Narelle completed a Bachelor of Arts (double major in psychology), followed by first class Honours in psychology, at the University of Queensland. Her PhD was based at the Queensland Institute of Medical Research (now known as QIMR Berghofer Medical Research Institute), where she merged her interest in psychology with that of behaviour genetics to investigate genetic influences on brain function and cognitive processing. In 2003 she took a post doctoral position with QIMR Berghofer where her work focussed on the genetic analysis of twin data and explored the extent of genetic and environmental influence on multiple behavioural traits, and more recently, brain structure and function. In January 2016 she took up a position as Research Fellow at the Queensland Brain Institute to work with A/Prof Margie Wright and the Imaging Genomics group on a range of imaging genetics projects, including a longitudinal twin study exploring neurodevelopment during early adolescence.
Other Outputs: Queensland Twin Adolescent Brain (QTAB) non-imaging phenotypes
Wright, Margie, Strike, Lachlan, Hansell, Narelle, Chuang, Kai-Hsiang, Miller, Jessica, de Zubicaray, Greig, Thompson, Paul M and McMahon, Katie L (2022). Queensland Twin Adolescent Brain (QTAB) non-imaging phenotypes. The University of Queensland. (Dataset) doi: 10.48610/e891597
Journal Article: Autism-related dietary preferences mediate autism-gut microbiome associations
Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I. ... Gratten, Jacob (2021). Autism-related dietary preferences mediate autism-gut microbiome associations. Cell, 184 (24), 5916-5931.e17. doi: 10.1016/j.cell.2021.10.015
Journal Article: 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
(2013) Doctor Philosophy
Autism-related dietary preferences mediate autism-gut microbiome associations
Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I. ... Gratten, Jacob (2021). Autism-related dietary preferences mediate autism-gut microbiome associations. Cell, 184 (24), 5916-5931.e17. doi: 10.1016/j.cell.2021.10.015
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
Are Sex Differences in Human Brain Structure Associated With Sex Differences in Behavior?
van Eijk, Liza, Zhu, Dajiang, Couvy-Duchesne, Baptiste, Strike, Lachlan T., Lee, Anthony J., Hansell, Narelle K., Thompson, Paul M., de Zubicaray, Greig I., McMahon, Katie L., Wright, Margaret J. and Zietsch, Brendan P. (2021). Are Sex Differences in Human Brain Structure Associated With Sex Differences in Behavior?. Psychological Science, 32 (8) 095679762199666, 1-15. doi: 10.1177/0956797621996664
Hofer, Edith, Roshchupkin, Gennady V., Adams, Hieab H. H., Knol, Maria J., Lin, Honghuang, Li, Shuo, Zare, Habil, Ahmad, Shahzad, Armstrong, Nicola J., Satizabal, Claudia L., Bernard, Manon, Bis, Joshua C., Gillespie, Nathan A., Luciano, Michelle, Mishra, Aniket, Scholz, Markus, Teumer, Alexander, Xia, Rui, Jian, Xueqiu, Mosley, Thomas H., Saba, Yasaman, Pirpamer, Lukas, Seiler, Stephan, Becker, James T., Carmichael, Owen, Rotter, Jerome I., Psaty, Bruce M., Lopez, Oscar L., Amin, Najaf ... Hansell, Narelle K. (2020). Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature Communications, 11 (1) 4796, 4796. doi: 10.1038/s41467-020-18367-y
Kong, Xiang-Zhen, ENIGMA Laterality Working Group, Francks, Clyde, Hansell, Narelle K. and Wright, Margaret J. (2020). Reproducibility in the absence of selective reporting: An illustration from large-scale brain asymmetry research. Human Brain Mapping, 43 (1) hbm.25154, 244-254. doi: 10.1002/hbm.25154
Region-specific sex differences in the hippocampus
van Eijk, Liza, Hansell, Narelle K., Strike, Lachlan T., Couvy-Duchesne, Baptiste, de Zubicaray, Greig I., Thompson, Paul M., McMahon, Katie L., Zietsch, Brendan P. and Wright, Margaret J. (2020). Region-specific sex differences in the hippocampus. NeuroImage, 215 116781, 116781. doi: 10.1016/j.neuroimage.2020.116781
The genetic architecture of the human cerebral cortex
Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Ching, Christopher R. K., McMahon, Mary Agnes B., Shatokhina, Natalia, Zsembik, Leo C. P., Thomopoulos, Sophia I., Zhu, Alyssa H., Strike, Lachlan T., Agartz, Ingrid, Alhusaini, Saud, Almeida, Marcio A. A., Alnæs, Dag, Amlien, Inge K., Andersson, Micael, Ard, Tyler, Armstrong, Nicola J., Ashley-Koch, Allison, Atkins, Joshua R., Bernard, Manon, Brouwer, Rachel M., Buimer, Elizabeth E. L., Bülow, Robin ... Medland, Sarah E. (2020). The genetic architecture of the human cerebral cortex. Science, 367 (6484) aay6690, eaay6690-+. doi: 10.1126/science.aay6690
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
Absolute and relative estimates of genetic and environmental variance in brain structure volumes
Strike, Lachlan T., Hansell, Narelle K., Thompson, Paul M., de Zubicaray, Greig I., McMahon, Katie L., Zietsch, Brendan P. and Wright, Margaret J. (2019). Absolute and relative estimates of genetic and environmental variance in brain structure volumes. Brain Structure and Function, 224 (8), 2805-2821. doi: 10.1007/s00429-019-01931-8
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
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
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
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
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
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
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
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. (2018). Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications, 9 (1) 2098, 2098. doi: 10.1038/s41467-018-04362-x
Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium
Kong, Xiang-Zhen, Mathias, Samuel R., Guadalupe, Tulio, Glahn, David C., Franke, Barbara, Crivello, Fabrice, Tzourio-Mazoyer, Nathalie, Fisher, Simon E., Thompson, Paul M., Francks, Clyde, ENIGMA Laterality Working Group, Hansell, Narelle K., van Eijk, Liza, Strike, Lachlan and Wright, Margaret Jane (2018). Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium. Proceedings of the National Academy of Sciences, 115 (22), E5154-E5163. doi: 10.1073/pnas.1718418115
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
Strike, Lachlan T., Hansell, Narelle K., Couvy-Duchesne, Baptiste, Thompson, Paul M., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2018). Genetic Complexity of Cortical Structure: Differences in Genetic and Environmental Factors Influencing Cortical Surface Area and Thickness. Cerebral Cortex (New York, N.Y. : 1991), 29 (3), 952-962. doi: 10.1093/cercor/bhy002
Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste, Witt, Stephanie H., Binz, Tina M., Bolton, Jennifer L., Hayward, Caroline, Direk, Nese, Anderson, Anna, Huffman, Jennifer, Wilson, James F., Campbell, Harry, Rudan, Igor, Wright, Alan, Hastie, Nicholas, Wild, Sarah H., Velders, Fleur P., Hofman, Albert, Uitterlinden, Andre G., Lahti, Jari, Räikkönen, Katri, Kajantie, Eero, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G., Kaakinen, Marika ... Rietschel, Marcella (2017). Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. Scientific Reports, 7 (1) 15351, 15351. doi: 10.1038/s41598-017-11852-3
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
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
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
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
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
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
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
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
Bates, Timothy C., Hansell, Narelle K., Martin, Nicholas G. and Wright, Margaret J. (2016). When does socioeconomic status (SES) moderate the heritability of IQ? No evidence for g × SES interaction for IQ in a representative sample of 1176 Australian adolescent twin pairs. Intelligence, 56 (2), 10-15. doi: 10.1016/j.intell.2016.02.003
The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume
Lupton, Michelle K., Strike, Lachlan, Hansell, Narelle K., Wen, Wei, Mather, Karen A., Armstrong, Nicola J., Thalamuthu, Anbupalam, McMahon, Katie L., de Zubicaray, Greig I., Assareh, Amelia A., Simmons, Andrew, Proitsi, Petroula, Powell, John F., Montgomery, Grant W., Hibar, Derrek P., Westman, Eric, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Velas, Bruno, Lovestone, Simon, Brodaty, Henry, Ames, David, Trollor, Julian N., Martin, Nicholas G., Thompson, Paul M., Sachdev, Perminder S. and Wright, Margaret J. (2016). The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume. Neurobiology of Aging, 40, 68-77. doi: 10.1016/j.neurobiolaging.2015.12.023
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
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept
Franke, Barbara, Stein, Jason L., Ripke, Stephan, Anttila, Verneri, Hibar, Derrek P., Van Hulzen, Kimm J. E., Arias-Vasquez, Alejandro, Smoller, Jordan W., Nichols, Thomas E., Neale, Michael C., McIntosh, Andrew M., Lee, Phil, McMahon, Francis J., Meyer-Lindenberg, Andreas, Mattheisen, Manuel, Andreassen, Ole A., Gruber, Oliver, Sachdev, Perminder S., Roiz-Santianez, Roberto, Saykin, Andrew J., Ehrlich, Stefan, Mather, Karen A., Turner, Jessica A., Schwarz, Emanuel, Thalamuthu, Anbupalam, Yao, Yin, Ho, Yvonne Y. W., Martin, Nicholas G., Wright, Margaret J. ... Hansell, Narelle (2016). Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience, 19 (3), 420-431. doi: 10.1038/nn.4228
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
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
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
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
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
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
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
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
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
Strike, Lachlan T, Couvy-Duchesne, Baptiste, Hansell, Narelle K, Cuellar-Partida, Gabriel, Medland, Sarah E and Wright, Margaret J (2015). Genetics and brain morphology. Neuropsychology Review, 25 (1), 63-96. doi: 10.1007/s11065-015-9281-1
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
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 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
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
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
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
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
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L
Benyamin, B., St Pourcain, B., Davis, O. S., Davies, G., Hansell, N. K., Brion, M. J., Kirkpatrick, R. M., Cents, R. A. M., Franic, S., Miller, M. B., Haworth, C. M. A., Meaburn, E., Price, T. S., Evans, D. M., Timpson, N., Kemp, J., Ring, S., McArdle, W., Medland, S. E., Yang, J., Harris, S. E., Liewald, D. C., Scheet, P., Xiao, X., Hudziak, J. J., de Geus, E. J. C., Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe, V. W. V., Starr, J. M. ... Visscher, P. M. (2014). Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, 19 (2), 253-258. doi: 10.1038/mp.2012.184
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
Heritability of resting state EEG functional connectivity patterns
Schutte, Nienke M., Hansell, Narelle K., de Geus, Eco J. C., Martin, Nicholas G., Wright, Margaret J. and Smit, Dirk J. A. (2013). Heritability of resting state EEG functional connectivity patterns. Twin Research and Human Genetics, 16 (5), 962-969. doi: 10.1017/thg.2013.55
The relationship of reading ability to creativity: positive, not negative associations
Ritchie, Stuart J., Luciano, Michelle, Hansell, Narelle K., Wright, Margaret J. and Bates, Timothy C. (2013). The relationship of reading ability to creativity: positive, not negative associations. Learning and Individual Differences, 26, 171-176. doi: 10.1016/j.lindif.2013.02.009
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
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
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
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
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
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
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
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
Identification of common variants associated with human hippocampal and intracranial volumes
Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Senstad, Rudy E., Winkler, Anderson M., Toro, Roberto, Appel, Katja, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Brown, Andrew A., Cannon, Dara M., Chakravarty, M. Mallar, Christoforou, Andrea, Domin, Martin, Grimm, Oliver, Hollinshead, Marisa, Holmes, Avram J., Homuth, Georg, Hottenga, Jouke-Jan, Langan, Camilla, Lopez, Lorna M., Hansell, Narelle K., Hwang, Kristy S., Kim, Sungeun, Laje, Gonzalo, Lee, Phil H., Liu, Xinmin ... Brown, Matthew A. (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44 (5), 552-561. doi: 10.1038/ng.2250
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
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
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
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
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
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 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Genetic covariation of pelvic organ and elbow mobility in twins and their sisters
Hansell, Narelle K, Dietz, Hans Peter, Treloar, Susan A, Clarke, Barton and Martin, Nicholas G (2004). Genetic covariation of pelvic organ and elbow mobility in twins and their sisters. Twin research : the official journal of the International Society for Twin Studies, 7 (3), 254-60.
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
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 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 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
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, Karlsson, Robert, Krapohl, Eva, Lam, Max, Nygaard, Marianne, Reynolds, Chandra A., Trampush, Joey W., Young, Hannah, Zabaneh, Delilah, Hagg, Sara, Hansell, Narelle K., Karlsson, Ida K., Linnarsson, Sten, Montgomery, Grant W., Munoz-Manchado, Ana B., Quinlan, Erin B., Schumann, Gunter ... Posthuma, Danielle (2018). GWAS meta-analysis (N=279,930) identifies new genes and functional links to general cognitive ability. Human Genome Meeting 2018, Yokohama, Japan, 12-15 March 2018. London, United Kingdom: Henry Stewart Publications. doi: 10.1186/s40246-018-0138-6
Smit, Dirk, Wright, Margareth, Meyers, Jacquelyn, Martin, Nicholas, Ho, Yvonne, Malone, Stephen, Zhang, Jian, Burwell, Scott, Chorlian, David, de Geus, Eco, Denys, Damiaan, Hansell, Narelle, Hottenga, Jouke-Jan, McGue, Matt, van Beijsterveldt, Catharina, Jehanshad, Neda, Thompson, Paul, Whelan, Chris, Medland, Sarah, Porjesz, Bernice, Iacono, William and Boomsma, Dorret (2018). Psychiatric Liability Genes are Linked to Oscillatory Brain Activity: A Genome-Wide Association Study. 73rd Annual Scientific Convention and Meeting of the Society-of-Biological-Psychiatry (SOBP), New York NY United States, 10-12 May 2017. New York NY United States: Elsevier . doi: 10.1016/j.biopsych.2018.02.865
A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait
Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, 24 November 2017.
Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder
Trung Ngo,, Renteria, Miguel E., Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Cuellar-Partida, Gabriel, Hansen, Narelle K., Medland, Sarah E., Miller, Steven M., Wright, Margaret J. and Martin, Nicholas G. (2017). Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto, Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier.
GWAS of complementary perceptual endophenotype measures: How do they rate?
Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). GWAS of complementary perceptual endophenotype measures: How do they rate?. Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, 15–17 September 2017.
Heritability of hair cortisol and genetic overlap with psychological variables
Streit, Fabian, Rietschel, Liz, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste, Witt, Stephanie H., Binz, Tina, McGrath, John, Hickie, Ian B., Hansell, Narelle K., Wright, Margaret J., Gillespie, Nathan, Forstner, Andreas J., Schulze, Thomas G., Wüst, Stefan, Nöthen, Markus M., Baumgartner, Markus, Walker, Brian R., Crawford, Andrew A., Conde, Lucia Colodro, Medland, Sarah E., Martin, Nicholas G. and Rietschel, Marcella (2017). Heritability of hair cortisol and genetic overlap with psychological variables. 47th Annual Conference of the International Society of Psychoneuroendocrinology, Zurich, Switzerland, 7-9 September, 2017. Pergamon.
Ngo, T. T., Couvy-Duchesne, B., Cuéllar-Partida, G., Rentería, M. E., Colodro Conde, L., Gordon, S. D., Hansell, N. K., Law, P. C. F., Miller, S. M., Medland, S. E., Wright, M. J. and Martin, N. G. (2016). Association of psychiatric profile measures with binocular rivalry rate (BRR): Implications for slow BRR as an endophenotype for bipolar disorder. International Society for Twin Studies Satellite Meeting, QIMR Berghofer Medical Research Institute, Brisbane, Australia, 20 June 2016. Cambridge, United Kingdom: Cambridge University Press. doi: 10.1017/thg.2016.66
Genetic contributions to brain structure
Strike, Lachlan, Hansell, Narelle, Couvy-Duchesne, Baptiste, Thompson, Paul, Martin, Nicholas, de Zubicaray, Greig, McMahon, Katie and Wright, Margaret (2016). Genetic contributions to brain structure. 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, 20-23 June 2016. New York, United States: Springer New York LLC. doi: 10.1007/s10519-016-9812-4
Genetic covariation among hippocampal subfields
Hansell, Narelle, Strike, Lachlan, McMahon, Katie, Martin, Nicholas, de Zubicaray, Greig, Thompson, Paul and Wright, Margaret (2016). Genetic covariation among hippocampal subfields. 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, 20-23 June 2016. New York, United States: Springer New York LLC. doi: 10.1007/s10519-016-9812-4
Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Hansell, Narelle K., Wright, Margie, McGrath, John J., Witt, Stephanie, Rietschel, Marcella and Martin, Nicholas G. (2016). Hair cortisol and its Association with Symptoms of Depression, Neuroticism and Perceived Stress in Adolescent Twins. IEPA 10th International Conference on Early Intervention in Mental Health – “Looking Back, Moving Forward”, Milan, Italy, 20th – 22nd October, 2016. Richmond, Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/eip.12397
Power of multivariate GWAS: real case scenarios using brain phenotypes from MRI
Couvy-Duchesne, Baptiste, Strike, Lachlan, Hansell, Narelle, Martin, Nicholas, McMahon, Katie, de Zubicaray, Greig, Thompson, Paul and Wright, Margaret (2016). Power of multivariate GWAS: real case scenarios using brain phenotypes from MRI. 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, 20-23 June 2016. New York, United States: Springer New York LLC. doi: 10.1007/s10519-016-9812-4
Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder
Ngo, Trung, Rentería, Miguel E., Colodro Conde, Lucia, Couvy-Duchesne, Baptiste, Cuéllar-Partida, Gabriel, Hansell, Narelle K., Medland, Sarah E., Miller, Steven M., Wright, Margaret J. and Martin, Nicholas G. (2015). Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder. XXIII rd World Congress of Psychiatric Genetics (WCPG), Toronto, Canada, 16–20 October 2015. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2015.09.010
Pol, Hilleke Hulshoff, Brouwer, Rachel, Glahn, David, Hibar, Derrek, Hua, Xue, Jahanshad, Neda, Abramovic, Lucija, Franz, Carol, Hansell, Narelle, Koenis, Marinka, Mather, Karen, Panizzon, Matthew, Strike, Lachlan, Swagerman, Suzanne, Wen, Wei, Boomsma, Dorret, Gilmore, John, Gogtay, Nitin, Kahn, Rene S., Kremen, William, Sachdev, Perminder, Wright, Margaret and Thompson, Paul (2015). Genetic influences on longitudinal changes in subcortical volumes: results of the ENIGMA Plasticity Working Group. 45th Annual Meeting of the Behavior Genetics Association, San Diego, United States, Jun 20, 2015. New York, United States: Springer New York LLC.
Genome-wide association for reading and language abilities in two population cohorts
Luciano, Michelle, Evans, David, Hansell, Narelle, Medland, Sarah, Montgomery, Grant, Martin, Nick G., Wright, Margaret and Bates, Timothy (2013). Genome-wide association for reading and language abilities in two population cohorts. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille, France, 28 June-2 July 2013. New York, NY United States: Springer New York.
Hill, William, Davies, Gail, Van de Lagemaat, Louie, Christoforou, Andrea, Fernandes, Carla, Liewald, David, Croning, Mike, Payton, Antony, Craig, Leone, Whalley, Lawrence, Horan, Michael, Ollier, William, Hansell, Narelle, Wright, Margaret, Martin, Nick G., Montgomery, Grant, Steen, Vidar, Le Hellard, Stephanie, Espeseth, Thomas, Lundervold, Astri, Reinvang, Ivar, Starr, John, Pendleton, Neil, Grant, Seth, Bates, Timothy and Deary, Ian (2013). Human cognitive ability is influenced by genetic variation in components of postsynaptic signaling complexes assembled by MAGUK proteins. 43rd Annual Meeting of the Behavior Genetics Association, Marseille, France, 28 June - 2 July 2013 3. New York, NY, United States : Springer.
Diffusion imaging protocol effects on genetic associations
Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Diffusion imaging protocol effects on genetic associations. International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. NEW YORK: IEEE. doi: 10.1109/ISBI.2012.6235712
Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome
Jahanshad, Neda, Hibar, Derrek, Ryles, April, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansel, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235605
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry rate, an endophenotype for bipolar disorder. 5th Biennial Conference of the International Society for Bipolar Disorders, Istanbul, Turkey, 14–17 March 2012. Hoboken, NJ United States: Wiley-Blackwell. doi: 10.1111/j.1399-5618.2012.00981.x
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder. 5th Biennial Conference of the International-Society-for-Bipolar-Disorders, Istanbul, Turkey, 14-17 March 2012. Malden, MA, United States: Wiley-Blackwell. doi: 10.1111/j.1399-5618.2012.00981.x
Wheland, D., Joshi, A., McMahon, K., Hansell, N., Martin, N., Wright, M., Thompson, P., Shattuck, D. and Leahy, R. (2012). Robust identification of partial-correlation based networks with applications to cortical thickness data. 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2012, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ United States: I E E E. doi: 10.1109/ISBI.2012.6235869
Increasing GWAS sample size using item response theory: A pilot study of the personality consortium
de Moor, Marleen, van den Berg, Stephanie, Wouda, Jasper, Verweij, Karin, Hansell, Narelle, Martin, Nick G. and Boomsma, Dorret (2011). Increasing GWAS sample size using item response theory: A pilot study of the personality consortium. 41st Annual Meeting of the Behaviour-Genetics-Association, Newport Ri, Jun 06-09, 2011. NEW YORK: SPRINGER.
Hansell, Narelle K., Hickie, Ian B., Davenport, Tracey A., Hadzi-Pavlovic, Dusan, Wray, Naomi R., Martin, Nicholas G. and Wright, Margaret J. (2010). A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults. 40th Annual Meeting of Behavior Genetics Association, Pennsylvania, PA, U.S.A., May 2009. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7
Genetic contribution to individual variation in binocular rivalry rate
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Martin, N. G. and Wright, M. J. (2010). Genetic contribution to individual variation in binocular rivalry rate. ANS/AuPS 2010 — 30th Annual Meeting of the Australian Neuroscience Society, in conjunction with the 50th Anniversary Meeting of the Australian Physiological Society, Sydney Convention & Exhibition Centre, Darling Harbour, Sydney, 31 January – 3 February 2010. Australian Neuroscience Society.
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Martin, N. G. and Wright, M. J. (2010). Genetic contribution to individual variation in binocular rivalry rate, an endophenotype for bipolar disorder. 18th World Congress of Psychiatric Genetics, Athens, Greece, 3–7 October 2010. International Society of Psychiatric Genetics.
The genetics of binocular rivalry
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Martin, N. G. and Wright, M. J. (2010). The genetics of binocular rivalry. 7th FENS Forum of European Neuroscience, Amsterdam, The Netherlands, 3–7 July, 2010. Federation of European Neuroscience Societies.
de Moor, Marleen H. M., Boomsma, Dorret, I, de Geus, Eco J. C., Willemsen, Gonneke, Hottenga, Jouke-Jan, Distel, Marijn A., Abecasis, Goncalo R., Terracciano, Antonio, McCrae, Robert R., Costa, Paul T., Hartman, Catharina A., Spinhoven, Philip, Penninx, Brenda W., Esko, Tonu, Allik, Jueri, Realo, Anu, Metspalu, Andres, Hansell, Narelle K., Medland, Sarah E., Wray, Naomi R., Wright, Margie J., Martin, Nicholas G., Amin, Najaf, Aulchenko, Yurii S., Janssens, A. Cecile, Oostra, Ben A. and van Duijn, Cornelia M. (2009). Meta-analysis of genome-wide association results in > 10.000 individuals for the big five personality traits. 39th Annual Meeting of the Behavior Genetics Association, Mineapolis, MN, United States, 17-20 June 2009 . New York, NY, United States: Springer.
Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology
Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2006). Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology. World Congress on Alcohol Research (ISBRA 2006), Sydney, Australia, 10 - 13 September 2006. Oxford: Blackwell Publishing. doi: 10.1111/j.1530-0277.2006.00197.x
A genomic wide screen of the P3(00) ERP component: Preliminary findings
Wright, M. J., Luciano, M., Hansell, N. K., Geffen, G. M. and Martin, N. G. (2004). A genomic wide screen of the P3(00) ERP component: Preliminary findings. Behavior Genetics Association 34th Annual Meeting , Aix en Provence, France, June 2004. New York, NY United States: Springer.
Linkage analyses of ERP slow wave measures of working memory
Hansell, Narelle K., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2004). Linkage analyses of ERP slow wave measures of working memory. 34th Annual Meeting of the Behavior Genetics Association, Provence, France, 27 - 30 June 2004. New York, NY, United States: Springer New York. doi: 10.1007/s10519-004-5590-5
Bladder neck mobility is a heritable trait
Dietz, H. P., Hansell, N., Grace, M., Eldridge, A., Martin, N. and Clarke, B. (2003). Bladder neck mobility is a heritable trait. 28th Annual IUGA Meeting, Buenos Aires, Argentina, 28-31 October, 2003. Surrey, U.K.: Springer-Verlag London Ltd. doi: 10.1007/s00192-003-1108-6
ERP endophenotypes of cognitive ability: A genetic study
Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2003). ERP endophenotypes of cognitive ability: A genetic study. 3rd Victorian Postgraduates in Psychology Conference, RMIT University, Victoria, 23 Nov 2002. Melbourne, VIC, Australia: John Wiley & Sons.
Genetic variation in brain function
de Geus, E, Posthuma, D, Hansell, N, Malone, SM and Mulder, E (2002). Genetic variation in brain function. HOBOKEN: WILEY-BLACKWELL.
ERP phenotypes in a genetic study of working memory
Wright, M. J., Hansell, N. K., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2000). ERP phenotypes in a genetic study of working memory. -, -, 2000. Hoboken, NJ United States: Wiley-Blackwell.
Genetic influences on ERP slow wave measures of working memory in adolescent twins
Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2000). Genetic influences on ERP slow wave measures of working memory in adolescent twins. Behavior Genetics Association Meeting, -, 2000. New York, NY United States: Springer.
Psychophysiological phenotypes of cognition: The P3 and SW components
Wright, M. J., Hansell, N., Geffen, G. M., Geffen, L., Smith, G. and Martin, N. (2000). Psychophysiological phenotypes of cognition: The P3 and SW components. 30th Annual Meeting of the Behavior Genetics Association, Burlington, Vermont, USA, June 29 - July 1, 2000. Westport, United States: Kluwer. doi: 10.1023/A:1017371222025
Reliability and stability of P3 and slow wave elicited in a working memory task
Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2000). Reliability and stability of P3 and slow wave elicited in a working memory task. -, -, 2000. Amsterdam, Netherlands: Elsevier.
Queensland Twin Adolescent Brain (QTAB) non-imaging phenotypes
Wright, Margie, Strike, Lachlan, Hansell, Narelle, Chuang, Kai-Hsiang, Miller, Jessica, de Zubicaray, Greig, Thompson, Paul M and McMahon, Katie L (2022). Queensland Twin Adolescent Brain (QTAB) non-imaging phenotypes. The University of Queensland. (Dataset) doi: 10.48610/e891597
QTAB phenotypic and metagenomic data
Wright, Margie, Strike, Lachlan and Hansell, Narelle (2021). QTAB phenotypic and metagenomic data. The University of Queensland. (Dataset) doi: 10.14264/e803a68
A genetic investigation of brain function and cognitive ability
Hansell, Narelle Kaye (2003). A genetic investigation of brain function and cognitive ability. PhD Thesis, School of Psychology, The University of Queensland.
(2013) Doctor Philosophy — Associate Advisor