B. Ruddle, Paul G. Sanfilippo, Cong Sun, Christopher J. Hammond, Terri L. Young, Nicholas G. Martin and Alex W. Hewitt (2009). Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins. Twin Research and Human Genetics, 12 (5), 441-454. doi: 10.1375/twin.12.5.441

Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence Symptoms

Arpana Agrawal, Carolyn E. Sartor, Michael T. Lynskey, Julia D. Grant, Michele L. Pergadia, Richard Grucza, Kathleen K. Bucholz, Elliot C. Nelson, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence Symptoms. Alcoholism: Clinical and Experimental Research, 33 (12), 2047-2056. doi: 10.1111/j.1530-0277.2009.01044.x

Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents

E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009). Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 (11), 2359-2368. doi: 10.1007/s00125-009-1510-9

A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability

Shekar, SN, Duffy, DL, Youl, P, Baxter, AJ, Kvaskoff, M, Whiteman, DC, Green, AC, Hughes, MC, Hayward, NK, Coates, M and Martin, NG (2009). A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability. Journal of Investigative Dermatology, 129 (9), 2211-2219. doi: 10.1038/jid.2009.48

Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures

Naomi R. Wray, Michael R. James, Scott D. Gordon, Troy Dumenil, Leanne Ryan, William L. Coventry, Dixie J. Statham, Michele L. Pergadia, Pamela A.F. Madden, Andrew C. Heath, Grant W. Montgomery and Nicholas G. Martin (2009). Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality Measures. Biological Psychiatry, 66 (5), 468-476. doi: 10.1016/j.biopsych.2009.04.030

Association Study of Common Mitochondrial Variants and Cognitive Ability

Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009). Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 (5), 504-512. doi: 10.1007/s10519-009-9276-x

Is There a "Party" in Your Genes?

Hatemi, Peter K., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2009). Is There a "Party" in Your Genes?. Political Research Quarterly, 62 (3), 584-600. doi: 10.1177/1065912908327606

Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci

J Kettunen, M Perola, N G Martin, B K Cornes, S G Wilson, G W Montgomery, B Benyamin, J R Harris, D Boomsma, G Willemsen, J-J Hottenga, P E Slagboom, K Christensen, K O Kyvik, T I A Sørensen, N L Pedersen, P K E Magnusson, T Andrew, T D Spector, E Widen, K Silventoinen, J Kaprio, A Palotie and L Peltonen (2009). Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci. International Journal of Obesity, 33 (11), 1235-1242. doi: 10.1038/ijo.2009.168

Smoking and Illicit Drug Use Associations With Early Versus Delayed Reproduction: Findings in a Young Adult Cohort of Australian Twins

Mary Waldron, , , ,, ,, Andrew C. Heath, Michael T. Lynskey, Elliot C. Nelson, Kathleen K. Bucholz, Pamela A.F. Madden and Nicholas G. Martin (2009). Smoking and Illicit Drug Use Associations With Early Versus Delayed Reproduction: Findings in a Young Adult Cohort of Australian Twins. Journal of Studies on Alcohol and Drugs, 70 (5), 786-796. doi: 10.15288/jsad.2009.70.786

Timing of first alcohol use and alcohol dependence: evidence of common genetic influences

Carolyn E. Sartor, Michael T. Lynskey, Kathleen K. Bucholz, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Timing of first alcohol use and alcohol dependence: evidence of common genetic influences. Addiction, 104 (9), 1512-1518. doi: 10.1111/j.1360-0443.2009.02648.x

Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.

Matthew C. Keller, Allan F. McRae, Julie M. McGaughran, Peter M. Visscher, Nicholas G. Martin and Grant W. Montgomery (2009). Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.. American Journal of Medical Genetics. Part A, 149A (8), 1823-1826. doi: 10.1002/ajmg.a.32973

Genome-wide association study identifies three loci associated with melanoma risk

Bishop, DT, Demenais, F, Iles, MM, Harland, M, Taylor, JC, Corda, E, Randerson-Moor, J, Aitken, JF, Avril, MF, Azizi, E, Bakker, B, Bianchi-Scarra, G, Bressac-de Paillerets, B, Calista, D, Cannon-Albright, LA, Chin-A-Woeng, T, Debniak, T, Galore-Haskel, G, Ghiorzo, P, Gut, I, Hansson, J, Hocevar, M, Hoiom, V, Hopper, JL, Ingvar, C, Kanetsky, PA, Kefford, RF, Landi, MT, Lang, J ... Bishop, JAN (2009). Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics, 41 (8), 920-925. doi: 10.1038/ng.411

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

Falchi, M, Bataille, V, Hayward, NK, Duffy, DL, Bishop, JAN, Pastinen, T, Cervino, A, Zhao, ZZ, Deloukas, P, Soranzo, N, Elder, DE, Barrett, JH, Martin, NG, Bishop, DT, Montgomery, GW and Spector, TD (2009). Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nature Genetics, 41 (8), 915-919. doi: 10.1038/ng.410

A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries

Claire M. A. Haworth, Margaret J. Wright, Nicolas W. Martin, Nicholas G. Martin, Dorret I. Boomsma, Meike Bartels, Danielle Posthuma, Oliver S. P. Davis, Angela M. Brant, Robin P. Corley, John K. Hewitt, William G. Iacono, Matthew McGue, Lee A. Thompson, Sara A. Hart, Stephen A. Petrill, David Lubinski and Robert Plomin (2009). A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries. Behavior Genetics, 39 (4), 359-370. doi: 10.1007/s10519-009-9262-3

Genetic and Environmental Transmission of Political Attitudes Over a Life Time

Hatemi, Peter K., Funk, Carolyn L., Medland, Sarah E., Maes, Hermine M., Silberg, Judy L., Martin, Nicholas G. and Eaves, Lindon J. (2009). Genetic and Environmental Transmission of Political Attitudes Over a Life Time. Journal of Politics, 71 (3), 1141-1156. doi: 10.1017/S0022381609090938

Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?

Martin, Nicolas W., Hansell, Narelle K., Wainwright, Mark A., Shekar, Sri N., Medland, Sarah E., Bates, Timothy C., Burt, Jennifer S., Martin, Nicholas G. and Wright, Margaret J. (2009). Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?. Behavior Genetics, 39 (4), 417-426. doi: 10.1007/s10519-009-9275-y

Genetic variation in female BMI increases with number of children born but failure to replicate association between GN beta 3 variants and increased BMI in parous females

Cornes, Belinda K., Medland, Sarah E., Lind, Penelope A., Nyholt, Dale R., Montgomery, Grant W. and Martin, Nicholas G. (2009). Genetic variation in female BMI increases with number of children born but failure to replicate association between GN beta 3 variants and increased BMI in parous females. Twin Research and Human Genetics, 12 (3), 276-285. doi: 10.1375/twin.12.3.276

The Establishment of the GENEQOL Consortium to Investigate the Genetic Disposition of Patient-Reported Quality-of-Life Outcomes

Sprangers, Mirjam A. G., Sloan, Jeff A., Veenhoven, Ruut, Cleeland, Charles S., Halyard, Michele Y., Abertnethy, Amy R., Baas, Frank, Barsevick, Andrea M., Bartels, Meike, Boomsma, Dorret I., Chauhan, Cynthia, Dueck, Amylou C., Frost, Marlene H., Hall, Per, Klepstad, Pal, Martin, Nicholas G., Miaskowski, Christine, Mosing, Miriam, Movsas, Benjamin, Van Noorden, Cornelis J. F., Patrick, Donald L., Pedersen, Nancy L., Ropka, Mary E., Shi, Quiling, Shinozaki, Gen, Singh, Jasvinder A., Yang, Ping and Zwinderman, Ailko H. (2009). The Establishment of the GENEQOL Consortium to Investigate the Genetic Disposition of Patient-Reported Quality-of-Life Outcomes. Twin Research and Human Genetics, 12 (3), 301-311. doi: 10.1375/twin.12.3.301

No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples

Penelope A. Lind, Michelle Luciano, Michael A. Horan, Riccardo E. Marioni, Margaret J. Wright, Timothy C. Bates, Patrick Rabbitt, Sarah E. Harris, Yvonne Davidson, Ian J. Deary, Linda Gibbons, Andrew Pickles, William Ollier, Neil Pendleton, Jackie F. Price, Antony Payton and Nicholas G. Martin (2009). No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples. Behavior Genetics, 39 (5), 513-523. doi: 10.1007/s10519-009-9274-z

Geographical structure and differential natural selection among North European populations

Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108

Bayesian latent trait modeling of migraine symptom data

Carla Chia Ming Chen, Jonathan M. Keith, Dale R. Nyholt, Nicholas G. Martin and Kerrie L. Mengersen (2009). Bayesian latent trait modeling of migraine symptom data. Human Genetics, 126 (2), 277-288. doi: 10.1007/s00439-009-0671-4

Familial Resemblance of Borderline Personality Disorder Features: Genetic or Cultural Transmission?

Marijn A. Distel, Irene Rebollo-Mesa, Gonneke Willemsen, Catherine A. Derom, Timothy J. Trull, Nicholas G. Martin and Dorret I. Boomsma (2009). Familial Resemblance of Borderline Personality Disorder Features: Genetic or Cultural Transmission?. PLoS One, 4 (4) e5334, e5334. doi: 10.1371/journal.pone.0005334

Heritability and Linkage Analysis of Appendicitis Utilizing Age at Onset

Christopher Oldmeadow, Kerrie Mengersen, Nicholas Martin and David L. Duffy (2009). Heritability and Linkage Analysis of Appendicitis Utilizing Age at Onset. Twin Research and Human Genetics, 12 (2), 150-157. doi: 10.1375/twin.12.2.150

Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma

Zhao, ZZ, Duffy, DL, Thomas, SA, Martin, NG, Hayward, NK and Montgomery, GW (2009). Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma. Melanoma Research, 19 (2), 80-85. doi: 10.1097/CMR.0b013e328322fc45

Relative Finger Lengths, Sex Differences, and Psychological Traits

Loehlin, JC, Medland, SE and Martin, NG (2009). Relative Finger Lengths, Sex Differences, and Psychological Traits. Archives of Sexual Behavior, 38 (2), 298-305. doi: 10.1007/s10508-007-9303-z

Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data

Chen, Carla C. M., Mengersen, Kerrie L., Keith, Jonathan M., Martin, Nicholas G. and Nyholt, Dale R. (2009). Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data. Human Genetics, 125 (5-6), 591-604. doi: 10.1007/s00439-009-0652-7

Genome-wide Association Study of Smoking Initiation and Current Smoking

Jacqueline M. Vink1, August B. Smit, Eco J.C. de Geus, Patrick Sullivan, Gonneke Willemsen, Jouke-Jan Hottenga, Johannes H. Smit, Witte J. Hoogendijk, Frans G. Zitman, Leena Peltonen, Jaakko Kaprio, Nancy L. Pedersen, Patrik K. Magnusson, Tim D. Spector, Kirsten Ohm Kyvik, Katherine I. Morley, Andrew C. Heath, Nicholas G. Martin, Rudi G.J. Westendorp, P. Eline Slagboom, Henning Tiemeier, Albert Hofman, Andre G. Uitterlinden, Yurii S. Aulchenko, Najaf Amin, Cornelia van Duijn, Brenda W. Penninx and Dorret I. Boomsma (2009). Genome-wide Association Study of Smoking Initiation and Current Smoking. American Journal of Human Genetics, 84 (3), 367-379. doi: 10.1016/j.ajhg.2009.02.001

The Role of Harsh Discipline in Explaining Sex Differences in Conduct Disorder: a Study of Opposite-Sex Twin Pairs

Madeline H. Meier, Wendy S. Slutske, Andrew C. Heath and Nicholas G. Martin (2009). The Role of Harsh Discipline in Explaining Sex Differences in Conduct Disorder: a Study of Opposite-Sex Twin Pairs. Journal of Abnormal Child Psychology, 37 (5), 653-664. doi: 10.1007/s10802-009-9309-1

Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerstrom test for nicotine dependence

Agrawal, Arpana, Pergadia, Michele L., Balasubramanian, Sumitra, Saccone, Scott F., Hinrichs, Anthony L., Saccone, Nancy L., Breslau, Naomi, Johnson, Eric O., Hatsukami, Dorothy, Martin, Nicholas G., Montgomery, Grant W., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A.F. (2009). Further evidence for an association between the gamma-aminobutyric acid receptor A, subunit 4 genes on chromosome 4 and Fagerstrom test for nicotine dependence. Addiction, 104 (3), 471-477. doi: 10.1111/j.1360-0443.2008.02445.x

Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults

Nelson, E. C., Agrawal, A., Pergadia, M. L., Lynskey, M. T., Todorov, A. A., Wang, J. C., Todd, R. D., Martin, N. G., Heath, A. C., Goate, A. M., Montgomery, G. W. and Madden, P. A. F. (2009). Association of childhood trauma exposure and GABRA2 polymorphisms with risk of posttraumatic stress disorder in adults. Molecular Psychiatry, 14 (3), 234-235. doi: 10.1038/mp.2008.81

Variation in the dysbindin gene and normal cognitive function in three independent population samples

M. Luciano, F. Miyajima, P. A. Lind, T. C. Bates, M. Horan, S. E. Harris, M. J. Wright, W. E. Ollier, C. Hayward, N. Pendleton, A. J. Gow, P. M. Visscher, J. M. Starr, I. J. Deary, N. G. Martin and A. Payton (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes, Brain and Behavior, 8 (2), 218-227. doi: 10.1111/j.1601-183X.2008.00462.x

An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeating

Tracey D. Wade, Susan A. Treloar, Andrew C. Heath and Nicholas G. Martin (2009). An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeating. International Journal of Eating Disorders, 42 (6), 492-497. doi: 10.1002/eat.20668

ADH single nucleotide polymorphism associations with alcohol metabolism in vivo

Andrew J. Birley, Michael R. James, Peter A. Dickson, Grant W. Montgomery, Andrew C. Heath, Nicholas G. Martin and John B. Whitfield (2009). ADH single nucleotide polymorphism associations with alcohol metabolism in vivo. Human Molecular Genetics, 18 (8), 1533-1542. doi: 10.1093/hmg/ddp060

Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis

Stuart Macgregor, Penelope A. Lind, Kathleen K. Bucholz, Narelle K. Hansell, Pamela A.F. Madden, Melinda M. Richter, Grant W. Montgomery, Nicholas G. Martin, Andrew C. Heath and John B. Whitfield (2009). Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Human Molecular Genetics, 18 (3), 580-593. doi: 10.1093/hmg/ddn372

Common genetic influences underlie comorbidity of migraine and endometriosis

Nyholt, Dale R., Gillespie, Nathan G., Merikangas, Kathleen R., Treloar, Susan A., Martin, Nicholas G. and Montgomery, Grant W. (2009). Common genetic influences underlie comorbidity of migraine and endometriosis. Genetic Epidemiology, 33 (2), 105-113. doi: 10.1002/gepi.20361

Flexible Mx Specification of Various Extended Twin Kinship Designs

Hermine H. Maes, Michael C. Neale, Sarah E. Medland, Matthew C. Keller, Nicholas G. Martin, Andrew C. Heath and Lindon J. Eaves (2009). Flexible Mx Specification of Various Extended Twin Kinship Designs. Twin Research and Human Genetics, 12 (1), 26-34. doi: 10.1375/twin.12.1.26

Shared aetiology of risky sexual behaviour and adolescent misconduct : Genetic and environmental influences

Verweij, K. J. H., Zietsch, B. P., Bailey, J. M. and Martin, N. G. (2009). Shared aetiology of risky sexual behaviour and adolescent misconduct : Genetic and environmental influences. Genes, Brain And Behavior, 8 (1), 107-113. doi: 10.1111/j.1601-183X.2008.00456.x

The Australian twin study of gambling (OZ-GAM): Rationale, sample description, predictors of participation, and a first look at sources of individual differences in gambling involvement

Wendy S. Slutske, Madeline H. Meier, Gu Zhu, Dixie J. Statham, Alex Blaszczynski and Nicholas G. Martin (2009). The Australian twin study of gambling (OZ-GAM): Rationale, sample description, predictors of participation, and a first look at sources of individual differences in gambling involvement. Twin Research and Human Genetics, 12 (1), 63-78. doi: 10.1375/twin.12.1.63

Genetic linkage findings for DSM-IV nicotine withdrawal in two populations

Michele L. Pergadia, Arpana Agrawal, Anu Loukola, Grant W. Montgomery, Ulla Broms, Scott F. Saccone, Jen C. Wang, Alexandre A. Todorov, Kauko Heikkilä, Dixie J. Statham, Anjali K. Henders, Megan J. Campbell, John P. Rice, Richard D. Todd, Andrew C. Heath, Alison M. Goate, Leena Peltonen, Jaakko Kaprio, Nicholas G. Martin and Pamela A.F. Madden (2009). Genetic linkage findings for DSM-IV nicotine withdrawal in two populations. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 150b (7), 950-959. doi: 10.1002/ajmg.b.30924

Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?

Narelle K. Hansell, Arpana Agrawal, John B. Whitfield, Katherine I. Morley, Scott D. Gordon, Penelope A. Lind, Michele L. Pergadia, Grant W. Montgomery, Pamela A. F. Madden, Richard D. Todd, Andrew C. Heath and Nicholas G. Martin (2009). Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?. Alcoholism: Clinical and Experimental Research, 33 (4), 729-739. doi: 10.1111/j.1530-0277.2008.00890.x

DNA methylation profiles in monozygotic and dizygotic twins

Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286

Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels

Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

Accumulation of trauma over time and risk for depression in a twin sample

V. V. McCutcheon, A. C. Heath, E. C. Nelson, K. K. Bucholz, P. A. F. Madden and N. G. Martin (2009). Accumulation of trauma over time and risk for depression in a twin sample. Psychological Medicine, 39 (3), 431-441. doi: 10.1017/S0033291708003759

Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families

Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M., Hay, David A., Levy, Florence, Van-Beijsterveldt, Catherina E.M., Willemsen, Gonneke, Townsend, Grant C., White, Vicki, Hewitt, Alex W., Mackey, David A., Bailey, J. Michael, Slutske, Wendy S., Nyholt, Dale R., Treloar, Susan A., Martin, Nicholas G. and Boomsma, Dorret I. (2009). Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families. Neuropsychologia, 47 (2), 330-337. doi: 10.1016/j.neuropsychologia.2008.09.005

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., Martin, N. G., Wray, N. R., Boomsma, D. I. and Penninx, B. W. J. H. (2009). Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14 (4), 359-375. doi: 10.1038/mp.2008.125

Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders

Psychiatric GWAS Consortium Coordinating Committee, Martin, N., Wray, N., Mowry, B. and Holliday, E. (2009). Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders. American Journal of Psychiatry, 166 (5), 540-556. doi: 10.1176/appi.ajp.2008.08091354

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

Yurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, Dorret Boomsma, Iris M Heid, Peter P Pramstaller, Brenda W J H Penninx, A Cecile J W Janssens, James F Wilson, Tim Spector, Nicholas G Martin, Nancy L Pedersen, Kirsten Ohm Kyvik, Jaakko Kaprio, Albert Hofman, Nelson B Freimer, Marjo-Riitta Jarvelin, Ulf Gyllensten, Harry Campbell, Igor Rudan, Åsa Johansson, Fabio Marroni, Caroline Hayward, Veronique Vitart, Inger Jonasson, Cristian Pattaro, Alan Wright, Nick Hastie, Irene Pichler ... Jouke-Jan Hottenga (2009). Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, 41 (1), 47-55. doi: 10.1038/ng.269

Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction

Cornes, B., Lind, P. A., Medland, S. E., Montgomery, G. W ., Nyholt, D. R. and Martin, N. G . (2009). Replication of the association of common rs9939609 variant of FTO with increased BMI in an Australian adult twin population but no evidence for gene by environment (G × E) interaction. International Journal of Obesity, 33 (1), 75-79. doi: 10.1038/ijo.2008.223

Autosomal linkage analysis for cannabis use behaviors in Australian adults

Agrawal, Arpana, Morley, Katherine I., Hansell, Narelle K., Pergadia, Michele L., Montgomery, Grant W., Statham, Dixie J., Todd, Richard D., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John, Martin, Nicholas G. and Lynskey, Michael T. (2008). Autosomal linkage analysis for cannabis use behaviors in Australian adults. Drug and Alcohol Dependence, 98 (3), 185-190. doi: 10.1016/j.drugalcdep.2008.05.009

Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins

Reiersen, Angela M., Constantino, John N., Grimmer, Marisa, Martin, Nicholas G. and Todd, Richard D. (2008). Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins. Twin Research and Human Genetics, 11 (6), 579-585. doi: 10.1375/twin.11.6.579

Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence

Middelberg, Rita P., Gordon, Scott D., Zhu, Gu, McRae, Allan, Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2008). Linkage and Association Analyses of Longitudinally Measured Lipid Phenotypes in Adolescence. Twin Research and Human Genetics, 11 (6), 603-620. doi: 10.1375/twin.11.6.603

Meeting the challenges of neuroimaging genetics

De Zubicaray, Greig I., Chiang, Ming-Chang, McMahon, Katie L., Shattuck, David W., Toga, Arthur W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2008). Meeting the challenges of neuroimaging genetics. Brian Imaging and Behavior, 2 (4), 258-263. doi: 10.1007/s11682-008-9029-0

A high-density association screen of 155 ion transport genes for involvement with common migraine

Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Farkkila, Markus, Hamalainen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Goebel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W. M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M. J. M. ... Palotie, Aarno (2008). A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17 (21), 3318-3331. doi: 10.1093/hmg/ddn227

Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts

Waldron, Mary, Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts. Alcoholism-Clinical and Experimental Research, 32 (11), 1865-1874. doi: 10.1111/j.1530-0277.2008.00771.x

Early cannabis use and DSM-IV nicotine dependence: A twin study

Agrawal, Arpana, Lynskey, Michael T., Pergadia, Michele L., Bucholz, Kathleen K., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2008). Early cannabis use and DSM-IV nicotine dependence: A twin study. Addiction, 103 (11), 1896-1904. doi: 10.1111/j.1360-0443.2008.02354.x

Genetic factors predisposing to homosexuality may increase mating success in heterosexuals

Zietsch, Brendan P., Morley, Katherine I., Shekar, Sri N., Verweij, Karin J. H., Keller, Matthew C., Macgregor, Stuart, Wright, Margaret J., Bailey, J. Michael and Martin, Nicholas G. (2008). Genetic factors predisposing to homosexuality may increase mating success in heterosexuals. Evolution and Human Behavior, 29 (6), 424-433. doi: 10.1016/j.evolhumbehav.2009.07.002

Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language

Bates, Timothy C., Luciano, Michelle, Lind, Penelope A., Wright, Margaret J., Montgomery, Grant W. and Martin, Nicholas G. (2008). Recently-derived variants of brain-size genes ASPM, MCPH1, CDK5RAP and BRCA1 not associated with general cognition, reading or language. Intelligence, 36 (6), 689-693. doi: 10.1016/j.intell.2008.04.001

Susceptibility variants for male-pattern baldness on chromosome 20p11

Hillmer, Axel M., Brockschmidt, Felix F., Hanneken, Sandra, Eigelshoven, Sibylle, Steffens, Michael, Flaquer, Antonia, Herms, Stefan, Becker, Tim, Kortuem, Anne-Katrin, Nyholt, Dale R., Zhao, Zhen Zhen, Montgomery, Grant W., Martin, Nicholas G., Muehleisen, Thomas W., Alblas, Margrieta A., Moebus, Susanne, Joeckel, Karl-Heinz, Broecker-Preuss, Martina, Erbel, Raimund, Reinartz, Roman, Betz, Regina C., Cichon, Sven, Propping, Peter, Baur, Max P., Wienker, Thomas F., Kruse, Roland and Noethen, Markus M. (2008). Susceptibility variants for male-pattern baldness on chromosome 20p11. Nature Genetics, 40 (11), 1279-1281. doi: 10.1038/ng.228

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies

Byrne, Enda M., Mcrae, Allan F., Zhao, Zhen-Zhen, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies. European Journal of Human Genetics, 16 (11), 1396-1403. doi: 10.1038/ejhg.2008.117

A genome-wide linkage scan for age at menarche in three populations of European descent

Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M. and Montgomery, Grant W. (2008). A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism., 93 (10), 3965-3970. doi: 10.1210/jc.2007-2568

Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins

Hur, Y-M, Kaprio, J., Iacono, W. G., Boomsma, D. I., McGgue, M., Silventoinen, K., Martin, N. G., Luciano, M., Visscher, P. M., Rose, R. J., He, M., Ando, J., Ooki, S., Nonaka, K., Lin, C. C. H., Lajunen, H. R., Cornes, B. K., Bartels, M., van Beijsterveldt, C. E. M., Cherny, S. S. and Mitchell, K. (2008). Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity, 32 (10), 1455-1467. doi: 10.1038/ijo.2008.144

Phenotypic, Genetic, and Environmental Properties of the Portrait Values Questionnaire

Schermer, Julie Aitken, Feather, N. T., Zhu, Gu and Martin, Nicholas G. (2008). Phenotypic, Genetic, and Environmental Properties of the Portrait Values Questionnaire. Twin Research and Human Genetics, 11 (5), 531-537. doi: 10.1375/twin.11.5.531

Shared and unique risk factors between lifetime purging and objective binge eating: A twin study

Wade, T. D., Treloar, S. and Martin, N. G. (2008). Shared and unique risk factors between lifetime purging and objective binge eating: A twin study. Psychological Medicine, 38 (10), 1455-1464. doi: 10.1017/S0033291708002791

The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample

Lind, Penelope A., Macgregor, Stuart, Agrawal, Arpana, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). The role of GABRA2 in alcohol dependence, smoking, and illicit drug use in an Australian population sample. Alcoholism: Clinical and Experimental Research, 32 (10), 1721-1731. doi: 10.1111/j.1530-0277.2008.00768.x

Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning

Zhao, Zhen Zhen, Painter, Jodie N., Palmer, James S., Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Boomsma, Dorret I., Martin, Nicholas G., Duffy, David L. and Montgomery, Grant W. (2008). Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction, 23 (10), 2372-2379. doi: 10.1093/humrep/den268

Vitamin D receptor gene polymorphisms have negligible effect on human height

Macgregor, Stuart, Hottenga, Jouke-Jan, Lind, Penelope A., Suchiman, H. Eka D., Willemsen, Gonneke, Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G., Visscher, Peter M. and Boomsma, Dorret I. (2008). Vitamin D receptor gene polymorphisms have negligible effect on human height. Twin Research and Human Genetics, 11 (5), 488-494. doi: 10.1375/twin.11.5.488

Evaluation of HapMap data in six populations of European descent

Lundmark, Per E., Liljedahl, Ulrika, Boomsma, Dorret I., Mannila, Heikki, Martin, Nicholas G., Palotie, Aarno, Peltonen, Leena, Perola, Markus, Spector, Tim D. and Syvanen, Ann-Christine (2008). Evaluation of HapMap data in six populations of European descent. European Journal of Human Genetics, 16 (9), 1142-1150. doi: 10.1038/ejhg.2008.77

Heritability of borderline personality disorder features is similar across three countries

Distel, M. A., Trull, T. J., Derom, C. A., Thiery, E. W., Grimmer, M. A., Martin, N. G., Willemsen, G. and Boomsma, D. I. (2008). Heritability of borderline personality disorder features is similar across three countries. Psychological Medicine, 38 (9), 1219-1229. doi: 10.1017/S0033291707002024

Homocysteine, folates, and the eye

Wright, A. D., Martin, N. and Dodson, P. M. (2008). Homocysteine, folates, and the eye. Eye, 22 (8), 989-993. doi: 10.1038/sj.eye.6703061

Investigation of the relationship between smoking and appendicitis in Australian twins

Oldmeadow, Chris, Wood, Ian, Mengersen, Kerrie, Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2008). Investigation of the relationship between smoking and appendicitis in Australian twins. Annals of Epidemiology, 18 (8), 631-636. doi: 10.1016/j.annepidem.2008.04.004

Searching for an environmental effect of parental alcoholism on offspring alcohol use disorder: A genetically informed study of children of alcoholics

Slutske, Wendy S., D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2008). Searching for an environmental effect of parental alcoholism on offspring alcohol use disorder: A genetically informed study of children of alcoholics. Journal of Abnormal Psychology, 117 (3), 534-551. doi: 10.1037/a0012907

Welcome - Human genetics society of Australasia

Martin, Nick (2008). Welcome - Human genetics society of Australasia. Twin Research and Human Genetics, 11 (4), III-III. doi: 10.1375/twin.11.4.iii

Heritability and genome-wide linkage in US and Australian twins identify novel genomic regions controlling chromogranin A

O'Connor, Daniel T., Zhu, Gu, Rao, Fangwen, Taupenot, Laurent, Fung, Maple M., Das, Madhusudan, Mahata, Sushil K., Mahata, Manjula, Wang, Lei, Zhang, Kuixing, Greenwood, Tiffany A., Shih, Pei-an Betty, Cockburn, Myles G, Ziegler, Michael G., Stridsberg, Mats, Martin, Nicholas G. and Whitfield, John B. (2008). Heritability and genome-wide linkage in US and Australian twins identify novel genomic regions controlling chromogranin A. Circulation, 118 (3), 247-257. doi: 10.1161/CIRCULATIONAHA.107.709105

Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression

Middeldorp, CM, Sullivan, PF, Wray, NR, Hottenga, JJ, de Geus, EJC, van den Berg, M, Montgomery, GW, Coventry, WL, Statham, DJ, Andrews, G, Slagboom, PE, Boomsma, DI and Martin, NG (2008). Suggestive linkage on chromosome 2, 8, and 17 for lifetime major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 150B (3), 352-358. doi: 10.1002/ajmg.b.30817

Common sequence variants on 20q11.22 confer melanoma susceptibility

Brown, K. M., MacGregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D. C., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Newton Bishop, J., Kefford, R. F. ... Hayward, N. (2008). Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 (7), 838-840. doi: 10.1038/ng.163

Does teenage childbearing increase smoking, drinking and body size?

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2008). Does teenage childbearing increase smoking, drinking and body size?. Journal of Health Economics, 27 (4), 888-903. doi: 10.1016/j.jhealeco.2008.02.005

Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake

Whitfield, John B., Day, Veronica, Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G. and Montgomery, Grant W. (2008). Measuring carbohydrate-deficient transferrin by direct immunoassay: factors affecting diagnostic sensitivity for excessive alcohol intake. Clinical Chemistry, 54 (7), 1158-1165. doi: 10.1373/clinchem.2007.101733

An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project

Agrawal, Arpana, Pergadia, Michele. L., Saccone, Scott F., Lynskey, Michael T., Wang, Jen C., Martin, Nicholas G., Statham, Dixie, Henders, Anjali, Campbell, Megan, Garcia, Robertino, Broms, Ulla, Todd, Richard D., Goate, Alison M., Rice, John, Kaprio, Jaakko, Heath, Andrew C., Montgomery, Grant W. and Madden, Pamela A. F. (2008). An autosomal linkage scan for cannabis use disorders in the nicotine addiction genetics project. Archives of General Psychiatry, 65 (6), 713-722. doi: 10.1001/archpsyc.65.6.713

Gamma-aminobutyric acid receptor genes and nicotine dependence: Evidence for association from a case-control study

Agrawal, Arpana, Pergadia, Michele L., Saccone, Scott F., Hinrichs, Anthony L., Lessov-Schlaggar, Christina N., Saccone, Nancy L., Neuman, Rosalind J., Breslau, Naomi, Johnson, Eric, Hatsukami, Dorothy, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G., Goate, Alison M., Rice, John P., Bierut, Laura J. and Madden, Pamela A. F. (2008). Gamma-aminobutyric acid receptor genes and nicotine dependence: Evidence for association from a case-control study. Addiction, 103 (6), 1027-1038. doi: 10.1111/j.1360-0443.2008.02236.x

Genetic Dissection of Myopia Evidence for Linkage of Ocular Axial Length to Chromosome 5q

Zhu, Gu, Hewitt, Alex W., Ruddle, Jonathan B., Kearns, Lisa S., Brown, Shayne A., Mackinnon, Jane R., Chen, Christine Y., Hammond, Christopher J., Craig, Jamie E., Montgomery, Grant W., Martin, Nicholas G. and Mackey, David A. (2008). Genetic Dissection of Myopia Evidence for Linkage of Ocular Axial Length to Chromosome 5q. Ophthalmology, 115 (6), 1053-1057. doi: 10.1016/j.ophtha.2007.08.013

Genetic covariation among facets of openness to experience and general cognitive ability

Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Geffen, Gina M. and Martin, Nicholas G. (2008). Genetic covariation among facets of openness to experience and general cognitive ability. Twin Research and Human Genetics, 11 (3), 275-286. doi: 10.1375/twin.11.3.275

Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence

Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Zhu, Gu, Lind, Penelope A., Pergadia, Michele L., Madden, Pamela A., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2008). Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence. Twin Research and Human Genetics, 11 (3), 287-305. doi: 10.1375/twin.11.3.287

Consistently replicating locus linked to migraine on 10q22-q23

Anttila, Verneri, Nyholt, Dale R., Kallela, Mikko, Artto, Ville, Vepsalainen, Salli, Jakkula, Eveliina, Wennerstrom, Annika, Tikka-Kleemola, Paeivi, Kaunisto, Mari A., Hamalainen, Eija, Widen, Elisabeth, Terwilliger, Joseph, Merikangas, Kathleen, Montgomery, Grant W., Martin, Nicholas G., Daly, Mark, Kaprio, Jaakko, Peltonen, Leena, Farkkila, Markus, Wessman, Maija and Palotie, Aarno (2008). Consistently replicating locus linked to migraine on 10q22-q23. American Journal of Human Genetics, 82 (5), 1051-1063. doi: 10.1016/j.ajhg.2008.03.003

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

Han, J., Kraft, P., Nan, H., Guo, Q., Chen, C., Qureshi, A., Hankinson, S.E., Hu, F.B., Duffy, D., Zhao, Z.Z., Martin, N. G., Montgomery, G., Hayward, N., Thomas, G., Hoover, R.N., Chanock, S. and Hunter, D.J. (2008). A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Plos Genetics, 4 (5) e1000074, e1000074. doi: 10.1371/journal.pgen.1000074

Genetic and environmental influences on individual differences in attidues toward homosexuality: An Australian twin study

Verweji, Karin J. H., Shekar, Sri N., Zietsch, Brendan P., Eaves, Lindon J., Bailey, J. Michael, Boomsma, Dorret I. and Martin, Nicholas G. (2008). Genetic and environmental influences on individual differences in attidues toward homosexuality: An Australian twin study. Behavior Genetics, 38 (3), 257-265. doi: 10.1007/s10519-008-9200-9

Spectrophotometric methods for quantifying pigmentation in human hair - influence of MC1R genotype and environment

Shekar, Sri N., Duffy, David L., Frudakis, Tony, Montgomery, Grant W., James, Michael R., Sturm, Richard A. and Martin, Nicholas G. (2008). Spectrophotometric methods for quantifying pigmentation in human hair - influence of MC1R genotype and environment. Photochemistry and Photobiology, 84 (3), 719-726. doi: 10.1111/j.1751-1097.2007.00237.x

Correlates of cigarette smoking during pregnancy and its genetic and environmental overlap with nicotine dependence

Agrawal, Arpana, Knopik, Valerie S., Pergadia, Michele L., Waldron, Mary, Bucholz, Kathleen K., Martin, Nicholas G., Heath, Andrew C. and Madden, Pamela A. F. (2008). Correlates of cigarette smoking during pregnancy and its genetic and environmental overlap with nicotine dependence. Nicotine and Tobacco Research, 10 (4), 567-578. doi: 10.1080/14622200801978672

Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the Alcohol Challenge Twin Study

Lind, Penelope A., MacGregor, Stuart, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G. and Whitfield, John B. (2008). Effects of GABRA2 variation on physiological, psychomotor and subjective responses in the Alcohol Challenge Twin Study. Twin Research and Human Genetics, 11 (2), 174-182. doi: 10.1375/twin.11.2.174

No effects of prenatal hormone transfer on digit ratio in a large sample of same- and opposite-sex dizygotic twins

Medland, Sarah E., Loehlin, John C. and Martin, Nicholas G. (2008). No effects of prenatal hormone transfer on digit ratio in a large sample of same- and opposite-sex dizygotic twins. Personality and Individual Differences, 44 (5), 1225-1234. doi: 10.1016/j.paid.2007.11.017

Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs

Benyamin, Beben, Perola, Markus, Cornes, Belinda K., Madden, Pamela A. F., Palotie, Aarno, Nyholt, Dale R., Montgomery, Grant W., Peltonen, Leena, Martin, Nicholas G. and Visscher, Peter M. (2008). Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. European Journal of Human Genetics, 16 (4), 516-524. doi: 10.1038/sj.ejhg.5201992

Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: The effects of OCA2 and HERC2

Shekar, Sri N., Duffy, David L., Frudakis, Tony, Sturm, Richard A., Zhao, Zhen Z., Montgomery, Grant W. and Martin, Nicholas G. (2008). Linkage and association analysis of spectrophotometrically quantified hair color in Australian adolescents: The effects of OCA2 and HERC2. Journal of Investigative Dermatology, 128 (12), 2807-2814. doi: 10.1038/jid.2008.147

Genetic and environmental contributions to perceived intensity and pleasantness of androstenone odor: an international twin study

Knaapila, Antti, Tuorila, Hely, Silventoinen, Karri, Wright, Margaret J., Kyvik, Kirsten O., Cherkas, Lynn F., Keskitalo, Kaisu, Hansen, Jonathan, Martin, Nicholas G., Spector, Tim D., Kaprio, Jaakko and Perola, Markus (2008). Genetic and environmental contributions to perceived intensity and pleasantness of androstenone odor: an international twin study. Chemosensory Perception, 1 (1), 34-42. doi: 10.1007/s12078-007-9005-x

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour

Sturm, Richard A., Duffy, David L., Zhao, Zhen Zhen, Leite, Fabio P.N., Stark, Mitchell S., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2008). A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour. The American Journal of Human Genetics, 82 (2), 424-431. doi: 10.1016/j.ajhg.2007.11.005

A study of diabetes mellitus within a large sample of Australian twins

Condon, Julianne, Shaw, Joanne E., Luciano, Michelle, Kyvik, Kirsten O., Martin, Nicholas G. and Duffy, David L. (2008). A study of diabetes mellitus within a large sample of Australian twins. Twin Research and Human Genetics, 11 (1), 28-40. doi: 10.1375/twin.11.1.28

A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie

Gillespie, Nathan A., Zhu, Gu, Evans, David M., Medland, Sarah E., Wright, Margie J. and Martin, Nick G. (2008). A genome-wide scan for Eysenckian personality dimensions in adolescent twin sibships: Psychoticism, Extraversion, Neuroticism, and Lie. Journal of Personality, 76 (6), 1415-1445. doi: 10.1111/j.1467-6494.2008.00527.x

A whole genome association study of neuroticism using DNA pooling

Shifman, S., Bhomra, A., Smiley, S., Wray, N. R., James, M. R., Martin, N. G., Hettema, J. M., An, S. S., Neale, M. C., van den Oord, E. J., Kendler, K. S., Chen, X., Boomsma, D. I., Middeldorp, C. M., Hottenga, J. J., Slagboom, P. E. and Flint, J. (2008). A whole genome association study of neuroticism using DNA pooling. Molecular Psychiatry, 13 (3), 302-312. doi: 10.1038/sj.mp.4002048

Association of the gastric alcohol dehydrogenase gene Adh7 with variation in alcohol metabolism

Birley, Andrew J., James, Michael R., Dickson, Peter A., Montgomery, Grant W., Heath, Andrew C., Whitfield, John B. and Martin, Nicholas G. (2008). Association of the gastric alcohol dehydrogenase gene Adh7 with variation in alcohol metabolism. Human Molecular Genetics, 17 (2), 179-189. doi: 10.1093/hmg/ddm295

Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression

Wray, Naomi R., James, Michael R., Handoko, Herlina Y., Dumenil, Troy, Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008). Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression. Psychiatric Genetics, 18 (5), 219-225. doi: 10.1097/YPG.0b013e3283050aee

Association study of candidate variants of COMT with neuroticism, anxiety and depression

Wray, Naomi, James, Michael R., Dumenil, Troy, Handoko, Herlina Y., Lind, Penelope A., Montgomery, Grant W. and Martin, Nicholas G. (2008). Association study of candidate variants of COMT with neuroticism, anxiety and depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B (7), 1314-1318. doi: 10.1002/ajmg.b.30744

Childhood sexual abuse moderates genetic influences on age at first consensual sexual intercourse in women

Waldron, Mary, Heath, Andrew C., Turkheimer, Eric N., Emery, Robert E., Nelson, Elliot, Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Childhood sexual abuse moderates genetic influences on age at first consensual sexual intercourse in women. Behavior Genetics, 38 (1), 1-10. doi: 10.1007/s10519-007-9176-x

Dizygotic twinning

Hoekstra, Chantal, Zhao, Zhen Zhen, Lambalk, Cornelius B., Willemsen, Gonneke, Martin, Nicholas G., Boomsma, Dorret I. and Montgomery, Grant W. (2008). Dizygotic twinning. Human Reproduction Update, 14 (1), 37-47. doi: 10.1093/humupd/dmm036

Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands

Wray, Naomi R., Middeldorp, Christel M., Birley, Andrew J., Gordon, Scott D., Sullivan, Patrick F., Visscher, Peter M., Nyholt, Dale R, Willemsen, Gonneke, de Geus, Eco J.C., Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G. and Boomsma, Dorret I. (2008). Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Archives of General Psychiatry, 65 (6), 649-658. doi: 10.1001/archpsyc.65.6.649

Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background

Loukola, A., Broms, U., Maunu, H., Widen, E., Heikkila, K., Siivola, M., Salo, A., Pergadia, M. L., Nyman, E., Sammalisto, S., Perola, M., Agrawal, A., Heath, A. C., Martin, N. G., Madden, P. A., Peltonen, L. and Kaprio, J. (2008). Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background. The Pharmacogenomics Journal, 8 (3), 209-219. doi: 10.1038/sj.tpj.6500464

QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes

Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas (2008). QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes. Biological Psychiatry, 63 (9), 864-873. doi: 10.1016/j.biopsych.2007.09.002

Quantifying the heritability of task-related brain activation and performance during the N-back working memory task: a twin fMRI study

Blokland, Gabriella A.M., McMahon, Katie L., Hoffman, Jan, Zhu, Gu, Meredith, Matthew, Martin, Nicholas G., Thompson, Paul M., De Zubicaray, Greig I. and Wright, Margaret J. (2008). Quantifying the heritability of task-related brain activation and performance during the N-back working memory task: a twin fMRI study. Biological Psychology, 79 (1), 70-79. doi: 10.1016/j.biopsycho.2008.03.006

Shared temperament risk factors for anorexia nervosa: a twin study

Wade, T. D., Tiggemann, M., Bulik, C. M., Fairburn, C. G., Wray, N. R. and Martin, N. G. (2008). Shared temperament risk factors for anorexia nervosa: a twin study. Psychosomatic Medicine, 70 (2), 239-244. doi: 10.1097/PSY.0b013e31815c40f1

Testing replication of a 5-SNP set for general cognitive ability in six population samples

Luciano, Michelle, Lind, Penelope A., Deary, Ian J., Payton, Antony, Posthuma, Danielle, Butcher, Lee M., Bochdanovits, Zoltan, Whalley, Lawrence J., Visscher, Peter M., Harris, Sarah E., Polderman, Tinca J. C., Davis, Oliver S. P., Wright, Margaret J., Starr, John M., de Geus, Eco J. C., Bates, Timothy C., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G. and Plomin, Robert (2008). Testing replication of a 5-SNP set for general cognitive ability in six population samples. European Journal of Human Genetics, 16 (11), 1388-1395. doi: 10.1038/ejhg.2008.100

The Queensland study of melanoma:Environmental and genetic associations (Q_MEGA): study design, baseline characteristics, and repeatability of phenotype and sun exposure measures

Baxter, A.J., Hughes, M.C., Kvaskoff, M, Siskind, V., Shekar, S., Aitken, J. F., Green, A. C., Duffy, D., Hayward, N., Martin, N. G. and Whiteman, D. C. (2008). The Queensland study of melanoma:Environmental and genetic associations (Q_MEGA): study design, baseline characteristics, and repeatability of phenotype and sun exposure measures. Twin Research and Human Genetics, 11 (2), 183-196. doi: 10.1375/twin.11.2.183

A comparison of early family life events amongst monozygotic twin women with lifetime anorexia nervosa, bulimia nervosa, or major depression

Wade, T. D., Gillespie, N. and Martin, N. G. (2007). A comparison of early family life events amongst monozygotic twin women with lifetime anorexia nervosa, bulimia nervosa, or major depression. International Journal of Eating Disorders, 40 (8), 679-686. doi: 10.1002/eat.20461

Genome partitioning of genetic variation for height from 11,214 sibling pairs

Visscher, Peter M., Macgregor, Stuart, Benyamin, Beben, Zhu, Gu, Gordon, Scott, Medland, Sarah, Hill, William G., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Liu, Yao-Zhong, Deng, Hong-Wen, Montgomery, Grant W. and Martin, Nicholas G. (2007). Genome partitioning of genetic variation for height from 11,214 sibling pairs. American Journal of Human Genetics, 81 (5), 1104-1110. doi: 10.1086/522934

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

Luciano, Michelle, Lind, Penelope A., Duffy, David L., Castles, Anne, Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G. and Bates, Timothy C. (2007). A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability. Biological Psychiatry, 62 (7), 811-817. doi: 10.1016/j.biopsych.2007.03.007

A longitudinal genetic study of uric Acid and liver enzymes in adolescent twins

Middelberg, Rita P. S., Medland, Sarah E., Martin, Nicholas G. and Whitfield, John B. (2007). A longitudinal genetic study of uric Acid and liver enzymes in adolescent twins. Twin Research and Human Genetics, 10 (5), 757-764. doi: 10.1375/twin.10.5.757

Gene-interleaving patterns of synteny in the Saccharomyces cerevisiae genome: Are they proof of an ancient genome duplication event?

Martin, Nicolas, Ruedi, Elizabeth A., LeDuc, Richard, Sun, Feng-Jie and Caetano-Anollés, Gustavo (2007). Gene-interleaving patterns of synteny in the Saccharomyces cerevisiae genome: Are they proof of an ancient genome duplication event?. Biology Direct, 2 (1) 23. doi: 10.1186/1745-6150-2-23

Sex differences in genetic variation in weight: a longitudinal study of body mass index in adolescent twins

Cornes, B. K., Zhu, G. and Martin, N. G. (2007). Sex differences in genetic variation in weight: a longitudinal study of body mass index in adolescent twins. Behavior Genetics, 37 (5), 648-660. doi: 10.1007/s10519-007-9165-0

Estimation of variance components for age at menarche in twin families

Anderson, Carl A., Duffy, David L., Martin, Nicholas G. and Visscher, Peter M. (2007). Estimation of variance components for age at menarche in twin families. Behavior Genetics, 37 (5), 668-677. doi: 10.1007/s10519-007-9163-2

A genetically informed study of the intergenerational transmission of marital instability

D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2007). A genetically informed study of the intergenerational transmission of marital instability. Journal of Marriage and Family, 69 (3), 793-809. doi: 10.1111/j.1741-3737.2007.00406.x

Linkage analysis of a model quantitative trait in humans: Finger ridge count shows significant multivariate linkage to 5q14.1

Medland, Sarah E., Loesch, Danuta Z., Mdzewski, Bogdan, Zhu, Gu, Montgomery, Grant W. and Martin, Nicholas G. (2007). Linkage analysis of a model quantitative trait in humans: Finger ridge count shows significant multivariate linkage to 5q14.1. PLoS Genetics, 3 (9), 1736-1744. doi: 10.1371/journal.pgen.0030165

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Francks, C., Maegawa, S., Lauren, J., Abrahams, B. S., Velayos-Baeza, A., Medland, S. E., Colella, S., Groszer, M., McAuley, E. Z., Caffrey, T. M., Timmusk, T., Pruunsild, P., Koppel, I., Lind, P. A., Matsumoto-Itaba, N., Nicod, J., Xiong, L., Joober, R., Enard, W., Krinsky, B., Nanba, E., Richardson, A. J., Riley, B. P., Martin, N. G., Strittmatter, S. M., Moller, H. J., Rujescu, D., St Clair, D., Muglia, P. and Roos, J. L. (2007). LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Molecular Psychiatry, 12 (12), 1129-1139. doi: 10.1038/sj.mp.4002053

Intergenerational transmission of childhood conduct problems: a children of twins study

D'Onofrio, Brian M., Slutske, Wendy S., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2007). Intergenerational transmission of childhood conduct problems: a children of twins study. Archives of General Psychiatry, 64 (7), 820-829. doi: 10.1001/archpsyc.64.7.820

Evidence of genetic effects on blood lead concentration

Whitfield, John B., Dy, Veronica, McQuilty, Robert, Zhu, Gu, Montgomery, Grant W., Ferreira, Manuel A. R., Duffy, David L., Neale, Michael C., Heijmans, Bas T., Heath, Andrew C. and Martin, Nicholas G. (2007). Evidence of genetic effects on blood lead concentration. Environmental Health Perspectives, 115 (8), 1224-1230. doi: 10.1289/ehp.8847

Variants in EMX2 and PTEN do not contribute to risk of endometriosis

Treloar, S. A., Zhao, Z. Z., Le, L., Zondervan, K. T., Martin, N. G., Kennedy, S., Nyholt, D. R. and Montgomery, G. W. (2007). Variants in EMX2 and PTEN do not contribute to risk of endometriosis. Molecular Human Reproduction, 13 (8), 587-594. doi: 10.1093/molehr/gam023

Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci

Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick G., Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R., Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Karre, Kyvik, Kirsten Ohm, Sorensen, Thorkild I., Pedersen, Nancy L., Magnusson, Patrik K., Spector, Tim D., Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno, Peltonen, Leena and GenomEUtwin Project (2007). Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097

Heritability of NEO PI-R extraversion facets and their relationship with IQ

Pincombe, Jennifer L., Luciano, Michelle, Martin, Nicholas G. and Wright, Margaret J. (2007). Heritability of NEO PI-R extraversion facets and their relationship with IQ. Twin Research and Human Genetics, 10 (3), 462-469. doi: 10.1375/twin.10.3.462

Cohort Trends in Prevalence and Spousal Concordance for Smoking

Kuo, P. H., Wood, P., Morley, K. I., Madden, P., Martin, N. G. and Heath, A. C. (2007). Cohort Trends in Prevalence and Spousal Concordance for Smoking. Drug & Alcohol Dependence, 88 (2-3), 122-129. doi: 10.1016/j.drugalcdep.2006.09.021

Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta

Zietsch, Brendan P., Hansen, Jonathan L., Hansell, Narelle K, Geffen, Gina M., Martin, Nicholas G. and Wright, Margaret J. (2007). Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta. Biological Psychology, 75 (2), 154-164. doi: 10.1016/j.biopsycho.2007.01.004

Spousal concordance for alcohol dependence: evidence for assortative mating or spousal interaction effects?

Grant, J. D., Heath, A. C., Bucholz, K. K., Madden, P. A., Agrawal, A., Statham, D. J. and Martin, N. G. (2007). Spousal concordance for alcohol dependence: evidence for assortative mating or spousal interaction effects?. Alcoholism: Clinical & Experimental Research, 31 (5), 717-728. doi: 10.1111/j.1530-0277.2007.00356.x

The Genetics of Voting: an Australian Twin Study

Hatemi, P. K., Medland, S. E., Morley, K. I., Heath, A. C. and Martin, N. G. (2007). The Genetics of Voting: an Australian Twin Study. Behavior Genetics, 37 (3) 435, 435-448. doi: 10.1007/s10519-006-9138-8

Effect of the BDNF V166M polymorphism on working memory in healthy adolescents

Hansell, N. K., James, M. R., Duffy, D. L., Birley, A. J., Luciano, M., Geffen, G. M., Wright, M. J., Montgomery, G. W. and Martin, N. G. (2007). Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes, Brain and Behavior, 6 (3), 260-268. doi: 10.1111/j.1601-183X.2006.00254.x

Height and 2D : 4D within and between ethnic groups: Reply to Hurd and van Anders (2007)

Loehlin, John C., McFadden, Dennis, Medland, Sarah E. and Martin, Nicholas G. (2007). Height and 2D : 4D within and between ethnic groups: Reply to Hurd and van Anders (2007). Archives of Sexual Behavior, 36 (2), 143-143. doi: 10.1007/s10508-006-9153-0

Anxiety and comorbid measures associated with PLXNA2

Wray, Naomi R., James, Michael R., Mah, Steven P., Nelson, Matthew, Andrews, Gavin, Sullivan, Patrick F., Montgomery, Grant W., Birley, Andrew J., Braun, Andreas and Martin, Nicholas G. (2007). Anxiety and comorbid measures associated with PLXNA2. Archives of General Psychiatry, 64 (3), 318-326. doi: 10.1001/archpsyc.64.3.318

A longitudinal genetic study of plasma lipids in adolescent twins

Middelberg, Rita P. S., Martin, Nicholas G. and Whitfield, John B. (2007). A longitudinal genetic study of plasma lipids in adolescent twins. Twin Research & Human Genetics, 10 (1), 127-135. doi: 10.1375/twin.10.1.127

Prevalence of premature ovarian failure in monozygotic and dizygotic twins

Gosden, R. G., Treloar, S. A., Martin, N. G., Cherkas, L. F., Spector, T. D., Faddy, M. J. and Silber, S. J. (2007). Prevalence of premature ovarian failure in monozygotic and dizygotic twins. Human Reproduction, 22 (2), 610-615. doi: 10.1093/humrep/del382

Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines

McRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007). Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics, 16 (4), 364-373. doi: 10.1093/hmg/ddl456

Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17

Bates, Timothy C., Luciano, Michelle, Castles, Anne, Coltheart, Max, Wright, Margaret J. and Martin, Nicholas G. (2007). Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. European Journal of Human Genetics, 15 (2), 194-203. doi: 10.1038/sj.ejhg.5201739

The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence

Mekel-Bobrov, Nitzan, Posthuma, Danielle, Gilbert, Sandra L., Lind, Penelope, Gosso, M. Florencia, Luciano, Michelle, Harris, Sarah E., Bates, Timothy C., Polderman, Tinca J., Whalley, Lawrence J., Fox, Helen, Starr, John M., Evans, Patrick D., Montgomery, Grant W., Fernandes, Croydon, Heutink, Peter, Martin, Nicholas G., Boomsma, Dorret I., Deary, Ian J., Wright, Margaret J., de Geus, Eco J. and Lahn, Bruce T. (2007). The ongoing adaptive evolution of ASPM and microcephalin is not explained by increased intelligence. Human Molecular Genetics, 16 (6), 600-608. doi: 10.1093/hmg/ddl487

"No thanks, it keeps me awake". The genetics of coffee-attributed sleep disturbance

Luciano, M., Ghu, Z., Kirk, K. M., Gordon, S. D., Heath, A. C., Montgomery, G. W. and Martin, N. G. (2007). "No thanks, it keeps me awake". The genetics of coffee-attributed sleep disturbance. Sleep, 30 (10), 1378-1386. doi: 10.1093/sleep/30.10.1378

A behavior genetic investigation of adolescent motherhood and offspring mental health problems

Harden, K. P., Lynch, S. K., Turkheimer, E., Emery, R. E., D'Onofrio, B. M., Slutske, W. S., Waldron, M. D., Statham, D. J. and Martin, N. G. (2007). A behavior genetic investigation of adolescent motherhood and offspring mental health problems. Journal of Abnormal Psychology, 116 (4), 667-683. doi: 10.1037/0021-843X.116.4.667

A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions

Zhu, Gu, Montgomery, Grant W., James, Michael R., Trent, Jeff M., Hayward, Nicholas K., Martin, Nicholas G. and Duffy, David L. (2007). A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics, 15 (1), 94-102. doi: 10.1038/sj.ejhg.5201729

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

Duffy, D. L., Montgomery, G. W., Chen, W., Zhao, Z. Z., Le, L., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2007). A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. American Journal of Human Genetics, 80 (2), 241-252. doi: 10.1086/510885

Age at first sexual intercourse and teenage pregnancy in Australian female twins

Waldron, M., Heath, A. C., Turkheimer, E., Emery, R., Bucholz, K. K., Madden, P. A. and Martin, N. G. (2007). Age at first sexual intercourse and teenage pregnancy in Australian female twins. Twin Research & Human Genetics, 10 (3), 440-449. doi: 10.1375/twin.10.3.440

Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs

Saccone, S. F., Hinrichs, A. L., Saccone, N. L., Chase, G. A., Konvicka, K., Madden, P. A., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O., Swan, G. E., Goate, A. M., Rutter, J., Bertelsen, S., Fox, L., Fugman, D., Martin, N. G., Montgomery, G. W., Wang, J. C., Ballinger, D. G., Rice, J. P. and Bierut, L. J. (2007). Cholinergic nicotinic receptor genes implicated in a nicotine dependence association study targeting 348 candidate genes with 3713 SNPs. Human Molecular Genetics, 16 (1), 36-49. doi: 10.1093/hmg/ddl438

Contrasting models of genetic co-morbidity for cannabis and other illicit drugs in adult Australian twins

Agrawal, A., Lynskey, M. T., Bucholz, K. K., Martin, N. G., Madden, P. A. and Heath, A. C. (2007). Contrasting models of genetic co-morbidity for cannabis and other illicit drugs in adult Australian twins. Psychological Medicine, 37 (1), 49-60. doi: 10.1017/S0033291706009287

Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins

Luciano, M, Hine, E., Wright, M. J., Duffy, D. L., MacMillan, J. and Martins, N. G. (2007). Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 144B (1), 95-100. doi: 10.1002/ajmg.b.30413

Exploring the inter-relationship of smoking age-at-onset, cigarette consumption and smoking persistence: Genes or environment?

Morley, K. I., Lynskey, M. T., Madden, P. A., Treloar, S. A., Heath, A. C. and Martin, N. G. (2007). Exploring the inter-relationship of smoking age-at-onset, cigarette consumption and smoking persistence: Genes or environment?. Psychological Medicine, 37 (9), 1357-1367. doi: 10.1017/S0033291707000748

Genetic and phenotypic stability of measures of neuroticism over 22 years

Wray, N. R., Birley, A. J., Sullivan, P. F., Visscher, P. M. and Martin, N. G. (2007). Genetic and phenotypic stability of measures of neuroticism over 22 years. Twin Research & Human Genetics, 10 (5), 695-702. doi: 10.1375/twin.10.5.695

Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples

Saccone, Scott F., Pergadia, Michele L., Loukola, Anu, Broms, Ula, Montgomery, Grant W., Wang, Jen C., Agrawal, Arpana, Dick, Danielle M., Heath, Andrew C., Todorov, Alexandre A., Maunu, Heidi, Heikkila, Kauko, Morley, Katherine I., Rice, John P., Todd, Richard D., Kaprio, Jaakko, Peltonen, Leena, Martin, Nicholas G., Goate, Alison M. and Madden, Pamela A. (2007). Genetic linkage to chromosome 22q12 for a heavy-smoking quantitative trait in two independent samples. American Journal of Human Genetics, 80 (5), 856-866. doi: 10.1086/513703

Genome-wide scan for blood pressure in Australian and Dutch subjects suggests linkage at 5P, 14Q, and 17P

Hottenga, Jouke-Jan, Whitfield, John B., Posthuma, Danielle, Willemsen, Gonneke, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2007). Genome-wide scan for blood pressure in Australian and Dutch subjects suggests linkage at 5P, 14Q, and 17P. Hypertension, 49 (4), 832-838. doi: 10.1161/01.HYP.0000260092.93964.ed

Genomewide scans of red cell indices suggest linkage on chromosome 6q23

Iliadou, A., Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2007). Genomewide scans of red cell indices suggest linkage on chromosome 6q23. Journal of Medical Genetics, 44 (1), 24-30. doi: 10.1136/jmg.2006.043521

Marital conflict and conduct problems in Children of Twins

Harden, K. P., Turkheimer, E., Emery, R. E., D'Onofrio, B. M., Slutske, W. S., Heath, A. C. and Martin, N. G. (2007). Marital conflict and conduct problems in Children of Twins. Child Development, 78 (1), 1-18. doi: 10.1111/j.1467-8624.2007.00982.x

Novel genes identified in a high-density genome wide association study for nicotine dependence

Bierut, L. J., Madden, P. A., Breslau, N., Johnson, E. O., Hatsukami, D., Pomerleau, O. F., Swan, G. E., Rutter, J., Bertelsen, S., Fox, L., Fugman, D., Goate, A. M., Hinrichs, A. L., Konvicka, K., Martin, N. G., Montgomery, G. W., Saccone, N. L., Saccone, S. F., Wang, J. C., Chase, G. A., Rice, J. P. and Ballinger, D. G. (2007). Novel genes identified in a high-density genome wide association study for nicotine dependence. Human Molecular Genetics, 16 (1), 24-35. doi: 10.1093/hmg/ddl441

Ridgecounter: A program for obtaining semi-automated finger ridge counts

Medland, S. E., Park, D. A., Loesch, D. Z. and Martin, N. G. (2007). Ridgecounter: A program for obtaining semi-automated finger ridge counts. Annals of Human Biology, 34 (4), 504-517. doi: 10.1080/03014460701431896

Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15

Zondervan, K. T., Treloar, S. A., Lin, J., Weeks, D. E., Nyholt, D. R., Mangion, J., MacKay, I. J., Cardon, L. R., Martin, N. G., Kennedy, S. H. and Montgomery, G. W. (2007). Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15. Human Reproduction, 22 (3), 717-728. doi: 10.1093/humrep/del446

Stimulant use and symptoms of abuse/dependence: epidemiology and associations with cannabis use--a twin study

Lynskey, Michael T., Grant, Julia D., Li, Lia, Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F., Statham, Dixie, Martin, Nicholas G. and Heath, Andrew C. (2007). Stimulant use and symptoms of abuse/dependence: epidemiology and associations with cannabis use--a twin study. Drug & Alcohol Dependence, 86 (2-3), 147-153. doi: 10.1016/j.drugalcdep.2006.05.023

Genetic Influences on Exercise Participation in 37.051 Twin Pairs from Seven Countries

Stubbe, Janine H., Boomsma, Dorret I., Vink, Jacqueline M., Cornes, Belinda K., Martin, Nicholas G., Skytthe, Axel, Kyvik, Kirsten O., Rose, Richard J., Kujala, Urho M., Harris, Jennifer R., Pedersen, Nancy L., Hunkin, Janice, Spector, Tin D. and De Geus, Eco J. C. (2006). Genetic Influences on Exercise Participation in 37.051 Twin Pairs from Seven Countries. PLoS ONE, 1 (1) e22, e22. doi: 10.1371/journal.pone.0000022

Use of latent profile analysis to identify eating disorder phenotypes in an adult Australian twin cohort

Wade, Tracey D., Crosby, Ross D. and Martin, Nicholas G. (2006). Use of latent profile analysis to identify eating disorder phenotypes in an adult Australian twin cohort. Archives of General Psychiatry, 63 (12), 1377-1384. doi: 10.1001/archpsyc.63.12.1377

Genetic and Cultural Transmission of Smoking Initiation: An Extended Twin Kinship Model

Maes, Hermine H., Neale, Michael C., Kendler, Kenneth S., Martin, Nicholas G., Heath, Andrew C. and Eaves, Lindon J. (2006). Genetic and Cultural Transmission of Smoking Initiation: An Extended Twin Kinship Model. Behavior Genetics, 36 (6), 795-808. doi: 10.1007/s10519-006-9085-4

Childhood sexual abuse and risks for licit and illicit drug-related outcomes: a twin study

Nelson, Elliot C., Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F., Statham, Dixie J. and Martin, Nicholas G. (2006). Childhood sexual abuse and risks for licit and illicit drug-related outcomes: a twin study. Psychological Medicine, 36 (10), 1473-1483. doi: 10.1017/S0033291706008397

A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits

Ferreira, Manuel A. R., Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2006). A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits. European Journal of Human Genetics, 14 (8), 953-962. doi: 10.1038/sj.ejhg.5201646

Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample

Smit, Christine M., Wright, Margaret J., Hansell, Narelle K., Geffen, Gina M. and Martin, Nicholas G. (2006). Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample. International Journal of Psychophysiology, 61 (2), 235-243. doi: 10.1016/j.ijpsycho.2005.10.004

Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly

Oates, N. A., van Vliet, J., Duffy, D. L., Kroes, H. Y., Martin, N. G., Boomsma, D. I., Campbell, M., Coulthard, M. G., Whitelaw, E. and Chong, S. (2006). Increased DNA Methylation at the AXIN1 Gene in a Monozygotic Twin from a Pair Discordant for a Caudal Duplication Anomaly. American Journal of Human Genetics, 79 (1), 155-162. doi: 10.1086/505031

Duration of cannabis use - a novel phenotype?

Lynskey, Michael T., Grant, Julia D., Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F., Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2006). Duration of cannabis use - a novel phenotype?. Addictive Behaviors, 31 (6), 984-994. doi: 10.1016/j.addbeh.2006.03.048

Heritability and genetic covariation of sensitivity to PROP, SOA, quinine HCl, and caffeine

Hansen, Jonathan L., Reed, Danielle R., Wright, Margaret J., Martin, Nicholas G. and Breslin, Paul. A. S. (2006). Heritability and genetic covariation of sensitivity to PROP, SOA, quinine HCl, and caffeine. Chemical Senses, 31 (3), 403-413. doi: 10.1093/chemse/bjj044

The heritability of conscientiousness facets and their relationship to IQ and academic achievement

Luciano, Michelle, Wainwright, Mark A., Wright, Margaret J. and Martin, Nicholas G. (2006). The heritability of conscientiousness facets and their relationship to IQ and academic achievement. Personality and Individual Differences, 40 (6), 1189-1199. doi: 10.1016/j.paid.2005.10.013

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A. R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Plos Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041

Cognitive modelling and the behaviour genetics of reading

Castles, Anne, Bates, Timothy, Coltheart, Max, Luciano, Michelle and Martin, Nicholas G. (2006). Cognitive modelling and the behaviour genetics of reading. Journal of Research In Reading, 29 (1), 92-103. doi: 10.1111/j.1467-9817.2006.00294.x

Handedness in twins: Joint analysis of data from 35 samples

Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M. and Martin, Nicholas G. (2006). Handedness in twins: Joint analysis of data from 35 samples. Twin Research and Human Genetics, 9 (1), 46-53. doi: 10.1375/183242706776402885

A Transdiagnostic Approach to Understanding Eating Disorders

Wade, Tracey D., Bergin, Jacqueline L., Martin, Nicholas G., Gillespie, Nathan A. and Fairburn, Christopher G. (2006). A Transdiagnostic Approach to Understanding Eating Disorders. Journal of Nervous And Mental Disease, 194 (7), 510-517. doi: 10.1097/01.nmd.0000225067.42191.b0

A genetically informed study of the association between harsh punishment and offspring behavioral problems

Lynch, Stacy K., Turkheimer, Eric, D'Onofrio, Brian M., Mendle, Jane, Emery, Robert E., Slutske, Wendy S. and Martin, Nicholas G. (2006). A genetically informed study of the association between harsh punishment and offspring behavioral problems. Journal of Family Psychology, 20 (2), 190-198. doi: 10.1037/0893-3200.20.2.190

A genetically informed study of the processes underlying the association between parental marital instability and offspring adjustment

Donofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. and Martin, Nicholas G. (2006). A genetically informed study of the processes underlying the association between parental marital instability and offspring adjustment. Developmental Psychology, 42 (3), 486-499. doi: 10.1037/0012-1649.42.3.486

A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31

Shekar, Sri Niranjan, Duffy, David L., Montgomery, Grant W. and Martin, Nicholas G. (2006). A genome scan for epidermal skin pattern in adolescent twins reveals suggestive linkage on 12p13.31. Journal of Investigative Dermatology, 126 (2), 277-282. doi: 10.1038/sj.jid.5700067

A linkage study of academic skills defined by the Queensland Core Skills Test

Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas G. (2006). A linkage study of academic skills defined by the Queensland Core Skills Test. Behavior Genetics, 36 (1), 56-64. doi: 10.1007/s10519-005-9013-z

A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families

Morley, Katherine I., Medland, Sarah E., Ferreira, Manuel A. R., Lynskey, Michael T., Montgomery, Grant W., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2006). A possible smoking susceptibility locus on chromosome 11p12: Evidence from sex-limitation linkage analyses in a sample of Australian twin families. Behavior Genetics, 36 (1), 87-99. doi: 10.1007/s10519-005-9004-0

Assortative Mating for Cigarette Smoking and for Alcohol Consumption in Female Australian Twins and their Spouses

Agrawal, Arpana, Heath, Andrew C., Grant, Julia D., Pergadia, Michele L., Statham, Dixie J., Bucholz, Kathleen K., Martin, Nicholas G. and Madden, Pamela A. F. (2006). Assortative Mating for Cigarette Smoking and for Alcohol Consumption in Female Australian Twins and their Spouses. Behavior Genetics, 36 (4), 553-566. doi: 10.1007/s10519-006-9081-8

Bias, precision and heritability of self-reported and clinically measured height in Australian twins

Macgregor, Stuart, Cornes, Belinda K., Martin, Nicholas G. and Visscher, Peter M. (2006). Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics, 120 (4), 571-580. doi: 10.1007/s00439-006-0240-z

Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity

Valle, Anne, OConnor, Daniel T., Taylor, Palmer, Zhu, Gu, Montgomery, Grant W., Slagboom, P. Eline, Martin, Nicholas G. and Whitfield, John B. (2006). Butyrylcholinesterase: Association with the metabolic syndrome and identification of 2 gene loci affecting activity. Clinical Chemistry, 52 (6), 1014-1020. doi: 10.1373/clinchem.2005.065052

Effects of Variation at the ALDH2 Locus on Alcohol Metabolism, Sensitivity, Consumption, and Dependence in Europeans

Dickson, Peter A., James, Michael R., Heath, Andrew C., Montgomery, Grant W., Martin, Nicholas G., Whitfield, John B. and Birley, Andrew J. (2006). Effects of Variation at the ALDH2 Locus on Alcohol Metabolism, Sensitivity, Consumption, and Dependence in Europeans. Alcoholism - Clinical And Experimental Research, 30 (7), 1093-1100. doi: 10.1111/j.1530-0277.2006.00128.x

Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers

Sullivan, Patrick F., Montgomery, Grant W., Hottenga, Jouke J., Wray, Naomi R., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Empirical Evaluation of the Genetic Similarity of Samples From Twin Registries in Australia and the Netherlands Using 359 STRP Markers. Twin Research And Human Genetics, 9 (4), 600-602. doi: 10.1375/183242706778025026

Family structure and age at menarche: A children-of-twins approach

Mendle, Jane, Turkheimer, Eric, D'Onofrio, Brian M., Lynch, Stacy K., Emery, Robert E., Slutske, Wendy S. and Martin, Nicholas G. (2006). Family structure and age at menarche: A children-of-twins approach. Developmental Psychology, 42 (3), 533-542. doi: 10.1037/0012-1649.42.3.533

Genetic analyses of DSM-IV nicotine withdrawal in adult twins

Pergadia, Michele L., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2006). Genetic analyses of DSM-IV nicotine withdrawal in adult twins. Psychological Medicine, 36 (7), 963-972. doi: 10.1017/S0033291706007495

Genetic and environmental influences on extreme personality dispositions in adolescent female twins

Pergadia, Michele L., Madden, Pamela A. F., Lessov, Christina N., Todorov, Alexandre A., Bucholz, Kathleen K., Martin, Nicholas G. and Heath, Andrew C. (2006). Genetic and environmental influences on extreme personality dispositions in adolescent female twins. Journal of Child Psychology And Psychiatry, 47 (9), 902-909. doi: 10.1111/j.1469-7610.2005.01568.x

Genome-wide linkage scan for loci influencing plasma triglycerides

Middelberg, Rita P., Martin, Nicholas G., Montgomery, Grant W. and Whitfield, John B. (2006). Genome-wide linkage scan for loci influencing plasma triglycerides. Clinica Chimica Acta, 374 (1-2), 87-92. doi: 10.1016/j.cca.2006.05.033

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q

Luciano, M., Wright, M. J., Duffy, D. L., Wainwright, M. A., Zhu, G., Evans, D. M., Geffen, G. M., Montgomery, G. W. and Martin, N. G. (2006). Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q. Behavior Genetics, 36 (1), 45-55. doi: 10.1007/s10519-005-9003-1

HLA and Genomewide Allele Sharing in Dizygotic Twins

Montgomery, Grant W., Zhu, Gu, Hottenga, Jouke J., Duffy, David L., Heath, Andrew C., Boomsma, Dorret I., Martin, Nicholas G. and Visscher, Peter M. (2006). HLA and Genomewide Allele Sharing in Dizygotic Twins. American Journal of Human Genetics, 79 (6), 1052-1058. doi: 10.1086/510136

Heritability and Stability of Resting Blood Pressure in Australian Twins

Hottenga, Jouke-Jan, Whitfield, John B., de Geus, Eco J. C., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Heritability and Stability of Resting Blood Pressure in Australian Twins. Twin Research And Human Genetics, 9 (2), 205-209. doi: 10.1375/183242706776382455

Heritability and nineteen-year stability of long and short EPQ-R Neuroticism scales

Birley, Andrew J., Gillespie, Nathan A., Heath, Andrew C., Sullivan, Patrick F., Boomsma, Dorret I. and Martin, Nicholas G. (2006). Heritability and nineteen-year stability of long and short EPQ-R Neuroticism scales. Personality And Individual Differences, 40 (4), 737-747. doi: 10.1016/j.paid.2005.09.005

KRAS variation and risk of endometriosis

Zhao, Z. Z., Nyholt, D. R., Le, L., Martin, N. G., James, M. R., Treloar, S. A. and Montgomery, G. W. (2006). KRAS variation and risk of endometriosis. Molecular Human Reproduction, 12 (11), 671-676. doi: 10.1093/molehr/gal078

Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task

Hansell, N. K., Medland, S. E., Ferreira, A. R., Geffen, G. M., Zhu, G., Montgomery, G. W., Duffy, D. L., Wright, M.J. and Martin, N. G. (2006). Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task. Behavior Genetics, 36 (1), 29-44. doi: 10.1007/s10519-005-9002-2

Longitudinal Genetic Analysis of Plasma Lipids

Middelberg, Rita P., Martin, Nicholas G. and Whitfield, John B. (2006). Longitudinal Genetic Analysis of Plasma Lipids. Twin Research And Human Genetics, 9 (4), 550-557. doi: 10.1375/183242706778024946

Maternal alcohol use disorder and offspring ADHD: disentangling genetic and environmental effects using a children-of-twins design

Knopik, Valerie S., Heath, Andrew C., Jacob, Theodore, Slutske, Wendy S., Bucholz, Kathleen K., Madden, Pamela A. F., Waldron, Mary and Martin, Nicholas G. (2006). Maternal alcohol use disorder and offspring ADHD: disentangling genetic and environmental effects using a children-of-twins design. Psychological Medicine, 36 (10), 1461-1471. doi: 10.1017/S0033291706007884

Migraine With Aura and Migraine Without Aura Are Not Distinct Entities: Further Evidence From a Large Dutch Population Study

Ligthart, Lannie, Boomsma, Dorret I., Martin, Nicholas G., Stubbe, Janine H. and Nyholt, Dale R. (2006). Migraine With Aura and Migraine Without Aura Are Not Distinct Entities: Further Evidence From a Large Dutch Population Study. Twin Research And Human Genetics, 9 (1), 54-63. doi: 10.1375/183242706776403019

Novel variants in growth differentiation factor 9 in mothers of dizygotic twins

Palmer, J. S., Zhao, Z. Z., Hoekstra, C., Hayward, N. K., Webb, P. M., Whiteman, D. C., Martin, N. G., Boomsma, D. I., Duffy, D. L. and Montgomery, G. W. (2006). Novel variants in growth differentiation factor 9 in mothers of dizygotic twins. Journal of Clinical Endocrinology And Metabolism, 91 (11), 4713-4716. doi: 10.1210/jc.2006-0970

Population differences in finger-length ratios: Ethnicity or latitude?

Loehlin, John C., McFadden, Dennis, Medland, Sarah E. and Martin, Nicholas G. (2006). Population differences in finger-length ratios: Ethnicity or latitude?. Archives of Sexual Behavior, 35 (6), 739-742. doi: 10.1007/s10508-006-9039-1

Rapid screening of 4000 individuals for germ-line variations in the BRAF gene

James, Michael R., Dumeni, Troy, Stark, Mitchell S., Duffy, David L., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2006). Rapid screening of 4000 individuals for germ-line variations in the BRAF gene. Clinical Chemistry, 52 (9), 1675-1678. doi: 10.1373/clinchem.2006.070169

Replicated linkage for eye color on 15q using comparative ratings of sibling pairs

Posthuma, D., Visscher, P. M., Willemsen, G., Zhu, G., Martin, N. G., Slagboom, P. E., de Geus, E. J. C. and Boomsma, D. I. (2006). Replicated linkage for eye color on 15q using comparative ratings of sibling pairs. Behavior Genetics, 36 (1), 12-17. doi: 10.1007/s10519-005-9007-x

Sex Differences in Symptoms of Depression in Unrelated Individuals and Opposite-Sex Twin and Sibling Pairs

Middeldorp, Christel M., Wray, Naomi R., Andrews, Gavin, Martin, Nicholas G. and Boomsma, Dorret I. (2006). Sex Differences in Symptoms of Depression in Unrelated Individuals and Opposite-Sex Twin and Sibling Pairs. Twin Research And Human Genetics, 9 (5), 632-636. doi: 10.1375/183242706778553507

Subtypes of Illicit Drug Users: A Latent Class Analysis of Data From an Australian Twin Sample

Lynskey, Michael T., Agrawal, Arpana, Bucholz, Kathleen K., Nelson, Elliot C., Madden, Pamela A. F., Todorov, Alexandre A., Grant, Julia D., Martin, Nicholas G. and Heath, Andrew C. (2006). Subtypes of Illicit Drug Users: A Latent Class Analysis of Data From an Australian Twin Sample. Twin Research And Human Genetics, 9 (4), 523-530. doi: 10.1375/183242706778024964

The implications of simultaneous smoking initiation for inferences about the genetics of smoking behavior from twin data

Pergadia, Michele L., Heath, Andrew C., Agrawal, Arpana, Bucholz, Kathleen K., Martin, Nicholas G. and Madden, Pamela A. F. (2006). The implications of simultaneous smoking initiation for inferences about the genetics of smoking behavior from twin data. Behavior Genetics, 36 (4), 567-576. doi: 10.1007/s10519-005-9042-7

The return to schooling: Estimates from a sample of young Australian twins

Miller, Paul, Mulvey, Charles and Martin, Nick (2006). The return to schooling: Estimates from a sample of young Australian twins. Labour Economics, 13 (5), 571-587. doi: 10.1016/j.labeco.2004.10.008

Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband

Ferreira, M. A. R., OGorman, L., Souef, P. L., Burton, P. R., Toelle, B. G., Robertson, C. F., Martin, N. G. and Duffy, D. L. (2006). Variance components analyses of multiple asthma traits in a large sample of Australian families ascertained through a twin proband. Allergy, 61 (2), 245-253. doi: 10.1111/j.1398-9995.2005.00954.x

ViewPoint and ViewDist: Utilities for rapid graphing of linkage distributions and identification of outliers

Beeby, Harry N., Medland, Sarah E. and Martin, Nicholas G. (2006). ViewPoint and ViewDist: Utilities for rapid graphing of linkage distributions and identification of outliers. Behavior Genetics, 36 (1), 7-11. doi: 10.1007/s10519-006-9045-z

A comparison of twin birthweight data from Australia, the Netherlands, the United States, Japan, and South Korea: Are genetic and environmental variations in birthweight similar in Caucasians and East Asians?

Hur, YM, Luciano, M, Martin, NG, Boomsma, DI, Iacono, WG, McGue, M, Shin, JS, Jun, JK, Ooki, S, van Beijsterveldt, CEM and Han, JY (2005). A comparison of twin birthweight data from Australia, the Netherlands, the United States, Japan, and South Korea: Are genetic and environmental variations in birthweight similar in Caucasians and East Asians?. Twin Research and Human Genetics, 8 (6), 638-648. doi: 10.1375/twin.8.6.638

BRAF Polymorphisms and Risk of Melanocytic Neoplasia

James, Michael R., Roth, Richard B., Shi, Michael M., Kammerer, Stefan, Nelson, Matthew R., Stark, Mitchell S., Dumenil, Troy, Montgomery, Grant W., Hayward, Nicholas K., Martin, Nicholas G., Braun, Andreas and Duffy, David L. (2005). BRAF Polymorphisms and Risk of Melanocytic Neoplasia. Journal of Investigative Dermatology, 125 (6), 1252-1258. doi: 10.1111/j.0022-202X.2005.23937.x

Familial clustering of major depression and anxiety disorders in Australian and Dutch twins and siblings

Middledorp, Christel M., Birley, Andrew J., Cath, Danielle C., Gillespie, Nathan A., Willemsen, Gonneke, Statham, Dixie J., de Geus, Eco J. C., Andrews, J. Gavin, van Dyck, Richard, Beem, A. Leo, Sullivan, Patrick F., Martin, Nicholas G. and Boomsma, Dorret I. (2005). Familial clustering of major depression and anxiety disorders in Australian and Dutch twins and siblings. Twin Research and Human Genetics, 8 (6), 609-615. doi: 10.1375/183242705774860123

Genetic and environmental influences on skin pattern deterioration

Shekar, Sri Niranjan, Luciano, Michelle, Duffy, David L. and Martin, Nicholas G. (2005). Genetic and environmental influences on skin pattern deterioration. Journal of Investigative Dermatology, 125 (6), 1119-1129. doi: 10.1111/j.0022-202X.2005.23961.x

Limitations of DSM-IV operationalizations of alcohol abuse and dependence in a sample of Australian twins

Lynskey, Michael T., Nelson, Elliot C., Neuman, Rosalind J., Bucholz, Kathleen K., Madden, Pamela A. F., Knopik, Valerie S., Slutske, Wendy, Whitfield, John B., Martin, Nicholas G. and Heath, Andrew C. (2005). Limitations of DSM-IV operationalizations of alcohol abuse and dependence in a sample of Australian twins. Twin Research and Human Genetics, 8 (6), 574-584. doi: 10.1375/183242705774860178

Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13

Ferreira, MAR, O'Gorman, L, Le Souef, P, Burton, PR, Toelle, BG, Robertson, CF, Visscher, PM, Martin, NG and Duffy, DL (2005). Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13. American Journal of Human Genetics, 77 (6), 1075-1085. doi: 10.1086/497997

Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families

Cornes, BK, Medland, SE, Ferreira, MAR, Morley, KI, Duffy, DL, Heijmans, BT, Montgomery, GW and Martin, NG (2005). Sex-limited genome-wide linkage scan for body mass index in an unselected sample of 933 Australian twin families. Twin Research and Human Genetics, 8 (6), 616-632. doi: 10.1375/183242705774860240

A genetically informed study of marital instability and its association with offspring psychopathology

D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. and Martin, Nicholas G. (2005). A genetically informed study of marital instability and its association with offspring psychopathology. Journal of Abnormal Psychology, 114 (4), 570-586. doi: 10.1037/0021-843X.114.4.570

Correlates of regular cigarette smoking in a population-based sample of Australian twins

Agrawal, Arpana, Madden, Pamela A. F., Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K. and Martin, Nicholas G. (2005). Correlates of regular cigarette smoking in a population-based sample of Australian twins. Addiction, 100 (11), 1709-1719. doi: 10.1111/j.1360-0443.2005.01217.x

Genetic covariation between event-related potential (ERP) and behavioral non-ERP measures of working-memory, processing speed, and IQ

Hansell, N. K., Wright, M. J., Luciano, M., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2005). Genetic covariation between event-related potential (ERP) and behavioral non-ERP measures of working-memory, processing speed, and IQ. Behavior Genetics, 35 (6), 695-706. doi: 10.1007/s10519-005-6188-2

Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females

Medland, Sarah E., Duffy, David L., Spurdle, Amanda B., Wright, Margaret J., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2005). Opposite effects of androgen receptor CAG repeat length on increased risk of left-handedness in males and females. Behavior Genetics, 35 (6), 735-744. doi: 10.1007/s10519-005-6187-3

Widespread evidence for non-additive genetic variation in Cloninger's and Eysenck's personality dimensions using a twin plus sibling design

Keller, MC, Coventry, WL, Heath, AC and Martin, NG (2005). Widespread evidence for non-additive genetic variation in Cloninger's and Eysenck's personality dimensions using a twin plus sibling design. Behavior Genetics, 35 (6), 707-721. doi: 10.1007/s10519-005-6041-7

Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions

Heijmans, BT, Beekman, M, Putter, H, Lakenberg, N, van der Wijk, HJ, Whitfield, JB, Posthuma, D, Pedersen, NL, Martin, NG, Boomsma, DI and Slagboom, PE (2005). Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions. European Journal of Human Genetics, 13 (10), 1143-1153. doi: 10.1038/sj.ejhg.5201466

Psychological masculinity-femininity via the gender diagnosticity approach: heritability and consistency across ages and populations

Loehlin, John C., Jonsson, Erik G., Gustavsson, J. Petter, Stallings, Michael C., Gillespie, Nathan A., Wright, Margaret J. and Martin, Nicholas G. (2005). Psychological masculinity-femininity via the gender diagnosticity approach: heritability and consistency across ages and populations. Journal of Personality, 73 (5), 1295-1320. doi: 10.1111/j.1467-6494.2005.00350.x

The genetics of tea and coffee drinking and preference for source of caffeine in a large community sample of Australian twins

Luciano, Michelle, Kirk, Katherine M., Heath, Andrew C. and Martin, Nicholas G. (2005). The genetics of tea and coffee drinking and preference for source of caffeine in a large community sample of Australian twins. Addiction, 100 (10), 1510-1517. doi: 10.1111/j.1360-0443.2005.01223.x

Genomewide significant linkage to migrainous Hheadache on chromosome 5q21

Nyholt, Dale R., Morley, Katherine I., Ferreira, Manual A. R., Medland, Sarah E., Boomsma, Dorret I., Heath, Andrew C., Merikangas, Kathleen R., Montgomery, Grant W. and Martin, Nicholas G. (2005). Genomewide significant linkage to migrainous Hheadache on chromosome 5q21. American Journal Of Human Genetics, 77 (3), 500-512. doi: 10.1086/444510

A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p

Posthuma, Danielle, Luciano, Michelle, de Geus, Eco J. C., Wright, Margie J., Slagboom, P. Eline, Montgomery, Grant W., Boomsma, Dorret I. and Martin, Nicholas G. (2005). A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p. American Journal of Human Genetics, 77 (2), 318-326. doi: 10.1086/432647

Evidence of age-dependent genetic influences on plasma total cholesterol

Middelberg, R, Heath, AC, Martin, NG and Whitfield, JB (2005). Evidence of age-dependent genetic influences on plasma total cholesterol. European Journal of Cardiovascular Prevention & Rehabilitation, 12 (4), 380-386. doi: 10.1097/01.hjr.0000160602.41762.9f

Eysenck's Psychoticism and the X-linked androgen receptor gene CAG polymorphism in additional Australian samples

Loehlin, JC, Medland, SE, Montgomery, GW and Martin, NG (2005). Eysenck's Psychoticism and the X-linked androgen receptor gene CAG polymorphism in additional Australian samples. Personality and Individual Differences, 39 (3), 661-667. doi: 10.1016/j.paid.2005.02.016

An analysis of risk factors for cutaneous melanoma by anatomical site (Australia)

Siskind, Victor, Whiteman, David C., Aitken, Joanne F., Martin, Nicholas G. and Green, Adele C. (2005). An analysis of risk factors for cutaneous melanoma by anatomical site (Australia). Cancer Causes and Control, 16 (3), 193-199. doi: 10.1007/s10552-004-4325-5

New concepts for distinguishing the hidden patterns of linkage disequilibrium which underlie association between genotypes and complex phenotypes

Wicks, Jacqueline, Treloar, Susan A., Martin, Nicholas G and Duffy, David L. (2005). New concepts for distinguishing the hidden patterns of linkage disequilibrium which underlie association between genotypes and complex phenotypes. Twin Research And Human Genetics, 8 (2), 95-100. doi: 10.1375/1832427053738737

Birth weight and schooling and earnings: estimates from a sample of twins

Miller, P, Mulvey, C and Martin, N (2005). Birth weight and schooling and earnings: estimates from a sample of twins. Economics Letters, 86 (3), 387-392. doi: 10.1016/j.econlet.2004.10.002

Bladder neck mobility is a heritable trait

Dietz, H. P., Hansell, N. K., Grace, M. E., Eldridge, A.M., Clarke, B. and Martin, N. G. (2005). Bladder neck mobility is a heritable trait. BJOG: An International Journal of Obstetrics and Gynaecology, 112 (3), 334-339. doi: 10.1111/j.1471-0528.2004.00428.x

Multivariate Genetic Analysis of Chronic Pelvic Pain and Associated Phenotypes

Zondervan, K., Kennedy, S., Cardon, L., Martin, N. G. and Treloar, S. (2005). Multivariate Genetic Analysis of Chronic Pelvic Pain and Associated Phenotypes. Behavior Genetics, 35 (2), 177-188. doi: 10.1007/s10519-004-1017-6

Teenage acne is influenced by genetic factors

Evans, D. M., Kirk, K. M., Nyholt, D. R., Novac, C. and Martin, N. G. (2005). Teenage acne is influenced by genetic factors. British Journal of Dermatology, 152 (3), 579-581. doi: 10.1111/j.1365-2133.2005.06387.x

The genetic basis of academic achievement on the Queensland Core Skills Test and its shared genetic variance with IQ

Wainwright, Mark A., Wright, Margaret J., Geffen, Gina M., Luciano, Michelle and Martin, Nicholas G. (2005). The genetic basis of academic achievement on the Queensland Core Skills Test and its shared genetic variance with IQ. Behavior Genetics, 35 (2), 133-145. doi: 10.1007/s10519-004-1014-9

Choice of residential location: Chance, family influences, or genes?

Whitfield, John B., Zhu, Gu, Heath, Andrew C. and Martin, Nicholas G. (2005). Choice of residential location: Chance, family influences, or genes?. Twin Research and Human Genetics, 8 (1), 22-26. doi: 10.1375/twin.8.1.22

Discordant MZ twins with cleft lip and palate: A model for identifying genes in complex traits

Mansilla, MA, Kimani, J, Mitchell, LE, Christensen, K, Boomsma, DI, Daack-Hirsch, S, Nepomucena, B, Wyszynski, DF, Felix, TM, Martin, NG and Murray, JC (2005). Discordant MZ twins with cleft lip and palate: A model for identifying genes in complex traits. Twin Research and Human Genetics, 8 (1), 39-46. doi: 10.1375/1832427053435373

Early childhood behaviours, schooling and labour market outcomes: estimates from a sample of twins

Le, AT, Miller, PW, Heath, AC and Martin, N (2005). Early childhood behaviours, schooling and labour market outcomes: estimates from a sample of twins. Economics of Education Review, 24 (1), 1-17. doi: 10.1016/j.econedurev.2004.04.004

Genetic and environmental influences on the frequency of female orgasm

Dawood, Khytam, Kirk, Katherine M., Bailey, J. Michael, Andrews, Paul W. and Martin, Nicholas G. (2005). Genetic and environmental influences on the frequency of female orgasm. Twin Research and Human Genetics, 8 (1), 27-33. doi: 10.1375/1832427053435427

Association between polymorphisms in the progesterone receptor gene and endometriosis

Treloar, Susan A., Zhao, Zhen Zhen, Armitage, Trudi, Duffy, David L., Wicks, Jacqueline, O'Connor, Daniel T., Martin, Nicholas G. and Montgomery, Grant W. (2005). Association between polymorphisms in the progesterone receptor gene and endometriosis. Molecular Human Reproduction, 11 (9), 641-647. doi: 10.1093/molehr/gah221

Erythrocyte aldehyde dehydrogenase activity: Lack of association with alcohol use and dependence or alcohol reactions in Australian twins

Hansell, NK, Pang, D, Heath, AC, Martin, NG and Whitfield, JB (2005). Erythrocyte aldehyde dehydrogenase activity: Lack of association with alcohol use and dependence or alcohol reactions in Australian twins. Alcohol and Alcoholism, 40 (5), 343-348. doi: 10.1093/alcalc/agh168

Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues

Montgomery, GW, Campbell, MJ, Dickson, P, Herbert, S, Siemering, K, Ewen-White, KR, Visscher, PM and Martin, NG (2005). Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues. Twin Research and Human Genetics, 8 (4), 346-352. doi: 10.1375/1832427054936673

Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan

Dickson, PA, Montgomery, GW, Henders, A, Campbell, MJ, Martin, NG and James, MR (2005). Evaluation of multiple displacement amplification in a 5 cM STR genome-wide scan. Nucleic Acids Research, 33 (13), 1-4. doi: 10.1093/nar/gni126

Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci

Birley, A. J., Whitfield, J. B., Neale, M. C., Duffy, D. L., Heath, A. C., Boomsma, D. I. and Martin, N. G. (2005). Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci. Behavior Genetics, 35 (5), 509-524. doi: 10.1007/s10519-005-3851-6

Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26

Treloar, Susan A., Wicks, Jacqueline, Nyholt, Dale R., Montgomery, Grant W., Bahlo, Melanie, Smith, Vicki, Dawson, Gary, Mackay, Ian J., Weeks, Daniel E., Bennett, Simon T., Carey, Alisoun, Ewen-White, Kelly R., Duffy, David L., O'Connor, Daniel T., Barlow, David H., Martin, Nicholas G. and Kennedy, Stephen H. (2005). Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. American Journal of Human Genetics, 77 (3), 365-376. doi: 10.1086/432960

Multivariate genetic analysis of academic skills of the Queensland Core Skills Test and IQ highlight the importance of genetic g

Wainwright, Mark A., Wright, Margaret J., Luciano, Michelle, Geffen, Gina M. and Martin, Nicholas G. (2005). Multivariate genetic analysis of academic skills of the Queensland Core Skills Test and IQ highlight the importance of genetic g. Twin Research and Human Genetics, 8 (6), 602-608. doi: 10.1375/183242705774860259

Perceptual speed does not cause intelligence, and intelligence does not cause perceptual speed

Luciano, Michelle, Posthuma, Danielle, Wright, Margaret J., de Geus, Eco J. C., Smith, Glen A., Geffen, Gina M., Boomsma, Dorret I. and Martin, Nicholas G. (2005). Perceptual speed does not cause intelligence, and intelligence does not cause perceptual speed. Biological Psychology, 70 (1), 1-8. doi: 10.1016/j.biopsycho.2004.11.011

The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression

Gillespie, NA, Whitfield, JB, Williams, B, Heath, AC and Martin, NG (2005). The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression. Psychological Medicine, 35 (1), 101-111. doi: 10.1017/S0033291704002727

A test of the sorting model of education in Australia

Miller, PW, Mulvey, C and Martin, N (2004). A test of the sorting model of education in Australia. Economics of Education Review, 23 (5), 473-482. doi: 10.1016/j.econedurev.2004.04.003

Major Depressive Disorder, Suicidal Ideation, and Suicide Attempt in Twins Discordant for Cannabis Dependence and Early-Onset Cannabis Use

Lynskey, Michael T., Glowinski, Anne L., Todorov, Alexandr A., Bucholz, Kathleen K., Madden, Pamela A. F., Nelson, Elliot C., Statham, Dixie J., Martin, Nicholas G. and Heath, Andrew C. (2004). Major Depressive Disorder, Suicidal Ideation, and Suicide Attempt in Twins Discordant for Cannabis Dependence and Early-Onset Cannabis Use. Archives of General Psychiatry, 61 (10), 1026-1032. doi: 10.1001/archpsyc.61.10.1026

Major quantitative trait locus for eosinophil count is located on chromosome 2q

Evans, DM, Zhu, G, Duffy, DL, Montgomery, GW, Frazer, IH and Martin, NG (2004). Major quantitative trait locus for eosinophil count is located on chromosome 2q. Journal of Allergy And Clinical Immunology, 114 (4), 826-830. doi: 10.1016/j.jaci.2004.05.060

Personality, arousal theory and the relationship to cognitive ability as measured by inspection time and IQ

Luciano, Michelle, Leisser, Romana, Wright, Margaret J. and Martin, Nicholas G. (2004). Personality, arousal theory and the relationship to cognitive ability as measured by inspection time and IQ. Personality and Individual Differences, 37 (5), 1081-1089. doi: 10.1016/j.paid.2003.11.016

Behaviour genetic analyses of reading and spelling: a component processes approach

Bates, Timothy C., Castles, Anne, Coltheart, Max, Gillespie, Nathan, Wright, Margie and Martin, Nicholas G. (2004). Behaviour genetic analyses of reading and spelling: a component processes approach. Australian Journal of Psychology, 56 (2), 115-126. doi: 10.1080/00049530410001734847

Brisbane adolescent twin study: outline of study methods and research projects

Wright, Margaret J. and Martin, Nicholas G. (2004). Brisbane adolescent twin study: outline of study methods and research projects. Australian Journal of Psychology, 56 (2), 65-78. doi: 10.1080/00049530410001734865

Genetic influences on cognitive processes associated with distraction: An event-related potential study of the slow wave

Hansell, Narelle K., Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B. and Martin, Nicholas G. (2004). Genetic influences on cognitive processes associated with distraction: An event-related potential study of the slow wave. Australian Journal of Psychology, 56 (2), 89-98. doi: 10.1080/0049530410001734856

Monozygotic twin pairs discordant for lifetime anorexia nervosa: an exploratory investigation

Wade, Tracey, Treloar, Susan A., Martin, Nicholas G., Statham, Dixie and Heath, Andrew C. (2004). Monozygotic twin pairs discordant for lifetime anorexia nervosa: an exploratory investigation. Australian Journal of Psychology, 56 (2), 127-132. doi: 10.1080/00049530410001734810

Genetic and environmental sources of covariance between reading tests used in neuropsychological assessment and IQ subtests

Wainwright, Mark, Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B., Luciano, Michelle and Martin, Nicholas G. (2004). Genetic and environmental sources of covariance between reading tests used in neuropsychological assessment and IQ subtests. Behavior Genetics, 34 (4), 365-376. doi: 10.1023/B:BEGE.0000023642.34853.cb

Using identity-by-de scent information in affected sib pairs to increase the efficiency of genetic association studies

Wicks, Jacqueline, Treloar, Susan A. and Martin, Nicholas G. (2004). Using identity-by-de scent information in affected sib pairs to increase the efficiency of genetic association studies. Twin Research, 7 (2), 211-216. doi: 10.1375/136905204323016195

Copulas in QTL mapping

Basrak, Bojan, Klaassen, Chris A. J., Beekman, Marion, Martin, Nicholas G. and Boomsma, Dorret I. (2004). Copulas in QTL mapping. Behavior Genetics, 34 (2), 161-171. doi: 10.1023/B:BEGE.0000013730.63991.ba

Genetic Epidemiology of Alcohol-Induced Blackouts

Nelson, Elliot C., Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F., Fu, Qiang, Knopik, Valerie, Lynskey, Michael T., Whitfield, John B., Statham, Dixie J. and Martin, Nicholas G. (2004). Genetic Epidemiology of Alcohol-Induced Blackouts. Archives of General Psychiatry, 61 (3), 257-263. doi: 10.1001/archpsyc.61.3.257

A deletion mutation in GDF9 in sisters with spontaneous DZ twins

Montgomery, G. W., Zhao, Z. Z., Marsh, A. J., Mayne, R., Treloar, S. A., James, M., Martin, N. G., Boomsma, D. I. and Duffy, D. L. (2004). A deletion mutation in GDF9 in sisters with spontaneous DZ twins. Twin Research, 7 (6), 548-555. doi: 10.1375/1369052042663823

A genetic investigation of the covariation among Inspection Time, Choice Reaction Time, and IQ subtest scores

Luciano, Michelle, Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B., Smith, Glen A. and Martin, Nicholas G. (2004). A genetic investigation of the covariation among Inspection Time, Choice Reaction Time, and IQ subtest scores. Behavior Genetics, 34 (1), 41-50. doi: 10.1023/B:BEGE.0000009475.35287.9d

A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q

Zhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M. and Martin, N. G. (2004). A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q. Twin Research, 7 (2), 197-210. doi: 10.1375/136905204323016186

A major quantitative trait locus for CD4-CD8 ratio is located on chromosome 11

Evans, D. M., Zhu, G., Duffy, D. L., Frazer, I. H., Montgomery, G. W. and Martin, N. G. (2004). A major quantitative trait locus for CD4-CD8 ratio is located on chromosome 11. Genes and Immunity, 5 (7), 548-552. doi: 10.1038/sj.gene.6364126

Analysis of Melanoma Onset: Assessing Familial Aggregation by Using Estimating Equations and Fitting Variance Components via Bayesian Random Effects Models

Do, Kim-Anh, Aitken, Joanne F., Green, Adele C and Martin, Nicholas G. (2004). Analysis of Melanoma Onset: Assessing Familial Aggregation by Using Estimating Equations and Fitting Variance Components via Bayesian Random Effects Models. Twin Research, 7 (1), 98-113. doi: 10.1375/13690520460741480

CCR5-Delta 32 mutation is strongly associated with primary sclerosing cholangitis

Eri, R, Jonsson, JR, Pandeya, N, Purdie, DM, Clouston, AD, Martin, N, Duffy, D, Powell, EE, Fawcett, J, Florin, THJ and Radford-Smith, GL (2004). CCR5-Delta 32 mutation is strongly associated with primary sclerosing cholangitis. Genes And Immunity, 5 (6), 444-450. doi: 10.1038/sj.gene.6364113

Defining nicotine dependence for genetic research: evidence from Australian twins

Lessov, Christina N., Martin, Nicholas G., Statham, Dixie J., Todorov, Alexandre A., Slutske, Wendy S., Bucholz, Kathleen K., Heath, Andrew C. and Madden, Pamela A. F. (2004). Defining nicotine dependence for genetic research: evidence from Australian twins. Psychological Medicine, 34 (5), 865-879. doi: 10.1017/S0033291703001582

Do the Genetic or Environmental Determinants of Anxiety and Depression Change with Age? A Longitudinal Study of Australian Twins

Gillespie, Nathan A., Kirk, Katherine M., Evans, David M., Heath, Andrew C., Hickie, Ian B. and Martin, Nicholas G. (2004). Do the Genetic or Environmental Determinants of Anxiety and Depression Change with Age? A Longitudinal Study of Australian Twins. Twin Research, 7 (1), 39-53. doi: 10.1375/13690520460741435

Effects of dopamine receptor D4 variation on alcohol and tobacco use and on novelty seeking: Multivariate linkage and association analysis

Luciano, Michelle, Zhu, Gu, Kirk, K. M., Whitfield, J. B., Butler, R., Heath, A. C., Madden, P. A. F. and Martin, N. G. (2004). Effects of dopamine receptor D4 variation on alcohol and tobacco use and on novelty seeking: Multivariate linkage and association analysis. American Journal of Medical Genetics Part B-neuropsychiatric Genetics, 124B (1), 113-123. doi: 10.1002/ajmg.b.20077

Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay

James, Michael R., Hayward, Nicholas K., Dumenil, Troy, Montgomery, Grant W., Martin, Nicholas G. and Duffy, David L. (2004). Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay. Journal of Investigative Dermatology, 123 (4), 760-762. doi: 10.1111/j.0022-202X.2004.23305.x

Exploring the Etiology of the Association Between Birthweight and IQ in an Adolescent Twin Sample

Luciano, Michelle, Wright, Margaret J. and Martin, Nicholas G. (2004). Exploring the Etiology of the Association Between Birthweight and IQ in an Adolescent Twin Sample. Twin Research, 7 (1), 62-71. doi: 10.1375/13690520460741453

Gender diagnosticity and androgen receptor gene CAG repeat sequence

Loehlin, John C., Jonsson, Erik G., Gustavsson, J. Petter, Schalling, Martin, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2004). Gender diagnosticity and androgen receptor gene CAG repeat sequence. Twin Research, 7 (5), 456-461. doi: 10.1375/1369052042335359

Genetic Simplex Modeling of Eysenck's Dimensions of Personality in a Sample of Young Australian Twins

Gillespie, Nathan A., Evans, David E., Wright, Margie M. and Martin, Nicholas G. (2004). Genetic Simplex Modeling of Eysenck's Dimensions of Personality in a Sample of Young Australian Twins. Twin Research, 7 (6), 637-648. doi: 10.1375/1369052042663814

Genetic covariation of pelvic organ and elbow mobility in twins and their sisters

Hansell, N. K., Dietz, H. P., Treloar, S. A., Clarke, B. and Martin, N. G. (2004). Genetic covariation of pelvic organ and elbow mobility in twins and their sisters. Twin Research, 7 (3), 254-260. doi: 10.1375/136905204774200532

Genetic effects on alcohol dependence risk: re-evaluating the importance of psychiatric and other heritable risk factors

Knopik, Valerie S., Heath, Andrew C., Madden, Pamela A. F., Bucholz, Kathleen K., Slutske, Wendy S., Nelson, Ellieo C., Statham, Dixie, Whitfield, John B. and Martin, Nicholas G. (2004). Genetic effects on alcohol dependence risk: re-evaluating the importance of psychiatric and other heritable risk factors. Psychological Medicine, 34 (8), 1519-1530. doi: 10.1017/S0033291704002922

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

Duffy, D. L., Box, N. F., Chen, W., Palmer, J. S., Montgomery, G. W., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2004). Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Human Molecular Genetics, 13 (4), 447-461. doi: 10.1093/hmg/ddh043

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities

Nyholt, Dale R., Gillespie, Nathan G., Heath, Andrew C., Merikangas, Kathleen R., Duffy, David L. and Martin, Nicholas G. (2004). Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities. Genetic Epidemiology, 26 (3), 231-244. doi: 10.1002/gepi.10311

Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q

Evans, D. M., Zhu, G., Duffy, D. L., Montgomery, G. W., Frazer, IH and Martin, NG (2004). Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q. European Journal of Human Genetics, 12 (10), 835-842. doi: 10.1038/sj.ejhg.5201248

Multivariate genetic analysis of cognitive abilities in an adolescent twin sample

Luciano, M., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2004). Multivariate genetic analysis of cognitive abilities in an adolescent twin sample. Australian Journal of Psychology, 56 (2), 79-88. doi: 10.1080/00049530410001734874

Perceived social support in a large community sample - Age and sex differences

Coventry, W. L., Gillespie, N. A., Heath, A. C. and Martin, N. G. (2004). Perceived social support in a large community sample - Age and sex differences. Social Psychiatry And Psychiatric Epidemiology, 39 (8), 625-636. doi: 10.1007/s00127-004-0795-8

Quantitative Association Tests of Immune Responses to Antigens of Mycobacterium Tuberculosis: A Study of Twins in West Africa

Wiart, Amanda, Jepson, Annette, Banya, Winston, Bennett, Steve, Whittle, Hilton, Martin, Nicholas G. and Hill, Adrain V. S. (2004). Quantitative Association Tests of Immune Responses to Antigens of Mycobacterium Tuberculosis: A Study of Twins in West Africa. Twin Research, 7 (6), 578-588. doi: 10.1375/1369052042663887

The epidemiology and genetics of smoking initiation and persistence: Crosscultural comparisons of twin study results

Madden, Pamela A. F., Pedersen, Nancy L., Kaprio, Jaakko, Koskenvuo, Markku J . and Martin, Nicholas G. (2004). The epidemiology and genetics of smoking initiation and persistence: Crosscultural comparisons of twin study results. Twin Research, 7 (1), 82-97. doi: 10.1375/13690520460741471

The genetics of alcohol intake and of alcohol dependence

Whitfield, John B., Zhu, Gu, Madden, Pamela A., Neale, Michael C., Heath, Andrew C. and Martin, Nicholas G. (2004). The genetics of alcohol intake and of alcohol dependence. Alcoholism-clinical And Experimental Research, 28 (8), 1153-1160. doi: 10.1097/01.ALC.0000134221.32773.69

Genetic Basis of Male Pattern Baldness [Letter to the editor]

Nyholt, Dale R., Gillespie, Nathan A., Heath, Andrew C. and Martin, Nicholas G. (2003). Genetic Basis of Male Pattern Baldness [Letter to the editor]. Journal of Investigative Dermatology, 121 (6), 1561-1564. doi: 10.1111/j.1523-1747.2003.12615.x

The genetic and environmental relationship between Cloninger's dimensions of temperament and character

Gillespie, NA, Cloninger, CR, Heath, AC and Martin, NG (2003). The genetic and environmental relationship between Cloninger's dimensions of temperament and character. Personality and Individual Differences, 35 (8), 1931-1946. doi: 10.1016/S0191-8869(03)00042-4

A role for the appendix in inflammatory bowel disease? Cut it out

Edwards, J. E., Florin, T. H., Green, A, Martin, N. G., Newman, B., Pandeya, N., Purdie, D. M., Radford-Smith, G. L. and Watson, M. (2003). A role for the appendix in inflammatory bowel disease? Cut it out. Gastroenterology, 125 (4), 1270-1272. doi: 10.1016/j.gastro.2003.05.002

Ocular melanoma is not associated with CDKN2A or MC1R variants - a population-based study

Vajdic, C, Kricker, A, Duffy, DL, Aitken, JF, Stark, M, ter Huurne, JAC, Martin, NG, Armstrong, BK and Hayward, NK (2003). Ocular melanoma is not associated with CDKN2A or MC1R variants - a population-based study. Melanoma Research, 13 (4), 409-413. doi: 10.1097/01.cmr.0000056244.56735.28

Direction of Causation Modeling Between Cross-Sectional Measures of Parenting and Psychological Distress in Female Twins

Gillespie, Nathan A., Zhu, Gu, Neale, Michael C., Heath, Andrew C. and Martin, Nicholas G. (2003). Direction of Causation Modeling Between Cross-Sectional Measures of Parenting and Psychological Distress in Female Twins. Behavior Genetics, 33 (4), 383-396. doi: 10.1023/A:1025365325016

The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes

Sturm, R. A., Duffy, D. L., Box, N. F., Chen, W., Smit, D. J., Brown, D. L., Stow, J. L., Leonard, J. H. and Martin, N. G. (2003). The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes. Pigment Cell Research, 16 (3), 266-272. doi: 10.1034/j.1600-0749.2003.00041.x

Escalation of Drug Use in Early-Onset Cannabis Users vs Co-twin Controls

Lynskey, Michael T., Heath, Andrew C., Bucholz, Kathleen K., Slutske, Wendy S., Madden, Pamela A. F., Nelson, Elliot C., Statham, Dixie J. and Martin, Nicholas G. (2003). Escalation of Drug Use in Early-Onset Cannabis Users vs Co-twin Controls. JAMA : The Journal of the American Medical Association, 289 (4), 427-433. doi: 10.1001/jama.289.4.427

A genetic two-factor model of the covariation among a subset of Multidimensional Aptitude Battery and Wechsler Adult Intelligence Scale - Revised subtests

Luciano, M., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A., Evans, D. M. and Martin, N. G. (2003). A genetic two-factor model of the covariation among a subset of Multidimensional Aptitude Battery and Wechsler Adult Intelligence Scale - Revised subtests. Intelligence, 31 (6), 589-605. doi: 10.1016/S0160-2896(03)00057-6

ADH genotype does not modify the effects of alcohol on high-density lipoprotein

Whitfield, John B., OBrien, Martin E., Nightingale, Brian N., Zhu, Gu, Heath, Andrew C. and Martin, Nicholas G. (2003). ADH genotype does not modify the effects of alcohol on high-density lipoprotein. Alcoholism-clinical And Experimental Research, 27 (3), 509-514. doi: 10.1097/01.ALC.0000057940.57330.70

Accuracy of Mothers' Retrospective Reports of Smoking During Pregnancy: Comparison with Twin Sister Informant Ratings

Heath, Andrew C., Knopik, Valerie S., Madden, Pamela A., Neuman, Rosalind J., Lynskey, Michael J., Slutske, Wendy S., Jacob, Theodore and Martin, Nicholas G. (2003). Accuracy of Mothers' Retrospective Reports of Smoking During Pregnancy: Comparison with Twin Sister Informant Ratings. Twin Research, 6 (4), 297-301. doi: 10.1375/136905203322296656

Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes

Montgomery, Grant W., Zhao, Zhen Zehn, Morley, Katherine I., Marsh, Anna J., Boomsma, Dorret I., Martin, Nicholas G. and Duffy, David L. (2003). Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes. Human Reproduction, 18 (11), 2460-2464. doi: 10.1093/humrep/deg441

Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population

Beekman, Marian, Heijmans, Bastian T., Martin, Nicholas G., Whitfield, John B., Pedersen, Nancy L., DeFaire, Ulf, Snieder, Harold, Lakenberg, Nico, Suchiman, H. Eka D., De Knijff, Peter, Frants, Rune R., van Ommen, Gert Jan B., Kluft, Cornelis, Vogler, George P., Boomsma, Dorret I. and Slagboom, P. Eline (2003). Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population. European Journal of Human Genetics, 11 (11), 845-850. doi: 10.1038/sj.ejhg.5201053

Genetic and Environmental Influences on Migraine: A Twin Study Across Six Countries

Mulder, Elles J., van Baal, Caroline, Gaistz, David, Kallela, Mikko, Kaprio, Jaakko, Svensson, Dan A., Nyholt, Dale R., Martin, Nicholas G., MacGregor, Alex J., Cherkas, Lynn F., Boomsma, Dorret I. and Palotie, Aarno (2003). Genetic and Environmental Influences on Migraine: A Twin Study Across Six Countries. Twin Research, 6 (5), 422-431. doi: 10.1375/136905203770326420

Heritability of adult body height: A comparative study of twin cohorts in eight countries

Silventoinen, K., Sammalisto, S., Perola, M., Boomsma, D. I., Cornes, B. K., Davis, C., Dunkel, L., deLange, M., Harris, J. R., Hjelmborg, J. V. B., Luciano, M., Martin, N. G., Mortensen, J., Nistico, L. and Pedersen, N. L. (2003). Heritability of adult body height: A comparative study of twin cohorts in eight countries. Twin Research, 6 (5), 399-408. doi: 10.1375/136905203770326402

Linkage and Association Analysis of Radiation Damage Repair Genes XRCC3 and XRCC5 with Nevus Density in Adolescent Twins

Zhu, Gu, Duffy, David L., Turner, David R., Ewen, Kelly R., Montgomery, Grant W. and Martin, Nicholas G. (2003). Linkage and Association Analysis of Radiation Damage Repair Genes XRCC3 and XRCC5 with Nevus Density in Adolescent Twins. Twin Research, 6 (4), 315-321. doi: 10.1375/136905203322296683

Localization of a novel melanoma susceptibility locus to 1p22

Gillanders, Elizabeth, Juo, Suh-Hang Hank, Holland, Elizabeth A., Jones, MaryPat, Nancarrow, Derek, Freas-Lutz, Diana, Sood, Raman, Park, Naeun, Faruque, Mezbah, Markey, Carol, Kefford, Richard F., Palmer, Jane, Bergman, Wilma, Bishop, D. Timothy, Tucker, Margaret A., Bressac-de Paillerets, Brigitte, Hansson, Johan, The Lund Melanoma Study Group, Stark, Mitchell, Gruis, Nelleke, Newton Bishop, Julia, Goldstein, Alisa M., Bailey-Wilson, Joan E., Mann, Graham J., Hayward, Nicholas, Trent, Jeffrey, Martin, Nicholas G. and The Melanoma Genetics Consortium (2003). Localization of a novel melanoma susceptibility locus to 1p22. American Journal of Human Genetics, 73 (2), 301-313. doi: 10.1086/377140

Osteoarthritis of the hands, hips and knees in an Australian twin sample - Evidence of association with the aggrecan VNTR polymorphism

Kirk, K. M., Doege, K. J., Hecht, J., Bellamy, N. and Martin, N. G. (2003). Osteoarthritis of the hands, hips and knees in an Australian twin sample - Evidence of association with the aggrecan VNTR polymorphism. Twin Research, 6 (1), 62-66. doi: 10.1375/136905203762687915

Relative importance of female-specific and non-female-specific effects on variation in iron stores between women

Whitfield, John B., Treloar, Susan, Zhu, Gu, Powell, Lawrie W. and Martin, Nicholas G. (2003). Relative importance of female-specific and non-female-specific effects on variation in iron stores between women. British Journal of Haematology, 120 (5), 860-866. doi: 10.1046/j.1365-2141.2003.04224.x

Serum inhibin A and B concentrations during the menstrual cycle in mothers of spontaneous dizygotic twins

Gilfillan, Christopher P., Montgomery, Grant W., Zhu, Gu, Martin, Nicholas G., Groome, N. P. and Robertson, David M. (2003). Serum inhibin A and B concentrations during the menstrual cycle in mothers of spontaneous dizygotic twins. Twin Research, 6 (1), 27-33. doi: 10.1375/136905203762687870

Sex differences in heritability of BMI: A comparative study of results from twin studies in eight countries

Schousboe, K., Willemsen, G., Kyvik, K. O., Mortensen, J., Boomsma, D. I., Cornes, B. K., Davis, C. J., Fagnani, C., Hjelmborg, J., Kaprio, J., de Lange, M., Luciano, M., Martin, N. G., Pedersen, N. and Pietilainen, K. H. (2003). Sex differences in heritability of BMI: A comparative study of results from twin studies in eight countries. Twin Research, 6 (5), 409-421. doi: 10.1375/136905203770326411

Special twin environments, genetic influences and their effects on the handedness of twins and their siblings

Medland, S. E., Wright, M. J., Geffen, G. M., Hay, D. A., Levy, F., Martin, N. G. and Duffy, D. L. (2003). Special twin environments, genetic influences and their effects on the handedness of twins and their siblings. Twin Research, 6 (2), 119-130. doi: 10.1375/136905203321536245

The genetics of coronary heart disease: the contribution of twin studies

Evans, Alun, van Baal, G. Caroline M., McCarron, Peter, deLange, Marlies, Soerensen, Thorkild I. A., De Geus, Eco J. C., Kyvik, Kirsten, Pedersen, Nancy L., Spector, Tim D., Andrew, Toby, Patterson, Christopher, Whitfield, John B., Zhu, Gu, Martin, Nicholas G., Kaprio, Jaakko and Boomsma, Dorret I. (2003). The genetics of coronary heart disease: the contribution of twin studies. Twin Research, 6 (5), 432-441. doi: 10.1375/136905203770326439

Two-locus Linkage Analysis Applied to Putative Quantitative Trait Loci for Lipoprotein(a) Levels

Beekman, Marian, Heijmans, Bastiaan T., Martin, Nicholas G., Whitfield, John B., Pedersen, Nancy L., DeFaire, Ulf, Snieder, Harold, Lakenberg, Nico, Knijff, Peter, Frants, Rune R., van Ommen, Gert Jan B., Kluft, Cornelis, Vogler, George R., Slagboom, P. Eline and Boomsma, Dorret I. (2003). Two-locus Linkage Analysis Applied to Putative Quantitative Trait Loci for Lipoprotein(a) Levels. Twin Research and Human Genetics, 6 (4), 322-324. doi: 10.1375/136905203322296692

Zygosity Diagnosis in the Absence of Genotypic Data: An Approach Using Latent Class Analysis

Heath, Andrew C., Nyholt, Dale R., Neuman, Rosalind, Madden, Pamela A. F., Bucholz, Kathleen K., Todd, Richard D., Nelson, Elliot C., Montgomery, Grant W. and Martin, Nicholas G. (2003). Zygosity Diagnosis in the Absence of Genotypic Data: An Approach Using Latent Class Analysis. Twin Research and Human Genetics, 6 (1), 22-26. doi: 10.1375/136905203762687861

Protective role of appendicectomy on onset and severity of ulcerative colitis and Crohn's disease

Radford-Smith, GL, Edwards, JE, Purdie, DM, Pandeya, N, Watson, M, Martin, NG, Green, A, Newman, B and Florin, THJ (2002). Protective role of appendicectomy on onset and severity of ulcerative colitis and Crohn's disease. Gut, 51 (6), 808-813. doi: 10.1136/gut.51.6.808

Biometrical Genetics

Evans, David M., Gillespie, N. A. and Martin, N. G. (2002). Biometrical Genetics. Biological Psychology, 61 (1-2), 33-51. doi: 10.1016/S0301-0511(02)00051-0

Genetic sources of covariation among P3(00) and online performance variables in a delayed-response working memory task

Wright, M. J., Luciano, M., Hansell, N. K., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2002). Genetic sources of covariation among P3(00) and online performance variables in a delayed-response working memory task. Biological Psychology, 61 (1-2), 183-202. doi: 10.1016/S0301-0511(02)00058-3

Genetic Covariation between Serum {gamma}-Glutamyltransferase Activity and Cardiovascular Risk Factors

Whitfield, John B., Zhu, Gu, Nestler, John E., Heath, Andrew C. and Martin, Nicholas G. (2002). Genetic Covariation between Serum {gamma}-Glutamyltransferase Activity and Cardiovascular Risk Factors. Clinical Chemistry, 48 (9), 1426-1431. doi: 10.1093/clinchem/48.9.1426

Repeated blood pressure measurements in a sample of Swedish twins: heritabilities and associations with polymorphisms in the renin-angiotensin-aldosterone system Iliadou, Anastasia, Lichtenstein, Paul, Morgenstern, Ralf, Forsberg, Lena, Svensson, Richard,

Iliadou, Anastasi, Lichtenstein, Paul, Morgenstern, Ralf, Forsberg, Lena, Svensson, Richard, de Faire, Ulf, Martin, Nicholas and Pedersen, Nancy (2002). Repeated blood pressure measurements in a sample of Swedish twins: heritabilities and associations with polymorphisms in the renin-angiotensin-aldosterone system Iliadou, Anastasia, Lichtenstein, Paul, Morgenstern, Ralf, Forsberg, Lena, Svensson, Richard,. Journal of Hypertension, 20 (8), 1543-1550. doi: 10.1097/00004872-200208000-00017

Association Between Self-reported Childhood Sexual Abuse and Adverse Psychosocial Outcomes: Results From a Twin Study

Nelson, Elliott C., Heath, Andrew C., Madden, Pamela A. F., Cooper, M. Lynne, Dinwiddie, Stephen H., Bucholz, Kathleen K., Glowinski, Anne, McLaughlin, Tara, Dunne, Michael P., Statham, Dixie J. and Martin, Nicholas G. (2002). Association Between Self-reported Childhood Sexual Abuse and Adverse Psychosocial Outcomes: Results From a Twin Study. Archives of General Psychiatry, 59 (2), 139-145. doi: 10.1001/archpsyc.59.2.139

Estimating Two-Stage Models for Genetic Influences on Alcohol, Tobacco or Drug Use Initiation and Dependence Vulnerability in Twin and Family Data

Heath, Andrew C., Martin, Nicholas G., Lynskey, Michael T., Todorov, Alexandre A. and Madden, Pamela A. F. (2002). Estimating Two-Stage Models for Genetic Influences on Alcohol, Tobacco or Drug Use Initiation and Dependence Vulnerability in Twin and Family Data. Twin Research, 5 (2), 113-124. doi: 10.1375/1369052022983

Gene-Environment Interaction Effects on Behavioral Variation and Risk of Complex Disorders: The Example of Alcoholism and Other Psychiatric Disorders

Heath, Andrew C., Todorov, Alexandre A., Nelson, Elliot C., Madden, Pamela A. F., Bucholz, Kathleen K. and Martin, Nicholas G. (2002). Gene-Environment Interaction Effects on Behavioral Variation and Risk of Complex Disorders: The Example of Alcoholism and Other Psychiatric Disorders. Twin Research, 5 (1), 30-37. doi: 10.1375/1369052022875

Genetic and environmental contributions to cannabis dependence in a national young adult twin sample

Lynskey, M. T., Heath, A. C., Nelson, E. C., Bucholz, K. K., Madden, P. A. F., Slutske, W. S., Statham, D. J. and Martin, N. G. (2002). Genetic and environmental contributions to cannabis dependence in a national young adult twin sample. Psychological Medicine, 32 (2), 195-207. doi: 10.1017/S0033291701005062

Genetic and environmental influences on premenstrual symptoms in an Australian twin sample

Treloar, S. A., Heath, A. C. and Martin, N. G. (2002). Genetic and environmental influences on premenstrual symptoms in an Australian twin sample. Psychological Medicine, 32 (1), 25-38. doi: 10.1017/S0033291701004901

Genetics of Serum Dehydroepiandrosterone Sulfate and Its Relationship to Insulin in a Population-Based Cohort of Twin Subjects

Nestler, John E., Whitfield, John B., Williams, Terre Y., Zhu, Gu, Condon, Juliann, Kirk, Katherine M., Heath, Andrew C., Montgomery, Grant W. and Martin, Nicholas G. (2002). Genetics of Serum Dehydroepiandrosterone Sulfate and Its Relationship to Insulin in a Population-Based Cohort of Twin Subjects. Journal of Clinical Endocrinology And Metabolism, 87 (2), 682-686. doi: 10.1210/jc.87.2.682

Heritabilities of Apolipoprotein and Lipid Levels in Three Countries

Beekman, Marian, Heijmans, Bastiaan T., Martin, Nicholas G., Pedersen, Nancy L., Whitfield, John B., DeFaire, Ulf, van Baal, G. Caroline M., Snieder, Harold, Vogler, George P., Slagboom, P. Eline and Boomsma, Dorret . (2002). Heritabilities of Apolipoprotein and Lipid Levels in Three Countries. Twin Research, 5 (2), 87-97. doi: 10.1375/1369052022956

Melanoma in adolescents: A case-control study of risk factors in Queensland, Australia

Youl, Philippa, Aitken, Joanne, Hayward, Nicholas, Hogg, David, Liu, Ling, Lassam, Norman, Martin, Nicholas and Green, Adele (2002). Melanoma in adolescents: A case-control study of risk factors in Queensland, Australia. International Journal of Cancer, 98 (1), 92-98. doi: 10.1002/ijc.10117

Personality and the genetic risk for alcohol dependence

Slutske, Wendy S., Heath, Andrew C., Madden, Pamela A. F., Bucholz, Kathleen K., Statham, Dixie J. and Martin, Nicholas G. (2002). Personality and the genetic risk for alcohol dependence. Journal of Abnormal Psychology, 111 (1), 124-133. doi: 10.1037//0021-843X.111.1.124

Sun exposure and interaction with family history in risk of melanoma, Queensland, Australia

Siskind, Victor, Aitken, Joanne, Green, Adele and Martin, Nicholas (2002). Sun exposure and interaction with family history in risk of melanoma, Queensland, Australia. International Journal of Cancer, 97 (1), 90-95. doi: 10.1002/ijc.1563

The validity and heritability of self-report osteoarthritis in an Australian older twin sample

Kirk, K. M., Bellamy, N., O'Gorman, L. E., Kuhnert, P. M., Klestov, A., Muirden, K., Tesar, P., Walker, D. and Martin, N. G. (2002). The validity and heritability of self-report osteoarthritis in an Australian older twin sample. Twin Research, 5 (2), 98-106. doi: 10.1375/1369052022965

Genetic covariation of neuroticism with monoamine oxidase activity and smoking

Kirk, Katherine M., Whitfield, John B., Pang, Dona, Heath, Andrew C. and Martin, Nicholas G. (2001). Genetic covariation of neuroticism with monoamine oxidase activity and smoking. American Journal of Medical Genetics, 105 (8), 700-706. doi: 10.1002/ajmg.1555

(Book Review) Retrieving the 'eu' from eugenics

Martin, Nick (2001). (Book Review) Retrieving the 'eu' from eugenics. Nature, 414 (6864), 583-583. doi: 10.1038/414583a

Genetic covariance among measures of information processing speed, working memory, and IQ

Luciano, M., Wright, M. J., Smith, G. A., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Genetic covariance among measures of information processing speed, working memory, and IQ. Behavior Genetics, 31 (6), 581-592. doi: 10.1023/A:1013397428612

Genetic influence on ERP slow wave measures of working memory

Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2001). Genetic influence on ERP slow wave measures of working memory. Behavior Genetics, 31 (6), 603-614. doi: 10.1023/A:1013301629521

Genetic influence on the variance in P3 amplitude and latency

Wright, M. J., Hansell, N. K., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2001). Genetic influence on the variance in P3 amplitude and latency. Behavior Genetics, 31 (6), 555-565. doi: 10.1023/A:1013393327704

Genetics of brain function and cognition

Eco, D., Wright, M. J., Martin, N. G. and Boomsa, D. I. (2001). Genetics of brain function and cognition. Behavior Genetics, 31 (6), 498-500. doi: 10.1023/A:1013360909048

On the heritability of inspection time and its covariance with IQ: A twin study

Luciano, M., Smith, G. A., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). On the heritability of inspection time and its covariance with IQ: A twin study. Intelligence, 29 (6), 443-457. doi: 10.1016/S0160-2896(01)00071-X

The genetic and environmental relationship between the interpersonal sensitivity measure (IPSM) and the personality dimensions of Eysenck and Cloninger

Gillespie, Nathan A., Johnstone, Stuart J., Boyce, Philip, Heath, Andrew C. and Martin, Nicholas G. (2001). The genetic and environmental relationship between the interpersonal sensitivity measure (IPSM) and the personality dimensions of Eysenck and Cloninger. Personality And Individual Differences, 31 (7), 1039-1051. doi: 10.1016/S0191-8869(00)00200-2

Relating body mass index to figural stimuli: population-based normative data for Caucasians

Bulik, C. M., Wade, T. D., Heath, A. C., Martin, N. G., Stunkard, A. J. and Eaves, L. J. (2001). Relating body mass index to figural stimuli: population-based normative data for Caucasians. International Journal of Obesity, 25 (10), 1517-1524. doi: 10.1038/sj.ijo.0801742

Mutation analysis of the CDKN2A promoter in Australian melanoma families

Pollock, Pamela M., Stark, Mitchell S., Palmer, Jane M., Walters, Marilyn K., Aitken, Joanne F., Martin, Nicholas G. and Hayward, Nicholas K. (2001). Mutation analysis of the CDKN2A promoter in Australian melanoma families. Genes Chromosomes and Cancer, 32 (1), 89-94. doi: 10.1002/gcc.1170

Variation in Alcohol Pharmacokinetics as a Risk Factor for Alcohol Dependence

Whitfield, J. B., Zhu, Gu, Duffy, D. L., Birley, A. J., Madden, P. A. F., Heath, A. C. and Martin, N. G. (2001). Variation in Alcohol Pharmacokinetics as a Risk Factor for Alcohol Dependence. Alcoholism-clinical And Experimental Research, 25 (9), 1257-1263. doi: 10.1111/j.1530-0277.2001.tb02345.x

Lack of Genetic and Epigenetic Changes in CDKN2A in Melanocytic Nevi [Letter to the editor]

Welch, John, Millar, Doug, Goldman, Alana, Heenan, Peter, Stark, Mitchell, Eldon, Michael, Clark, Susan, Martin, Nicholas G. and Hayward, Nicholas K. (2001). Lack of Genetic and Epigenetic Changes in CDKN2A in Melanocytic Nevi [Letter to the editor]. Journal of Investigative Dermatology, 117 (2), 383-384. doi: 10.1046/j.0022-202x.2001.01391.x

A comparison of family functioning, temperament, and childhood conditions in monozygotic twin pairs discordant for lifetime bulimia nervosa

Treloar, S. A., Wade, T. D. and Martin, N. G. (2001). A comparison of family functioning, temperament, and childhood conditions in monozygotic twin pairs discordant for lifetime bulimia nervosa. American Journal of Psychiatry, 158 (7), 1155-1157. doi: 10.1176/appi.ajp.158.7.1155

Effects of alcohol consumption on indices of iron stores and of iron stores on alcohol intake markers

Whitfield, John B., Zhu, Gu, Heath, Andrew C., Martin, Nicholas G. and Powell, Lawrie W. (2001). Effects of alcohol consumption on indices of iron stores and of iron stores on alcohol intake markers. Alcoholism: Clinical and Experimental Research, 25 (7), 1037-1045. doi: 10.1097/00000374-200107000-00014

Genetic and environmental contributions to educational attainment in Australia

Miller, Paul, Mulvey, Charles and Martin, Nick (2001). Genetic and environmental contributions to educational attainment in Australia. Economics of Education Review, 20 (3), 211-224. doi: 10.1016/S0272-7757(00)00018-2

Age changes in personality traits and their heritabilities during the adult years: evidence from Australian Twin Registry samples

Loehlin, J. C. and Martin, N. G. (2001). Age changes in personality traits and their heritabilities during the adult years: evidence from Australian Twin Registry samples. Personality and Individual Differences, 30 (7), 1147-1160. doi: 10.1016/S0191-8869(00)00099-4

Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecB

Duffy, David L., Montgomery, Grant W., Hall, Jeff, Mayne, Carol, Healey, Sue C., Brown, Joy, Boomsma, Dorret I. and Martin, Nicholas G. (2001). Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecB. American Journal of Medical Genetics Part A, 100 (3), 182-186. doi: 10.1002/ajmg.1255

Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning

Montgomery, Grant W., Duffy, David L., Hall, Jeff, Kudo, Masataka, Martin, Nicholas G. and Hsueh, Aaron J. (2001). Mutations in the follicle-stimulating hormone receptor and familial dizygotic twinning. Lancet, 357 (9258), 773-774. doi: 10.1016/S0140-6736(00)04164-7

Natural selection and quantitative genetics of life-history traits in Western women: A twin study

Kirk, K. M., Blomberg, S. P., Duffy, D. L., Heath, A. C., Owens, I. P. and Martin, N. G. (2001). Natural selection and quantitative genetics of life-history traits in Western women: A twin study. Evolution, 55 (2), 423-435. doi: 10.1554/0014-3820(2001)055[0423:NSAQGO]2.0.CO;2

Natural selection and quantitative genetics of life-history traits in Western women: a twin study

Kirk, Katherine M., Blomberg, Simon P., Duffy, David L., Heath, Andrew C., Owens, Ian P. and Martin, Nick G. (2001). Natural selection and quantitative genetics of life-history traits in Western women: a twin study. Evolution, 55 (2), 423-435. doi: 10.1111/j.0014-3820.2001.tb01304.x

A twin study of the etiology of prolonged fatigue and immune activation

Hickie, I. B., Bansal, A. S., Kirk, K. M., Lloyd, A. R. and Martin, N. G. (2001). A twin study of the etiology of prolonged fatigue and immune activation. Twin Research, 4 (2), 94-102. doi: 10.1375/twin.4.2.94

An Australian twin study of the genetic basis of preeclampsia and eclampsia

Treloar, Susan A., Cooper, Desmond W., Brennecke, Shaun P., Grehan, Madonna M. and Martin, Nicholas G. (2001). An Australian twin study of the genetic basis of preeclampsia and eclampsia. American Journal of Obstetrics And Gynecology, 184 (3), 374-381. doi: 10.1067/mob.2001.109400

An integrative approach for studying the etiology of alcoholism and other addictions

Jacob, T., Sher, K. J., Bucholz, K. K., True, W. T., Sirevaag, E. J., Rohrbaugh, J. W., Nelson, E., Neuman, R. J., Todd, R. D., Slutske, W. S., Whitfield, J. B., Kirk, K. M., Martin, N. G., Madden, P. A. F. and Heath, A. C. (2001). An integrative approach for studying the etiology of alcoholism and other addictions. Twin Research, 4 (2), 103-118. doi: 10.1375/twin.4.2.103

Developmental genetics of red cell indices during puberty: A longitudinal twin study

Evans, D. M., Frazer, I. H., Boomsma, D. I. and Martin, N. G. (2001). Developmental genetics of red cell indices during puberty: A longitudinal twin study. International Journal of Human Genetics, 1 (1), 41-53. doi: 10.1080/09723757.2001.11885735

Genetic and non-genetic factors affecting birth-weight and adult body mass index

Whitfield, John B., Treloar, Susan A., Zhu, Gu and Martin, Nicholas G. (2001). Genetic and non-genetic factors affecting birth-weight and adult body mass index. Twin Research, 4 (5), 365-370. doi: 10.1375/twin.4.5.365

Genetic influence on the relationship between choice reaction time and IQ: A twin study

Luciano, M., Smith, G., Wright, M., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2001). Genetic influence on the relationship between choice reaction time and IQ: A twin study. Foreign Psychology, 14, 49-59.

Genetics of cognition: Outline of a collaborative twin study

Wright, M. J., Eco, D., Ando, J, Luciano, M., Posthuma, D., Ono, Y., Hansell, N. K., Van Baal, C., Hiraishi, K., Hasegawa, T., Smith, G., Geffen, G. M., Geffen, L. B., Kanba, S., Miyake, A., Martin, N. G. and Boomsa, D. I. (2001). Genetics of cognition: Outline of a collaborative twin study. Twin Research, 4 (1), 48-56. doi: 10.1375/twin.4.1.48

Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genes

Healey, S. C., Kirk, K. M., Hyland, V. J., Munns, C., Henders, A. K., Batch, J. A., Heath, A. C., Martin, N. G. and Glass, I. A. (2001). Height discordance in monozygotic females is not attributable to discordant inactivation of X-linked stature determining genes. Twin Research, 4 (1), 19-24. doi: 10.1375/twin.4.1.19

Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study

Wachsmuth, R. C., Gaut, R. M., Barrett, J. H., Saunders, C. L., Randerson-Moor, J. A., Eldridge, A., Martin, N. G., Bishop, T. D. and Newton Bishop, J. A. (2001). Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study. Journal of Investigative Dermatology, 117 (2), 348-352. doi: 10.1046/j.0022-202x.2001.01415.x

IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers

Duffy, David, Montgomery, Grant, Treloar, Susan, Birley, Andrew, Kirk, Katherine, Boomsma, Dorret, Beem, Leo, de Geus, Eco, Slagboom, Eline, Knighton, Joharna, Reed, Peter and Martin, Nicholas (2001). IBD sharing around the PPARG locus is not increased in dizygotic twins or their mothers. Nature Genetics, 28 (4), 315-315. doi: 10.1038/91074

Increasing the response rate to a mailed questionnaire by including more stamps on the return envelope: A cotwin control study

Duffy, D. L. and Martin, N. G. (2001). Increasing the response rate to a mailed questionnaire by including more stamps on the return envelope: A cotwin control study. Twin Research, 4 (2), 71-72. doi: 10.1375/twin.4.2.71

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

Box, N. F., Duffy, D. L., Chen, W., Stark, M., Martin, N. G., Sturm, R. A. and Hayward, N. K. (2001). MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. American Journal of Human Genetics, 69 (4), 765-773. doi: 10.1086/323412

Phenotypic and genetic analyses of a short measure of psychosis-proneness in a large-scale Australian twin study

Hay, D., Martin, N. G., Foley, D., Treloar, S. A., Kirk, K. M. and Heath, A. C. (2001). Phenotypic and genetic analyses of a short measure of psychosis-proneness in a large-scale Australian twin study. Twin Research, 4 (1), 30-40. doi: 10.1375/twin.4.1.30

Predictors of non-response to a questionnaire survey of a volunteer twin panel: Findings from the Australian 1989 twin cohort

Heath, A. C., Howells, W., Kirk, K. M., Madden, P. A., Bucholz, K. K., Nelson, E. C., Slutske, W. S., Statham, D. B. and Martin, N. G. (2001). Predictors of non-response to a questionnaire survey of a volunteer twin panel: Findings from the Australian 1989 twin cohort. Twin Research, 4 (2), 73-80. doi: 10.1375/twin.4.2.73

The influence of genetic and environmental factors in estimations of current body size, desired body size, and body dissatisfaction

Wade, Tracey D., Bulik, Cynthia M., Heath, Andrew C., Martin, Nicholas G. and Eaves, Lindon J. (2001). The influence of genetic and environmental factors in estimations of current body size, desired body size, and body dissatisfaction. Twin Research, 4 (4), 260-265. doi: 10.1375/twin.4.4.260

Towards a molecular epidemiology of alcohol dependence analysing the interplay of genetic and environmental risk factors

Heath, A. C., Whitfield, J. B., Madden, P. A., Bucholz, K. K., Dinwiddie, S. H., Slutske, W.S., Bierut, L. J., Statham, D. B. and Martin, N. G. (2001). Towards a molecular epidemiology of alcohol dependence analysing the interplay of genetic and environmental risk factors. British Journal of Psychiatry, 178 (40), S33-S40. doi: 10.1192/bjp.178.40.s33

The subtlety of sex-atypicality

Dunne, M. P., Bailey, J. M., Kirk, K. M. and Martin, N. G. (2000). The subtlety of sex-atypicality. Archives of Sexual Behavior, 29 (6), 549-565. doi: 10.1023/A:1002002420159

Childhood sexual abuse and pathogenic parenting in the childhood recollections of adult twin pairs

McLaughlin, T. L., Heath, A. C., Bucholz, K. K., Madden, P. A. F., Bierut, L. J., Slutske, W. S., Dinwiddie, S., Statham, D. J., Dunne, M. P. and Martin, N. G. (2000). Childhood sexual abuse and pathogenic parenting in the childhood recollections of adult twin pairs. Psychological Medicine, 30 (6), 1293-1302. doi: 10.1017/S0033291799002809

A study of the genetic and environmental etiology of stuttering in a selected twin sample

Felsenfeld, S, Kirk, KM, Zhu, G, Statham, DJ, Neale, MC and Martin, NG (2000). A study of the genetic and environmental etiology of stuttering in a selected twin sample. Behavior Genetics, 30 (5), 359-366. doi: 10.1023/A:1002765620208

Dizygotic Twinning Is Not Linked to Variation at the {alpha}-Inhibin Locus on Human Chromosome 2

Montgomery, Grant W., Duffy, David L., Hall, Jeff, Haddon, Barbara R., Kudo, Masataka, McGee, Elizabeth A., Palmer, James S., Hsueh, Aaron J., Boomsma, Dorrett I. and Martin, Nicholas G. (2000). Dizygotic Twinning Is Not Linked to Variation at the {alpha}-Inhibin Locus on Human Chromosome 2. Journal of Clinical Endocrinology & Metabolism, 85 (9), 3391-3395. doi: 10.1210/jc.85.9.3391

Twin study of adolescent genetic susceptibility to mosquito bites using ordinal and comparative rating data

Kirk, K. M., Eaves, L. J., Meyer, J. M., Saul, A. and Martin, N. G. (2000). Twin study of adolescent genetic susceptibility to mosquito bites using ordinal and comparative rating data. Genetic Epidemiology, 19 (2), 178-190. doi: 10.1002/1098-2272(200009)19:2<178::AID-GEPI5>3.0.CO;2-3

Etiology of male sexual orientation in an Australian twin sample

Bailey, J. M., Kirk, M. and Martin, N. G. (2000). Etiology of male sexual orientation in an Australian twin sample. Psychology, Evolution & Gender, 2 (Dec 3), 301-311. doi: 10.1093/pubmed/fdw069

Measurement models for sexual orientation in a community twin sample

Kirk, KM, Bailey, JM, Dunne, MP and Martin, NG (2000). Measurement models for sexual orientation in a community twin sample. Behavior Genetics, 30 (4), 345-356. doi: 10.1023/A:1026557719181

The validity of twin studies

Evans, David M. and Martin, Nicholas G. (2000). The validity of twin studies. GeneScreen, 1 (2), 77-79. doi: 10.1046/j.1466-9218.2000.00027.x

Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models

Do, K. A., Broom, B. M., Kuhnert, P., Duffy, D. L., Todorov, A. A., Treloar, S. A. and Martin, N. G. (2000). Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models. Statistics in Medicine, 19 (9), 1217-1235. doi: 10.1002/(SICI)1097-0258(20000515)19:9<1217::AID-SIM421>3.3.CO;2-H

Further Evidence Against the Environmental Transmission of Individual Differences in Neuroticism from a Collaborative Study of 45,850 Twins and Relatives on Two Continents

Lake, Robert I. E., Eaves, Lindon J., Maes, Hermine M., Heath, Andrew C. and Martin, Nicholas G. (2000). Further Evidence Against the Environmental Transmission of Individual Differences in Neuroticism from a Collaborative Study of 45,850 Twins and Relatives on Two Continents. Behavior Genetics, 30 (3), 223-233. doi: 10.1023/A:1001918408984

CYP17 promotor polymorphism and ovarian cancer risk

Spurdle, Amanda B., Chen, Xiaoqing, Abbazadegan, Mohammed, Martin, Nicholas, Khoo, Soo-Keat, Hurst, Terry, Ward, Bruce, Webb, Penelope M. and Chenevix-Trench, Georgia (2000). CYP17 promotor polymorphism and ovarian cancer risk. International Journal of Cancer, 89 (2), 436-439.

Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins

Whitfield, J. B., Cullen, L. M., Jazwinska, E. C., Powell, L. W., Heath, A. C., Zhu, Gu, Duffy, D. L. and Martin, N. G. (2000). Effects of HFE C282Y and H63D Polymorphisms and Polygenic Background on Iron Stores in a Large Community Sample of Twins. American Journal of Human Genetics, 66 (4), 1246-1258. doi: 10.1086/302862

Genetic and environmental risk factors shared between disordered eating, psychological and family variables

Wade, T., Martin, N. G., Tiggemann, M., Abraham, S., Treloar, S. A. and Heath, A. C. (2000). Genetic and environmental risk factors shared between disordered eating, psychological and family variables. Personality & Individual Differences, 28 (4), 729-740. doi: 10.1016/S0191-8869(99)00134-8

Monoamine oxidase: associations with alcohol dependence, smoking and other measures of psychopathology

Whitfield, J. B., Pang, D., Bucholz, K. K., Madden, P. A. F., Heath, A. C., Statham, D. J. and Martin, N. G. (2000). Monoamine oxidase: associations with alcohol dependence, smoking and other measures of psychopathology. Psychological Medicine, 30 (2), 443-454. doi: 10.1017/S0033291799001798

Androgen receptor EXON 1 CAG repeat length and risk of ovarian cancer

Spurdle, A. B., Webb, P. M., Chen, X. D., Martin, N. G., Giles, G. G., Hopper, J. L. and Chenevix-Trench, G. (2000). Androgen receptor EXON 1 CAG repeat length and risk of ovarian cancer. International Journal of Cancer, 87 (5), 637-643. doi: 10.1002/1097-0215(20000901)87:5<637::AID-IJC3>3.0.CO;2-R

Anxiety and depression in twin and sib pairs extremely discordant and concordant for neuroticism: Prodromus to a linkage study

Kirk, Katherine M., Birley, Andrew J., Statham, Dixie J., Haddon, Barbara, Lake, Robert I. E., Andrews, J Gavin and Martin, Nicholas G. (2000). Anxiety and depression in twin and sib pairs extremely discordant and concordant for neuroticism: Prodromus to a linkage study. Twin Research, 3 (4), 299-309. doi: 10.1375/twin.3.4.299

Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis

Treloar, S. A., Sadrzadeh, S., Do, K. A., Martin, N. G. and Lambalk, C. B. (2000). Birth weight and age at menopause in Australian female twin pairs: exploration of the fetal origin hypothesis. Human Reproduction, 15 (1), 55-59. doi: 10.1093/humrep/15.1.55

CYP17 promotor polymorphism and ovarian cancer risk

Spurdle, Amanda B., Chen, Xiaoqing, Abbazadegan, Mohammed, Martin, Nicholas, Khoo, Soo-Keat, Hurst, Terry, Ward, Bruce, Webb, Penelope M. and Chenevix-Trench, Georgia (2000). CYP17 promotor polymorphism and ovarian cancer risk. International Journal of Cancer, 86 (3), 436-439. doi: 10.1002/(SICI)1097-0215(20000501)86:3<436::AID-IJC21>3.0.CO;2-A

Dimensions of psychological masculinity-femininity in adult twins from opposite-sex and same-sex pairs

Loehlin, John C. and Martin, Nicholas G. (2000). Dimensions of psychological masculinity-femininity in adult twins from opposite-sex and same-sex pairs. Behavior Genetics, 30 (1), 19-28. doi: 10.1023/A:1002082325784

Do individual differences in sociosexuality represent genetic or environmentally contingent strategies? Evidence from the Australian twin registry

Bailey, J. M., Kirk, K. M., Zhu, G., Dunne, M. P. and Martin, N. G. (2000). Do individual differences in sociosexuality represent genetic or environmentally contingent strategies? Evidence from the Australian twin registry. Journal of Personality & Social Psychology, 78 (3), 537-545. doi: 10.1037/0022-3514.78.3.537

Early sexual abuse and lifetime psychopathology: a co-twin-control study

Dinwiddie, S., Heath, A. C., Dunne, M. P., Bucholz, K. K., Madden, P. A. F., Slutske, W. S., Bierut, L. J., Statham, D. B. and Martin, N. G. (2000). Early sexual abuse and lifetime psychopathology: a co-twin-control study. Psychological Medicine, 30 (1), 41-52. doi: 10.1017/S0033291799001373

Genetic and environmental influences on sexual orientation and its correlates in an Australian twin sample

Bailey, J. M., Dunne, M. P. and Martin, N. G. (2000). Genetic and environmental influences on sexual orientation and its correlates in an Australian twin sample. Journal of Personality & Social Psychology, 78 (3), 524-536. doi: 10.1037//0022-3514.78.3.524

Genetic influence on the variance in coincidence timing and its covariance with IQ: A twin study

Wright, Margaret J., Smith, Glen A., Geffen, Gina M., Geffen, Laurie B. and Martin, Nicholas G. (2000). Genetic influence on the variance in coincidence timing and its covariance with IQ: A twin study. Intelligence, 28 (4), 239-250. doi: 10.1016/S0160-2896(99)00036-7

Genetic influences on premature parturition in an Australian twin sample

Treloar, S. A., Macones, G. A., Mitchell, L. A. M. and Martin, N. G. (2000). Genetic influences on premature parturition in an Australian twin sample. Twin Research, 3 (2), 80-82. doi: 10.1375/twin.3.2.80

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

Palmer, JS, Duffy, DL, Box, NF, Aitken, JF, O'Gorman, LE, Green, AC, Hayward, NK, Martin, NG and Sturm, RA (2000). Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?. American Journal of Human Genetics, 66 (1), 176-186. doi: 10.1086/302711

Shared and unique environmental factors determine the ecology of methanogens in humans and rats

Florin, T. H. J., Zhu, G., Kirk, K. M. and Martin, N. G. (2000). Shared and unique environmental factors determine the ecology of methanogens in humans and rats. American Journal of Gastroenterology, 95 (10), 2872-2879. doi: 10.1016/S0002-9270(00)01111-4

Smoking and the genetic contribution to alcohol-dependence risk

Madden, PAF, Bucholz, KK, Martin, NG and Heath, AC (2000). Smoking and the genetic contribution to alcohol-dependence risk. Alcohol Research & Health, 24 (4), 209-214.

Taxometric analyses of sexual orientation and gender identity

Gangestad, S. W., Bailey, J. M. and Martin, N. G. (2000). Taxometric analyses of sexual orientation and gender identity. Journal of Personality and Social Psychology, 78 (6), 1109-1121. doi: 10.1037//0022-3514.78.6.1109

The effect of apolipoprotein(a)-, apolipoprotein E-, and apolipoprotein A4- polymorphisms on quantitative lipoprotein(a) concentrations

Boomsma, D. I., Knijff, P., Kaptein, A., Labeur, C., Martin, N. G., Havekes, L. M. and Princen, H. M. (2000). The effect of apolipoprotein(a)-, apolipoprotein E-, and apolipoprotein A4- polymorphisms on quantitative lipoprotein(a) concentrations. Twin Research, 3 (3), 152-158. doi: 10.1375/twin.3.3.152

The genetic aetiology of somatic distress

Gillespie, N. A., Zhu, G., Heath, A. C., Hickie, I. B. and Martin, N. G. (2000). The genetic aetiology of somatic distress. Psychological Medicine, 30 (5), 1051-1061. doi: 10.1017/S0033291799002640

Perceptual variation in grading hand, hip and knee radiographs: observations based on an Australian twin registry study of osteoarthritis

Bellamy, N., Tesar, P., Walker, D., Klestov, A., Muirden, K., Kuhnert, P., Do, K. A., O'Gorman, L. and Martin, N. (1999). Perceptual variation in grading hand, hip and knee radiographs: observations based on an Australian twin registry study of osteoarthritis. Annals of the Rheumatic Diseases, 58 (12), 766-769. doi: 10.1136/ard.58.12.766

An assessment of the genetic relationship between alcohol metabolism and alcoholism risk in Australian twins of European ancestry

Grant, JD, Heath, AC, Madden, PAF, Bucholz, KK, Whitfield, JB and Martin, NG (1999). An assessment of the genetic relationship between alcohol metabolism and alcoholism risk in Australian twins of European ancestry. Behavior Genetics, 29 (6), 463-472. doi: 10.1023/A:1021683106532

Melanocytic naevi in eastern Australia: Latitude is important but most variation is within cities

MacLennan, Robert, Kelly, John W. and Martin, Nicholas G. (1999). Melanocytic naevi in eastern Australia: Latitude is important but most variation is within cities. Australasian Journal of Dermatology, 40 (3), 167-167.

The genetics of smoking persistence in men and women: A multicultural study

Madden, PAF, Heath, AC, Pedersen, NL, Kaprio, J, Koskenvuo, MJ and Martin, NG (1999). The genetics of smoking persistence in men and women: A multicultural study. Behavior Genetics, 29 (6), 423-431. doi: 10.1023/A:1021674804714

Somatic distress as a distinct psychological dimension

Gillespie, N., Kirk, K. M., Heath, A. C., Martin, N. G. and Hickie, I. (1999). Somatic distress as a distinct psychological dimension. Social Psychiatry & Psychiatric Epidemiology, 34 (9), 451-458. doi: 10.1007/s001270050219

A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs

Zhu, G, Duffy, DL, Eldridge, A, Grace, M, Mayne, C, O'Gorman, L, Aitken, JF, Neale, MC, Hayward, NK, Green, AC and Martin, NG (1999). A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. American Journal of Human Genetics, 65 (2), 483-492. doi: 10.1086/302494

Genetic and environmental causes of variation in basal levels of blood cells

Evans, David M., Frazer, Ian H. and Martin, Nicholas G. (1999). Genetic and environmental causes of variation in basal levels of blood cells. Twin Research, 2 (4), 250-257. doi: 10.1375/twin.2.4.250

Distinguishing population stratification from genuine allelic effects with Mx: association of ADH2 with alcohol consumption

Neale, M. C., Cherny, S. S., Sham, P. C., Whitfield, J. B., Heath, A. C., Birley, A. J. and Martin, N. G. (1999). Distinguishing population stratification from genuine allelic effects with Mx: association of ADH2 with alcohol consumption. Behavior Genetics, 29 (4), 233-243. doi: 10.1023/A:1021638122693

Major depressive disorder in a community-based twin sample: are there different genetic and environmental contributions for men and women

Bierut, Laura Jean, Heath, Andrew C., Bucholz, Kathleen K., Dinwiddie, Stephen H., Madden, Pamela A. F., Statham, Dixie. J., Dunne, Michael P. and Martin, Nicholas G. (1999). Major depressive disorder in a community-based twin sample: are there different genetic and environmental contributions for men and women. Archives of General Psychiatry, 56 (6), 557-563.

Predictors of hysterectomy: an Australian study

Treloar, Susan A., Do, Kim-Anh, O'Connor, Vivienne M., O'Connor, Daniel T., Yeo, Margaret A. and Martin, Nicholas G. (1999). Predictors of hysterectomy: an Australian study. American Journal of Obstetrics & Gynecology, 180 (4), 945-954. doi: 10.1016/S0002-9378(99)70666-6

Fatigue as related to anxiety and depression in a community-based sample of twins aged over 50.

Kirk, K. M., Hickie, I. B. and Martin, N. G. (1999). Fatigue as related to anxiety and depression in a community-based sample of twins aged over 50.. Social Psychiatry & Psychiatric Epidemiology, 34 (2), 85-90. doi: 10.1007/s001270050116

Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci

MacMillan, J., Voisey, J., Healey, S. C. and Martin, N. G. (1999). Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci. Journal of Medical Genetics, 36 (3), 258-259. doi: 10.1136/jmg.36.3.258

Perceptual variation in categorizing individual peripheral joints for the presence or absence of osteoarthritis: observations based on an Australian Twin Reigstry study of osteoarthritis

Bellamy, N., Klestov, A., Muirden, K. D., Kuhnert, P., Do, K. A., O'Gorman, L. and Martin, N. G. (1999). Perceptual variation in categorizing individual peripheral joints for the presence or absence of osteoarthritis: observations based on an Australian Twin Reigstry study of osteoarthritis. Inflammopharmacology, 7 (1), 37-46. doi: 10.1007/s10787-999-0024-x

A genetic analysis of the eating and attitudes associated with bulimia nervosa: dealing with the problem of ascertainment in twin studies.

Wade, T., Neale, M. C., Lake, R. I. and Martin, N. G. (1999). A genetic analysis of the eating and attitudes associated with bulimia nervosa: dealing with the problem of ascertainment in twin studies.. Behavior Genetics, 29 (1), 1-10. doi: 10.1023/A:1021429604095

CDKN2A variants in a population-based sample of Queensland families with melanoma

Aitken, J., Welch, J., Duffy, D., Milligan, A., Green, A., Martin, N. G. and Hayward, N. (1999). CDKN2A variants in a population-based sample of Queensland families with melanoma. Journal of the National Cancer Institute, 91 (5), 446-452. doi: 10.1093/jnci/91.5.446

Comparing the biological and cultural inheritance of personality and social attitudes in the Virginia 30,000 study of twins and their relatives

Eaves, Lindon, Heath, Andrew, Martin, Nicholas, Maes, Hermine, Neale, Michael, Kendler, Kenneth, Kirk, Katherine and Corey, Linda (1999). Comparing the biological and cultural inheritance of personality and social attitudes in the Virginia 30,000 study of twins and their relatives. Twin Research, 2 (2), 62-80. doi: 10.1375/136905299320565933

Complex genetic and environmental relationships between psychological distress, fatigue and immune functioning: a twin study

Hickie, I., Bennett, B., Lloyd, A., Heath, A. and Martin, N. (1999). Complex genetic and environmental relationships between psychological distress, fatigue and immune functioning: a twin study. Psychological Medicine, 29 (2), 269-277. doi: 10.1017/S0033291798007922

Frequency of church attendance in Australia and the United States: models of family resemblance

Kirk, K. M., Maes, H., Neale, M. C., Heath, A., Martin, N. G. and Eaves, L. J. (1999). Frequency of church attendance in Australia and the United States: models of family resemblance. Twin Research, 2 (2), 99-107. doi: 10.1375/twin.2.2.99

Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins.

McGregor, B., Pfitzner, J., Zhu, G., Grace, M., Eldridge, A., Pearson, J., Mayne, C., Aitken, J. F., Green, A. C. and Martin, N. G. (1999). Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins.. Genetic Epidemiology, 16 (1), 40-53. doi: 10.1002/(SICI)1098-2272(1999)16:1<40::AID-GEPI4>3.0.CO;2-1

Genetic differences in alcohol sensitivity and the inheritance of alcoholism risk.

Heath, A., Madden, P. A., Bucholz, K. K., Dinwiddie, S. H., Slutske, W. W., Bierut, L. J., Rohrbaugh, J. W., Statham, D. J., Dunne, M. P., Whitfield, J. B. and Martin, N. G. (1999). Genetic differences in alcohol sensitivity and the inheritance of alcoholism risk.. Psychological Medicine, 29 (5), 1069-1081. doi: 10.1017/S0033291799008909

Genetic influences on endometriosis in an Australian twin sample.

Treloar, S. A., O'Connor, D. T., O'Connor, V. M. and Martin, N. G. (1999). Genetic influences on endometriosis in an Australian twin sample.. Fertility & Sterility, 71 (4), 701-710. doi: 10.1016/S0015-0282(98)00540-8

Genetic influences on post-natal depressive symptoms: findings from an Australian twin sample.

Treloar, S. A., Martin, N. G., Bucholz, K. K., Madden, P. A. and Heath, A. (1999). Genetic influences on post-natal depressive symptoms: findings from an Australian twin sample.. Psychological Medicine, 29 (3), 645-654. doi: 10.1017/S0033291799008387

Genetics of early cancer detection behaviours in Australian female twins

Treloar, S. A., McDonald, C. A. and Martin, N. G. (1999). Genetics of early cancer detection behaviours in Australian female twins. Twin Research, 2 (1), 33-42. doi: 10.1375/twin.2.1.33

How accurate is the family history method for assessing siblings' sexual orientation?

Kirk, Katherine M., Bailey, J. Michael and Martin, Nicholas G. (1999). How accurate is the family history method for assessing siblings' sexual orientation?. Archives of Sexual Behaviour, 28 (2), 129-137. doi: 10.1023/A:1018715821801

Number of X-linked androgen receptor gene CAG repeats and femininity in women.

Loehlin, J. C., Spurdle, A. B., Treloar, S. A. and Martin, N. G. (1999). Number of X-linked androgen receptor gene CAG repeats and femininity in women.. Personality & Individual Differences, 27 (5), 887-899. doi: 10.1016/S0191-8869(99)00038-0

Perceptual variation in categorizing individuals according to American College of Rheumatology classification criteria for hand, knee, and hip osteoarthritis (OA): observations based on an Australian Twin Registry study of OA

Bellamy, N., Klestov, A., Muirden, K., Kuhnert, P., Do, K. A., O'Gorman, L. and Martin, N. (1999). Perceptual variation in categorizing individuals according to American College of Rheumatology classification criteria for hand, knee, and hip osteoarthritis (OA): observations based on an Australian Twin Registry study of OA. Journal of Rheumatology, 26 (12), 2654-2658.

Religious attendance and frequency of alcohol use: same genes or same environments: a bivariate extended twin kinship model

Maes, Hermine H., Neale, Michael C., Martin, Nicholas G., Heath, Andrew C. and Eaves, Lindon J. (1999). Religious attendance and frequency of alcohol use: same genes or same environments: a bivariate extended twin kinship model. Twin Research, 2 (2), 169-179. doi: 10.1375/twin.2.2.169

Self-transcendence as a measure of spirituality in a sample of older Australian twins

Kirk, Katherine M., Eaves, Lindon J. and Martin, Nicholas G. (1999). Self-transcendence as a measure of spirituality in a sample of older Australian twins. Twin Research, 2 (2), 81-87. doi: 10.1375/136905299320565942

Some implications of chaos theory for the genetic analysis of human development and variation.

Eaves, L. J., Kirk, K. M., Martin, N. G. and Russell, R. J. (1999). Some implications of chaos theory for the genetic analysis of human development and variation.. Twin Research, 2 (1), 43-48. doi: 10.1375/twin.2.1.43

The structure of genetic and environmental risk factors for three measures of disordered eating

Wade, T., Martin, N. G., Neale, M. C., Tiggemann, M., Treloar, S. A., Bucholz, K. K., Madden, P. A. F. and Heath, A. C. (1999). The structure of genetic and environmental risk factors for three measures of disordered eating. Psychological Medicine, 29 (4), 925-934. doi: 10.1017/S0033291799008740

Unique genetic and environmental determinants of prolonged fatigue: a twin study

Hickie, I., Kirk, K. and Martin, N. (1999). Unique genetic and environmental determinants of prolonged fatigue: a twin study. Psychological Medicine, 29 (2), 259-268. doi: 10.1017/S0033291798007934

Predictive factors of age at menopause in a large Australian twin study

Do, Kim-Anh, Treloar, Susan A., Pandeya, Nirmala, Purdie, David, Green, Adele C., Heath, Andrew C. and Martin, Nicholas G. (1998). Predictive factors of age at menopause in a large Australian twin study. Human Biology, 70 (6), 1073-1091.

Smoking, obesity, and hypertension alter the dose-response curve and test sensitivity of carbohydrate-deficient transferrin as a marker of alcohol intake

Whitfield, JB, Fletcher, LM, Murphy, TL, Powell, LW, Halliday, J, Heath, AC and Martin, NG (1998). Smoking, obesity, and hypertension alter the dose-response curve and test sensitivity of carbohydrate-deficient transferrin as a marker of alcohol intake. Clinical Chemistry, 44 (12), 2480-2489.

Assessing the effects of cooperation bias and attrition in behavioral genetic research using data-weighting

Heath, AC, Madden, PAF and Martin, NG (1998). Assessing the effects of cooperation bias and attrition in behavioral genetic research using data-weighting. Behavior Genetics, 28 (6), 415-427. doi: 10.1023/A:1021633127604

Genetic influences on the age at menopause

Treloar, SA, Do, KA and Martin, NG (1998). Genetic influences on the age at menopause. Lancet, 352 (9134), 1084-1085. doi: 10.1016/S0140-6736(05)79753-1

ADH genotypes and alcohol use and dependence in Europeans

Whitfield, JB, Nightingale, BN, Bucholz, KK, Madden, PAF, Heath, AC and Martin, NG (1998). ADH genotypes and alcohol use and dependence in Europeans. Alcoholism-Clinical and Experimental Research, 22 (7), 1463-1469. doi: 10.1111/j.1530-0277.1998.tb03936.x

The Short Interpersonal Reactions Inventory, Self-regulation and Differentiation scales in an older Australian twin sample

Kirk, KM and Martin, NG (1998). The Short Interpersonal Reactions Inventory, Self-regulation and Differentiation scales in an older Australian twin sample. Personality and Individual Differences, 25 (3), 591-604. doi: 10.1016/S0191-8869(98)00116-0

Genetic and environmental risk factors for the weight and shape concerns characteristic of bulimia nervosa

Wade, T., Martin, N. G. and Tiggemann, M. (1998). Genetic and environmental risk factors for the weight and shape concerns characteristic of bulimia nervosa. Psychological Medicine, 28 (4), 761-771. doi: 10.1017/S0033291798006989

Suicidal behaviour: an epidemiological and genetic study

Statham, DJ, Heath, AC, Madden, PAF, Bucholz, KK, Bierut, L, Dinwiddie, SH, Slutske, WS, Dunne, MP and Martin, NG (1998). Suicidal behaviour: an epidemiological and genetic study. Psychological Medicine, 28 (4), 839-855. doi: 10.1017/S0033291798006916