Professor Grant Montgomery

Professorial Research Fellow

Institute for Molecular Bioscience

Affiliate Professorial Research Fe

Queensland Brain Institute
g.montgomery1@uq.edu.au
+61 7 334 62612

Overview

Professor Grant Montgomery was born in New Zealand, completed PhD studies in Animal Science at Massey University and post-doctoral research in France. In 1987, he cofounded the New Zealand Sheep Genomics Program in the Biochemistry Department at the University of Otago and pioneered the introduction of genome mapping methods in farm animals. He moved to Australia in 1999 and joined the Queensland Institute of Medical Research where he ran a successful genome mapping program for human complex disease. In 2016, he moved to the University of Queensland and holds joint appointments at the Institute for Molecular Bioscience (IMB) and the Queensland Brain Institute (QBI). He is a National Health and Medical Research Council Principal Research Fellow and was elected a Fellow the Society for Reproductive Biology in 2012, Fellow of the Australian Academy of Health and Medical Sciences in 2015, and Honorary Fellow of the Royal Society of New Zealand in 2016. His research focusses on discovery of critical genes and pathways increasing risk for common diseases especially endometriosis.

Research Impacts

Professor Montgomery has made substantial contributions to the worldwide effort to map genomic regions contributing to risk for complex traits and diseases, including endometriosis, age at menarche and menopause, cancers of the reproductive tract, melanoma and inflammatory bowel disease. He is conducting systems genetics and functional studies to identify the genes and pathways affected by these genetic risk factors.

Qualifications

  • PhD, Massey University

Publications

  • Fung, Jenny N., Girling, Jane E., Lukowski, Samuel W., Sapkota, Yadav, Wallace, Leanne, Holdsworth-Carson, Sarah J., Henders, Anjali K., Healey, Martin, Rogers, Peter A. W., Powell, Joseph E. and Montgomery, Grant W. (2017) The genetic regulation of transcription in human endometrial tissue. Human Reproduction, 32 4: 893-904. doi:10.1093/humrep/dex006

  • Lloyd-Jones, Luke R., Holloway, Alexander, McRae, Allan, Yang, Jian, Small, Kerrin, Zeng, Biao, Bakshi, Andrew, Metspalu, Andres, Dermitzakis, Manolis, Gibson, Greg, Spector, Tim, Montgomery, Grant, Esko, Tonu, Visscher, Peter M. and Powell, Joseph E. (2017) The genetic architecture of gene expression in peripheral blood. American Journal of Human Genetics, 100 2: 228-237. doi:10.1016/j.ajhg.2016.12.008

  • Powell, Joseph E., Fung, Jenny N., Shakhbazov, Konstantin, Sapkota, Yadav, Cloonan, Nicole, Hemani, Gibran, Hillman, Kristine M., Kaufmann, Susanne, Luong, Hien T., Bowdler, Lisa, Painter, Jodie N., Holdsworth-Carson, Sarah J., Visscher, Peter M., Dinger, Marcel E., Healey, Martin, Nyholt, Dale R., French, Juliet D., Edwards, Stacey L., Rogers, Peter A. W. and Montgomery, Grant W. (2016) Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human Molecular Genetics, 25 22: 5046-5058. doi:10.1093/hmg/ddw320

  • Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander, Ekici, Arif B., Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Doerk, Thilo, Duerst, Matthias, Hillemanns, Peter, Runnebaum, Ingo, Amant, Frederic, Schrauwen, Stefanie, Zhao, Hui, Lambrechts, Diether, Depreeuw, Jeroen, Dowdy, Sean C., Goode, Ellen L., Fridley, Brooke L., Winham, Stacey J., Njolstad, Tormund S., Salvesen, Helga B., Trovik, Jone, Werner, Henrica M. J., Ashton, Katie, Otton, Geoffrey, Proietto, Tony, Liu, Tao, Mints, Miriam, Tham, Emma, Li, Mulin Jun, Yip, Shun H., Wang, Junwen, Bolla, Manjeet K., Michailidou, Kyriaki, Wang, Qin, Tyrer, Jonathan P., Dunlop, Malcolm, Houlston, Richard, Palles, Claire, Hopper, John L., Peto, Julian, Swerdlow, Anthony J., Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Chang-Claude, Jenny, Couch, Fergus J., Giles, Graham G., Kristensen, Vessela N., Cox, Angela, Cunningham, Julie M., Pharoah, Paul D. P., Dunning, Alison M., Edwards, Stacey L., Easton, Douglas F., Tomlinson, Ian and Spurdle, Amanda B. (2016) Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 6: 667-674. doi:10.1038/ng.3562

  • 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, Montgomery, Grant W., McGue , Matt, Ong, Ken K., Perry, John R.B., Martin, Nicholas G., Stefansson, Hreinn, Stefansson, Kari and 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

  • Zhu, Zhihong, Zhang, Futao, Hu, Han, Bakshi, Andrew, Robinson, Matthew R., Powell, Joseph E., Montgomery,Grant W., Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2016) Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. Nature Genetics, 48 5: 481-487. doi:10.1038/ng.3538

  • Day, Felix R., Ruth, Katherine S., Thompson, Deborah J., Lunetta, Kathryn L., Pervjakova, Natalia, Chasman, Daniel I., Stolk, Lisette, Finucane, Hilary K., Sulem, Patrick, Bulik-Sullivan, Brendan, Esko, Tonu, Johnson, Andrew D., Elks, Cathy E., Franceschini, Nora, He, Chunyan, Altmaier, Elisabeth, Brody, Jennifer A., Franke, Lude L., Huffman, Jennifer E., Keller, Margaux F., McArdle, Patrick F., Nutile, Teresa, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M., Schick, Ursula M., Smith, Jennifer A., Teumer, Alexander, Traglia, Michela, Vuckovic, Dragana, Yao, Jie, Zhao, Wei, Albrecht, Eva, Amin, Najaf, Corre, Tanguy, Hottenga, Jouke-Jan, Mangino, Massimo, Smith, Albert V., Tanaka, Toshiko, Abecasis, Goncalo R., Andrulis, Irene L., Anton-Culver, Hoda, Antoniou, Antonis C., Arndt, Volker, Arnold, Alice M., Barbieri, Caterina, Beckmann, Matthias W., Beeghly-Fadiel, Alicia, Benitez, Javier, Bernstein, Leslie, Bielinski, Suzette J., Blomqvist, Carl, Boerwinkle, Eric, Bogdanova, Natalia V., Bojesen, Stig E., Bolla, Manjeet K., Borresen-Dale, Anne-Lise, Boutin, Thibaud S., Brauch, Hiltrud, Brenner, Hermann, Bruening, Thomas, Burwinkel, Barbara, Campbell, Archie, Campbell, Harry, Chanock, Stephen J., Chapman, J. Ross, Chen, Yii-Der Ida, Chenevix-Trench, Georgia, Couch, Fergus J., Coviello, Andrea D., Cox, Angela, Czene, Kamila, Darabi, Hatef, De Vivo, Immaculata, Demerath, Ellen W., Dennis, Joe, Devilee, Peter, Doerk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M., Eicher, John D., Fasching, Peter A., Faul, Jessica D., Figueroa, Jonine, Flesch-Janys, Dieter, Gandin, Ilaria, Garcia, Melissa E., Garcia-Closas, Montserrat, Giles, Graham G., Girotto, Giorgia G., Goldberg, Mark S., Gonzalez-Neira, Anna, Goodarzi, Mark O., Grove, Megan L., Gudbjartsson, Daniel F., Guenel, Pascal, Guo, Xiuqing, Haiman, Christopher A., Hall, Per, Hamann, Ute, Henderson, Brian E., Hocking, Lynne J., Hofman, Albert, Homuth, Georg, Hooning, Maartje J., Hopper, John L., Hu, Frank B., Huang, Jinyan, Humphreys, Keith, Hunter, David J., Jakubowska, Anna, Jones, Samuel E., Kabisch, Maria, Karasik, David, Knight, Julia A., Kolcic, Ivana, Kooperberg, Charles, Kosma, Veli-Matti, Kriebel, Jennifer, Kristensen, Vessela, Lambrechts, Diether, Langenberg, Claudia, Li, Jingmei, Li, Xin, Lindstroem, Sara, Liu, Yongmei, Luan, Jian'an, Lubinski, Jan, Maegi, Reedik, Mannermaa, Arto, Manz, Judith, Margolin, Sara, Marten, Jonathan, Martin, Nicholas G., Masciullo, Corrado, Meindl, Alfons, Michailidou, Kyriaki, Mihailov, Evelin, Milani, Lili, Milne, Roger L., Mueller-Nurasyid, Martina, Nalls, Michael, Neale, Benjamin M., Nevanlinna, Heli, Neven, Patrick, Newman, Anne B., Nordestgaard, Borge G., Olson, Janet E., Padmanabhan, Sandosh, Peterlongo, Paolo, Peters, Ulrike, Petersmann, Astrid, Peto, Julian, Pharoah, Paul D. P., Pirastu, Nicola N., Pirie, Ailith, Pistis, Giorgio, Polasek, Ozren, Porteous, David, Psaty, Bruce M., Pylkas, Katri, Radice, Paolo, Raffel, Leslie J., Rivadeneira, Fernando, Rudan, Igor, Rudolph, Anja, Ruggiero, Daniela, Sala, Cinzia F., Sanna, Serena, Sawyer, Elinor J., Schlessinger, David, Schmidt, Marjanka K., Schmidt, Frank, Schmutzler, Rita K., Schoemaker, Minouk J., Scott, Robert A., Seynaeve, Caroline M., Simard, Jacques, Sorice, Rossella, Southey, Melissa C., Stoeckl, Doris, Strauch, Konstantin, Swerdlow, Anthony, Taylor, Kent D., Thorsteinsdottir, Unnur, Toland, Amanda E., Tomlinson, Ian, Truong, Therese, Tryggvadottir, Laufey, Turner, Stephen T., Vozzi, Diego, Wang, Qin, Wellons, Melissa, Willemsen, Gonneke, Wilson, James F., Winqvist, Robert, Wolffenbuttel, Bruce B. H. R., Wright, Alan F., Yannoukakos, Drakoulis, Zemunik, Tatijana, Zheng, Wei, Zygmunt, Marek, Bergmann, Sven, Boomsma, Dorret I., Buring, Julie E., Ferrucci, Luigi, Montgomery, Grant W., Gudnason, Vilmundur, Spector, Tim D., van Duijn, Cornelia M., Alizadeh, Behrooz Z., Ciullo, Marina, Crisponi, Laura, Easton, Douglas F., Gasparini, Paolo P., Gieger, Christian, Harris, Tamara B., Hayward, Caroline, Kardia, Sharon L. R., Kraft, Peter, McKnight, Barbara, Metspalu, Andres, Morrison, Alanna C., Reiner, Alex P., Ridker, Paul M., Rotter, Jerome I., Toniolo, Daniela, Uitterlinden, Andre G., Ulivi, Sheila, Voelzke, Henry, Wareham, Nicholas J., Weir, David R., Yerges-Armstrong, Laura M., Price, Alkes L., Stefansson, Kari, Visser, Jenny A., Ong, Ken K., Chang-Claude, Jenny, Murabito, Joanne M., Perry, John R. B. and Murray, Anna (2015) Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics, 47 11: 1294-1305. doi:10.1038/ng.3412

  • Fung, Jenny N., Holdsworth-Carson, Sarah J., Sapkota, Yadav, Zhao, Zhen Zhen, Jones, Lincoln, Girling, Jane E., Paiva, Premila, Healey, Martin, Nyholt, Dale R., Rogers, Peter A. W. and Montgomery, Grant W. (2015) Functional evaluation of genetic variants associated with endometriosis near GREB1. Human Reproduction, 30 5: 1263-1275. doi:10.1093/humrep/dev051

  • Fung, Jenny N., Rogers, Peter A. W. and Montgomery, Grant W. (2015) Identifying the biological basis of GWAS hits for endometriosis. Biology of Reproduction, 92 4: . doi:10.1095/biolreprod.114.126458

  • Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L., Shu X.-O., Long J., Zheng W., Xiang Y.-B., Montgomery G.W., Webb P.M., Scott R.J., McEvoy M., Attia J., Holliday E., Martin N.G., Nyholt D.R., Henders A.K., Fasching P.A., Hein A., Beckmann M.W., Renner S.P., Dork T., Hillemanns P., Durst M., Runnebaum I., Lambrechts D., Coenegrachts L., Schrauwen S., Amant F., Winterhoff B., Dowdy S.C., Goode E.L., Teoman A., Salvesen H.B., Trovik J., Njolstad T.S., Werner H.M.J., Ashton K., Proietto T., Otton G., Tzortzatos G., Mints M., Tham E., Hall P., Czene K., Liu J., Li J., Hopper J.L., Southey M.C., Ekici A.B., Ruebner M., Johnson N., Peto J., Burwinkel B., Marme F., Brenner H., Dieffenbach A.K., Meindl A., Brauch H., Lindblom A., Depreeuw J., Moisse M., Chang-Claude J., Rudolph A., Couch F.J., Olson J.E., Giles G.G., Bruinsma F., Cunningham J.M., Fridley B.L., Borresen-Dale A.L., Kristensen V.N., Cox A., Swerdlow A.J., Orr N., Bolla M.K., Wang Q., Weber R.P., Chen Z., Shah M., French J.D., Pharoah P.D.P., Dunning A.M., Tomlinson I., Easton D.F., Edwards S.L., Thompson D.J. and Spurdle A.B. (2015) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 5: 1478-1492. doi:10.1093/hmg/ddu552

  • 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

  • Perry, John R. B., Day, Felix, Elks, Cathy E., Sulem, Patrick, Thompson, Deborah J., Ferreira, Teresa, He, Chunyan, Chasman, Daniel I., Esko, Toenu, Thorleifsson, Gudmar, Albrecht, Eva, Ang, Wei Q., Corre, Tanguy, Cousminer, Diana L., Feenstra, Bjarke, Franceschini, Nora, Ganna, Andrea, Johnson, Andrew D., Kjellqvist, Sanela, Lunetta, Kathryn L., McMahon, George, Nolte, Ilja M., Paternoster, Lavinia, Porcu, Eleonora, Smith, Albert V., Stolk, Lisette, Teumer, Alexander, Tsernikova, Natalia, Tikkanen, Emmi, Ulivi, Sheila, Wagner, Erin K., Amin, Najaf, Bierut, Laura J., Byrne, Enda M., Hottenga, Jouke-Jan, Koller, Daniel L., Mangino, Massimo, Pers, Tune H., Yerges-Armstrong, Laura M., Zhao, Jing Hua, Andrulis, Irene L., Anton-Culver, Hoda, Atsma, Femke, Bandinelli, Stefania, Beckmann, Matthias W., Benitez, Javier, Blomqvist, Carl, Bojesen, Stig E., Bolla, Manjeet K., Bonanni, Bernardo, Brauch, Hiltrud, Brenner, Hermann, Buring, Julie E., Chang-Claude, Jenny, Chanock, Stephen, Chen, Jinhui, Chenevix-Trench, Georgia, Collee, J. Margriet, Couch, Fergus J., Couper, David, Coviello, Andrea D., Cox, Angela, Czene, Kamila, D'adamo, Adamo Pio, Smith, George Davey, De Vivo, Immaculata, Demerath, Ellen W., Dennis, Joe, Devilee, Peter, Dieffenbach, Aida K., Dunning, Alison M., Eiriksdottir, Gudny, Eriksson, Johan G., Fasching, Peter A., Ferrucci, Luigi, Flesch-Janys, Dieter, Flyger, Henrik, Foroud, Tatiana, Franke, Lude, Garcia, Melissa E., Garcia-Closas, Montserrat, Geller, Frank, de Geus, Eco E. J., Giles, Graham G., Gudbjartsson, Daniel F., Gudnason, Vilmundur, Guenel, Pascal, Guo, Suiqun, Hall, Per, Hamann, Ute, Haring, Robin, Hartman, Catharina A., Heath, AndrewC., Hofman, Albert, Hooning, Maartje J., Hopper, John L., Hu, Frank B., Hunter, David J., Karasik, David, Kiel, Douglas P., Knight, Julia A., Kosma, Veli-Matti, Kutalik, Zoltan, Lai, Sandra, Lambrechts, Diether, Lindblom, Annika, Maegi, Reedik, Magnusson, Patrik K., Mannermaa, Arto, Martin, Nicholas G., Masson, Gisli, McArdle, Patrick F., McArdle, Wendy L., Melbye, Mads, Michailidou, Kyriaki, Mihailov, Evelin, Milani, Lili, Milne, Roger L., Nevanlinna, Heli, Neven, Patrick, Nohr, Ellen A., Oldehinkel, Albertine J., Oostra, Ben A., Palotie, Aarno, Peacock, Munro, Pedersen, Nancy L., Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Postma, Dirkje S., Pouta, Anneli, Pylkaes, Katri, Radice, Paolo, Ring, Susan, Rivadeneira, Fernando, Robino, Antonietta, Rose, Lynda M., Rudolph, Anja, Salomaa, Veikko, Sanna, Serena, Schlessinger, David, Schmidt, Marjanka K., Southey, Mellissa C., Sovio, Ulla, Stampfer, Meir J., Stoeckl, Doris, Storniolo, Anna M., Timpson, Nicholas J., Tyrer, Jonathan, Visser, Jenny A., Vollenweider, Peter, Voelzke, Henry, Waeber, Gerard, Waldenberger, Melanie, Wallaschofski, Henri, Wang, Qin, Willemsen, Gonneke, Winqvist, Robert, Wolffenbuttel, Bruce H. R., Wright, Margaret J., Australian Ovarian Cancer Study, The GENICA Network, kConFab, The LifeLines Cohort Study, The InterAct Consortium, Early Growth Genetics (EGG) Consortium, Boomsma, Dorret I., Econs, Michael J., Khaw, Kay-Tee, Loos, Ruth J. F., McCarthy, Mark I., Montgomery, Grant W., Rice, John P., Streeten, Elizabeth A., Thorsteinsdottir, Unnur, van Duijn, Cornelia M., Alizadeh, Behrooz Z., Bergmann, Sven, Boerwinkle, Eric, Boyd, Heather A., Crisponi, Laura, Gasparini, Paolo, Gieger, Christian, Harris, Tamara B., Ingelsson, Erik, Jaervelin, Marjo-Riitta, Kraft, Peter, Lawlor, Debbie, Metspalu, Andres, Pennell, Craig E., Ridker, Paul M., Snieder, Harold, Sorensen, Thorkild I. A., Spector, Tim D., Strachan, David P., Uitterlinden, Andre G., Wareham, Nicholas J., Widen, Elisabeth, Zygmunt, Marek, Murray, Anna, Easton, Douglas F., Stefansson, Kari, Murabito, Joanne M., Ong, Ken K., the ReproGen Consortium and Middeldorp, Christel (2014) Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature, 514 7520: 92-97. doi:10.1038/nature13545

  • Rahmioglu, Nilufer, Nyholt, Dale R., Morris, Andrew P., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2014) Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human Reproduction Update, 20 5: 702-716. doi:10.1093/humupd/dmu015

  • 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

  • Westra, Harm-Jan, Peters, Marjolein J., Esko, Tonu, Yaghootkar, Hanieh, Schurmann, Claudia, Kettunen, Johannes, Christiansen, Mark W., Fairfax, Benjamin P., Schramm, Katharina, Powell, Joseph E., Zhernakova, Alexandra, Zhernakova, Daria V., Veldink, Jan H., Van den Berg, Leonard H., Karjalainen, Juha, Withoff, Sebo, Uitterlinden, Andre G., Hofman, Albert, Rivadeneira, Fernando, Hoen, Peter A. C't, Reinmaa, Eva, Fischer, Krista, Nelis, Mari, Milani, Lili, Melzer, David, Ferrucci, Luigi, Singleton, Andrew B., Hernandez, Dena G., Nalls, Michael A., Homuth, Georg, Nauck, Matthias, Radke, Doerte, Voelker, Uwe, Perola, Markus, Salomaa, Veikko, Brody, Jennifer, Suchy-Dicey, Astrid, Gharib, Sina A., Enquobahrie, Daniel A., Lumley, Thomas, Montgomery, Grant W., Makino, Seiko, Prokisch, Holger, Herder, Christian, Roden, Michael, Grallert, Harald, Meitinger, Thomas, Strauch, Konstantin, Li, Yang, Jansen, Ritsert C., Visscher, Peter M., Knight, Julian C., Psaty, Bruce M., Ripatti, Samuli, Teumer, Alexander, Frayling, Timothy M., Metspalu, Andres, van Meurs, Joyce B. J. and Franke, Lude (2013) Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics, 45 10: 1238-U195. doi:10.1038/ng.2756

  • 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

  • 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, 22 456-466. doi:10.1101/gr.126540.111

  • 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., Boerwinkle E., Broekmans F.J., Burri A., Campbell H., Chanock S.J., Chen C., Cornelis M.C., Corre T., Coviello A.D., D'Adamo P., Davies G., De Faire U., De Geus E.J.C., Deary I.J., Dedoussis G.V.Z., Deloukas P., Ebrahim S., Eiriksdottir G., Emilsson V., Eriksson J.G., Fauser B.C.J.M., Ferreli L., Ferrucci L., Fischer K., Folsom A.R., Garcia M.E., Gasparini P., Gieger C., Glazer N., Grobbee D.E., Hall P., Haller T., Hankinson S.E., Hass M., Hayward C., Heath A.C., Hofman A., Ingelsson E., Janssens A.C.J.W., Johnson A.D., Karasik D., Kardia S.L.R., Keyzer J., Kiel D.P., Kolcic I., Kutalik Z., Lahti J., Lai S., Laisk T., Laven J.S.E., Lawlor D.A., Liu J., Lopez L.M., Louwers Y.V., Magnusson P.K.E., Marongiu M., Martin N.G., Klaric I.M., Masciullo C., McKnight B., Medland S.E., Melzer D., Mooser V., Navarro P., Newman A.B., Nyholt D.R., Onland-Moret N.C., Palotie A., Pare G., Parker A.N., Pedersen N.L., Peeters P.H.M., Pistis G., Plump A.S., Polasek O., Pop V.J.M., Psaty B.M., R Currency Signikkonen K., Rehnberg E., Rotter J.I., Rudan I., Sala C., Salumets A., Scuteri A., Singleton A., Smith J.A., Snieder H., Soranzo N., Stacey S.N., Starr J.M., Stathopoulou M.G., Stirrups K., Stolk R.P., Styrkarsdottir U., Sun Y.V., Tenesa A., Thorand B., Toniolo D., Tryggvadottir L., Tsui K., Ulivi S., Van Dam R.M., Van Der Schouw Y.T., Van Gils C.H., Van Nierop P., Vink J.M., Visscher P.M., Voorhuis M., Waeber G., Wallaschofski H., Wichmann H.E., Widen E., Wijnands-Van Gent C.J.M., Willemsen G., Wilson J.F., Wolffenbuttel B.H.R., Wright A.F., Yerges-Armstrong L.M., Zemunik T., Zgaga L., Zillikens M.C., Zygmunt M., Arnold A.M., Boomsma D.I., Buring J.E., Crisponi L., Demerath E.W., Gudnason V., Harris T.B., Hu F.B., Hunter D.J., Launer L.J., Metspalu A., Montgomery G.W., Oostra B.A., Ridker P.M., Sanna S., Schlessinger D., Spector T.D., Stefansson K., Streeten E.A., Thorsteinsdottir U., Uda M., Uitterlinden A.G., Van Duijn C.M., Volzke H., Murray A., Murabito J.M., Visser J.A. and 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

  • 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

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Publications

Featured Publications

  • Fung, Jenny N., Girling, Jane E., Lukowski, Samuel W., Sapkota, Yadav, Wallace, Leanne, Holdsworth-Carson, Sarah J., Henders, Anjali K., Healey, Martin, Rogers, Peter A. W., Powell, Joseph E. and Montgomery, Grant W. (2017) The genetic regulation of transcription in human endometrial tissue. Human Reproduction, 32 4: 893-904. doi:10.1093/humrep/dex006

  • Lloyd-Jones, Luke R., Holloway, Alexander, McRae, Allan, Yang, Jian, Small, Kerrin, Zeng, Biao, Bakshi, Andrew, Metspalu, Andres, Dermitzakis, Manolis, Gibson, Greg, Spector, Tim, Montgomery, Grant, Esko, Tonu, Visscher, Peter M. and Powell, Joseph E. (2017) The genetic architecture of gene expression in peripheral blood. American Journal of Human Genetics, 100 2: 228-237. doi:10.1016/j.ajhg.2016.12.008

  • Powell, Joseph E., Fung, Jenny N., Shakhbazov, Konstantin, Sapkota, Yadav, Cloonan, Nicole, Hemani, Gibran, Hillman, Kristine M., Kaufmann, Susanne, Luong, Hien T., Bowdler, Lisa, Painter, Jodie N., Holdsworth-Carson, Sarah J., Visscher, Peter M., Dinger, Marcel E., Healey, Martin, Nyholt, Dale R., French, Juliet D., Edwards, Stacey L., Rogers, Peter A. W. and Montgomery, Grant W. (2016) Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339. Human Molecular Genetics, 25 22: 5046-5058. doi:10.1093/hmg/ddw320

  • Cheng, Timothy H. T., Thompson, Deborah J., O'Mara, Tracy A., Painter, Jodie N., Glubb, Dylan M., Flach, Susanne, Lewis, Annabelle, French, Juliet D., Freeman-Mills, Luke, Church, David, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Webb, Penelope M., Attia, John, Holliday, Elizabeth G., McEvoy, Mark, Scott, Rodney J., Henders, Anjali K., Martin, Nicholas G., Montgomery, Grant W., Nyholt, Dale R., Ahmed, Shahana, Healey, Catherine S., Shah, Mitul, Dennis, Joe, Fasching, Peter A., Beckmann, Matthias W., Hein, Alexander, Ekici, Arif B., Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Doerk, Thilo, Duerst, Matthias, Hillemanns, Peter, Runnebaum, Ingo, Amant, Frederic, Schrauwen, Stefanie, Zhao, Hui, Lambrechts, Diether, Depreeuw, Jeroen, Dowdy, Sean C., Goode, Ellen L., Fridley, Brooke L., Winham, Stacey J., Njolstad, Tormund S., Salvesen, Helga B., Trovik, Jone, Werner, Henrica M. J., Ashton, Katie, Otton, Geoffrey, Proietto, Tony, Liu, Tao, Mints, Miriam, Tham, Emma, Li, Mulin Jun, Yip, Shun H., Wang, Junwen, Bolla, Manjeet K., Michailidou, Kyriaki, Wang, Qin, Tyrer, Jonathan P., Dunlop, Malcolm, Houlston, Richard, Palles, Claire, Hopper, John L., Peto, Julian, Swerdlow, Anthony J., Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Chang-Claude, Jenny, Couch, Fergus J., Giles, Graham G., Kristensen, Vessela N., Cox, Angela, Cunningham, Julie M., Pharoah, Paul D. P., Dunning, Alison M., Edwards, Stacey L., Easton, Douglas F., Tomlinson, Ian and Spurdle, Amanda B. (2016) Five endometrial cancer risk loci identified through genome-wide association analysis. Nature Genetics, 48 6: 667-674. doi:10.1038/ng.3562

  • 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, Montgomery, Grant W., McGue , Matt, Ong, Ken K., Perry, John R.B., Martin, Nicholas G., Stefansson, Hreinn, Stefansson, Kari and 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

  • Zhu, Zhihong, Zhang, Futao, Hu, Han, Bakshi, Andrew, Robinson, Matthew R., Powell, Joseph E., Montgomery,Grant W., Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2016) Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. Nature Genetics, 48 5: 481-487. doi:10.1038/ng.3538

  • Day, Felix R., Ruth, Katherine S., Thompson, Deborah J., Lunetta, Kathryn L., Pervjakova, Natalia, Chasman, Daniel I., Stolk, Lisette, Finucane, Hilary K., Sulem, Patrick, Bulik-Sullivan, Brendan, Esko, Tonu, Johnson, Andrew D., Elks, Cathy E., Franceschini, Nora, He, Chunyan, Altmaier, Elisabeth, Brody, Jennifer A., Franke, Lude L., Huffman, Jennifer E., Keller, Margaux F., McArdle, Patrick F., Nutile, Teresa, Porcu, Eleonora, Robino, Antonietta, Rose, Lynda M., Schick, Ursula M., Smith, Jennifer A., Teumer, Alexander, Traglia, Michela, Vuckovic, Dragana, Yao, Jie, Zhao, Wei, Albrecht, Eva, Amin, Najaf, Corre, Tanguy, Hottenga, Jouke-Jan, Mangino, Massimo, Smith, Albert V., Tanaka, Toshiko, Abecasis, Goncalo R., Andrulis, Irene L., Anton-Culver, Hoda, Antoniou, Antonis C., Arndt, Volker, Arnold, Alice M., Barbieri, Caterina, Beckmann, Matthias W., Beeghly-Fadiel, Alicia, Benitez, Javier, Bernstein, Leslie, Bielinski, Suzette J., Blomqvist, Carl, Boerwinkle, Eric, Bogdanova, Natalia V., Bojesen, Stig E., Bolla, Manjeet K., Borresen-Dale, Anne-Lise, Boutin, Thibaud S., Brauch, Hiltrud, Brenner, Hermann, Bruening, Thomas, Burwinkel, Barbara, Campbell, Archie, Campbell, Harry, Chanock, Stephen J., Chapman, J. Ross, Chen, Yii-Der Ida, Chenevix-Trench, Georgia, Couch, Fergus J., Coviello, Andrea D., Cox, Angela, Czene, Kamila, Darabi, Hatef, De Vivo, Immaculata, Demerath, Ellen W., Dennis, Joe, Devilee, Peter, Doerk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M., Eicher, John D., Fasching, Peter A., Faul, Jessica D., Figueroa, Jonine, Flesch-Janys, Dieter, Gandin, Ilaria, Garcia, Melissa E., Garcia-Closas, Montserrat, Giles, Graham G., Girotto, Giorgia G., Goldberg, Mark S., Gonzalez-Neira, Anna, Goodarzi, Mark O., Grove, Megan L., Gudbjartsson, Daniel F., Guenel, Pascal, Guo, Xiuqing, Haiman, Christopher A., Hall, Per, Hamann, Ute, Henderson, Brian E., Hocking, Lynne J., Hofman, Albert, Homuth, Georg, Hooning, Maartje J., Hopper, John L., Hu, Frank B., Huang, Jinyan, Humphreys, Keith, Hunter, David J., Jakubowska, Anna, Jones, Samuel E., Kabisch, Maria, Karasik, David, Knight, Julia A., Kolcic, Ivana, Kooperberg, Charles, Kosma, Veli-Matti, Kriebel, Jennifer, Kristensen, Vessela, Lambrechts, Diether, Langenberg, Claudia, Li, Jingmei, Li, Xin, Lindstroem, Sara, Liu, Yongmei, Luan, Jian'an, Lubinski, Jan, Maegi, Reedik, Mannermaa, Arto, Manz, Judith, Margolin, Sara, Marten, Jonathan, Martin, Nicholas G., Masciullo, Corrado, Meindl, Alfons, Michailidou, Kyriaki, Mihailov, Evelin, Milani, Lili, Milne, Roger L., Mueller-Nurasyid, Martina, Nalls, Michael, Neale, Benjamin M., Nevanlinna, Heli, Neven, Patrick, Newman, Anne B., Nordestgaard, Borge G., Olson, Janet E., Padmanabhan, Sandosh, Peterlongo, Paolo, Peters, Ulrike, Petersmann, Astrid, Peto, Julian, Pharoah, Paul D. P., Pirastu, Nicola N., Pirie, Ailith, Pistis, Giorgio, Polasek, Ozren, Porteous, David, Psaty, Bruce M., Pylkas, Katri, Radice, Paolo, Raffel, Leslie J., Rivadeneira, Fernando, Rudan, Igor, Rudolph, Anja, Ruggiero, Daniela, Sala, Cinzia F., Sanna, Serena, Sawyer, Elinor J., Schlessinger, David, Schmidt, Marjanka K., Schmidt, Frank, Schmutzler, Rita K., Schoemaker, Minouk J., Scott, Robert A., Seynaeve, Caroline M., Simard, Jacques, Sorice, Rossella, Southey, Melissa C., Stoeckl, Doris, Strauch, Konstantin, Swerdlow, Anthony, Taylor, Kent D., Thorsteinsdottir, Unnur, Toland, Amanda E., Tomlinson, Ian, Truong, Therese, Tryggvadottir, Laufey, Turner, Stephen T., Vozzi, Diego, Wang, Qin, Wellons, Melissa, Willemsen, Gonneke, Wilson, James F., Winqvist, Robert, Wolffenbuttel, Bruce B. H. R., Wright, Alan F., Yannoukakos, Drakoulis, Zemunik, Tatijana, Zheng, Wei, Zygmunt, Marek, Bergmann, Sven, Boomsma, Dorret I., Buring, Julie E., Ferrucci, Luigi, Montgomery, Grant W., Gudnason, Vilmundur, Spector, Tim D., van Duijn, Cornelia M., Alizadeh, Behrooz Z., Ciullo, Marina, Crisponi, Laura, Easton, Douglas F., Gasparini, Paolo P., Gieger, Christian, Harris, Tamara B., Hayward, Caroline, Kardia, Sharon L. R., Kraft, Peter, McKnight, Barbara, Metspalu, Andres, Morrison, Alanna C., Reiner, Alex P., Ridker, Paul M., Rotter, Jerome I., Toniolo, Daniela, Uitterlinden, Andre G., Ulivi, Sheila, Voelzke, Henry, Wareham, Nicholas J., Weir, David R., Yerges-Armstrong, Laura M., Price, Alkes L., Stefansson, Kari, Visser, Jenny A., Ong, Ken K., Chang-Claude, Jenny, Murabito, Joanne M., Perry, John R. B. and Murray, Anna (2015) Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nature Genetics, 47 11: 1294-1305. doi:10.1038/ng.3412

  • Fung, Jenny N., Holdsworth-Carson, Sarah J., Sapkota, Yadav, Zhao, Zhen Zhen, Jones, Lincoln, Girling, Jane E., Paiva, Premila, Healey, Martin, Nyholt, Dale R., Rogers, Peter A. W. and Montgomery, Grant W. (2015) Functional evaluation of genetic variants associated with endometriosis near GREB1. Human Reproduction, 30 5: 1263-1275. doi:10.1093/humrep/dev051

  • Fung, Jenny N., Rogers, Peter A. W. and Montgomery, Grant W. (2015) Identifying the biological basis of GWAS hits for endometriosis. Biology of Reproduction, 92 4: . doi:10.1095/biolreprod.114.126458

  • Painter J.N., O'Mara T.A., Batra J., Cheng T., Lose F.A., Dennis J., Michailidou K., Tyrer J.P., Ahmed S., Ferguson K., Healey C.S., Kaufmann S., Hillman K.M., Walpole C., Moya L., Pollock P., Jones A., Howarth K., Martin L., Gorman M., Hodgson S., De Polanco M.M.E., Sans M., Carracedo A., Castellvi-Bel S., Rojas-Martinez A., Santos E., Teixeira M.R., Carvajal-Carmona L., Shu X.-O., Long J., Zheng W., Xiang Y.-B., Montgomery G.W., Webb P.M., Scott R.J., McEvoy M., Attia J., Holliday E., Martin N.G., Nyholt D.R., Henders A.K., Fasching P.A., Hein A., Beckmann M.W., Renner S.P., Dork T., Hillemanns P., Durst M., Runnebaum I., Lambrechts D., Coenegrachts L., Schrauwen S., Amant F., Winterhoff B., Dowdy S.C., Goode E.L., Teoman A., Salvesen H.B., Trovik J., Njolstad T.S., Werner H.M.J., Ashton K., Proietto T., Otton G., Tzortzatos G., Mints M., Tham E., Hall P., Czene K., Liu J., Li J., Hopper J.L., Southey M.C., Ekici A.B., Ruebner M., Johnson N., Peto J., Burwinkel B., Marme F., Brenner H., Dieffenbach A.K., Meindl A., Brauch H., Lindblom A., Depreeuw J., Moisse M., Chang-Claude J., Rudolph A., Couch F.J., Olson J.E., Giles G.G., Bruinsma F., Cunningham J.M., Fridley B.L., Borresen-Dale A.L., Kristensen V.N., Cox A., Swerdlow A.J., Orr N., Bolla M.K., Wang Q., Weber R.P., Chen Z., Shah M., French J.D., Pharoah P.D.P., Dunning A.M., Tomlinson I., Easton D.F., Edwards S.L., Thompson D.J. and Spurdle A.B. (2015) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics, 24 5: 1478-1492. doi:10.1093/hmg/ddu552

  • 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

  • Perry, John R. B., Day, Felix, Elks, Cathy E., Sulem, Patrick, Thompson, Deborah J., Ferreira, Teresa, He, Chunyan, Chasman, Daniel I., Esko, Toenu, Thorleifsson, Gudmar, Albrecht, Eva, Ang, Wei Q., Corre, Tanguy, Cousminer, Diana L., Feenstra, Bjarke, Franceschini, Nora, Ganna, Andrea, Johnson, Andrew D., Kjellqvist, Sanela, Lunetta, Kathryn L., McMahon, George, Nolte, Ilja M., Paternoster, Lavinia, Porcu, Eleonora, Smith, Albert V., Stolk, Lisette, Teumer, Alexander, Tsernikova, Natalia, Tikkanen, Emmi, Ulivi, Sheila, Wagner, Erin K., Amin, Najaf, Bierut, Laura J., Byrne, Enda M., Hottenga, Jouke-Jan, Koller, Daniel L., Mangino, Massimo, Pers, Tune H., Yerges-Armstrong, Laura M., Zhao, Jing Hua, Andrulis, Irene L., Anton-Culver, Hoda, Atsma, Femke, Bandinelli, Stefania, Beckmann, Matthias W., Benitez, Javier, Blomqvist, Carl, Bojesen, Stig E., Bolla, Manjeet K., Bonanni, Bernardo, Brauch, Hiltrud, Brenner, Hermann, Buring, Julie E., Chang-Claude, Jenny, Chanock, Stephen, Chen, Jinhui, Chenevix-Trench, Georgia, Collee, J. Margriet, Couch, Fergus J., Couper, David, Coviello, Andrea D., Cox, Angela, Czene, Kamila, D'adamo, Adamo Pio, Smith, George Davey, De Vivo, Immaculata, Demerath, Ellen W., Dennis, Joe, Devilee, Peter, Dieffenbach, Aida K., Dunning, Alison M., Eiriksdottir, Gudny, Eriksson, Johan G., Fasching, Peter A., Ferrucci, Luigi, Flesch-Janys, Dieter, Flyger, Henrik, Foroud, Tatiana, Franke, Lude, Garcia, Melissa E., Garcia-Closas, Montserrat, Geller, Frank, de Geus, Eco E. J., Giles, Graham G., Gudbjartsson, Daniel F., Gudnason, Vilmundur, Guenel, Pascal, Guo, Suiqun, Hall, Per, Hamann, Ute, Haring, Robin, Hartman, Catharina A., Heath, AndrewC., Hofman, Albert, Hooning, Maartje J., Hopper, John L., Hu, Frank B., Hunter, David J., Karasik, David, Kiel, Douglas P., Knight, Julia A., Kosma, Veli-Matti, Kutalik, Zoltan, Lai, Sandra, Lambrechts, Diether, Lindblom, Annika, Maegi, Reedik, Magnusson, Patrik K., Mannermaa, Arto, Martin, Nicholas G., Masson, Gisli, McArdle, Patrick F., McArdle, Wendy L., Melbye, Mads, Michailidou, Kyriaki, Mihailov, Evelin, Milani, Lili, Milne, Roger L., Nevanlinna, Heli, Neven, Patrick, Nohr, Ellen A., Oldehinkel, Albertine J., Oostra, Ben A., Palotie, Aarno, Peacock, Munro, Pedersen, Nancy L., Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Postma, Dirkje S., Pouta, Anneli, Pylkaes, Katri, Radice, Paolo, Ring, Susan, Rivadeneira, Fernando, Robino, Antonietta, Rose, Lynda M., Rudolph, Anja, Salomaa, Veikko, Sanna, Serena, Schlessinger, David, Schmidt, Marjanka K., Southey, Mellissa C., Sovio, Ulla, Stampfer, Meir J., Stoeckl, Doris, Storniolo, Anna M., Timpson, Nicholas J., Tyrer, Jonathan, Visser, Jenny A., Vollenweider, Peter, Voelzke, Henry, Waeber, Gerard, Waldenberger, Melanie, Wallaschofski, Henri, Wang, Qin, Willemsen, Gonneke, Winqvist, Robert, Wolffenbuttel, Bruce H. R., Wright, Margaret J., Australian Ovarian Cancer Study, The GENICA Network, kConFab, The LifeLines Cohort Study, The InterAct Consortium, Early Growth Genetics (EGG) Consortium, Boomsma, Dorret I., Econs, Michael J., Khaw, Kay-Tee, Loos, Ruth J. F., McCarthy, Mark I., Montgomery, Grant W., Rice, John P., Streeten, Elizabeth A., Thorsteinsdottir, Unnur, van Duijn, Cornelia M., Alizadeh, Behrooz Z., Bergmann, Sven, Boerwinkle, Eric, Boyd, Heather A., Crisponi, Laura, Gasparini, Paolo, Gieger, Christian, Harris, Tamara B., Ingelsson, Erik, Jaervelin, Marjo-Riitta, Kraft, Peter, Lawlor, Debbie, Metspalu, Andres, Pennell, Craig E., Ridker, Paul M., Snieder, Harold, Sorensen, Thorkild I. A., Spector, Tim D., Strachan, David P., Uitterlinden, Andre G., Wareham, Nicholas J., Widen, Elisabeth, Zygmunt, Marek, Murray, Anna, Easton, Douglas F., Stefansson, Kari, Murabito, Joanne M., Ong, Ken K., the ReproGen Consortium and Middeldorp, Christel (2014) Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature, 514 7520: 92-97. doi:10.1038/nature13545

  • Rahmioglu, Nilufer, Nyholt, Dale R., Morris, Andrew P., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2014) Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human Reproduction Update, 20 5: 702-716. doi:10.1093/humupd/dmu015

  • 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

  • Westra, Harm-Jan, Peters, Marjolein J., Esko, Tonu, Yaghootkar, Hanieh, Schurmann, Claudia, Kettunen, Johannes, Christiansen, Mark W., Fairfax, Benjamin P., Schramm, Katharina, Powell, Joseph E., Zhernakova, Alexandra, Zhernakova, Daria V., Veldink, Jan H., Van den Berg, Leonard H., Karjalainen, Juha, Withoff, Sebo, Uitterlinden, Andre G., Hofman, Albert, Rivadeneira, Fernando, Hoen, Peter A. C't, Reinmaa, Eva, Fischer, Krista, Nelis, Mari, Milani, Lili, Melzer, David, Ferrucci, Luigi, Singleton, Andrew B., Hernandez, Dena G., Nalls, Michael A., Homuth, Georg, Nauck, Matthias, Radke, Doerte, Voelker, Uwe, Perola, Markus, Salomaa, Veikko, Brody, Jennifer, Suchy-Dicey, Astrid, Gharib, Sina A., Enquobahrie, Daniel A., Lumley, Thomas, Montgomery, Grant W., Makino, Seiko, Prokisch, Holger, Herder, Christian, Roden, Michael, Grallert, Harald, Meitinger, Thomas, Strauch, Konstantin, Li, Yang, Jansen, Ritsert C., Visscher, Peter M., Knight, Julian C., Psaty, Bruce M., Ripatti, Samuli, Teumer, Alexander, Frayling, Timothy M., Metspalu, Andres, van Meurs, Joyce B. J. and Franke, Lude (2013) Systematic identification of trans eQTLs as putative drivers of known disease associations. Nature Genetics, 45 10: 1238-U195. doi:10.1038/ng.2756

  • 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

  • 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, 22 456-466. doi:10.1101/gr.126540.111

  • 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., Boerwinkle E., Broekmans F.J., Burri A., Campbell H., Chanock S.J., Chen C., Cornelis M.C., Corre T., Coviello A.D., D'Adamo P., Davies G., De Faire U., De Geus E.J.C., Deary I.J., Dedoussis G.V.Z., Deloukas P., Ebrahim S., Eiriksdottir G., Emilsson V., Eriksson J.G., Fauser B.C.J.M., Ferreli L., Ferrucci L., Fischer K., Folsom A.R., Garcia M.E., Gasparini P., Gieger C., Glazer N., Grobbee D.E., Hall P., Haller T., Hankinson S.E., Hass M., Hayward C., Heath A.C., Hofman A., Ingelsson E., Janssens A.C.J.W., Johnson A.D., Karasik D., Kardia S.L.R., Keyzer J., Kiel D.P., Kolcic I., Kutalik Z., Lahti J., Lai S., Laisk T., Laven J.S.E., Lawlor D.A., Liu J., Lopez L.M., Louwers Y.V., Magnusson P.K.E., Marongiu M., Martin N.G., Klaric I.M., Masciullo C., McKnight B., Medland S.E., Melzer D., Mooser V., Navarro P., Newman A.B., Nyholt D.R., Onland-Moret N.C., Palotie A., Pare G., Parker A.N., Pedersen N.L., Peeters P.H.M., Pistis G., Plump A.S., Polasek O., Pop V.J.M., Psaty B.M., R Currency Signikkonen K., Rehnberg E., Rotter J.I., Rudan I., Sala C., Salumets A., Scuteri A., Singleton A., Smith J.A., Snieder H., Soranzo N., Stacey S.N., Starr J.M., Stathopoulou M.G., Stirrups K., Stolk R.P., Styrkarsdottir U., Sun Y.V., Tenesa A., Thorand B., Toniolo D., Tryggvadottir L., Tsui K., Ulivi S., Van Dam R.M., Van Der Schouw Y.T., Van Gils C.H., Van Nierop P., Vink J.M., Visscher P.M., Voorhuis M., Waeber G., Wallaschofski H., Wichmann H.E., Widen E., Wijnands-Van Gent C.J.M., Willemsen G., Wilson J.F., Wolffenbuttel B.H.R., Wright A.F., Yerges-Armstrong L.M., Zemunik T., Zgaga L., Zillikens M.C., Zygmunt M., Arnold A.M., Boomsma D.I., Buring J.E., Crisponi L., Demerath E.W., Gudnason V., Harris T.B., Hu F.B., Hunter D.J., Launer L.J., Metspalu A., Montgomery G.W., Oostra B.A., Ridker P.M., Sanna S., Schlessinger D., Spector T.D., Stefansson K., Streeten E.A., Thorsteinsdottir U., Uda M., Uitterlinden A.G., Van Duijn C.M., Volzke H., Murray A., Murabito J.M., Visser J.A. and 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

  • 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

Journal Article

  • Mills, Natalie, 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

  • 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

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  • Rahmioglu, Nilufer, Nyholt, Dale R., Morris, Andrew P., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2014) Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets. Human Reproduction Update, 20 5: 702-716. doi:10.1093/humupd/dmu015

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  • 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

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  • Dumenil, Troy D., Wockner, Leesa F., Bettington, Mark, Mckeone, Diane M., Klein, Kerenaftali, Bowdler, Lisa M., Montgomery, Grant W., Leggett, Barbara A. and Whitehall, Vicki L. J. (2014) Genome-wide DNA methylation analysis of formalin-fixed paraffin embedded colorectal cancer tissue. Genes Chromosomes and Cancer, 53 7: 537-548. doi:10.1002/gcc.22164

  • 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

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  • 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., Nicholson, George, Clegg, Deborah J., Person, Thomas, Krohn, Jon P., Bauer, Sabrina, Buechler, Christa, Eisinger, Kristina, Bonnefond, Amelie, Froguel, Philippe, Hottenga, Jouke-Jan, Prokopenko, Inga, Waite, Lindsay L., Harris, Tamara B., Smith, Albert Vernon, Shuldiner, Alan R., McArdle, Wendy L., Caulfield, Mark J., Munroe, Patricia B., Gronberg, Henrik, Chen, Yii-Der Ida, Li, Guo, Beckmann, Jacques S., Johnson, Toby, Thorsteinsdottir, Unnur, Teder-Laving, Maris, Khaw, Kay-Tee, Wareham, Nicholas J., Zhao, Jing Hua, Amin, Najaf, Oostra, Ben A., Kraja, Aldi T., Province, Michael A., Cupples, L. 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L., Leach, Irene Mateo, Navis, Gerjan, van der Harst, Pim, Martin, Nicholas G., Medland, Sarah E., Montgomery, Grant W., Yang, Jian, Chasman, Daniel I., Ridker, Paul M., Rose, Lynda M., Lehtimaki, Terho, Raitakari, Olli, Absher, Devin, Iribarren, Carlos, Basart, Hanneke, Hovingh, Kees G., Hyppoenen, Elina, Power, Chris, Anderson, Denise, Beilby, John P., Hui, Jennie, Jolley, Jennifer, Sager, Hendrik, Bornstein, Stefan R., Schwarz, Peter E. H., Kristiansson, Kati, Perola, Markus, Lindstrom, Jaana, Swift, Amy J., Uusitupa, Matti, Atalay, Mustafa, Lakka, Timo A., Rauramaa, Rainer, Bolton, Jennifer L., Fowkes, Gerry, Fraser, Ross M., Price, Jackie F., Fischer, Krista, KrjutAikov, Kaarel, Metspalu, Andres, Mihailov, Evelin, Langenberg, Claudia, Luan, Jian'an, Ong, Ken K., Chines, Peter S., Keinanen-Kiukaanniemi, Sirkka M., Saaristo, Timo E., Edkins, Sarah, Franks, Paul W., Hallmans, Goran, Shungin, Dmitry, Morris, Andrew David, Palmer, Colin N. A., Erbel, Raimund, Moebus, Susanne, Noethen, Markus M., Pechlivanis, Sonali, Hveem, Kristian, Narisu, Narisu, Hamsten, Anders, Humphries, Steve E., Strawbridge, Rona J., Tremoli, Elena, Grallert, Harald, Thorand, Barbara, Illig, Thomas, Koenig, Wolfgang, Mueller-Nurasyid, Martina, Peters, Annette, Boehm, Bernhard O., Kleber, Marcus E., Maerz, Winfried, Winkelmann, Bernhard R., Kuusisto, Johanna, Laakso, Markku, Arveiler, Dominique, Cesana, Giancarlo, Kuulasmaa, Kari, Virtamo, Jarmo, Yarnell, John W. G., Kuh, Diana, Wong, Andrew, Lind, Lars, de Faire, Ulf, Gigante, Bruna, Magnusson, Patrik K. E., Pedersen, Nancy L., Dedoussis, George, Dimitriou, Maria, Kolovou, Genovefa, Kanoni, Stavroula, Stirrups, Kathleen, Bonnycastle, Lori L., Njolstad, Inger, Wilsgaard, Tom, Ganna, Andrea, Rehnberg, Emil, Hingorani, Aroon, Kivimaki, Mika, Kumari, Meena, Assimes, Themistocles L., Barroso, Ine S., Boehnke, Michael, Borecki, Ingrid B., Deloukas, Panos, Fox, Caroline S., Frayling, Timothy, Groop, Leif C., Haritunians, Talin, Hunter, David, Ingelsson, Erik, Kaplan, Robert, Mohlke, Karen L., O'Connell, Jeffrey R., Schlessinger, David, Strachan, David P., Stefansson, Kari, van Duijn, Cornelia M., Abecasis, Goncalo R., McCarthy, Mark I., Hirschhorn, Joel N., Qi, Lu, Loos, Ruth J. F., Lindgren, Cecilia M., North, Kari E., Heid, Iris M., DIAGRAM Consortium and MAGIC Investigators (2013) Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. 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  • 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

  • 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

  • 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: e1003502.1-e1003502.10. doi:10.1371/journal.pgen.1003502

  • Rogers, Peter A. W., D'Hooghe, Thomas M., Fazleabas, Asgerally, Giudice, Linda C., Montgomery, Grant W., Petraglia, Felice and Taylor, Robert N. (2013) Defining future directions for endometriosis research: workshop report from the 2011 World Congress of Endometriosis in Montpellier, France. Reproductive Sciences, 20 5: 483-499. doi:10.1177/1933719113477495

  • 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

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A., Palotie, Aarno, Peden, John F., Pedersen, Nancy, Peters, Annette, Polasek, Ozren, Pouta, Anneli, Pramstaller, Peter P., Prokopenko, Inga, Puetter, Carolin, Radhakrishnan, Aparna, Raitakari, Olli, Rendon, Augusto, Rivadeneira, Fernando, Rudan, Igor, Saaristo, Timo E., Sambrook, Jennifer G., Sanders, Alan R., Sanna, Serena, Saramies, Jouko, Schipf, Sabine, Schreiber, Stefan, Schunkert, Heribert, Shin, So-Youn, Signorini, Stefano, Sinisalo, Juha, Skrobek, Boris, Soranzo, Nicole, Stancakova, Alena, Stark, Klaus, Stephens, Jonathan C., Stirrups, Kathleen, Stolk, Ronald P., Stumvoll, Michael, Swift, Amy J., Theodoraki, Eirini V., Thorand, Barbara, Tregouet, David-Alexandre, Tremoli, Elena, Van der Klauw, Melanie M., van Meurs, Joyce B. J., Vermeulen, Sita H., Viikari, Jorma, Virtamo, Jarmo, Vitart, Veronique, Waeber, Gerard, Wang, Zhaoming, Widen, Elisabeth, Wild, Sarah H., Willemsen, Gonneke, Winkelmann, Bernhard R., Witteman, Jacqueline C. M., Wolffenbuttel, Bruce H. 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A., Spector, Timothy D., Stefansson, Kari, Tonjes, Anke, Tuomilehto, Jaakko, Uitterlinden, Andre G., Uusitupa, Matti, van der Harst, Pim, Vollenweider, Peter, Wallaschofski, Henri, Wareham, Nicholas J., Watkins, Hugh, Wichmann, H-Erich, Wilson, James F., Abecasis, Goncalo R., Assimes, Themistocles L., Barroso, Ines, Boehnke, Michael, Borecki, Ingrid B., Deloukas, Panos, Fox, Caroline S., Frayling, Timothy, Groop, Leif C., Haritunian, Talin, Heid, Iris M., Hunter, David, Kaplan, Robert C., Karpe, Fredrik, Moffatt, Miriam F., Mohlke, Karen L., O'Connell, Jeffrey R., Pawitan, Yudi, Schadt, Eric E., Schlessinger, David, Steinthorsdottir, Valgerdur, Strachan, David P., Thorsteinsdottir, Unnur, van Duijn, Cornelia M., Visscher, Peter M., Di Blasio, Anna Maria, Hirschhorn, Joel N., Lindgren, Cecilia M., Morris, Andrew P., Meyre, David, Scherag, Andr, McCarthy, Mark I., Speliotes, Elizabeth K., North, Kari E., Loos, Ruth J. F. and 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

  • 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

  • Perry, John R. B., Corre, Tanguy, Esko, Tonu, Chasman, Daniel I., Fischer, Krista, Franceschini, Nora, He, Chunyan, Kutalik, Zoltan, Mangino, Massimo, Rose, Lynda M., Smith, Albert Vernon, Stolk, Lisette, Sulem, Patrick, Weedon, Michael N., Zhuang, Wei V., Arnold, Alice, Ashworth, Alan, Bergmann, Sven, Buring, Julie E., Burri, Andrea, Chen, Constance, Cornelis, Marilyn C., Couper, David J., Goodarzi, Mark O., Gudnason, Vilmundur, Harris, Tamara, Hofman, Albert, Jones, Michael, Kraft, Peter, Launer, Lenore, Laven, Joop S. E., Li, Guo, McKnight, Barbara, Masciullo, Corrado, Milani, Lili, Orr, Nicholas, Psaty, Bruce M., Ridker, Paul M., Rivadeneira, Fernando, Sala, Cinzia, Salumets, Andres, Schoemaker, Minouk, Traglia, Michela, Waeber, Gerard, Chanock, Stephen J., Demerath, Ellen W., Garcia, Melissa, Hankinson, Susan E., Hu, Frank B., Hunter, David J., Lunetta, Kathryn L., Metspalu, Andres, Montgomery, Grant W., Murabito, Joanne M., Newman, Anne B., Ong, Ken K., Spector, Tim D., Stefansson, Kari, Swerdlow, Anthony J., Thorsteinsdottir, Unnur, Van Dam, Rob M., Uitterlinden, Andre G., Visser, Jenny A., Vollenweider, Peter, Toniolo, Daniela and Murray, Anna (2013) A genome-wide association study of early menopause and the combined impact of identified variants. Human Molecular Genetics, 22 7: 1465-1472. doi:10.1093/hmg/dds551

  • 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

  • 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

  • Hacker, Elke, Nagore, Eduardo, Cerroni, Lorenzo, Woods, Susan L., Hayward, Nicholas K., Chapman, Brett, Montgomery, Grant W., Soyer, H. Peter and Whiteman, David C. (2013) NRAS and BRAF mutations in cutaneous melanoma and the association with MC1R genotype: findings from spanish and austrian populations. Journal of Investigative Dermatology, 133 4: 1027-1033. doi:10.1038/jid.2012.385

  • 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

  • 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

  • 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

  • Verhoeven V.J.M., Hysi P.G., Wojciechowski R., Fan Q., Guggenheim J.A., Hohn R., Macgregor S., Hewitt A.W., Nag A., Cheng C.-Y., Yonova-Doing E., Zhou X., Ikram M.K., Buitendijk G.H.S., Mcmahon G., Kemp J.P., Pourcain B.S., Simpson C.L., Makela K.-M., Lehtimaki T., Kahonen M., Paterson A.D., Hosseini S.M., Wong H.S., Xu L., Jonas J.B., Parssinen O., Wedenoja J., Yip S.P., Ho D.W.H., Pang C.P., Chen L.J., Burdon K.P., Craig J.E., Klein B.E.K., Klein R., Haller T., Metspalu A., Khor C.-C., Tai E.-S., Aung T., Vithana E., Tay W.-T., Barathi V.A., Chen P., Li R., Liao J., Zheng Y., Ong R.T., Doring A., Evans D.M., Timpson N.J., Verkerk A.J.M.H., Meitinger T., Raitakari O., Hawthorne F., Spector T.D., Karssen L.C., Pirastu M., Murgia F., Ang W., Mishra A., Montgomery G.W., Pennell C.E., Cumberland P.M., Cotlarciuc I., Mitchell P., Wang J.J., Schache M., Janmahasathian S., Igo Jr. R.P., Lass J.H., Chew E., Iyengar S.K., Gorgels T.G.M.F., Rudan I., Hayward C., Wright A.F., Polasek O., Vatavuk Z., Wilson J.F., Fleck B., Zeller T., Mirshahi A., Muller C., Uitterlinden A.G., Rivadeneira F., Vingerling J.R., Hofman A., Oostra B.A., Amin N., Bergen A.A.B., Teo Y.-Y., Rahi J.S., Vitart V., Williams C., Baird P.N., Wong T.-Y., Oexle K., Pfeiffer N., Mackey D.A., Young T.L., Van Duijn C.M., Saw S.-M., Bailey-Wilson J.E., Stambolian D., Klaver C.C. and Hammond C.J. (2013) Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nature Genetics, 45 3: 314-318. doi:10.1038/ng.2554

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  • 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

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  • 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, Robertson, Colin F., Viikari, Jorma, Widen, Elisabeth, Wjst, Matthias, Jarvis, Deborah L., Montgomery, Grant W., Thompson, Philip J., Wareham, Nick, Eriksson, Johan, Jousilahti, Pekka, Laitinen, Tarja, Pekkanen, Juha, Raitakari, Olli T., O'Connor, George T., Salomaa, Veikko, Jarvelin, Marjo-Riitta and 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: e44008-1-e44008-10. doi:10.1371/journal.pone.0044008

  • 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, Vermeulen, Sita H., Heath, Andrew C., Wright, Alan, Polasek, Ozren, Kovacevic, Sanja B., Hastie, Nicholas D., Franke, Barbara, Boomsma, Dorret I., Martin, Nicholas G., Rujescu, Dan, Wilson, James F., Buitelaar, Jan, Pendleton, Neil, Rudan, Igor and 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

  • 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, Thompson, John R., Vink, Jacqueline M., Vogelzangs, Nicole, Wenzlaff, Angela S., Wheeler, William, Xiao, Xiangjun, Yang, Bao-Zhu, Aggen, Steven H., Balmforth, Anthony J., Baumeister, Sebastian E., Beaty, Terri, Bennett, Siiri, Bergen, Andrew W., Boyd, Heather A., Broms, Ulla, Campbell, Harry, Chatterjee, Nilanjan, Chen, Jingchun, Cheng, Yu-Ching, Cichon, Sven, Couper, David, Cucca, Francesco, Dick, Danielle M., Foroud, Tatiana, Furberg, Helena, Giegling, Ina, Gu, Fangyi, Hall, Alistair S., Hallfors, Jenni, Han, Shizhong, Hartmann, Annette M., Hayward, Caroline, Heikkila, Kauko, Hewitt, John K., Hottenga, Jouke Jan, Jensen, Majken K., Jousilahti, Pekka, Kaakinen, Marika, Kittner, Steven J., Konte, Bettina, Korhonen, Tellervo, Landi, Maria-Teresa, Laatikainen, Tiina, Leppert, Mark, Levy, Steven M., Mathias, Rasika A., McNeil, Daniel W., Medland, Sarah E., Montgomery, Grant W., Muley, Thomas, Murray, Tanda, Nauck, Matthias, North, Kari, Pergadia, Michele, Polasek, Ozren, Ramos, Erin M., Ripatti, Samuli, Risch, Angela, Ruczinski, Ingo, Rudan, Igor, Salomaa, Veikko, Schlessinger, David, Styrkarsdottir, Unnur, Terracciano, Antonio, Uda, Manuela, Willemsen, Gonneke, Wu, Xifeng, Abecasis, Goncalo, Barnes, Kathleen, Bickeboeller, Heike, Boerwinkle, Eric, Boomsma, Dorret I., Caporaso, Neil, Duan, Jubao, Edenberg, Howard J., Francks, Clyde, Gejman, Pablo V., Gelernter, Joel, Grabe, Hans Joergen, Hops, Hyman, Jarvelin, Marjo-Riitta, Viikari, Jorma, Kahonen, Mika, Kendler, Kenneth S., Lehtimaki, Terho, Levinson, Douglas F., Marazita, Mary L., Marchini, Jonathan, Melbye, Mads, Mitchell, Braxton D., Murray, Jeffrey C., Nothen, Markus M., Penninx, Brenda W., Raitakari, Olli, Rietschel, Marcella, Rujescu, Dan, Samani, Nilesh J., Sanders, Alan R., Schwartz, Ann G., Shete, Sanjay, Shi, Jianxin, Spitz, Margaret, Stefansson, Kari, Swan, Gary E., Thorgeirsson, Thorgeir, Volzke, Henry, Wei, Qingyi, Wichmann, H. -Erich, Amos, Christopher I., Breslau, Naomi, Cannon, Dale S., Ehringer, Marissa, Grucza, Richard, Hatsukami, Dorothy, Heath, Andrew, Johnson, Eric O., Kaprio, Jaakko, Madden, Pamela, Martin, Nicholas G., Stevens, Victoria L., Stitzel, Jerry A., Weiss, Robert B., Kraft, Peter and 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

  • 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

  • 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

  • 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

  • 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, Lopez, Lorna M., Sala, Cinzia, Lahti, Jari, Laatikainen, Tiina, Prokopenko, Inga, Kals, Mart, Viikari, Jorma, Yang, Jian, Pouta, Anneli, Estrada, Karol, Hofman, Albert, Freimer, Nelson, Martin, Nicholas G., Kahonen, Mika, Milani, Lili, Heliovaara, Markku, Vartiainen, Erkki, Raikkonen, Katri, Masciullo, Corrado, Starr, John M., Hicks, Andrew A., Esposito, Laura, Kolcic, Ivana, Farrington, Susan M., Oostra, Ben, Zemunik, Tatijana, Campbell, Harry, Kirin, Mirna, Pehlic, Marina, Faletra, Flavio, Porteous, David, Pistis, Giorgio, Widen, Elisabeth, Salomaa, Veikko, Koskinen, Seppo, Fischer, Krista, Lehtimaki, Terho, Heath, Andrew, McCarthy, Mark I., Rivadeneira, Fernando, Montgomery, Grant W., Tiemeier, Henning, Hartikainen, Anna-Liisa, Madden, Pamela A. F., d'Adamo, Pio, Hastie, Nicholas D., Gyllensten, Ulf, Wright, Alan F., van Duijn, Cornelia M., Dunlop, Malcolm, Rudan, Igor, Gasparini, Paolo, Pramstaller, Peter P., Deary, Ian J., Toniolo, Daniela, Eriksson, Johan G., Jula, Antti, Raitakari, Olli T., Metspalu, Andres, Perola, Markus, Jarvelin, Marjo-Riitta, Uitterlinden, Andre, Visscher, Peter M. and Wilson, James F. (2012) Evidence of inbreeding depression on human height. Plos Genetics, 8 7: . doi:10.1371/journal.pgen.1002655

  • 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: 3050-3062. doi:10.1093/hmg/dds114

  • 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

  • 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

  • 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, Vollenweider, Peter, Spector, Tim D., Dedoussis, George, Martin, Nicholas G., Kiemeney, Lambertus A., Mooser, Vincent, Stefansson, Kari, Hinds, David A., Noethen, Markus M. and Richards, J. Brent (2012) Six novel susceptibility loci for early-onset androgenetic alopecia and their unexpected association with common diseases. PLoS Genetics, 8 5: . doi:10.1371/journal.pgen.1002746

  • 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 . doi:10.1038/tp.2012.37

  • van Koolwijk, Leonieke M. E., Ramdas, Wishal D., Ikram, M. Kamran, Jansonius, Nomdo M., Pasutto, Francesca, Hysi, Pirro G., Macgregor, Stuart, Janssen, Sarah F., Hewitt, Alex W., Viswanathan, Ananth C., ten Brink, Jacoline B., Hosseini, S. Mohsen, Amin, Najaf, Despriet, Dominiek D. G., Willemse-Assink, Jacqueline J. M., Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S., Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y., Gramer, Eugen, Welge-Luessen, Ulrich, Montgomery, Grant W., Carbonaro, Francis, Young, Terri L., The DCCT/EDIC Research Group, Bellenguez, Celine, McGuffin, Peter, Foster, Paul J., Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y., Czudowska, Monika A., Hofman, Albert, Uitterlinden, Andre G., Wolfs, Roger C. W., de Jong, Paulus T. V. M., Oostra, Ben A., Paterson, Andrew D., Wellcome Trust Case Control Consortium 2, Mackey, David A., Bergen, Arthur A. B., Reis, Andre, Hammond, Christopher J., Vingerling, Johannes R., Lemij, Hans G., Klaver, Caroline C. W., van Duijn, Cornelia M. and Brown, Matthew A. (2012) Common genetic determinants of intraocular pressure and primary open-angle glaucoma. PLoS Genetics, 8 5: e1002611.1-e1002611.13. doi:10.1371/journal.pgen.1002611

  • 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, Loth, Eva, Lourdusamy, Anbarasu, Mattingsdal, Morten, Mohnke, Sebastian, Maniega, Susana Muñoz, Nho, Kwangsik, Nugent, Allison C., O'Brien, Carol, Papmeyer, Martina, Pütz, Benno, Ramasamy, Adaikalavan, Rasmussen, Jerod, Rijpkema, Mark, Risacher, Shannon L., Roddey, J. Cooper, Rose, Emma J., Ryten, Mina, Shen, Li, Sprooten, Emma, Strengman, Eric, Teumer, Alexander, Trabzuni, Daniah, Turner, Jessica, van Eijk, Kristel, van Erp, Theo G. M., van Tol, Marie-Jose, Wittfeld, Katharina, Wolf, Christiane, Woudstra, Saskia, Aleman, Andre, Alhusaini, Saud, Almasy, Laura, Binder, Elisabeth B., Brohawn, David G., Cantor, Rita M., Carless, Melanie A., Corvin, Aiden, Czisch, Michael, Curran, Joanne E., Davies, Gail, de Almeida, Marcio A. A., Delanty, Norman, Depondt, Chantal, Duggirala, Ravi, Dyer, Thomas D., Erk, Susanne, Fagerness, Jesen, Fox, Peter T., Freimer, Nelson B., Gill, Michael, Göring, Harald H. H., Hagler, Donald J., Hoehn, David, Holsboer, Florian, Hoogman, Martine, Hosten, Norbert, Jahanshad, Neda, Johnson, Matthew P., Kasperaviciute, Dalia, Kent Jr., Jack W., Kochunov, Peter, Lancaster, Jack L., Lawrie, Stephen M., Liewald, David C., Mandl, René, Matarin, Mar, Mattheisen, Manuel, Meisenzahl, Eva, Melle, Ingrid, Moses, Eric K., Mühleisen, Thomas W., Nauck, Matthias, Nöthen, Markus M., Olvera, Rene L., Pandolfo, Massimo, Pike, G. Bruce, Puls, Ralf, Reinvang, Ivar, Rentería, Miguel E., Rietschel, Marcella, Roffman, Joshua L., Royle, Natalie A., Rujescu, Dan, Savitz, Jonathan, Schnack, Hugo G., Schnell, Knut, Seiferth, Nina, Smith, Colin, Steen, Vidar M., Hernández, Maria C. Valdés, Van den Heuvel, Martijn, van der Wee, Nic J., Van Haren, Neeltje E. M., Veltman, Joris A., Völzke, Henry, Walker, Robert, Westlye, Lars T., Whelan, Christopher D., Agartz, Ingrid, Boomsma, Dorret I., Cavalleri, Gianpiero L., Dale, Anders M., Djurovic, Srdjan, Drevets, Wayne C., Hagoort, Peter, Hall, Jeremy, Heinz, Andreas, Jack Jr., Clifford R., Foroud, Tatiana M, Le Hellard, Stephanie, Macciardi, Fabio, Montgomery, Grant W., Poline, Jean Baptiste, Porteous, David J., Sisodiya, Sanjay M., Starr, John M., Sussmann, Jessika, Toga, Arthur W., Veltman, Dick J., Walte, Henrik, Weiner, Michael W., the Alzheimer's Disease Neuroimaging Initiative (ADNI), EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth Study Group (SYS), Bis, Joshua C., Ikram, M. Arfan, Smith, Albert V., Gudnason, Vilmundur, Tzourio, Christophe, Vernooij, Meike W, Launer, Lenore J., DeCarli, Charles, Seshadri, Sudha, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Andreassen, Ole A., Apostolova, Liana G., Bastin, Mark E., Blangero, John, Brunner, Han G., Buckner, Randy L., Cichon, Sven, Coppola, Giovanni, de Zubicaray, Greig I., Deary, Ian J., Donohoe, Gary, de Geus, Eco J. C., Espeseth, Thomas, Fernández, Guillén, Glahn, David C., Grabe, Hans J., Hardy, John, Pol, Hilleke E. Hulshoff, Jenkinson, Mark, Kahn, René S., McDonald, Colm, McIntosh, Andrew M., McMahon, Francis J., McMahon, Katie L., Meyer-Lindenberg, Andreas, Morris, Derek W., Müller-Myhsok, Bertram, Nichols, Thomas E., Ophoff, Roel A., Paus, Tomas, Pausova, Zdenka, Penninx, Brenda W., Potkin, Steven G., Sämann, Philipp G., Saykin, Andrew J., Schumann, Gunter, Smoller, Jordan W., Wardlaw, Joanna M., Weale, Michael E., Martin, Nicholas G., Franke, Barbara, Wright, Margaret J., Thompson, Paul M., for the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium, Danoy, Patrick and 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

  • 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

  • Hollis-Moffatt, Jade E., Phipps-Green, Amanda J., Chapman, Brett, Jones, Gregory T., van Rij, Andre, Gow, Peter J., Harrison, Andrew A., Highton, John, Jones, Peter B., Montgomery, Grant W., Stamp, Lisa K., Dalbeth, Nicola and Merriman, Tony R. (2012) The renal urate transporter SLC17A1 locus: confirmation of association with gout. Arthritis Research and Therapy, 14 . doi:10.1186/ar3816

  • 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: . doi:10.1371/journal.pone.0035605

  • 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, Craig, Ian W., Lewis, Cathryn, Sham, Pak, Crowe, Raymond. R., Flint, Jonathan and 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

  • 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

  • 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

  • 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: . doi:10.1038/tp.2012.27

  • 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

  • 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: e35430.1-e35430.9. doi:10.1371/journal.pone.0035430

  • 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, 22 456-466. doi:10.1101/gr.126540.111

  • Tomlinson, Ian P. M., Houlston, Richard S., Montgomery, Grant W., Sieber, Oliver M. and Dunlop, Malcolm G. (2012) Investigation of the effects of DNA repair gene polymorphisms on the risk of colorectal cancer. Mutagenesis, 27 2: 219-223. doi:10.1093/mutage/ger070

  • 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, Houlston, Richard S. and 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: 934-946. doi:10.1093/hmg/ddr523

  • O'Callaghan, Michael E., MacLennan, Alastair H., Gibson, Catherine S., McMichael, Gai L., Haan, Eric A., Broadbent, Jessica L., Goldwater, Paul N., Painter, Jodie N., Montgomery, Grant W. and Dekker, Gus A. (2012) Fetal and maternal candidate single nucleotide polymorphism associations with cerebral palsy: a case-control study. Pediatrics, 129 2: E414-E423. doi:10.1542/peds.2011-0739

  • 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

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  • Sklar, Pamela, Ripke, Stephan, Scott, Laura J., Andreassen, Ole A., Cichon, Sven, Craddock, Nick, Edenberg, Howard J., Nurnberger, John I., Jr., Rietschel, Marcella, Blackwood, Douglas, Corvin, Aiden, Flickinger, Matthew, Guan, Weihua, Mattingsdal, Morten, McQuillin, Andrew, Kwan, Phoenix, Wienker, Thomas F., Daly, Mark, Dudbridge, Frank, Holmans, Peter A., Lin, Danyu, Burmeister, Margit, Greenwood, Tiffany A., Hamshere, Marian L., Muglia, Pierandrea, Smith, Erin N., Zandi, Peter P., Nievergelt, Caroline M., McKinney, Rebecca, Shilling, Paul D., Schork, Nicholas J., Bloss, Cinnamon S., Foroud, Tatiana, Koller, Daniel L., Gershon, Elliot S., Liu, Chunyu, Badner, Judith A., Scheftner, William A., Lawson, William B., Nwulia, Evaristus A., Hipolito, Maria, Coryell, William, Rice, John, Byerley, William, McMahon, Francis J., Schulze, Thomas G., Berrettini, Wade, Lohoff, Falk W., Potash, James B., Mahon, Pamela B., McInnis, Melvin G., Zoellner, Sebastian, Zhang, Peng, Craig, David W., Szelinger, Szabocls, Barrett, Thomas B., Breuer, Rene, Meier, Sandra, Strohmaier, Jana, Witt, Stephanie H., Tozzi, Federica, Farmer, Anne, McGuffin, Peter, Strauss, John, Xu, Wei, Kennedy, James L., Vincent, John B., Matthews, Keith, Day, Richard, Ferreira, Manuel A., O'Dushlaine, Colm, Perlis, Roy, Raychaudhuri, Soumya, Ruderfer, Douglas, Lee, Phil H., Smoller, Jordan W., Li, Jun, Absher, Devin, Bunney, William E., Barchas, Jack D., Schatzberg, Alan F., Jones, Edward G., Meng, Fan, Thompson, Robert C., Watson, Stanley J., Myers, Richard M., Akil, Huda, Boehnke, Michael, Chambert, Kim, Moran, Jennifer, Scolnick, Ed, Djurovic, Srdjan, Melle, Ingrid, Morken, Gunnar, Gill, Michael, Morris, Derek, Quinn, Emma, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Schumacher, Johannes, Maier, Wolfgang, Steffens, Michael, Propping, Peter, Noethen, Markus M., Anjorin, Adebayo, Bass, Nick, Gurling, Hugh, Kandaswamy, Radhika, Lawrence, Jacob, McGhee, Kevin, McIntosh, Andrew, McLean, Alan W., Muir, Walter J., Pickard, Benjamin S., Breen, Gerome, St Clair, David, Caesar, Sian, Gordon-Smith, Katherine, Jones, Lisa, Fraser, Christine, Green, Elaine K., Grozeva, Detelina, Jones, Ian R., Kirov, George, Moskvina, Valentina, Nikolov, Ivan, O'Donovan, Michael C., Owen, Michael J., Collier, David A., Elkin, Amanda, Williamson, Richard, Young, Allan H., Ferrier, I. Nicol, Stefansson, Kari, Stefansson, Hreinn, Porgeirsson, Porgeir, Steinberg, Stacy, Gustafsson, Omar, Bergen, Sarah E., Nimgaonkar, Vishwajit, Hultman, Christina, Landen, Mikael, Lichtenstein, Paul, Sullivan, Patrick, Schalling, Martin, Osby, Urban, Backlund, Lena, Frisen, Louise, Langstrom, Niklas, Jamain, Stephane, Leboyer, Marion, Etain, Bruno, Bellivier, Frank, Petursson, Hannes, Sigurosson, Engilbert, Mueller-Mysok, Bertram, Lucae, Susanne, Schwarz, Markus, Schofield, Peter R., Martin, Nick, Montgomery, Grant W., Lathrop, Mark, Oskarsson, Hogni, Bauer, Michael, Wright, Adam, Mitchell, Philip B., Hautzinger, Martin, Reif, Andreas, Kelsoe, John R. and Purcell, Shaun M. (2011) Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Nature Genetics, 43 10: 977-983. doi:10.1038/ng.943

  • 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

  • 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

  • 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: 1-9. doi:10.1186/1471-2350-12-123

  • 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

  • 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

  • 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: 3710-3717. doi:10.1093/hmg/ddr272

  • 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., Hirschhorn, Joel N., Walters, Haydn, Martin, Nicholas G., James, Alan, Jones, Graham, Abramson, Michael J., Robertson, Colin F., Dharmage, Shyamali C., Brown, Matthew A., Montgomery, Grant W., Thompson, Philip J. and for the Australian Asthma Genetics Consortium (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

  • 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

  • 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., Thorsteinsdottir, U., Stefansson, K., van Rooij, F. J. A., Aulchenko, Y. S., Hottenga, J. J., Rivadeneira, F. R., Hofman, A., Uitterlinden, A. G., Hammond, C. J., Shin, S- Y., Ikram, A., Witteman, J. C. M., Janssens, A. C. J. W., Snieder, H., Tiemeier, H., Wolfenbuttel, B. H. R., Oostra, B. A., Heath, A. C., Wichmann, E., Spector, T. D., Grabe, H. ., Boomsma, D. I., Martin, N. G. and 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

  • 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

  • Ligthart, Lannie, de Vries, Boukje, Smith, Albert V., Ikram, M. Arfan, Amin, Najaf, Hottenga, Jouke-Jan, Koelewijn, Stephany C., Kattenberg, V. Mathijs, de Moor, Marleen H. M., Janssens, A. Cecile J. W., Aulchenko, Yurii S., Oostra, Ben A., de Geus, Eco J. C., Smit, Johannes H., Zitman, Frans G., Uitterlinden, Andre G., Hofman, Albert, Willemsen, Gonneke, Nyholt, Dale R., Montgomery, Grant W., Terwindt, Gisela M., Gudnason, Vilmundur, Penninx, Brenda W. J. H., Breteler, Monique, Ferrari, Michel D., Launer, Lenore J., van Duijn, Cornelia M., van den Maagdenberg, Arn M. J. M. and Boomsma, Dorret I. (2011) Meta-analysis of genome-wide association for migraine in six population-based European cohorts. European Journal of Human Genetics, 19 8: 901-907. doi:10.1038/ejhg.2011.48

  • 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., Penninx, Brenda W., Wilson, James F., Rivadeneria, Fernando, Magnusson, Patrik K. E., Boomsma, Dorret I., Spector, Tim, Campbell, Harry, Hoehne, Birgit, Martin, Nicholas G., Oostra, Ben A., McCarthy, Mark, Peltonen-Palotie, Leena, Aulchenko, Yurii, Visscher, Peter M., Ripatti, Samuli, Janssens, A. Cecile J. W. and 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

  • 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

  • Tomlinson, Ian P. M., Carvajal-Carmona, Luis G., Dobbins, Sara E., Tenesa, Albert, Jones, Angela M., Howarth, Kimberley, Palles, Claire, Broderick, Peter, Jaeger, Emma E. M., Farrington, Susan, Lewis, Annabelle, Prendergast, James G. D., Pittman, Alan M., Theodoratou, Evropi, Olver, Bianca, Walker, Marion, Penegar, Steven, Barclay, Ella, Whiffin, Nicola, Martin, Lynn, Ballereau, Stephane, Lloyd, Amy, Gorman, Maggie, Lubbe, Steven, Howie, Bryan, Marchini, Jonathan, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Castells, Antoni, Carracedo, Angel, Castellvi-Bel, Sergi, Duggan, David, Conti, David, Cazier, Jean-Baptiste, Campbell, Harry, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G., Montgomery, Grant W., Young, Joanne, Baird, Paul N., Gallinger, Steven, Newcomb, Polly, Hopper, John, Jenkins, Mark A., Aaltonen, Lauri A., Kerr, David J., Cheadle, Jeremy, Pharoah, Paul, Casey, Graham, Houlston, Richard S. and Dunlop, Malcolm G. (2011) Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. PLoS Genetics, 7 6: . doi:10.1371/journal.pgen.1002105

  • 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: e20128.1-e20128.8. doi:10.1371/journal.pone.0020128

  • 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

  • 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

  • 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

  • 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

  • Spurdle, Amanda B., Thompson, Deborah J., Ahmed, Shahana, Ferguson, Kaltin, Healey, Catherine S., O'Mara, Tracy, Walker, Logan C., Montgomery, Stephen B., Dermitzakis, Emmanouil T., The Australian National Endometrial Cancer Study Group, Fahey, Paul, Montgomery, Grant W., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Lambrechts, Diether, Coenegrachts, Lieve, Vergote, Ignace, Amant, Frederic, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Helland, Harald, Scott, Rodney J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, National Study of Endometrial Cancer Genetics Group, Tomlinson, Ian, Gorman, Maggie, Howarth, Kimberley, Hodgson, Shirley, Garcia-Closas, Montserrat, Wentzensen, Nicolas, Yang, Hannah, Chanock, Stephen, Hall, Per, Czene, Kamila, Liu, Jianjun, Li, Jingmei, Shu, Xiao-Ou, Zheng, Wei, Long, Jirong, Xiang, Yong-Bing, Shah, Mitul, Morrison, Jonathan, Michailidou, Kyriaki, Pharoah, Paul D., Dunning, Alison M. and Easton, Douglas F. (2011) Genome-wide association study identifies a common variant associated with risk of endometrial cancer. Nature Genetics, 43 5: 451-454. doi:10.1038/ng.812

  • 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

  • Brennan, Patricia A., Hammen, Constance, Sylvers, Patrick, Bor, William, Najman, Jake, Lind, Penelope, Montgomery, Grant and Smith, Alicia K. (2011) Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes. Biological Psychology, 87 1: 99-105. doi:10.1016/j.biopsycho.2011.02.013

  • 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, Hamshere, Marian, O'Donovan, Michael C., Owen, Michael J., Craddock, Nick, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Reif, Andreas, Sasse, Johanna, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Mitchell, Philip B., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Gustafsson, Omar, Andreassen, Ole, Djurovic, Srdjan, Sigurdsson, Engilbert, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Kapur-Pojskic, Lejla, Oruc, Liliana, Rivas, Fabio, Mayoral, Fermin, Chuchalin, Alexander, Babadjanova, Gulja, Tiganov, Alexander S., Pantelejeva, Galina, Abramova, Lilia I., Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C., Czerski, Piotr M., Hauser, Joanna, Zimmer, Andreas, Lathrop, Mark, Schulze, Thomas G., Wienker, Thomas F., Schumacher, Johannes, Maier, Wolfgang, Propping, Peter, Rietschel, Marcella and 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

  • 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., Carr, J. Jeffrey, Feitosa, Mary F., Harris, Tamara B., Fox, Caroline S., Smith, Albert V., Kao, W. H. Linda, Hirschhorn, Joel N., Borecki, Ingrid B., GOLD Consortium, Martin, Nicholas G., Montgomery, Grant W., Yang, Jian and 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: e1001324.1-e1001324.14. doi:10.1371/journal.pgen.1001324

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  • 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

  • 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

  • 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, Uitterlinden, André G., Hofman, Albert, Tönjes, Anke, Kovacs, Peter, Hottenga, Jouke Jan, Willemsen, Gonneke, Vogelzangs, Nicole, Döring, Angela, Dahmen, Norbert, Nitz, Barbara, Pergadia, Michele L, Saez, Berta, De Diego, Veronica, Lezcano, Victoria, Garcia-Prats, Maria D., Ripatti, Samuli, Perola, Markus, Kettunen, Johannes, Hartikainen, Anna-Liisa, Pouta, Anneli, Laitinen, Jaana, Isohanni, Matti, Huei-Yi, Shen, Allen, Maxine, Krestyaninova, Maria, Hall, Alistair S., Jones, Gregory T., van Rij, Andre M., Mueller, Thomas, Dieplinger, Benjamin, Haltmayer, Meinhard, Jonsson, Steinn, Matthiasson, Stefan E., Oskarsson, Hogni, Tyrfingsson, Thorarinn, Kiemeney, Lambertus A., Mayordomo, Jose I., Lindholt, Jes S., Pedersen, Jesper Holst, Franklin, Wilbur A., Wolf, Holly, Montgomery, Grant W., Heath, Andrew C., Martin, Nicholas G., Madden, Pamela A. F., Giegling, Ina, Rujescu, Dan, Järvelin, Marjo-Riitta, Salomaa, Veikko, Stumvoll, Michael, Spector, Tim D., Wichmann, H.-Erich, Metspalu, Andres, Samani, Nilesh J., Penninx, Brenda W., Oostra, Ben A., Boomsma, Dorret I., Tiemeier, Henning, van Duijn, Cornelia M., Kaprio, Jaakko, Gulcher, Jeffrey R., The ENGAGE Consortium, McCarthy, Mark I., Peltonen, Leena, Thorsteinsdottir, Unnur and Stefansson, Kari (2010) Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nature Genetics, 42 5: 448-454. doi:10.1038/ng.573

  • 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

  • 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

  • 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

  • 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

  • Hoekstra, Chantal, Willemsen, Gonneke, van Beijsterveldt, Toos, Lambalk, Cornelius B., Montgomery, Grant W. and Boomsma, Dorret I. (2010) Body composition, smoking, and spontaneous dizygotic twinning. Fertility and Sterility, 93 3: 885-893. doi:10.1016/j.fertnstert.2008.10.012

  • 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

  • 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

  • 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

  • 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

  • Prodoehl, Mark J., Hatzirodos, Nicholas, Irving-Rodgers, Helen F., Zhao, Zhen Z., Painter, Jodie N., Hickey, Theresa E., Gibson, Mark A., Rainey, William E., Carr, Bruce R., Mason, Helen D., Norman, Robert J., Montgomery, Grant W. and Rodgers, Raymond J. (2009) Genetic and gene expression analyses of the polycystic ovary syndrome candidate gene fibrillin-3 and other fibrillin family members in human ovaries. Molecular Human Reproduction, 15 12: 829-841. doi:10.1093/molehr/gap072

  • 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

  • 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

  • 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

  • Visscher, Peter M. and Montgomery, Grant W. (2009) Genome-wide Association Studies and Human Disease From Trickle to Flood. Jama-Journal of the American Medical Association, 302 18: 2028-2029.

  • 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

  • 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

  • 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

  • Jamie E. Craig, Alex W. Hewitt, Amy E. McMellon, Anjali K. Henders, Lingjun Ma, Leanne Wallace, Shiwani Sharma, Kathryn P. Burdon, Peter M. Visscher, Grant W. Montgomery and Stuart MacGregor (2009) Rapid inexpensive genome-wide association using pooled whole blood. Genome Research, 19 11: 2075-2080. doi:10.1101/gr.094680.109

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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, Lubinski, J, Mackie, R, Malvehy, J, Mann, GJ, Martin, NG, Montgomery, GW, van Nieuwpoort, FA, Novakovic, S, Olsson, H, Puig, S, Weiss, M, van Workum, W, Zelenika, D, Brown, KM, Goldstein, AM, Gillanders, EM, Boland, A, Galan, P, Elder, DE, Gruis, NA, Hayward, NK, Lathrop, GM, Barrett, JH and 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

  • 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

  • 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

  • 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

  • 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

  • Rogers, Peter A. W., D'Hooghe, Thomas M., Fazleabas, Asgerally, Gargett, Caroline E., Giudice, Linda C., Montgomery, Grant W., Rombauts, Luk, Salamonsen, Lois A. and Zondervan, Krina T. (2009) Priorities for endometriosis research: recommendations from an international consensus workshop. Reproductive Sciences, 16 4: 335-346. doi:10.1177/1933719108330568

  • Woo, Jean, Tong, Stephen, Campbell, Megan J., Wallace, Leanne, Meagher, Simon, Montgomery, Grant W., Chao, Fay, Chan, Weng and Vollenhoven, Beverley (2009) Two Corpora Lutea Seen at 6-13 Weeks' Gestation Infers Dizygosity Among Spontaneous Same-Sexed Dichorionic Twins. Twin Research and Human Genetics, 12 2: 180-182.

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • Hoekstra, Chantal, Willemsen, Gonneke, van Beijsterveldt, Toos C. E. M., Montgomery, Grant W. and Boomsma, Dorret I. (2008) Familial twinning and fertility in Dutch mothers of twins. American Journal of Medical Genetics, Part A, 146A 24: 3147-3156. doi:10.1002/ajmg.a.32585

  • 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

  • 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

  • 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., Kubisch, Christian, Martin, Nicholas G., Wessman, Maija, Peltonen, Leena and 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

  • 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

  • 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

  • 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

  • Peters, Kirsten, Wiltshire, Steven, Henders, Anjali K., Dragovic, Milan, Badcock, Johanna C., Chandler, David, Howell, Sarah, Ellis, Chris, Bouwer, Sonja, Montgomery, Grant W., Palmer, Lyle J., Kalaydjieva, Luba and Jablensky, Assen (2008) Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 147B 7: 1159-1166. doi:10.1002/ajmg.b.30741

  • 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

  • Fowler, Elizabeth V., Doecke, James, Simms, Lisa A., Zhao, Zhen Zhen, Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Florin, Timothy H., Montgomery, Grant W., Cavanaugh, Juleen A. and Radford-Smith, Graham L. (2008) ATG16L1 T300A shows strong associations with disease subgroups in a large Australian IBD population: Further support for significant disease heterogeneity. The American Journal of Gastroenterology, 103 10: 2519-2526. doi:10.1111/j.1572-0241.2008.02023.x

  • 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

  • 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

  • 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

  • Zhao, Zhen Zhen, Nyholt, Dale R., Thomas, Shane, Treloar, Susan A. and Montgomery, Grant W. (2008) Polymorphisms in the vascular endothelial growth factor gene and the risk of familial endometriosis. Molecular Human Reproduction, 14 9: 531-538. doi:10.1093/molehr/gan043

  • Montgomery, Grant W., Nyholt, Dale R., Zhao, Zhen Zhen, Treloar, Susan A., Painter, Jodie N., Missmer, Stacey A., Zondervan, Krina T. and Kennedy, Stephen H. (2008) The search for genes contributing to endometriosis risk. Human Reproduction Update, 14 5: 447-457. doi:10.1093/humupd/dmn016

  • 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

  • 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., Giles, G. G., Armstrong, B. K., Aitken, J. F., Hopper, J. L., Martin, N. G., Trent, J. M., Mann, G. J. and Hayward, N. (2008) Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 7: 838-840. doi:10.1038/ng.163

  • Zhao, Zhu Zhen, Pollock, Pamela M., Thomas, Shane, Treloar, Susan A., Nyholt, Dale R. and Montgomery, Grant W. (2008) Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk. Human Reproduction, 23 7: 1661-1668. doi:10.1093/humrep/den035

  • 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

  • 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

  • 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

  • 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

  • van Beijsterveldt, C. E. M. Toos, Hoekstra, Chantal, Schats, Roel, Montgomery, Grant W., Willemsen, Gonneke and Boomsma, Dorret I. (2008) Mode of conception of twin pregnancies: willingness to reply to survey items and comparison of survey data to hospital records. Twin Research and Human Genetics, 11 3: 349-351. doi:10.1375/twin.11.3.349

  • McRae, Allan F., Byrne, Enda M., Zhao, Zhen Zhen, Montgomery, Grant W. and Visscher, Peter M. (2008) Power and SNP tagging in whole mitochondrial genome association studies. Genome Research, 18 6: 911-917. doi:10.1101/gr.074872.107

  • 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

  • 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. doi:10.1371/journal.pgen.1000074

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • Zhao, Zhen Zhen, Nyholt, Dale R., Le, Lien, Treloar, Susan A. and Montgomery, Grant W. (2008) Common variation in the CYP17A1 and IFIT1 genes on chromosome 10 does not contribute to the risk of endometriosis. The Open Reproductive Science Journal, 1 35-40. doi:10.2174/1874255600801010035

  • 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

  • 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

  • Macgregor, Stuart, Zhao, Zhen Zhen, Henders, Anjali, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008) Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays. Nucleic Acids Research, 36 6: . doi:10.1093/nar/gkm1060

  • 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

  • Doecke, J D, Zhao, Z Z, Stark, M S, Green, A C, Hayward, N K, Montgomery, G W, Webb, P M and Whiteman, D C (2008) Single nucleotide polymorphisms in obesity-related genes and the risk of esophageal cancers. Cancer Epidemiology, Biomarkers & Prevention, 17 4: 1007-1012. doi:10.1158/1055-9965.EPI-08-0023

  • 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

  • Ellis, MK, Zhao, ZZ, Chen, HG, Montgomery, GW, Li, YS and McManus, DP (2007) Analysis of the 5q31-33 locus shows an association between single nucleotide polymorphism variants in the IL-5 gene and symptomatic infection with the human blood fluke, Schistosoma japonicum. Journal of Immunology, 179 12: 8366-8371.

  • 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

  • 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

  • Zhao, Zhen Zhen, Nyholt, Dale R., Le, Lien, Thomas, Shane, Engwerda, Christian, Randall, Louise, Treloar, Susan A. and Montgomery, Grant W. (2007) Genetic variation in tumour necrosis factor and lymphotoxin is not associated with endometriosis in an Australian sample. Human Reproduction, 22 9: 2389-2397. doi:10.1093/humrep/dem182

  • 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

  • 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

  • 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

  • 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

  • Souter, Vivienne L., Parisi, Melissa A., Nyholt, Dale R., Kapur, Raj P., Henders, Anjali K., Opheim, Kent E., Gunther, Daniel F., Mitchell, Michael E., Glass, Ian A. and Montgomery, Grant W. (2007) A case of true hermaphroditism reveals an unusual mechanism of twinning. Human Genetics, 121 2: 179-185. doi:10.1007/s00439-006-0279-x

  • 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

  • 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

  • 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

  • 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.

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • Spring, Kevin, Zhao, Zhen Zhen, Karamatic, Rozemary, Walsh, Michael, Whitehall, Vicki, Pike, Tanya, Simms, Lisa, Young, Joanne, James, Michael, Montgomery, Grant, Appleyard, Mark, Hewett, David, Togashi, Kazutomo, Jass, Jeremy and Leggett, Barbara (2006) High prevalence of sessile serrated adenomas with BRAF mutations: A prospective study of patients undergoing colonoscopy. Gastroenterology, 131 5: 1400-1407. doi:10.1053/j.gastro.2006.08.038

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • Hansell, N. K., Medland, S. E., Ferreira, A. R., Geffen, G. M., Zhu, G., Montgomery, G. W., Duffy, D. L. 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

  • 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

  • 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

  • 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

  • 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.

  • 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

  • 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

  • Zhao, Zhen Zhen, Nyholt, Dale R., James, Michael R., Mayne, Renee, Treloar, Susan A. and Montgomery, Grant W. (2005) A comparison of DNA pools constructed following whole genome amplification for two-stage SNP genotyping designs. Twin Research and Human Genetics, 8 4: 353-361. doi:10.1375/1832427054936718

  • 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

  • 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

  • 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

  • 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

  • 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

  • Hoekstra, Chantal, Meijer, Piet, Kluft, Cornelis, Heutink, Peter, Smit, Guus, de Geus, Eco, Smit, Jan H., van Bruggen, Angelique, Montgomery, Grant W. and Boomsma, Dorret I. (2004) Genetics of dizygotic twinning: a feasibility study for a biobank. Twin Research and Human Genetics, 7 6: 556-563. doi:10.1375/1369052042663751

  • 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

  • Fleming, Jean S., Yu, Fu, McDonald, Robin M., Meyers, Stuart A., Montgomery, Grant W., Smith, John F. and Nicholson, Helen D. (2004) Effects of scrotal heating on sperm surface protein PH-20 expression in sheep. Molecular Reproduction and Development, 68 1: 103-114. doi:10.1002/mrd.20049

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • 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

  • Souter, Vivienne L., Kapur, Raj P., Nyholt, Dale R., Skogerboe, Kristen, Myerson, David, Ton, Carl C., Opheim, Kent E., Easterling, Thomas R., Shields, Laurence E., Montgomery, Grant W. and Glass, Ian A. (2003) A report of dizygous monochorionic twins. New England Journal of Medicine, 349 2: 154-158. doi:10.1056/NEJMoa030050

  • 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

  • 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

  • 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

  • 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

  • Haiman, Christopher A., Chen, Gary K., Vachon, Celine M., Canzian, Federico, Dunning, Alison, Millikan, Robert C., Wang, Xianshu, Ademuyiwa, Foluso, Ahmed, Shahana, Ambrosone, Christine B., Baglietto, Laura, Balleine, Rosemary, Bandera, Elisa V., Beckmann, Matthias W., Berg, Christine D., Bernstein, Leslie, Blomqvist, Carl, Blot, William J., Brauch, Hiltrud, Buring, Julie E., Carey, Lisa A., Carpenter, Jane E., Chang-Claude, Jenny, Chanock, Stephen J., Chasman, Daniel I., Clarke, Christine L., Cox, Angela, Cross, Simon S., Deming, Sandra L., Diasio, Robert B., Dimopoulos, Athanasios M., Driver, W. Ryan, Duennebier, Thomas, Durcan, Lorraine, Eccles, Diana, Edlund, Christopher K., Ekici, Arif B., Fasching, Peter A., Feigelson, Heather S., Flesch-Janys, Dieter, Fostira, Florentia, Foersti, Asta, Fountzilas, George, Gerty, Susan M., Giles, Graham G., Godwin, Andrew K., Goodfellow, Paul, Graham, Nikki, Greco, Dario, Hamann, Ute, Hankinson, Susan E., Hartmann, Arndt, Hein, Rebecca, Heinz, Judith, Holbrook, Andrea, Hoover, Robert N., Hu, Jennifer J., Hunter, David J., Ingles, Sue A., Irwanto, Astrid, Ivanovich, Jennifer, John, Esther M., Johnson, Nicola, Jukkola-Vuorinen, Arja, Kaaks, Rudolf, Ko, Yon-Dschun, Kolonel, Laurence N., Konstantopoulou, Irene, Kosma, Veli-Matti, Kulkarni, Swati, Lambrechts, Diether, Lee, Adam M., Le Marchand, Loic, Lesnick, Timothy, Liu, Jianjun, Lindstrom, Sara, Mannermaa, Arto, Margolin, Sara, Martin, Nicholas G., Miron, Penelope, Montgomery, Grant W., Nevanlinna, Heli, Nickels, Stephan, Nyante, Sarah, Olswold, Curtis, Palmer, Julie, Pathak, Harsh, Pectasides, Dimitrios, Perou, Charles M., Peto, Julian, Pharoah, Paul D. P., Pooler, Loreall C., Press, Michael F., Pylkas, Katri, Rebbeck, Timothy R., Rodriguez-Gil, Jorge L., Rosenberg, Lynn, Ross, Eric, Ruediger, Thomas, Silva, Isabel dos Santos, Sawyer, Elinor, Schmidt, Marjanka K., Schulz-Wendtland, Ruediger, Schumacher, Fredrick, Severi, Gianluca, Sheng, Xin, Signorello, Lisa B., Sinn, Hans-Peter, Stevens, Kristen N., Southey, Melissa C., Tapper, William J., Tomlinson, Ian, Hogervorst, Frans B. L., Wauters, Els, Weaver, JoEllen, Wildiers, Hans, Winqvist, Robert, Van Den Berg, David, Wan, Peggy, Xia, Lucy Y., Yannoukakos, Drakoulis, Zheng, Wei, Ziegler, Regina G., Siddiq, Afshan, Slager, Susan L., Stram, Daniel O., Easton, Douglas, Kraft, Peter, Henderson, Brian E. and Couch, Fergus J. (2002) Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nature Genetics, 32 2: 285-289. doi:10.1038/ng985

  • Treloar, Susan, Hadfield, Ruth, Montgomery, Grant, Lambert, ,Ann, Wicks, Jacki, Barlow, David H., O’Connor, Daniel T., Kennedy, Stephen and International Endogene Study Group (2002) The international endogene study: a collection of families for genetic research in endometriosis. Fertility and Sterility, 78 4: 679-685. doi:10.1016/S0015-0282(02)03341-1

  • 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

  • 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

  • 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

  • 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

  • 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

Conference Publication

  • Ebejer, Jane, Medland, Sarah, Martin, Nick G., Wright, Margaret, Montgomery, Grant, Powell, Joseph, Visscher, Peter and Duffy, David (2013). Clarification of varying genetic expression and structure within adolescent monozygotic and dizygotic twins discordant for high and low attention and activity. In: Behavior Genetics Association 43rd Annual Meeting Abstracts. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, (515-516). 28 June-02 July 2013. doi:10.1007/s10519-013-9623-9

  • Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Weiner, Michael W. and Thompson, Paul M. (2013). Exhaustive search of the SNP-SNP interactome identifies epistatic effects on brain volume in two cohorts. In: Medical Image Computing and Computer-Assisted Intervention, MICCAI 2013 - 16th International Conference, Proceedings. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, (600-607). 22-26 September 2013. doi:10.1007/978-3-642-40760-4_75

  • Hibar, Derrek P., Medland, Sarah E., Stein, Jason L., Kim, Sungeun, Shen, Li, Saykin, Andrew J., de Zubicaray, Greig I., McMahon, Katie L, Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Djurovic, Srdjan, Agartz, Ingrid A., Andreassen, Ole A. and Thompson, Paul M. (2013). Genetic clustering on the hippocampal surface for genome-wide association studies. In: Medical Image Computing and Computer-Assisted Intervention, MICCAI 2013 - 16th International Conference, Proceedings. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, (690-697). 22-26 September 2013. doi:10.1007/978-3-642-40763-5_85

  • Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., Johnson, Kori, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Changes in Anatomical Brain Connectivity Between Ages 12 and 30: A HARDI Study of 484 Adolescents and Adults. In: 2012 9th IEEE International Symposium on Biomedical Imaging : From Nano to Macro : proceedings. 9th IEEE International Symposium on Biomedical Imaging, Barcelona, Spain, (904-907). 2-5 May 2012. doi:10.1109/ISBI.2012.6235695

  • 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. In: International Symposium on Biomedical Imaging, Barcelona, Spain, (944-947). 2-5 May 2012. doi:10.1109/ISBI.2012.6235712

  • 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. In: 2012 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro: Proceedings. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, (542-545). 2-5 May 2012. doi:10.1109/ISBI.2012.6235605

  • Medland, S. E., Nyholt, D. R., Painter, J. N., McEvoy, B. P., McRae, A. F., Montgomery, G. W. and Martin, N. G. (2010). Common variants in the Trichohyalin gene are associated with straight hair in Europeans genetics and genodermatoses. In: 6th World Congress for Hair Research, Cairns, QLD, Australia, (563-563). 16-19 June 2010. doi:10.1111/j.1600-0625.2010.01097.x

  • Bates, Timothy C., Luciano, Michelle, Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2010). Genes for a component of the language acquisition mechanism: ROBO1 polymorphisms associated with phonological buffer deficits. In: Behavior Genetics Association 40th Annual Meeting Abstracts. Behavior Genetics Association 40th Annual Meeting, Seoul, Korea, (785-786). 2-5 June 2010. doi:10.1007/s10519-010-9392-7

  • Martin, N., Madden, P., Pergadia, M., Nelson, E., Bucholz, K., Whitfield, J.B., Montgomery, G. and Heath, G. (2010). Genomewide association study of quantitative alcohol phenotypes in community-ascertained families. In: Abstracts from the International Society for Biomedical Research on Alcoholism World Congress. 2010 World Congress on International Society for Biomedical Research on Alcoholism, Paris, France, (36A-36A). 13-16 September 2010. doi:10.1111/j.1530-0277.2010.01292_3.x

  • Montgomery, G. W., Treloar, S. A., Kennedy, S. H. and Zondervan, K. T. (2008). Genetic variation and endometriosis risk. In: Endometriosis 2008: The Proceedings of the 10th World Congress on Endometriosis. AGES XVIII Annual Scientific Meeting: Art and Science of Endometriosis. WCE 2008: 10th World Congress on Endometriosis, Melbourne, VIC, Australia, (37-48). 11-14 March 2008.

  • 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. In: Alcoholism-Clinical And Experimental Research: World Congress on Alcohol Research (ISBRA 2006). World Congress on Alcohol Research (ISBRA 2006), Sydney, Australia, (62A-62A). 10 - 13 September 2006. doi:10.1111/j.1530-0277.2006.00197.x

PhD and MPhil Supervision

Completed Supervision