Book Chapters
Odintsova, Veronika, Willemsen, Gonneke, Dolan, Conor V., Hottenga, Jouke-Jan, Martin, Nicholas G., Slagboom, P. Eline, Ordoñana, Juan R. and Boomsma, Dorret I. (2022). Establishing a resource for genetic, epidemiological, and biomarker studies: the important role of twin registers. Twin research for everyone: from biology to health, epigenetics, and psychology. (pp. 163-188) edited by Adam D. Tarnoki, David L. Tarnoki, Jennifer R. Harris and Nancy L. Segal. Amsterdam, Netherlands: Elsevier. doi: 10.1016/B978-0-12-821514-2.00011-8
Shen, Kaikai, Dore, Vincent, Fripp, Jurgen, Rose, Stephen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2018). Genetic correlation between cortical gray matter thickness and white matter connections. Imaging genetics. (pp. 85-100) edited by Adrian Dalca, Kayhan Batmanghelich, Mert Sabuncu and Li Shen. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-813968-4.00005-5
Gillespie, Nathan A. and Martin, Nicholas G. (2014). Direction of causation models. Wiley StatsRef: Statistics Reference Online. (pp. *-*) Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06685
Gillespie, Nathan A. and Martin, Nicholas G. (2014). Multivariate genetic analysis. Wiley StatsRef: statistics reference online. Chichester, United Kingdom: John Wiley & Sons. doi: 10.1002/9781118445112.stat06468
Zhan, L., Nie, Z., Ye, J., Wang, Y., Jin, Y., Jahanshad, N., Prasad, G., de Zubicaray, G. I., McMahan, K. L., Martin, N. G., Wright, M. J. and Thompson, P. M. (2014). Multiple stages classification of Alzheimer’s disease based on structural brain networks using generalized low rank approximations (GLRAM). Computational diffusion MRI: MICCAI Workshop, Boston, MA, USA, September 2014. (pp. 35-44) edited by Lauren O'Donnell, Gemma Nedjati-Gilani, Yogesh Rathi, Marco Reisert and Torben Schneider. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-11182-7_4
Eaves, Lindon J., Hatemi, Peter K., Heath, Andrew C. and Martin, Nicholas G. (2011). Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families. Man is by nature a political animal: evolution, biology, and politics. (pp. 101-184) edited by Peter K. Hatemi and Rose McDermott. Chicago, IL, United States: University of Chicago Press. doi: 10.7208/chicago/9780226319117.003.0005
Khytam Dawood, J. Michael Bailey and Nicholas G. Martin (2009). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics. (pp. 269-279) edited by Kim, Yong-Kyu. United Sates: Springer New York. doi: 10.1007/978-0-387-76727-7_19
Journal Articles
Scott, Jan, Crouse, Jacob J., Medland, Sarah E., Mitchell, Brittany L., Gillespie, Nathan A., Martin, Nicholas G. and Hickie, Ian B. (2025). Polygenic risk scores and help-seeking behaviour in young people with recent onset of mood and psychotic disorders. Journal of Affective Disorders, 372, 40-47. doi: 10.1016/j.jad.2024.11.067
Mosley, Philip E., van der Meer, Johan N., Hamilton, Lachlan H. W., Fripp, Jurgen, Parker, Stephen, Jeganathan, Jayson, Breakspear, Michael, Parker, Richard, Holland, Rebecca, Mitchell, Brittany L., Byrne, Enda, Hickie, Ian B., Medland, Sarah E., Martin, Nicholas G. and Cocchi, Luca (2025). Markers of positive affect and brain state synchrony discriminate melancholic from non-melancholic depression using naturalistic stimuli. Molecular Psychiatry, 30 (3) 11605, 848-860. doi: 10.1038/s41380-024-02699-y
Crouse, Jacob J., Park, Shin Ho, Mitchell, Brittany L., Byrne, Enda M., Medland, Sarah E., Lin, Tian, Scott, Jan, de Haan, Zsofi, Tonini, Emiliana, Iorfino, Frank, Wray, Naomi R., Martin, Nicholas G. and Hickie, Ian B. (2025). Mental health and sleep correlates of self-reported outdoor daylight exposure in over 13,000 adults with depression. European Psychiatry, 68 (1) e41, 1-34. doi: 10.1192/j.eurpsy.2025.20
Gustavson, Daniel E., The IGEMS Consortium, Bell, Tyler R., Buchholz, Erik J., Zellers, Stephanie, Luczak, Susan E., Reynolds, Chandra A., Finch, Brian K., Nygaard, Marianne, Catts, Vibeke S., Christensen, Kaare, Finkel, Deborah, Kremen, William S., Latvala, Antti, Martin, Nicholas G., McGue, Matt, Mewton, Louise, Mosing, Miriam A., Panizzon, Matthew S., Plassman, Brenda L., Kaprio, Jaakko, Gatz, Margaret and Franz, Carol E. (2025). Genetic and environmental influences on alcohol consumption in middle to late life. Psychology of Addictive Behaviors. doi: 10.1037/adb0001052
Monistrol-Mula, Anna, Felez-Nobrega, Mireia, Byrne, Enda M., Lind, Penelope A., Hickie, Ian B., Martin, Nicholas G., Medland, Sarah E., Colodro-Conde, Lucía and Mitchell, Brittany L. (2024). The effect of polygenic liability to mental disorders on COVID-19 outcomes in people with depression: the mediating role of anxiety. Psychological Medicine, 54 (15), 4140-4149. doi: 10.1017/s0033291724001983
Walker, Alicia, Karlsson, Robert, Szatkiewicz, Jin P., Thornton, Laura M., Yilmaz, Zeynep, Leppä, Virpi M., Savva, Androula, Lin, Tian, Sidorenko, Julia, McRae, Allan, Kirov, George, Davies, Helena L., Fundín, Bengt T., Chawner, Samuel J. R. A., Song, Jie, Borg, Stina, Wen, Jia, Watson, Hunna J., Munn-Chernoff, Melissa A., Baker, Jessica H., Gordon, Scott, Berrettini, Wade H., Brandt, Harry, Crawford, Steven, Halmi, Katherine A., Kaplan, Allan S., Kaye, Walter H., Mitchell, James, Strober, Michael ... Wray, Naomi R. (2024). Genome-wide copy number variation association study in anorexia nervosa. Molecular Psychiatry, 30 (5) 867, 1-8. doi: 10.1038/s41380-024-02811-2
Horton, Sarah, Jackson, Victoria, Boyce, Jessica, Franken, Marie-Christine, Siemers, Stephanie, John, Miya St, Hearps, Stephen, van Reyk, Olivia, Braden, Ruth, Parker, Richard, Vogel, Adam P., Eising, Else, Amor, David J., Irvine, Janelle, Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie, Scheffer, Ingrid and Morgan, Angela (2024). Self-reported stuttering severity is accurate: informing methods for large-scale data collection in stuttering. Journal of Speech, Language, and Hearing Research, 67 (10), 4015-4024. doi: 10.1044/2023_JSLHR-23-00081
Curtis, Madeleine, Colodro-Conde, Lucia, Medland, Sarah E., Gordon, Scott, Martin, Nicholas G., Wade, Tracey D. and Cohen-Woods, Sarah (2024). Anorexia nervosa polygenic risk, beyond diagnoses: relationship with adolescent disordered eating and behaviors in an Australian female twin population. Psychological Medicine, 54 (13), 3646-3654. doi: 10.1017/s0033291724001727
García-Marín, Luis M., Campos, Adrian I., Diaz-Torres, Santiago, Rabinowitz, Jill A., Ceja, Zuriel, Mitchell, Brittany L., Grasby, Katrina L., Thorp, Jackson G., Agartz, Ingrid, Alhusaini, Saud, Ames, David, Amouyel, Philippe, Andreassen, Ole A., Arfanakis, Konstantinos, Arias-Vasquez, Alejandro, Armstrong, Nicola J., Athanasiu, Lavinia, Bastin, Mark E., Beiser, Alexa S., Bennett, David A., Bis, Joshua C., Boks, Marco P. M., Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Burkhardt, Ralph, Cahn, Wiepke, Calhoun, Vince D. ... Rentería, Miguel E. (2024). Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. Nature Genetics, 56 (11), 1-12. doi: 10.1038/s41588-024-01951-z
Sidorenko, Julia, Couvy-Duchesne, Baptiste, Kemper, Kathryn E., Moen, Gunn-Helen, Bhatta, Laxmi, Åsvold, Bjørn Olav, Mägi, Reedik, Estonian Biobank Research Team, Ani, Alireza, Wang, Rujia, Nolte, Ilja M., Lifelines Cohort Study, Nolte, Ilja M., Gordon, Scott, Hayward, Caroline, Campbell, Archie, Benjamin, Daniel J., Cesarini, David, Evans, David M., Goddard, Michael E., Haley, Chris S., Porteous, David, Medland, Sarah E., Martin, Nicholas G., Snieder, Harold, Metspalu, Andres, Hveem, Kristian, Brumpton, Ben, Visscher, Peter M. and Yengo, Loic (2024). Genetic architecture reconciles linkage and association studies of complex traits. Nature Genetics, 56 (11), 2352-2360. doi: 10.1038/s41588-024-01940-2
Adams, Mark J., Thorp, Jackson G., Jermy, Bradley S., Kwong, Alex S. F., Kõiv, Kadri, Grotzinger, Andrew D., Nivard, Michel G., Marshall, Sally, Milaneschi, Yuri, Baune, Bernhard T., Müller-Myhsok, Bertram, Penninx, Brenda W. J. H., Boomsma, Dorret I., Levinson, Douglas F., Breen, Gerome, Pistis, Giorgio, Grabe, Hans J., Tiemeier, Henning, Berger, Klaus, Rietschel, Marcella, Magnusson, Patrik K., Uher, Rudolf, Hamilton, Steven P., Lucae, Susanne, Lehto, Kelli, Li, Qingqin S., Byrne, Enda M., Hickie, Ian B., Martin, Nicholas G. ... Derks, Eske M. (2024). Genome-wide meta-analysis of ascertainment and symptom structures of major depression in case-enriched and community cohorts. Psychological Medicine, 54 (12), 3459-3468. doi: 10.1017/s0033291724001880
Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Scott, Jan, Medland, Sarah E., Lin, Tian, Wray, Naomi R., Martin, Nicholas G. and Hickie, Ian B. (2024). Patterns of stressful life events and polygenic scores for five mental disorders and neuroticism among adults with depression. Molecular Psychiatry, 29 (9), 2765-2773. doi: 10.1038/s41380-024-02492-x
Ingold, Nathan, Seviiri, Mathias, Ong, Jue Sheng, Neale, Rachel E., Pandeya, Nirmala, Whiteman, David C., Olsen, Catherine M., Martin, Nicholas G., Duffy, David L., Khosrotehrani, Kiarash, Hayward, Nicholas, Montgomery, Grant W., MacGregor, Stuart and Law, Matthew H. (2024). Exploring the germline genetics of in situ and invasive cutaneous melanoma: a genome-wide association study meta-analysis. JAMA Dermatology, 160 (9), 964-971. doi: 10.1001/jamadermatol.2024.2601
Ciulkinyte, Austeja, Mountford, Hayley S., Fontanillas, Pierre, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bowes, Jonathan, Bryc, Katarzyna, Chaudhary, Ninad S., Coker, Daniella, Das, Sayantan, DelloRusso, Emily, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Freyman, Will, Fuller, Zach, German, Chris, Granka, Julie M., Heilbron, Karl, Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan ... 23andMe Research Team (2024). Genetic neurodevelopmental clustering and dyslexia. Molecular Psychiatry, 30 (1) e12648, 140-150. doi: 10.1038/s41380-024-02649-8
Kentistou, Katherine A., Kaisinger, Lena R., Stankovic, Stasa, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Walters, Robin G., Liu, Xiaoxi, Busch, Alexander S., Helgason, Hannes, Thompson, Deborah J., Santoni, Federico, Petricek, Konstantin M., Zouaghi, Yassine, Huang-Doran, Isabel, Gudbjartsson, Daniel F., Bratland, Eirik, Lin, Kuang, Gardner, Eugene J., Zhao, Yajie, Jia, Raina Y., Terao, Chikashi, Riggan, Marjorie J., Bolla, Manjeet K., Yazdanpanah, Mojgan, Yazdanpanah, Nahid, Bradfield, Jonathan P., Broer, Linda, Campbell, Archie ... The China Kadoorie Biobank Collaborative Group (2024). Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (8), 1-2. doi: 10.1038/s41588-024-01857-w
Kentistou, Katherine A., Kaisinger, Lena R., Stankovic, Stasa, Vaudel, Marc, Mendes de Oliveira, Edson, Messina, Andrea, Walters, Robin G., Liu, Xiaoxi, Busch, Alexander S., Helgason, Hannes, Thompson, Deborah J., Santoni, Federico, Petricek, Konstantin M., Zouaghi, Yassine, Huang-Doran, Isabel, Gudbjartsson, Daniel F., Bratland, Eirik, Lin, Kuang, Gardner, Eugene J., Zhao, Yajie, Jia, Raina Y., Terao, Chikashi, Riggan, Marjorie J., Bolla, Manjeet K., Yazdanpanah, Mojgan, Yazdanpanah, Nahid, Bradfield, Jonathan P., Broer, Linda, Campbell, Archie ... The China Kadoorie Biobank Collaborative Group (2024). Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nature Genetics, 56 (7), 1-15. doi: 10.1038/s41588-024-01798-4
Dash, Genevieve F., Gizer, Ian R., Martin, Nicholas G. and Slutske, Wendy S. (2024). Differential etiologic associations of heroin use and prescription opioid misuse with psychopathology. Journal of Psychopathology and Clinical Science, 133 (5), 378-391. doi: 10.1037/abn0000921
Nievergelt, Caroline M., Maihofer, Adam X., Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Daskalakis, Nikolaos P., Duncan, Laramie E., Polimanti, Renato, Aaronson, Cindy, Amstadter, Ananda B., Andersen, Soren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegoviç, Esmina, Babić, Dragan, Bacanu, Silviu-Alin, Baker, Dewleen G., Batzler, Anthony, Beckham, Jean C., Belangero, Sintia, Benjet, Corina, Bergner, Carisa, Bierer, Linda M., Biernacka, Joanna M., Bierut, Laura J., Bisson, Jonathan I. ... HUNT All-In Psychiatry (2024). Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. Nature Genetics, 56 (5), 792-808. doi: 10.1038/s41588-024-01707-9
Hatton, Alesha A., Cheng, Fei-Fei, Lin, Tian, Shen, Ren-Juan, Chen, Jie, Zheng, Zhili, Qu, Jia, Lyu, Fan, Harris, Sarah E., Cox, Simon R., Jin, Zi-Bing, Martin, Nicholas G., Fan, Dongsheng, Montgomery, Grant W., Yang, Jian, Wray, Naomi R., Marioni, Riccardo E., Visscher, Peter M. and McRae, Allan F. (2024). Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature Communications, 15 (1) 2713, 1-12. doi: 10.1038/s41467-024-47005-0
Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Guintivano, Jerry, Hickie, Ian B., Whiteman, David C., Olsen, Catherine M., Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Byrne, Enda M. (2024). Comprehensive sex-stratified genetic analysis of 28 blood biomarkers and depression reveals a significant association between depression and low levels of total protein in females. Complex Psychiatry, 10 (1-4), 19-34. doi: 10.1159/000538058
Hur, Yoon-Mi, Martin, Nick, Oginni, Olakunle, Boomsma, Dorret, Hubers, Nikki and Mbarek, Hamdi (2024). Family history of twinning and fertility traits in Nigerian mothers of dizygotic twins. Twin Research and Human Genetics, 27 (1), 12-17. doi: 10.1017/thg.2024.2
Sterenborg, Rosalie B. T. M., Steinbrenner, Inga, Li, Yong, Bujnis, Melissa N., Naito, Tatsuhiko, Marouli, Eirini, Galesloot, Tessel E., Babajide, Oladapo, Andreasen, Laura, Astrup, Arne, Åsvold, Bjørn Olav, Bandinelli, Stefania, Beekman, Marian, Beilby, John P., Bork-Jensen, Jette, Boutin, Thibaud, Brody, Jennifer A., Brown, Suzanne J., Brumpton, Ben, Campbell, Purdey J., Cappola, Anne R., Ceresini, Graziano, Chaker, Layal, Chasman, Daniel I., Concas, Maria Pina, Coutinho de Almeida, Rodrigo, Cross, Simone M., Cucca, Francesco, Deary, Ian J. ... Regeneron Genetics Center (2024). Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications. Nature Communications, 15 (1) 888, 1-18. doi: 10.1038/s41467-024-44701-9
Scholz, Markus, Horn, Katrin, Pott, Janne, Wuttke, Matthias, Kühnapfel, Andreas, Nasr, M. Kamal, Kirsten, Holger, Li, Yong, Hoppmann, Anselm, Gorski, Mathias, Ghasemi, Sahar, Li, Man, Tin, Adrienne, Chai, Jin-Fang, Cocca, Massimiliano, Wang, Judy, Nutile, Teresa, Akiyama, Masato, Åsvold, Bjørn Olav, Bansal, Nisha, Biggs, Mary L., Boutin, Thibaud, Brenner, Hermann, Brumpton, Ben, Burkhardt, Ralph, Cai, Jianwen, Campbell, Archie, Campbell, Harry, Chalmers, John ... Pattaro, Cristian (2024). X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. Nature Communications, 15 (1) 586, 1-17. doi: 10.1038/s41467-024-44709-1
Meng, Xiangrui, Navoly, Georgina, Giannakopoulou, Olga, Levey, Daniel F., Koller, Dora, Pathak, Gita A., Koen, Nastassja, Lin, Kuang, Adams, Mark J., Rentería, Miguel E., Feng, Yanzhe, Gaziano, J. Michael, Stein, Dan J., Zar, Heather J., Campbell, Megan L., van Heel, David A., Trivedi, Bhavi, Finer, Sarah, McQuillin, Andrew, Bass, Nick, Chundru, V. Kartik, Martin, Hilary C., Huang, Qin Qin, Valkovskaya, Maria, Chu, Chia-Yi, Kanjira, Susan, Kuo, Po-Hsiu, Chen, Hsi-Chung, Tsai, Shih-Jen ... BioBank Japan Project (2024). Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nature Genetics, 56 (2), 222-233. doi: 10.1038/s41588-023-01596-4
Davis, Christal N., Gizer, Ian R., Agrawal, Arpana, Statham, Dixie J., Heath, Andrew C., Martin, Nicholas G. and Slutske, Wendy S. (2024). Genetic and shared environmental factors explain the association between adolescent polysubstance use and high school noncompletion. Psychology of Addictive Behaviors, 38 (1), 114-123. doi: 10.1037/adb0000915
Mbarek, Hamdi, Gordon, Scott D., Duffy, David L., Hubers, Nikki, Mortlock, Sally, Beck, Jeffrey J., Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V., Actkins, Ky’Era V., Gerring, Zachary F., Van Dongen, Jenny, Ehli, Erik A., Iacono, William G., Mcgue, Matt, Chasman, Daniel I., Gallagher, C. Scott, Schilit, Samantha L. P., Morton, Cynthia C., Paré, Guillaume, Willemsen, Gonneke, Whiteman, David C., Olsen, Catherine M., Derom, Catherine, Vlietinck, Robert, Gudbjartsson, Daniel, Cannon-Albright, Lisa, Krapohl, Eva, Plomin, Robert ... Martin, Nicholas G. (2024). Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. Human Reproduction, 39 (1), 240-257. doi: 10.1093/humrep/dead247
Perugini, Ambra, Fontanillas, Pierre, Gordon, Scott D., Fisher, Simon E., Martin, Nicholas G., Bates, Timothy C and Luciano, Michelle (2024). Dyslexia polygenic scores show heightened prediction of verbal working memory and arithmetic. Scientific Studies of Reading, 28 (5), 1-15. doi: 10.1080/10888438.2024.2365697
Crouse, Jacob J., Park, Shin Ho, Byrne, Enda M., Mitchell, Brittany L., Chan, Karina, Scott, Jan, Medland, Sarah E., Martin, Nicholas G., Wray, Naomi R. and Hickie, Ian B. (2024). Evening chronotypes with depression report poorer outcomes of SSRIs: A survey-based study of self-ratings. Biological Psychiatry, 96 (1), 4-14. doi: 10.1016/j.biopsych.2023.12.023
García-Marín, Luis M., Ogonowski, Natalia S., Han, Laura K.M., Maya-Martínez, Mateo, Mitchell, Brittany L., Schmaal, Lianne, Martin, Nicholas G. and Rentería, Miguel E. (2024). Investigating the genetic relationship of intracranial and subcortical brain volumes with depression and other psychiatric disorders. Imaging Neuroscience, 2, 1-16. doi: 10.1162/imag_a_00291
Zhou, Hang, Kember, Rachel L., Deak, Joseph D., Xu, Heng, Toikumo, Sylvanus, Yuan, Kai, Lind, Penelope A., Farajzadeh, Leila, Wang, Lu, Hatoum, Alexander S., Johnson, Jessica, Lee, Hyunjoon, Mallard, Travis T., Xu, Jiayi, Johnston, Keira J. A., Johnson, Emma C., Nielsen, Trine Tollerup, Galimberti, Marco, Dao, Cecilia, Levey, Daniel F., Overstreet, Cassie, Byrne, Enda M., Gillespie, Nathan A., Gordon, Scott, Hickie, Ian B., Whitfield, John B., Xu, Ke, Zhao, Hongyu, Huckins, Laura M. ... Million Veteran Program (2023). Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. Nature Medicine, 29 (12), 3184-3192. doi: 10.1038/s41591-023-02653-5
Guintivano, Jerry, Byrne, Enda M., Kiewa, Jacqueline, Yao, Shuyang, Bauer, Anna E., Aberg, Karolina A., Adams, Mark J., Campbell, Archie, Campbell, Megan L., Choi, Karmel W., Corfield, Elizabeth C., Havdahl, Alexandra, Hucks, Donald, Koen, Nastassja, Lu, Yi, Maegbaek, Merete L., Mullaer, Jimmy, Peterson, Roseann E., Raffield, Laura M., Sallis, Hannah M., Sealock, Julia M., Walker, Alicia, Watson, Hunna J., Xiong, Ying, Yang, Jessica M. K., Anney, Richard J. L., Gordon-Smith, Katherine, Hubbard, Leon, Jones, Lisa A. ... Sullivan, Patrick (2023). Meta-analyses of genome-wide association studies for postpartum depression. American Journal of Psychiatry, 180 (12), 884-895. doi: 10.1176/appi.ajp.20230053
Gordon, Scott D., Duffy, David L., Whiteman, David C., Olsen, Catherine M., McAloney, Kerrie, Adsett, Jessica M., Garden, Natalie A., Cross, Simone M., List-Armitage, Susan E., Brown, Joy, Beck, Jeffrey J., Mbarek, Hamdi, Medland, Sarah E., Montgomery, Grant W. and Martin, Nicholas G. (2023). GWAS of dizygotic twinning in an enlarged Australian sample of mothers of DZ twins. Twin Research and Human Genetics, 26 (6), 327-338. doi: 10.1017/thg.2023.45
Garcia-Marin, Luis M., Mulcahy, Aoibhe, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Chafota, Freddy, Lind, Penelope A., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E. and Campos, Adrian I. (2023). Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants. Annals of General Psychiatry, 22 (1) 49, 1-8. doi: 10.1186/s12991-023-00480-z
Ingold, N., Zhu, G., Duffy, D. L., Mothershaw, A., Martin, N. G., MacGregor, S. and Law, M. H. (2023). Counting nevi on the outer arm provides an accurate and feasible alternative to total body nevus count. Journal of the European Academy of Dermatology and Venereology, 37 (11), e1302-e1304. doi: 10.1111/jdv.19279
Lind, Penelope A., Siskind, Dan J., Hickie, Ian B, Colodro-Conde, Lucía, Cross, Simone, Parker, Richard, Martin, Nicholas G. and Medland, Sarah E. (2023). Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohort. Australian and New Zealand Journal of Psychiatry, 57 (11), 1428-1442. doi: 10.1177/00048674231195571
Ong, Jue-Sheng, Seviiri, Mathias, Dusingize, Jean Claude, Wu, Yeda, Han, Xikun, Shi, Jianxin, Olsen, Catherine M., Neale, Rachel E., Thompson, John F., Saw, Robyn P. M., Shannon, Kerwin F., Mann, Graham J., Martin, Nicholas G., Medland, Sarah E., Gordon, Scott D., Scolyer, Richard A., Long, Georgina V., Iles, Mark M., Landi, Maria Teresa, Whiteman, David C., MacGregor, Stuart and Law, Matthew H. (2023). Uncovering the complex relationship between balding, testosterone and skin cancers in men. Nature Communications, 14 (1) 5962, 1-12. doi: 10.1038/s41467-023-41231-8
Mulder, Tessa A, Campbell, Purdey J, Taylor, Peter N, Peeters, Robin P, Wilson, Scott G, Medici, Marco, Dayan, Colin, Jaddoe, Vincent V W, Walsh, John P, Martin, Nicholas G, Tiemeier, Henning and Korevaar, Tim I M (2023). Genetic determinants of thyroid function in children. European Journal of Endocrinology, 189 (2), 164-174. doi: 10.1093/ejendo/lvad086
Gomez, Lina M., Mitchell, Brittany L., McAloney, Kerrie, Adsett, Jessica, Garden, Natalie, Wood, Madeline, Diaz-Torres, Santiago, Garcia-Marin, Luis M., Breakspear, Michael, Martin, Nicholas G. and Lupton, Michelle K. (2023). The effect of genetic predisposition to Alzheimer’s disease and related traits on recruitment bias in a study of cognitive aging. Twin Research and Human Genetics, 26 (3) PII S1832427423000269, 1-6. doi: 10.1017/thg.2023.26
Peng, Fuduan, Xiong, Ziyi, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Wu, Sijie, Adhikari, Kaustubh, Chen, Yan, Li, Yi, Gonzalez-José, Rolando, Schüler-Faccini, Lavinia, Bortolini, Maria-Cátira, Acuña-Alonzo, Victor, Canizales-Quinteros, Samuel, Gallo, Carla, Poletti, Giovanni, Bedoya, Gabriel, Rothhammer, Francisco, Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Ruiz-Linares, Andrés, Wang, Sijia, Walsh, Susan, Spector, Timothy D., Martin, Nicholas G., Kayser, Manfred and Liu, Fan (2023). GWAs identify DNA variants influencing eyebrow thickness variation in Europeans and across continental populations. Journal of Investigative Dermatology, 143 (7), 1317-1322. doi: 10.1016/j.jid.2022.11.026
Chundru, V. Kartik, Marioni, Riccardo E., Pendergast, James G. D., Lin, Tian, Beveridge, Allan J., Martin, Nicholas G, Montgomery, Grant W., Hume, David A., Deary, Ian J., Visscher, Peter M., Wray, Naomi R. and McRae, Allan F. (2023). Rare genetic variants underlie outlying levels of DNA methylation and gene-expression. Human Molecular Genetics, 32 (11), 1912-1921. doi: 10.1093/hmg/ddad028
Graham, Sarah E., Clarke, Shoa L., Wu, Kuan-Han H., Kanoni, Stavroula, Zajac, Greg J. M., Ramdas, Shweta, Surakka, Ida, Ntalla, Ioanna, Vedantam, Sailaja, Winkler, Thomas W., Locke, Adam E., Marouli, Eirini, Hwang, Mi Yeong, Han, Sohee, Narita, Akira, Choudhury, Ananyo, Bentley, Amy R., Ekoru, Kenneth, Verma, Anurag, Trivedi, Bhavi, Martin, Hilary C., Hunt, Karen A., Hui, Qin, Klarin, Derek, Zhu, Xiang, Thorleifsson, Gudmar, Helgadottir, Anna, Gudbjartsson, Daniel F., Holm, Hilma ... Global Lipids Genetics Consortium (2023). Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature, 618 (7965), E19-E20. doi: 10.1038/s41586-023-06194-2
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Pardiñas, Antonio F, Holmans, Peter, Pocklington, Andrew J, Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E, Bishop, Sophie, Cameron, Darren, Hamshere, Marian L, Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H, McCarroll, Steven A, Baune, Bernhard T, Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C, Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M, Plomin, Robert, Porteous, David J, Wray, Naomi R, Caballero, Armando ... CRESTAR Consortium (2018). Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics, 50 (3), 381-389. doi: 10.1038/s41588-018-0059-2
Gharahkhani, Puya, Burdon, Kathryn P., Cooke Bailey, Jessica N, Hewitt, Alex W., Law, Matthew H., Pasquale, Louis R., Kang, Jae H., Haines, Jonathan L., Souzeau, Emmanuelle, Zhou, Tiger, Siggs, Owen M., Landers, John, Awadalla, Mona, Sharma, Shiwani, Mills, Richard A., Ridge, Bronwyn, Lynn, David, Casson, Robert, Graham, Stuart L., Goldberg, Ivan, White, Andrew, Healey, Paul R., Grigg, John, Lawlor, Mitchell, Mitchell, Paul, Ruddle, Jonathan, Coote, Michael, Walland, Mark, Best, Stephen ... NEIGHBORHOOD consortium (2018). Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Scientific reports, 8 (1) 3124, 3124. doi: 10.1038/s41598-018-20435-9
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Scott, Jan, Davenport, Tracey A., Parker, Richard, Hermens, Daniel F., Lind, Penelope A., Medland, Sarah E., Wright, Margaret J., Martin, Nicholas G., Gillespie, Nathan A. and Hickie, Ian B. (2017). Pathways to depression by age 16 years: Examining trajectories for self-reported psychological and somatic phenotypes across adolescence. Journal of Affective Disorders, 230, 1-6. doi: 10.1016/j.jad.2017.12.007
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Ong, Jue-Sheng, Hwang, Liang-Dar, Cuellar-Partida, Gabriel, Martin, Nicholas G., Chenevix-Trench, Georgia, Quinn, Michael C. J., Cornelis, Marilyn C., Gharahkhani, Puya, Webb, Penelope M., MacGregor, Stuart and Ovarian Cancer Association Consortium (2017). Assessment of moderate coffee consumption and risk of epithelial ovarian cancer: a Mendelian randomization study. International Journal of Epidemiology, 47 (2), 450-459. doi: 10.1093/ije/dyx236
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Schermer, Julie Aitken, Martin, Rod A., Vernon, Philip A., Martin, Nicholas G., Conde, Lucia Colodro, Statham, Dixie and Lynskey, Michael T. (2017). Lonely people tend to make fun of themselves: A behavior genetic analysis of humor styles and loneliness. Personality and Individual Differences, 117, 71-73. doi: 10.1016/j.paid.2017.05.042
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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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Middelberg, Rita P. S., Ferreira, Manuel A. R., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. BMC Medical Genetics, 12 (123) 123, 1-9. doi: 10.1186/1471-2350-12-123
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Ferreira, Manuel A. R., Matheson, Melanie C., Duffy, David L., Marks, Guy B., Hui, Jennie, Le Souef, Peter, Danoy, Patrick, Baltic, Svetlana, Nyholt, Dale R., Jenkins, Mark, Hayden, Catherine, Willemsen, Gonneke, Ang, Wei, Kuokkanen, Mikko, Beilby, John, Cheah, Faang, de Geus, Eco J.C., Ramasamy, Adaikalavan, Vedantam, Sailaka, Salomaa, Veikko, Madden, Pamela A., Heath, Andrew C., Hopper, John L., Visscher, Peter M., Musk, Bill, Leeder, Stephen R., Jarvelin, Marjo-Riitta, Pennell, Craig, Boomsma, Dorret I. ... Wright, Margaret J. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378 (9795), 1006-1014. doi: 10.1016/S0140-6736(11)60874-X
Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M., McMahon, K. L., De Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack, C. R., Weiner, M. W., Toga, A. W. and Thompson, P. M. (2011). Genome-wide association reveals dopamine-related genetic effects on caudate volume. Molecular Psychiatry, 16 (9), 881-881. doi: 10.1038/mp.2011.98
Amin, N., Byrne, E., Johnson, J., Chenevix-Trench, G., Walter, S., Nolte, I. M., kConFab Investigators, Vink, J.M., Rawal, R., Mangino, M., Teumer, A., Keers, J. C., Verwoert, G., Baumeister, S., Biffar, R., Petersmann, A., Dahmen, N., Doering, A., Isaacs, A., Broer, L., Wray, N. R., Montgomery, G. W., Levy, D., Psaty, B. M., Gudnason, V., Chakravarti, A., Sulem, P., Gudbjartsson, D. F., Kiemeney, L. A. ... van Duijn, C. M. (2011). Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Molecular Psychiatry, 17 (11), 1116-1129. doi: 10.1038/mp.2011.101
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
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
Zietsch, Brendan P., Miller, Geoffrey F., Bailey, J. Michael and Martin, Nicholas G. (2011). Female orgasm rates are largely independent of other traits: Implications for "female orgasmic disorder" and evolutionary theories of orgasm. Journal of Sexual Medicine, 8 (8), 2305-2316. doi: 10.1111/j.1743-6109.2011.02300.x
Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Attitudes towards economic risk and the gender pay gap. Labour Economics, 18 (4), 555-561. doi: 10.1016/j.labeco.2010.12.007
Bedi, Saaniya, Nelson, Elliot C., Lynskey, Michael T., McCutcheon, Vivia V., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Risk for suicidal thoughts and behavior after childhood sexual abuse in women and men. Suicide and Life-Threatening Behavior, 41 (4), 406-415. doi: 10.1111/j.1943-278X.2011.00040.x
Slutske, Wendy S., Zhu, Gu, Meier, Madeline H. and Martin, Nicholas G. (2011). Disordered gambling as defined by the diagnostic and statistical manual of mental disorders and the South Oaks Gambling Screen: evidence for a common etiologic structure. Journal of Abnormal Psychology, 120 (3), 743-751. doi: 10.1037/a0022879
Blokland, Gabriella A. M., McMahon, Katie L., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I. and Wright, Margaret J. (2011). Heritability of working memory brain activation. Journal of Neuroscience, 31 (30), 10882-10890. doi: 10.1523/JNEUROSCI.5334-10.2011
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
Demirkan, Ayse, Amin, Najaf, Isaacs, Aaron, Jarvelin, Marjo-Riitta, Whitfield, John B., Wichmann, Heinz-Erich, Kyvik, Kirsten Ohm, Rudan, Igor, Gieger, Christian, Hicks, Andrew A., Johansson, Asa, Hottenga, Jouke-Jan, Smith, Johannes J., Wild, Sarah H., Pedersen, Nancy L., Willemsen, Gonneke, Mangino, Massimo, Hayward, Caroline, Uitterlinden, Andre G., Hofman, Albert, Witteman, Jacqueline, Montgomery, Grant W., Pietilainen, Kirsi H., Rantanen, Taina, Kaprio, Jaakko, Doering, Angela, Pramstaller, Peter P., Gyllensten, Ulf, de Geus, Eco J. C. ... van Duijn, Cornelia M. (2011). Genetic architecture of circulating lipid levels. European Journal of Human Genetics, 19 (7), 813-819. doi: 10.1038/ejhg.2011.21
Theodoraki, A., Jones, G., Parker, J., Woolman, E., Martin, N., Perera, S., Thomas, M., Bunn, C., Khoo, B., Bouloux, P. M. and Vanderpump, M. P. J. (2011). Performance of a third-generation TSH-receptor antibody in a UK clinic. Clinical Endocrinology, 75 (1), 127-133. doi: 10.1111/j.1365-2265.2011.04022.x
Slutske, Wendy S., Bascom, Elise N., Meier, Madeline H., Medland, Sarah E. and Martin, Nicholas G. (2011). Sensation seeking in females from opposite-versus same-sex twin pairs: hormone transfer or sibling imitation?. Behavior Genetics, 41 (4), 533-542. doi: 10.1007/s10519-010-9416-3
Singh, A. L., D'Onofrio, B. M., Slutske, W. S., Turkheimer, E., Emery, R. E., Harden, K. P., Heath, A. C., Madden, P. A. F., Statham, D. J. and Martin, N. G. (2011). Parental depression and offspring psychopathology: a Children of Twins study. Psychological Medicine, 41 (7), 1385-1395. doi: 10.1017/S0033291710002059
Sanfilippo, Paul G., Medland, Sarah E., Hewitt, Alex W., Kearns, Lisa S., Ruddle, Jonathan B., Sun, Cong, Hammond, Christopher J., Young, Terri L., Martin, Nicholas G. and Mackey, David A. (2011). Ophthalmic phenotypes and the representativeness of twin data for the general population. Investigative Ophthalmology & Visual Science, 52 (8), 5565-5572. doi: 10.1167/iovs.11-7258
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
Martin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Educational Attainment: A Genome Wide Association Study in 9538 Australians. PLoS One, 6 (6) e20128, e20128.1-e20128.8. doi: 10.1371/journal.pone.0020128
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
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
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
Beam, Christopher R., Horn, Erin E., Hunt, Stacy Karagis, Emery, Robert E., Turkheimer, Eric and Martin, Nick (2011). Revisiting the effect of marital support on depressive symptoms in mothers and fathers: a genetically informed study. Journal of Family Psychology, 25 (3), 336-344. doi: 10.1037/a0023758
Gehrman, Philip R., Byrne, Enda, Gillespie, Nathan and Martin, Nicholas G. (2011). Genetics of insomnia. Sleep Medicine Clinics, 6 (2), 191-202. doi: 10.1016/j.jsmc.2011.03.003
Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stephane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (vol 108, pg 7119, 2011). Proceedings of the National Academy of Sciences of the United States of America, 108 (22), 9316-9316. doi: 10.1073/pnas.1106917108
Braskie, Meredith N., Jahanshad, Neda, Stein, Jason L., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Ringman, John M., Toga, Arthur W. and Thompson, Paul M. (2011). Common Alzheimer's disease risk variant within the CLU gene affects white matter microstructure in young adults. The Journal of Neuroscience, 31 (18), 6764-6770. doi: 10.1523/JNEUROSCI.5794-10.2011
Zietsch, Brendan P., Verweij, Karin J. H., Heath, Andrew C. and Martin, Nicholas G. (2011). Variation in human mate choice: Simultaneously investigating heritability, parental influence, sexual imprinting, and assortative mating. The American Naturalist, 177 (5), 605-616. doi: 10.1086/659629
Meier, Madeline H., Slutske, Wendy S., Heath, Andrew C. and Martin, Nicholas G. (2011). Sex differences in the genetic and environmental influences on childhood conduct disorder and adult antisocial behavior. Journal of Abnormal Psychology, 120 (2), 377-388. doi: 10.1037/a0022303
Schumann, Gunter, Coin, Lachlan J., Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H., Stacey, David, Desrivieres, Sylvane, Aliev, Fazil A., Khan, Anokhi A., Amin, Najaf, Aulchenko, Yurii S., Bakalkin, Georgy, Bakker, Stephan J., Balkau, Beverley, Beulens, Joline W., Bilbao, Ainhoa, de Boer, Rudolf A., Beury, Delphine, Bots, Michiel L., Breetvelt, Elemi J., Cauchi, Stéphane, Cavalcanti-Proenca, Christine, Chambers, John C., Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J., Dick, Danielle, Ducci, Francesca, Easton, Alanna ... Elliott, Paul (2011). Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proceedings of the National Academy of Sciences of the United States of America, 108 (17), 7119-7124. doi: 10.1073/pnas.1017288108
Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2011). Does teenage childbearing reduce investment in human capital?. Journal of Population Economics, 24 (2), 701-730. doi: 10.1007/s00148-009-0270-7
Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Obstetrical and Gynecological Survey, 66 (4), 214-216. doi: 10.1097/OGX.0b013e318210cea1
Alford, John R., Hatemi, Peter K., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2011). The politics of mate choice. The Journal of Politics, 73 (2), 362-379. doi: 10.1017/S0022381611000016
Loehlin, John C. and Martin, Nicholas G. (2011). Corrigendum to: "The general factor of personality: questions and elaborations" [J. Res. Pers. 45 (2011) 44-49]. Journal of Research in Personality, 45 (2), 258-258. doi: 10.1016/j.jrp.2011.02.010
Waldron, Mary, Heath, Andrew C., Lynskey, Michael T., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2011). Alcoholic marriage: later start, sooner end. Alcoholism: Clinical and Experimental Research, 35 (4), 632-642. doi: 10.1111/j.1530-0277.2010.01381.x
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
Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Aexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics, 88 (3), 372-381. doi: 10.1016/j.ajhg.2011.01.017
Speliotes, Elizabeth K., Yerges-Armstrong, Laura M., Wu, Jun, Hernaez, Ruben, Kim, Lauren J., Palmer, Cameron D., Gudnason, Vilmundur, Eiriksdottir, Gudny, Garcia, Melissa E., Launer, Lenore J., Nalls, Michael A., Clark, Jeanne M., Mitchell, Braxton D., Shuldiner, Alan R., Butler, Johannah L., Tomas, Marta, Hoffmann, Udo, Hwang, Shih-Jen, Massaro, Joseph M., O'Donnell, Christopher J., Sahani, Dushyant V., Salomaa, Veikko, Schadt, Eric E., Schwartz, Stephen M., Siscovick, David S., NASH CRN, GIANT Consortium, MAGIC Investigators, Voight, Benjamin F. ... Coin, Lachlan (2011). Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genetics, 7 (3) e1001324, e1001324.1-e1001324.14. doi: 10.1371/journal.pgen.1001324
Luciano, Michelle, Hansell, Narelle K., Lahti, Jari, Davies, Gail, Medland, Sarah E., Raikkonen, Katri, Tenesa, Albert, Widen, Elisabeth, McGhee, Kevin A., Palotie, Aarno, Liewald, David, Porteous, David J., Starr, John M., Montgomery, Grant W., Martin, Nicholas G., Eriksson, Johan G., Wright, Margaret J. and Deary, Ian J. (2011). Whole genome association scan for genetic polymorphisms influencing information processing speed. Biological Psychology, 86 (3), 193-202. doi: 10.1016/j.biopsycho.2010.11.008
Chiang, M. C., Barysheva, M., Toga, A. W., Medland, S. E., Hansel, N. K., James, M. R., McMahon, K. L., de Zubicaray, G. I., Martin, N. G., Wright, M. J. and Thompson, P. M. (2011). BDNF gene effects on brain circuitry replicated in 455 twins. NeuroImage, 55 (2), 448-454. doi: 10.1016/j.neuroimage.2010.12.053
Cichon, Sven, Muehleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miro, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, Rene, Schmael, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H. -Erich, Schreiber, Stefan, Mueller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stephane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon ... Noethen, Markus M. (2011). Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011). American Journal of Human Genetics, 88 (3), 396-396. doi: 10.1016/j.ajhg.2011.03.001
Joshi, A.A., Lepore, N., Joshi, S.H., Lee, A.D., Barysheva, M., Stein, J.L., McMahon, K.L., Johnson, K., de Zubicaray, G.I., Martin, N.G., Wright, M.J., Toga, A.W. and Thompson, P.M. (2011). The contribution of genes to cortical thickness and volume. NeuroReport, 22 (3), 101-105. doi: 10.1097/WNR.0b013e3283424c84
Barakat, M., Doyon, J., Debas, K., Vandewalle, G., Morin, A., Poirier, G., Martin, N., Lafortune, M., Karni, A., Ungerleider, L. G., Benali, H. and Carrier, J. (2011). Fast and slow spindle involvement in the consolidation of a new motor sequence. Behavioural Brain Research, 217 (1), 117-121. doi: 10.1016/j.bbr.2010.10.019
Chiang, MC, McMahon, KL, de Zubicaray, GI, Martin, NG, Hickie, I, Toga, AW, Wright, MJ and Thompson, PM (2011). Genetics of white matter development: A DTI study of 705 twins and their siblings aged 12 to 29. NeuroImage, 54 (3), 2308-2317. doi: 10.1016/j.neuroimage.2010.10.015
Zietsch, Brendan P., Verweij, Karin J. H., Bailey, J. Michael, Wright, Margaret J. and Martin, Nicholas G. (2011). Sexual orientation and psychiatric vulnerability: A twin study of neuroticism and psychoticism. Archives of Sexual Behavior, 40 (1), 133-142. doi: 10.1007/s10508-009-9508-4
Ngo, Trung T., Mitchell, Philip B., Martin, Nicholas G. and Miller, Steven M. (2011). Psychiatric and genetic studies of binocular rivalry: an endophenotype for bipolar disorder?. Acta Neuropsychiatrica, 23 (1), 37-42. doi: 10.1111/j.1601-5215.2010.00510.x
Carrier, Julie, Viens, Isabelle, Poirier, Gaétan , Robillard, Rébecca , Lafortune, Marjolaine, Vandewalle, Gilles, Martin, Nicolas, Barakat, Marc, Paquet, Jean and Filipini, Daniel (2011). Sleep slow wave changes during the middle years of life. European Journal of Neuroscience, 33 (4), 758-766. doi: 10.1111/j.1460-9568.2010.07543.x
Fahy, Samantha J., Sun, Cong, Zhu, Gu, Healey, Paul R., Spector, Tim D., Martin, Nicolas G., Mitchell, Paul, Wong, Tien Y., Mackey, David A., Hammond, Christopher J. and Andrew, Toby (2011). The relationship between retinal arteriolar and venular calibers is genetically mediated, and each is associated with risk of cardiovascular disease. Investigative Ophthalmology & Visual Science, 52 (2), 975-981. doi: 10.1167/iovs.10-5927
Loehlin, John C. and Martin, Nicholas G. (2011). The general factor of personality: questions and elaborations. Journal of Research in Personality, 45 (1), 44-49. doi: 10.1016/j.jrp.2010.11.008
Vink, Jacqueline M., Boomsma, Dorret I., Medland, Sarah E., de Moor, Marleen H. M., Stubbe, Janine H., Cornes, Belinda K., Martin, Nicholas G., Skytthea, Axel, Kyvik, Kirsten O., Rose, Richard J., Kujala, Urho M., Kaprio, Jaakko, Harris, Jennifer R., Pedersen, Nancy L., Cherkas, Lynn, Spector, Tim D. and de Geus, Eco J. C. (2011). Variance components models for physical activity with age as modifier: a comparative twin study in seven countries. Twin Research and Human Genetics, 14 (1), 25-34. doi: 10.1375/twin.14.1.25
Siskind, Victor, Hughes, Maria Celia B., Palmer, Jane M., Symmons, Judith M., Aitken, Joanne F., Martin, Nicholas G., Hayward, Nicholas K. and Whiteman, David C. (2011). Nevi, family history, and fair skin increase the risk of second primary melanoma. The Journal of Investigative Dermatology, 131 (2), 461-467. doi: 10.1038/jid.2010.298
Hatemi, Peter K., Gillespie, Nathan A., Eaves, Lindon J., Maher, Brion S., Webb, Bradley T., Heath, Andrew C., Medland, Sarah E., Smyth, David C., Beeby, Harry N., Gordon, Scott D., Montgomery, Grant W., Zhu, Ghu, Byrne, Enda M. and Martin, Nicholas G. (2011). A genome-wide analysis of liberal and conservative political attitudes. Journal of Politics, 73 (1), 271-285. doi: 10.1017/S0022381610001015
Barrett, Jennifer H., Iles, Mark M., Harland, Mark, Taylor, John C., Aitken, Joanne F., Andresen, Per Arne, Akslen, Lars A., Armstrong, Bruce K., Avril, Marie-Francoise, Azizi, Esther, Bakker, Bert, Bergman, Wilma, Bianchi-Scarrà, Giovanna, Bressac-de Paillerets, Brigitte, Calista, Donato, Cannon-Albright, Lisa A., Corda, Eve, Cust, Anne E., Dębniak, Tadeusz, Duffy, David, Dunning, Alison M., Easton, Douglas F., Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Giles, Graham G., Hansson, Johan, Hocevar, Marko, Höiom, Veronica ... Bishop, D. Timothy (2011). Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics, 43 (11), 1108-1113. doi: 10.1038/ng.959
Martin, Nicolas W., Benyamin, Beben, Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011). Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50 (1), 55-62.e4. doi: 10.1016/j.jaac.2010.10.010
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
Wade, T. D., Zhu, G. and Martin, N. G. (2011). Undue influence of weight and shape: Is it distinct from body dissatisfaction and concern about weight and shape?. Psychological Medicine, 41 (4), 819-828. doi: 10.1017/S0033291710001066
Vinkhuyzen, A. A. E., Dumenil, T., Ryan, L., Gordon, S. D., Henders, A. K., Madden, P. A. F., Heath, A. C., Montgomery, G. W., Martin, N. G. and Wray, N. R. (2011). Identification of tag haplotypes for 5HTTLPR for different genome-wide SNP platforms. Molecular Psychiatry, 16 (11), 1073-1075. doi: 10.1038/mp.2011.68
Pergadia, Michele L., Glowinski, Anne L., Wray, Naomi, Agrawal, Arpana, Saccone, Scott F., Loukola, Anu, Broms, Ulla, Koronen, Tellervo, Penninx, Brenda W. J. H., Grant, Julia D., Nelson, Elliot C., Henders, Anjali K., Schrage, Andrew J., Chou, Yi-Ling, Keskitalo-Vuokko, Kaisu, Zhu, Qin, Gordon, Scott D., Vink, Jacqueline M., de Geus, Eco J. C., MacGregor, Stuart, Liu, Jimmy Z., Willemsen, Gonneke, Medland, Sarah E., Boomsma, Dorret I., Montgomery, Grant W., Rice, John P., Goate, Alison M., Heath, Andrew, C, Martin, Nicholas G. and Madden, Pamela A. F. (2011). A 3p26-3p25 genetic linkage finding for DSM-IV major depression in heavy smoking families. American Journal Psychiatry, 168 (8), 848-852. doi: 10.1176/appi.ajp.2011.10091319
Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J. ... Posthuma, Danielle (2011). The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 156 (2), 145-157. doi: 10.1002/ajmg.b.31149
Bates, Timothy C., Luciano, Michelle, Medland, Sarah E., Montgomery, Grant W., Wright, Margaret J. and Martin, Nicholas G. (2011). Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Behavior Genetics, 41 (1), 50-57. doi: 10.1007/s10519-010-9402-9
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Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Madden, Pamela A. F. and Martin, Nicholas G. (2010). A Family Study of Adult Twins with and without a History of Childhood Abuse: Stability of Retrospective Reports of Maltreatment and Associated Family Measures. Twin Research and Human Genetics, 13 (2), 121-130. doi: 10.1375/twin.13.2.121
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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
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McCutcheon, Vivia V., Heath, Andrew C., Nelson, Elliot C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2010). Clustering of trauma and associations with single and co-occurring depression and panic attack over twenty years. Twin Research And Human Genetics, 13 (1), 57-65. doi: 10.1375/twin.13.1.57
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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
Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2010). Does education reduce the probability of being overweight?. Journal of Health Economics, 29 (1), 29-38. doi: 10.1016/j.jhealeco.2009.11.013
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
Bouzigon, Emmanuelle, Forabosco, Paola, Koppelman, Gerard H., Cookson, William O. C. M., Dizier, Marie-Helene, Duffy, David L., Evans, David M., Ferreira, Manuel A. R., Kere, Juha, Laitinen, Tarja, Malerba, Giovanni, Meyers, Deborah A., Moffatt, Miriam, Martin, Nicholas G, Ng, Mandy Y., Pignatti, Pier Franco, Wjst, Mathias, Kauffmann, Francine, Demenais, Florence and Lewis, Cathryn M. (2010). Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy. European Journal of Human Genetics, 18 (6), 700-706. doi: 10.1038/ejhg.2009.224
Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Genetic and environmental influences on risky sexual behaviour and its relationship with personality. Behavior Genetics, 40 (1), 12-21. doi: 10.1007/s10519-009-9300-1
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
Dawood, Khytam, Bailey, J. Michael and Martin, Nicholas G. (2010). Genetic and Environmental Influences on Sexual Orientation. Handbook of Behavior Genetics, 269-279. doi: 10.1007/978-0-387-76727-7_19
Marijn A. Distel, Timothy J. Trull, Gonneke Willemsen, Jacqueline M. Vink, Catherine A. Derom, Michael Lynskey, Nicholas G. Martin and Dorret I. Boomsm (2009). The Five-Factor Model of Personality and Borderline Personality Disorder: A Genetic Analysis of Comorbidity. BIOLOGICAL PSYCHIATRY, 66 (12), 1131-1138. doi: 10.1016/j.biopsych.2009.07.017
Sachdev, Perminder S., Lammel, Andrea, Trollor, Julian N., Lee, Teresa, Wright, Margaret J., Ames, David, Wen, Wei, Martin, Nicholas G., Brodaty, Henry, Schofield, Peter R. and OATS Research Team (2009). A comprehensive neuropsychiatric study of elderly twins: The Older Australian Twins Study. Twin Research and Human Genetics, 12 (6), 573-582. doi: 10.1375/twin.12.6.573
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
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
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
Mosing, Miriam A., Zietsch, Brendan P., Shekar, Sri N., Wright, Margaret J. and Martin, Nicholas G. (2009). Genetic and environmental influences on optimism and its relationship to mental and self-rated health: A study of aging twins. Behavior Genetics, 39 (6), 597-604. doi: 10.1007/s10519-009-9287-7
Julia D. Grant, Arpana Agrawal, Kathleen K. Bucholz, Pamela A.F. Madden, Michele L. Pergadia, Elliot C. Nelson, Michael T. Lynskey, Richard D. Todd, Alexandre A. Todorov, Narelle K. Hansell, John B. Whitfield, Nicholas G. Martin and Andrew C. Heath (2009). Alcohol consumption indices of genetic risk for alcohol dependence. Biological Psychiatry, 66 (8), 795-800. doi: 10.1016/j.biopsych.2009.05.018
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
Sarah E. Medland, Gu Zhu and Nicholas G. Martin (2009). Estimating the Heritability of Hair Curliness in Twins of European Ancestry. Twin Research and Human Genetics, 12 (5), 514-518. doi: 10.1375/twin.12.5.514
David A. Mackey, Jane R. MacKinnon, Shayne A. Brown, Lisa S. Kearns, Jonathan B. Ruddle, Paul G. Sanfilippo, Cong Sun, Christopher J. Hammond, Terri L. Young, Nicholas G. Martin and Alex W. Hewitt (2009). Twins Eye Study in Tasmania (TEST): Rationale and Methodology to Recruit and Examine Twins. Twin Research and Human Genetics, 12 (5), 441-454. doi: 10.1375/twin.12.5.441
Mary Waldron, Nicholas G. Martin and Andrew C. Heath (2009). Parental Alcoholism and Offspring Behavior Problems: Findings in Australian Children of Twins. Twin Research and Human Genetics, 12 (5), 433-440. doi: 10.1375/twin.12.5.433
Wendy S. Slutske, Alex Blaszczynski and Nicholas G. Martin (2009). Sex Differences in the Rates of Recovery, Treatment-Seeking, and Natural Recovery in Pathological Gambling: Results From an Australian Community-Based Twin Survey. Twin Research and Human Genetics, 12 (5), 425-432. doi: 10.1375/twin.12.5.425
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
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
Arpana Agrawal, Carolyn E. Sartor, Michael T. Lynskey, Julia D. Grant, Michele L. Pergadia, Richard Grucza, Kathleen K. Bucholz, Elliot C. Nelson, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Evidence for an Interaction Between Age at First Drink and Genetic Influences on DSM-IV Alcohol Dependence Symptoms. Alcoholism: Clinical and Experimental Research, 33 (12), 2047-2056. doi: 10.1111/j.1530-0277.2009.01044.x
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
Shekar, SN, Duffy, DL, Youl, P, Baxter, AJ, Kvaskoff, M, Whiteman, DC, Green, AC, Hughes, MC, Hayward, NK, Coates, M and Martin, NG (2009). A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability. Journal of Investigative Dermatology, 129 (9), 2211-2219. doi: 10.1038/jid.2009.48
Mary Waldron, , , ,, ,, Andrew C. Heath, Michael T. Lynskey, Elliot C. Nelson, Kathleen K. Bucholz, Pamela A.F. Madden and Nicholas G. Martin (2009). Smoking and Illicit Drug Use Associations With Early Versus Delayed Reproduction: Findings in a Young Adult Cohort of Australian Twins. Journal of Studies on Alcohol and Drugs, 70 (5), 786-796. doi: 10.15288/jsad.2009.70.786
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
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
Hatemi, Peter K., Alford, John R., Hibbing, John R., Martin, Nicholas G. and Eaves, Lindon J. (2009). Is There a "Party" in Your Genes?. Political Research Quarterly, 62 (3), 584-600. doi: 10.1177/1065912908327606
Carolyn E. Sartor, Michael T. Lynskey, Kathleen K. Bucholz, Pamela A. F. Madden, Nicholas G. Martin and Andrew C. Heath (2009). Timing of first alcohol use and alcohol dependence: evidence of common genetic influences. Addiction, 104 (9), 1512-1518. doi: 10.1111/j.1360-0443.2009.02648.x
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
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
Bishop, DT, Demenais, F, Iles, MM, Harland, M, Taylor, JC, Corda, E, Randerson-Moor, J, Aitken, JF, Avril, MF, Azizi, E, Bakker, B, Bianchi-Scarra, G, Bressac-de Paillerets, B, Calista, D, Cannon-Albright, LA, Chin-A-Woeng, T, Debniak, T, Galore-Haskel, G, Ghiorzo, P, Gut, I, Hansson, J, Hocevar, M, Hoiom, V, Hopper, JL, Ingvar, C, Kanetsky, PA, Kefford, RF, Landi, MT, Lang, J ... Bishop, JAN (2009). Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics, 41 (8), 920-925. doi: 10.1038/ng.411
Claire M. A. Haworth, Margaret J. Wright, Nicolas W. Martin, Nicholas G. Martin, Dorret I. Boomsma, Meike Bartels, Danielle Posthuma, Oliver S. P. Davis, Angela M. Brant, Robin P. Corley, John K. Hewitt, William G. Iacono, Matthew McGue, Lee A. Thompson, Sara A. Hart, Stephen A. Petrill, David Lubinski and Robert Plomin (2009). A Twin Study of the Genetics of High Cognitive Ability Selected from 11,000 Twin Pairs in Six Studies from Four Countries. Behavior Genetics, 39 (4), 359-370. doi: 10.1007/s10519-009-9262-3
Martin, Nicolas W., Hansell, Narelle K., Wainwright, Mark A., Shekar, Sri N., Medland, Sarah E., Bates, Timothy C., Burt, Jennifer S., Martin, Nicholas G. and Wright, Margaret J. (2009). Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?. Behavior Genetics, 39 (4), 417-426. doi: 10.1007/s10519-009-9275-y
Hatemi, Peter K., Funk, Carolyn L., Medland, Sarah E., Maes, Hermine M., Silberg, Judy L., Martin, Nicholas G. and Eaves, Lindon J. (2009). Genetic and Environmental Transmission of Political Attitudes Over a Life Time. Journal of Politics, 71 (3), 1141-1156. doi: 10.1017/S0022381609090938
Sprangers, Mirjam A. G., Sloan, Jeff A., Veenhoven, Ruut, Cleeland, Charles S., Halyard, Michele Y., Abertnethy, Amy R., Baas, Frank, Barsevick, Andrea M., Bartels, Meike, Boomsma, Dorret I., Chauhan, Cynthia, Dueck, Amylou C., Frost, Marlene H., Hall, Per, Klepstad, Pal, Martin, Nicholas G., Miaskowski, Christine, Mosing, Miriam, Movsas, Benjamin, Van Noorden, Cornelis J. F., Patrick, Donald L., Pedersen, Nancy L., Ropka, Mary E., Shi, Quiling, Shinozaki, Gen, Singh, Jasvinder A., Yang, Ping and Zwinderman, Ailko H. (2009). The Establishment of the GENEQOL Consortium to Investigate the Genetic Disposition of Patient-Reported Quality-of-Life Outcomes. Twin Research and Human Genetics, 12 (3), 301-311. doi: 10.1375/twin.12.3.301
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
Penelope A. Lind, Michelle Luciano, Michael A. Horan, Riccardo E. Marioni, Margaret J. Wright, Timothy C. Bates, Patrick Rabbitt, Sarah E. Harris, Yvonne Davidson, Ian J. Deary, Linda Gibbons, Andrew Pickles, William Ollier, Neil Pendleton, Jackie F. Price, Antony Payton and Nicholas G. Martin (2009). No Association Between Cholinergic Muscarinic Receptor 2 (CHRM2) Genetic Variation and Cognitive Abilities in Three Independent Samples. Behavior Genetics, 39 (5), 513-523. doi: 10.1007/s10519-009-9274-z
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
Marijn A. Distel, Irene Rebollo-Mesa, Gonneke Willemsen, Catherine A. Derom, Timothy J. Trull, Nicholas G. Martin and Dorret I. Boomsma (2009). Familial Resemblance of Borderline Personality Disorder Features: Genetic or Cultural Transmission?. PLoS One, 4 (4) e5334, e5334. doi: 10.1371/journal.pone.0005334
Carla Chia Ming Chen, Jonathan M. Keith, Dale R. Nyholt, Nicholas G. Martin and Kerrie L. Mengersen (2009). Bayesian latent trait modeling of migraine symptom data. Human Genetics, 126 (2), 277-288. doi: 10.1007/s00439-009-0671-4
Christopher Oldmeadow, Kerrie Mengersen, Nicholas Martin and David L. Duffy (2009). Heritability and Linkage Analysis of Appendicitis Utilizing Age at Onset. Twin Research and Human Genetics, 12 (2), 150-157. doi: 10.1375/twin.12.2.150
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
Loehlin, JC, Medland, SE and Martin, NG (2009). Relative Finger Lengths, Sex Differences, and Psychological Traits. Archives of Sexual Behavior, 38 (2), 298-305. doi: 10.1007/s10508-007-9303-z
Chen, Carla C. M., Mengersen, Kerrie L., Keith, Jonathan M., Martin, Nicholas G. and Nyholt, Dale R. (2009). Linkage and heritability analysis of migraine symptom groupings: A comparison of three different clustering methods on twin data. Human Genetics, 125 (5-6), 591-604. doi: 10.1007/s00439-009-0652-7
Jacqueline M. Vink1, August B. Smit, Eco J.C. de Geus, Patrick Sullivan, Gonneke Willemsen, Jouke-Jan Hottenga, Johannes H. Smit, Witte J. Hoogendijk, Frans G. Zitman, Leena Peltonen, Jaakko Kaprio, Nancy L. Pedersen, Patrik K. Magnusson, Tim D. Spector, Kirsten Ohm Kyvik, Katherine I. Morley, Andrew C. Heath, Nicholas G. Martin, Rudi G.J. Westendorp, P. Eline Slagboom, Henning Tiemeier, Albert Hofman, Andre G. Uitterlinden, Yurii S. Aulchenko, Najaf Amin, Cornelia van Duijn, Brenda W. Penninx and Dorret I. Boomsma (2009). Genome-wide Association Study of Smoking Initiation and Current Smoking. American Journal of Human Genetics, 84 (3), 367-379. doi: 10.1016/j.ajhg.2009.02.001
Madeline H. Meier, Wendy S. Slutske, Andrew C. Heath and Nicholas G. Martin (2009). The Role of Harsh Discipline in Explaining Sex Differences in Conduct Disorder: a Study of Opposite-Sex Twin Pairs. Journal of Abnormal Child Psychology, 37 (5), 653-664. doi: 10.1007/s10802-009-9309-1
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
M. Luciano, F. Miyajima, P. A. Lind, T. C. Bates, M. Horan, S. E. Harris, M. J. Wright, W. E. Ollier, C. Hayward, N. Pendleton, A. J. Gow, P. M. Visscher, J. M. Starr, I. J. Deary, N. G. Martin and A. Payton (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes, Brain and Behavior, 8 (2), 218-227. doi: 10.1111/j.1601-183X.2008.00462.x
Tracey D. Wade, Susan A. Treloar, Andrew C. Heath and Nicholas G. Martin (2009). An examination of the overlap between genetic and environmental risk factors for intentional weight loss and overeating. International Journal of Eating Disorders, 42 (6), 492-497. doi: 10.1002/eat.20668
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
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
Wendy S. Slutske, Madeline H. Meier, Gu Zhu, Dixie J. Statham, Alex Blaszczynski and Nicholas G. Martin (2009). The Australian twin study of gambling (OZ-GAM): Rationale, sample description, predictors of participation, and a first look at sources of individual differences in gambling involvement. Twin Research and Human Genetics, 12 (1), 63-78. doi: 10.1375/twin.12.1.63
Hermine H. Maes, Michael C. Neale, Sarah E. Medland, Matthew C. Keller, Nicholas G. Martin, Andrew C. Heath and Lindon J. Eaves (2009). Flexible Mx Specification of Various Extended Twin Kinship Designs. Twin Research and Human Genetics, 12 (1), 26-34. doi: 10.1375/twin.12.1.26
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
Verweij, K. J. H., Zietsch, B. P., Bailey, J. M. and Martin, N. G. (2009). Shared aetiology of risky sexual behaviour and adolescent misconduct : Genetic and environmental influences. Genes, Brain And Behavior, 8 (1), 107-113. doi: 10.1111/j.1601-183X.2008.00456.x
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
Medland, Sarah E., Duffy, David L., Wright, Margaret J., Geffen, Gina M., Hay, David A., Levy, Florence, Van-Beijsterveldt, Catherina E.M., Willemsen, Gonneke, Townsend, Grant C., White, Vicki, Hewitt, Alex W., Mackey, David A., Bailey, J. Michael, Slutske, Wendy S., Nyholt, Dale R., Treloar, Susan A., Martin, Nicholas G. and Boomsma, Dorret I. (2009). Genetic influences on handedness: Data from 25,732 Australian and Dutch twin families. Neuropsychologia, 47 (2), 330-337. doi: 10.1016/j.neuropsychologia.2008.09.005
Psychiatric GWAS Consortium Coordinating Committee, Martin, N., Wray, N., Mowry, B. and Holliday, E. (2009). Genomewide Association Studies: History, Rationale, and Prospects for Psychiatric Disorders. American Journal of Psychiatry, 166 (5), 540-556. doi: 10.1176/appi.ajp.2008.08091354
Yurii S Aulchenko, Samuli Ripatti, Ida Lindqvist, Dorret Boomsma, Iris M Heid, Peter P Pramstaller, Brenda W J H Penninx, A Cecile J W Janssens, James F Wilson, Tim Spector, Nicholas G Martin, Nancy L Pedersen, Kirsten Ohm Kyvik, Jaakko Kaprio, Albert Hofman, Nelson B Freimer, Marjo-Riitta Jarvelin, Ulf Gyllensten, Harry Campbell, Igor Rudan, Åsa Johansson, Fabio Marroni, Caroline Hayward, Veronique Vitart, Inger Jonasson, Cristian Pattaro, Alan Wright, Nick Hastie, Irene Pichler ... Jouke-Jan Hottenga (2009). Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nature Genetics, 41 (1), 47-55. doi: 10.1038/ng.269
V. V. McCutcheon, A. C. Heath, E. C. Nelson, K. K. Bucholz, P. A. F. Madden and N. G. Martin (2009). Accumulation of trauma over time and risk for depression in a twin sample. Psychological Medicine, 39 (3), 431-441. doi: 10.1017/S0033291708003759
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
Sullivan, P. F., de Geus, E. J. C., Willemsen, G., James, M. R., Smit, J. H., Zandbelt, T., Martin, N. G., Wray, N. R., Boomsma, D. I. and Penninx, B. W. J. H. (2009). Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Molecular Psychiatry, 14 (4), 359-375. doi: 10.1038/mp.2008.125
De Zubicaray, Greig I., Chiang, Ming-Chang, McMahon, Katie L., Shattuck, David W., Toga, Arthur W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2008). Meeting the challenges of neuroimaging genetics. Brian Imaging and Behavior, 2 (4), 258-263. doi: 10.1007/s11682-008-9029-0
Reiersen, Angela M., Constantino, John N., Grimmer, Marisa, Martin, Nicholas G. and Todd, Richard D. (2008). Evidence for shared genetic influences on self-reported ADHD and autistic symptoms in young adult Australian twins. Twin Research and Human Genetics, 11 (6), 579-585. doi: 10.1375/twin.11.6.579
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
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
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
Nyholt, Dale R., LaForge, K. Steven, Kallela, Mikko, Alakurtti, Kirsi, Anttila, Verneri, Farkkila, Markus, Hamalainen, Eija, Kaprio, Jaakko, Kaunisto, Mari A., Heath, Andrew C., Montgomery, Grant W., Goebel, Hartmut, Todt, Unda, Ferrari, Michel D., Launer, Lenore J., Frants, Rune R., Terwindt, Gisela M., de Vries, Boukje, Verschuren, W. M. Monique, Brand, Jan, Freilinger, Tobias, Pfaffenrath, Volker, Straube, Andreas, Ballinger, Dennis G., Zhan, Yiping, Daly, Mark J., Cox, David R., Dichgans, Martin, van den Maagdenberg, Arn M. J. M. ... Palotie, Aarno (2008). A high-density association screen of 155 ion transport genes for involvement with common migraine. Human Molecular Genetics, 17 (21), 3318-3331. doi: 10.1093/hmg/ddn227
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
Zietsch, Brendan P., Morley, Katherine I., Shekar, Sri N., Verweij, Karin J. H., Keller, Matthew C., Macgregor, Stuart, Wright, Margaret J., Bailey, J. Michael and Martin, Nicholas G. (2008). Genetic factors predisposing to homosexuality may increase mating success in heterosexuals. Evolution and Human Behavior, 29 (6), 424-433. doi: 10.1016/j.evolhumbehav.2009.07.002
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
Agrawal, Arpana, Lynskey, Michael T., Pergadia, Michele L., Bucholz, Kathleen K., Heath, Andrew C., Martin, Nicholas G. and Madden, Pamela A. F. (2008). Early cannabis use and DSM-IV nicotine dependence: A twin study. Addiction, 103 (11), 1896-1904. doi: 10.1111/j.1360-0443.2008.02354.x
Waldron, Mary, Heath, Andrew C., Bucholz, Kathleen K., Madden, Pamela A. F. and Martin, Nicholas G. (2008). Alcohol Dependence and Reproductive Onset: Findings in Two Australian Twin Cohorts. Alcoholism-Clinical and Experimental Research, 32 (11), 1865-1874. doi: 10.1111/j.1530-0277.2008.00771.x
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
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
Wade, T. D., Treloar, S. and Martin, N. G. (2008). Shared and unique risk factors between lifetime purging and objective binge eating: A twin study. Psychological Medicine, 38 (10), 1455-1464. doi: 10.1017/S0033291708002791
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
Hur, Y-M, Kaprio, J., Iacono, W. G., Boomsma, D. I., McGgue, M., Silventoinen, K., Martin, N. G., Luciano, M., Visscher, P. M., Rose, R. J., He, M., Ando, J., Ooki, S., Nonaka, K., Lin, C. C. H., Lajunen, H. R., Cornes, B. K., Bartels, M., van Beijsterveldt, C. E. M., Cherny, S. S. and Mitchell, K. (2008). Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity, 32 (10), 1455-1467. doi: 10.1038/ijo.2008.144
Schermer, Julie Aitken, Feather, N. T., Zhu, Gu and Martin, Nicholas G. (2008). Phenotypic, Genetic, and Environmental Properties of the Portrait Values Questionnaire. Twin Research and Human Genetics, 11 (5), 531-537. doi: 10.1375/twin.11.5.531
Distel, M. A., Trull, T. J., Derom, C. A., Thiery, E. W., Grimmer, M. A., Martin, N. G., Willemsen, G. and Boomsma, D. I. (2008). Heritability of borderline personality disorder features is similar across three countries. Psychological Medicine, 38 (9), 1219-1229. doi: 10.1017/S0033291707002024
Lundmark, Per E., Liljedahl, Ulrika, Boomsma, Dorret I., Mannila, Heikki, Martin, Nicholas G., Palotie, Aarno, Peltonen, Leena, Perola, Markus, Spector, Tim D. and Syvanen, Ann-Christine (2008). Evaluation of HapMap data in six populations of European descent. European Journal of Human Genetics, 16 (9), 1142-1150. doi: 10.1038/ejhg.2008.77
Slutske, Wendy S., D'Onofrio, Brian M., Turkheimer, Eric, Emery, Robert E., Harden, K. Paige, Heath, Andrew C. and Martin, Nicholas G. (2008). Searching for an environmental effect of parental alcoholism on offspring alcohol use disorder: A genetically informed study of children of alcoholics. Journal of Abnormal Psychology, 117 (3), 534-551. doi: 10.1037/a0012907
Oldmeadow, Chris, Wood, Ian, Mengersen, Kerrie, Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2008). Investigation of the relationship between smoking and appendicitis in Australian twins. Annals of Epidemiology, 18 (8), 631-636. doi: 10.1016/j.annepidem.2008.04.004
Conference Papers
Ceja, Zuriel, Edwards, Alexis, Martin, Nick, Hickie, Ian, Medland, Sarah E. and Rentería, Miguel E. (2024). Genetic And Psychological Predictors Of Suicidal Behavior: Insights From Polygenic Risk Scores And Mental Health Diagnoses. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.324
Werwath, Kathryn, Lawn, Rebecca, Salem, Madeleine, Li, Tayden, Gordon, Scott, Shen, Hanyang, Mitchell, Brittany, Kung, Benson, Stafford, Ciera, Vemuri, Mytilee, Ratanatharathorn, Andrew, Meijsen, Joeri, Medland, Sarah E., Martin, Nicholas G. and Duncan, Laramie (2024). Trans-ancestry GWAS Of Hot Flushes Reveals Potent Treatment Target, Overlap With Psychiatric Disorders, And Cell Types Matching Known Hot Flash Neurons. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.207
Lind, Penelope A., Martin, Nicholas G. and Medland, Sarah E. (2024). A Genome-wide Association Meta-analysis Of Lithium Response Including The Recently Recruited Australian Genetics Of Bipolar Disorder Study. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.458
Mitchell, Brittany, Martin, Nick and Medland, Sarah E. (2024). Genetic and environmental predictors of treatment resistant depression. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.067
Lupton, Michelle K., Gomez, Lina, Mitchell, Brittany L., Adsett, Jessica, García‐Marín, Luis M., Renteria, Miguel E., McAloney, Kerrie, Ceslis, Amelia, Thienel, Renate, Robinson, Gail, Breakspear, Michael and Martin, Nicholas G (2023). Poorer online cognitive performance is associated with genetic risk for Alzheimer’s disease and brain phenotypes in healthy mid‐life and older adults. AAIC 2023 Abstracts, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ USA: Wiley. doi: 10.1002/alz.078078
Thienel, Renate, Borne, Léonie, Faucher, Caroline, Robinson, Gail, Fripp, Jurgen, Giorgio, Joseph, Martin, Nicholas G., Breakspear, Michael and Lupton, Michelle K. (2023). Can an online battery match in‐person cognitive testing in predicting age‐related cortical changes. Alzheimer’s Association International Conference AAIC 2023, Amsterdam, Netherlands, 16-20 July 2023. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.074476
Mitchell, Brittany, Morosoli, José, Martin, Nicholas G., Lind, Penelope A., Hickie, Ian B., Medland, Sarah E. and Wray, Naomi (2023). Characterising antidepressant usage based on electronic prescription records in the Australian Genetics of Depression Study. World Congress of Psychiatric Genetics (WCPG), Montreal, Canada, 10-14 October 2023. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2023.08.422
Ma, X., Shah, A., Fairlie, T., Martin, N., Jones, M., Koloski, N., Morrison, M. and Holtmann, G. (2023). Small intestinal bacterial overgrowth in patients with intestinal failure: A systematic review and meta-analysis. Gastroenterological Society of Australia (GESA) Australian Gastroenterology Week (AGW) 2023, Brisbane, QLD Australia, 2-5 September 2023. Richmond, VIC Australia: John Wiley & Sons.
Kholghi, Mahnoosh, Fazlollahi, Amir, Lupton, Michelle K., Bourgeat, Pierrick, Zhang, Qing, Martin, Nicholas G., Breakspear, Michael, Fripp, Jurgen and PISA (Prospective Imaging Study of Aging: Genes, Brain and Behaviour) (2023). The association between sleep restlessness and neuroimaging biomarkers of Alzheimer’s Disease in mid‐life to older adults and patients. Alzheimer's Association International Conference (AAIC) 2022, San Diego, CA United States, 31 July - 4 August 2022. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.062017
Mitchell, B., Saklatvala, J., Martin, N.G., Smith, C., Barker, J., Renteria, M. and Simpson, M. (2022). Exploring the relationship between acne and mental health. 51st Annual ESDR Meeting, Amsterdam, Netherlands, 28 September-1 October 2022. Oxford, United Kingdom: Elsevier. doi: 10.1016/j.jid.2022.09.318
Hopkins, Kristen L., Lind, Penelope A., Mitchell, Brittany L., Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian B., Martin, Nicholas G. and Medland, Sarah E. (2022). Can polygenic Risk Scores Predict Who Will Receive or Respond Better to Electroconvulsive Therapy for Treatment of Major Depressive Disorder?. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.
Medland, Sarah E., Mitchell, Brittany, Campos, Adrian, Whiteman, David C., Olsen, Catherine M., Siskind, Dan J., Hickie, Ian, Lind, Penelope A. and Martin, Nicholas G. (2022). Challenges to Incorporating Polygenic Risk Scores in Clinical Mental Health Practice. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Los Angeles Ca, Jun 22-25, 2022. NEW YORK: SPRINGER.
ter Kuile, Abigail, Mitchell, Brittany, Peel, Alicia, Mundy, Jessica, Hubel, Christopher, Zvrskovec, Johan, Palmos, Alish, Coleman, Jonathan, Davies, Molly, Martin, Nick, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Adey, Brett N., Lee, Sang Hyuck, Furtjes, Anna E., Morneau-Vaillancourt, Genevieve, Purves, Kirstin, Skelton, Megan, Hotopf, Matthew, Smith, Daniel J., Veale, David, Armour, Cherie, McIntosh, Andrew, Walters, James T. R., Jones, Ian R., Hirsch, Colette R., Kalsi, Gursharan, Breen, Gerome and Eley, Thalia (2022). Exploring the genome-wide genetic overlap between anxiety and fear disorders. World Congress of Psychiatric Genetics (WCPG), Florence, Italy, 13-17 September 2022. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2022.07.014
Campos, Adrian I., Garcia-Marin, Luis M., Christensen, Helen, Batterham, Philip J., van Velzen, Laura S., Schmaal, Lianne, Rabinowitz, Jill A., Jahanshad, Neda, Martin, Nicholas G., Cuellar-Partida, Gabriel, Ruderfer, Douglas M., Mullins, Niamh and Renteria, Miguel E. (2022). Genomics Driven Screening for Causal Determinants of Suicide Attempt. SOBP 77th Annual Scientific Meeting, New Orleans, LA United States, 28-30 April 2022. Philadelphia, PA United States: Elsevier.
Fazlollahi, Amir, Xia, Ying, Lupton, Michelle K., Raniga, Parnesh, Bourgeat, Pierrick, Martin, Nick, Dore, Vincent, Rose, Stephen, Salvado, Olivier, Breakspear, Michael and Fripp, Jurgen (2022). Early effects of amyloid-β on structural and vascular brain changes in mid-life cognitively unimpaired individuals. Alzheimer's Association International Conference (AAIC) 2021, Denver, CO United States, 26-30 July 2021. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.052681
Lupton, Michelle K., McAloney, Kerrie, Ceslis, Amelia, Robinson, Gail, Thienel, Renate, Breakspear, Michael and Martin, Nicholas G. (2021). The use of online testing to assess cognitive differences in healthy individuals at high genetic risk of Alzheimer's disease. 2021 Alzheimer's Association International Conference, Denver, CO United States, 26 - 30 July 2021. Hoboken, NJ United States: John Wiley & Sons. doi: 10.1002/alz.055369
Thorp, Jackson G., Campos, Adrian I., Grotzinger, Andrew D., Gerring, Zachary, An, Jiyuan, Ong, Jue-Sheng, Wang, Wei, Shringarpure, Suyash, Byrne, Enda M., MacGregor, Stuart, Martin, Nicholas G., Medland, Sarah E., Middeldorp, Christel M. and Derks, Eske M. (2020). Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression. 50th Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 26, 2020. NEW YORK: SPRINGER.
Campos, Adrián I., Roughan, William H., García-Marin, Luis M., Cuéllar-Partida, Gabriel, Lupton, Michelle K., Hickie, Ian B., Medland, Sarah E., Wray, Naomi R., Byrne, Enda M., Ngo, Trung T., Martin, Nicholas G. and Rentería, Miguel E. (2020). The relationship between comorbid chronic pain and poorer self-reported antidepressant efficacy is partly mediated by genetics. Virtual 2020 World Congress of Psychiatric Genetics (WCPG), Online, 16–22 October 2020.
Hubel, C., Watson, H. J., Yilmaz, Z., Landen, M., Martin, N. G., Mortensen, P., Sullivan, P. F., Breen, G. and Bulik, C. M. (2019). Anorexia nervosa genome-wide association study identifies eight loci and implicates psychiatric and metabolic origins. 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg Sweden, Jun 15-18, 2019. LONDON: NATURE PUBLISHING GROUP.
Hwang, Liang-Dar, Gharahkhani, Puya, Zhu, Gu, Gordon, Scott D., Breslin, Paul A. S., Martin, Nicholas G., Reed, Danielle R. and Wright, Margaret J. (2018). Replication and discovery of genetic variants influencing human bitter taste perception. 39th Annual Meeting of the Association for Chemoreception Sciences, Bonita Springs, FL, United States, 26 - 29 April 2017. Oxford, United Kingdom: Oxford University Press. doi: 10.1093/chemse/bjy003
Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, 24 November 2017.
Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). GWAS of complementary perceptual endophenotype measures: How do they rate?. Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, 15–17 September 2017.
Dennis, Emily L., Rashid, Faisal, Faskowitz, Josh, Jin, Yan, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Hickie, Ian B., Wright, Margaret J., Jahanshad, Neda and Thompson, Paul M. (2017). Mapping age effects along fiber tracts in young adults. 2017 IEEE 14th International Symposium on Biomedical Imaging (ISBI 2017),, Melbourne, VIC, Australia, 18-21 April 2017. NEW YORK: IEEE. doi: 10.1109/ISBI.2017.7950478
Pizzagalli, Fabrizio, Auzias, Guillaume, Kochunov, Peter, Faskowitz, Joshua I., McMahon, Katie L., De Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Jahanshad, Neda and Thompson, Paul M. (2016). Genetic analysis of cortical sulci in 1,009 adults. 2016 IEEE 13th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2016, Prague, Czech Republic, 13-16 April 2016. Piscataway, NJ, United States: Institute of Electrical and Electronics Engineers. doi: 10.1109/ISBI.2016.7493395
Shen, Kaikai, Dore, Vincent, Rose, Stephen, Fripp, Jurgen, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Thompson, Paul M., Wright, Margaret J. and Salvado, Olivier (2015). Heritability analysis of surface-based cortical thickness estimation on a large twin cohort. Medical Imaging 2015: Image Processing, Orlando, Florida, United States, Feb 24-26, 2015. Bellingham, WA United States: SPIE. doi: 10.1117/12.2081677
Zhan, L., Jahanshad, N., Faskowitz, J., Zhu, D., Prasad, G., Martin, N. G., de Zubicaray, G. I., McMahon, K. L., Wright, M. J. and Thompson, P. M. (2015). Heritability of brain network topology in 853 twins and siblings. IEEE 12th International Symposium on Biomedical Imaging, New York, United States, Apr 16-19, 2015. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2015.7163908
Zhu, Dajiang, Zhan, Liang, Faskowitz, Joshua, Daianu, Madelaine, Jahanshad, Neda, De Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2015). Genetic analysis of structural brain connectivity using DICCCOL models of diffusion MRI in 522 twins. IEEE 12th International Symposium on Biomedical Imaging, New York, United States, Apr 16-19, 2015. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2015.7164080
Hwang, Liang-Dar, Zhu, Gu, Wright, Margaret J., Martin, Nicholas G., Reed, Danielle R. and Breslin, Paul A. S. (2015). Genetic Modeling of Human Intensity Ratings of Four Sweeteners. 15th Scientific Meeting of the Australasian Association for ChemoSensory Science (AACSS), Brisbane, QLD Australia, 03-05 December 2014. Oxford, United Kingdom: Oxford University Press. doi: 10.1093/chemse/bjv008
Warstadt, Nicholus M., Jahanshad, Neda, Dennis, Emily L., Kohannim, Omid, McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Whitfield, John B., Wright, Margaret J. and Thompson, Paul M. (2014). Identifying candidate gene effects by restricting search space in a multivariate genetic analysis of white matter microstructure. Biomedical Imaging ISBI, Beijing, China, 29 April - 2 May, 2014. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2014.6867881
Jahanshad, Neda, Kochunov, Peter, Nichols, Thomas E., Sprooten, Emma, Mandl, Rene C., Almasy, Laura, Brouwer, Rachel M., Curran, Joanne E., de Zubicaray, Greig I., Dimitrova, Rali, Fox, Peter T., Hong, L. Elliot, Landman, Bennett A., Lemaitre, Herve, Lopez, Lorna, Martin, Nicholas G., McMahon, Katie L., Mitchell, Braxton D., Olvera, Rene L., Peterson, Charles P., Sussmann, Jessika E., Toga, Arthur W., Wardlaw, Joanna M., Wright, Margaret J., Wright, Susan N., Bastin, Mark E., McIntosh, Andrew M., Boomsma, Dorret I., Kahn, Rene S. ... Thompson, Paul M. (2014). Combining meta- and mega- analytic approaches for multi-site diffusion imaging based genetic studies: From the ENIGMA-DTI working group. 11th IEEE International Symposium on Biomedical Imaging (ISBI), Beijing, Peoples Republic of China, 29 April-02 May 2014. Piscataway, NJ., United States: IEEE. doi: 10.1109/ISBI.2014.6868099
Mitchem, Dorian, Purkey, Alicia, Grebe, Nicholas, Carey, Greg, Garver-Apgar, Christine, Bates, Timothy, Arden, Rosalind, Hewitt, John, Medland, Sarah, Martin, Nick G., Zietsch, Brendan and Keller, Matthew (2013). Estimating the sex-specific effects of genes on facial attractiveness and sexual dimorphism. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, Jun 28-Jul 02, 2013. NEW YORK: SPRINGER.
Jin, Yan, Shi, Yonggang, Zhan, Liang, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Labeling white matter tracts in hardi by fusing multiple tract atlases with applications to genetics. 2013 IEEE 10th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2013, San Francisco, CA, United States, 7-11 April 2013. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2013.6556524
Zhan, Liang, Jahanshad, Neda, Jin, Yan, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Brain network efficiency and topology depend on the fiber tracking method: 11 tractography algorithms compared in 536 subjects. 2013 IEEE 10th International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2013, San Francisco, CA, United States, 7-11 April 2013. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2013.6556679
Jahanshad, Neda, Bhatt, Priya, Hibar, Derrek P., Villalon, Julio E., Nir, Talia M., Toga, Arthur W., Jack Jr., Clifford R., Bernstein, Matt A. B, Weiner, Michael W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2013). Bivariate genome-wide association study of genetically correlated neuroimaging phenotypes from DTI and MRI through a seemingly unrelated regression model. 3rd International Workshop on Multimodal Brain Image Analysis, MBIA 2013, Held in Conjunction with the 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22 September 2013. Heidelberg, Germany: Springer. doi: 10.1007/978-3-319-02126-3_19
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. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9
Jahanshad, Neda, Kochunov, Peter, Glahn, David C., Blangero, John, Nichols, Thomas E., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Jack, Jr., Clifford R., Bernstein, Matt A., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013). Power estimates for voxel-based genetic association studies using diffusion imaging. MMBC 2013: Mathematical Methods for Brain Connectivity. Held in conjunction with MICCAI 2013: The 16th International Conference on Medical Image Computing and Computer Assisted Intervention Workshops, Nagoya, Japan, 22 September, 2013. Cham, Switzerland: Springer International Publishing. doi: 10.1007/978-3-319-02475-2_21
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. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40763-5_85
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. 16th International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2013, Nagoya, Japan, 22-26 September 2013. Berlin, Germany: Springer. doi: 10.1007/978-3-642-40760-4_75
Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Diffusion imaging protocol effects on genetic associations. International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. NEW YORK: IEEE. doi: 10.1109/ISBI.2012.6235712
Daianu, Madelaine, Jahanshad, Neda, Dennis, Emily L., Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Hickie, Ian B. and Thompson, Paul M. (2012). Left versus right hemisphere differences in brain connectivity: 4-Tesla HARDI tractography in 569 twins. 9th IEEE International Symposium on Biomedical Imaging (ISBI) - From Nano to Macro, Barcelona Spain, 2 - 5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235601
Jin, Yan, Shi, Yonggang, Zhan, Liang, Li, Junning, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Automatic population HARDI white matter tract clustering by label fusion of multiple tract atlases. Second International Multimodal Brain Image Analysis Workshop (MBIA 2012) in Conjunction with MICCAI 2012, Nice, France, 1 - 5 October 2012. Heidelberg, Germany: Springer. doi: 10.1007/978-3-642-33530-3_12
Joshi, S. H., Joshi, A. A., Gutman, B., Toga, A. W., McMahon, K., de Zubicaray, G., Martin, N., Wright, M. and Thompson, P. M. (2012). Genetic influences on sulcal patterns of the brain. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235572
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. 9th IEEE International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway NJ, United States: IEEE. doi: 10.1109/ISBI.2012.6235695
Wheland, D., Joshi, A., McMahon, K., Hansell, N., Martin, N., Wright, M., Thompson, P., Shattuck, D. and Leahy, R. (2012). Robust identification of partial-correlation based networks with applications to cortical thickness data. 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2012, Barcelona, Spain, 2 - 5 May 2012. Piscataway, NJ United States: I E E E. doi: 10.1109/ISBI.2012.6235869
Jahanshad, Neda, Hibar, Derrek, Ryles, April, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansel, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, 2-5 May 2012. Piscataway, NJ, United States: IEEE (Institute for Electrical and Electronic Engineers). doi: 10.1109/ISBI.2012.6235605
Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder. 5th Biennial Conference of the International-Society-for-Bipolar-Disorders, Istanbul, Turkey, 14-17 March 2012. Malden, MA, United States: Wiley-Blackwell. doi: 10.1111/j.1399-5618.2012.00981.x
Dennis, Emily L., Jahanshad, Neda, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Test-retest reliability of graph theory measures of structural brain connectivity. 15th International Conference on Medical Image Computing and Computer Assisted Intervention (MICCAI 2012), Nice, France, 1-5 October 2012. Springer: Heidelberg, Germany. doi: 10.1007/978-3-642-33454-2_38
Chiang, Ming-Chang, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Johnson, Kori, Martin, Nicholas G., Toga, Arthur W., Wright, Margaret J. and Thompson, Paul M. (2011). Hierarchical clustering of the genetic connectivity matrix reveals the network topology of gene action on brain microstructure: An N=531 twin study. 2011 IEEE 8th International Symposium on Biomedical Imaging (ISBI 2011), Chicago, United States, 30 March - 2 April 2011. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2011.5872533
Jahanshad, Neda, Aganj, Iman, Lenglet, Christophe, Joshi, Anand, Jin, Yan, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright Margaret J., Toga, Arthur W., Sapiro, Guillermo and Thompson, Paul M. (2011). Sex differences in the human connectome: 4-Tesla High Angular Resolution Diffusion Imaging (HARDI) tractography in 234 young adult twins. 2011 IEEE 8th International Symposium on Biomedical Imaging (ISBI 2011), Chicago, United States, 30 March - 2 April 2011. Piscataway, NJ, United States: IEEE. doi: 10.1109/ISBI.2011.5872558
Jin, Yan, Shi, Yonggang, Joshi, Shantanu, Jahanshad, Neda, Zhan, Lian, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W. and Thompson, Paul M. (2011). Heritability of white matter fiber tract shapes: A HARDI study of 198 twins. Multimodal Brain Image Analysis: First International Workshop, MBIA 2011. Held in Conjunction with MICCAI 2011, Toronto, Canada, 18-22 September 2011. Heidelberg, Germany: Springer. doi: 10.1007/978-3-642-24446-9_5
Prasad, Gautam, Joshi, Shantanu H,, Jahanshad, Neda, Villalon, Julio, Aganj, Iman, Lenglet, Christophe, Sapiro, Guillermo, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W and Thompson, Paul M. (2011). White matter tract analysis in 454 adults using maximum density paths. CDMRI'11 - Workshop on Computational Diffusion MRI, Toronto, Canada, 22 September 2011.
Prasad, Gautam, Joshi, Anand A., Feng, Albert, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Terzopoulos, Demetri and Thompson, Paul M. (2011). Brain segmentation using deformable organisms and error learning. 3rd MICCAI Workshop on Mathematical Foundations of Computational Anatomy (MFCA 2011), Toronto, Canada, 22 September 2011. Toronto, Canada: MFCA.
Le, Anh T., Miller, Paul W., Slutske, Wendy S. and Martin, Nicholas G. (2011). Opportunity and Educational Outcomes in Australia. 39th Australian Conference of Economists, Sydney Australia, 27-29 September 2010. Richmond, VIC., Australia: Wiley-Blackwell Publishing. doi: 10.1111/j.1475-4932.2011.00749.x
Staffieri, S. E., Ruddle, J. B., Hewitt, A. W., Kearns, L. S., Sanfilippo, P. G., MacGregor, S., Martin, N. G., Young, T. L., Hammond, C. J. and Mackey, D. A. (2010). Genome Wide Analysis Identifies Putative Loci Associated With Interpupillary Distance. ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
Kearns, L. S., Hewitt, A. W., Ruddle, J. B., Bigault, O., Staffieri, S. E., Sanfillipo, P., Martin, N. G., Hammond, C. J., Young, T. L. and Mackey, D. A. (2010). Up to What Age is a Cyclopleged Refraction Required? Results From the Twins Eye Study Tasmania(TEST). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
Aganj, Iman, Jahanshad, Neda, Lenglet, Christophe, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Wright, Margaret J., Martin, Nicholas G., Sapiro, Guillermo and Thompson, Paul M. (2010). Relating fiber crossing in HARDI to intellectual function. 16th annual meeting of the Organization for Human Brain Mapping, Barcelona, Spain, 6-10 June 2010.
Zietsch, B. P., Verweij, K. J. H., Bailey, J. M., Wright, M. J. and Martin, N. G. (2010). Psychiatric vulnerability in nonheterosexuals. The 40th Annual Behavior Genetics Association meeting, Seoul, Korea, 2-5 June 2010. New York, NY, U.S.A.: Springer New York. doi: 10.1007/s10519-010-9392-7
Hansell, Narelle K., Hickie, Ian B., Davenport, Tracey A., Hadzi-Pavlovic, Dusan, Wray, Naomi R., Martin, Nicholas G. and Wright, Margaret J. (2010). A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults. 40th Annual Meeting of Behavior Genetics Association, Pennsylvania, PA, U.S.A., May 2009. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7
Brant, Angela M., Boomsma, Dorret I., Corley, Robin P., DeFries, John C., Haworth, Clare M. A., Hewitt, John K., Martin, Nicholas G., McGue, Matthew, Petrill, Stephen A., Plomin, Robert, Wadsworth, Sally J. and Wright, Margaret J. (2010). Ability and heritability: Investigating the continuous effect of IQ score on IQ etiology in multiple samples. The 40th Annual Behavior Genetic Association Meeting, Seoul, Korea, 2- 5 June 2010. New York, NY, U.S.A.: Springer New York LLC. doi: 10.1007/s10519-010-9392-7
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. Behavior Genetics Association 40th Annual Meeting, Seoul, Korea, 2-5 June 2010. New York, U.S.A.: Springer New York LLC. 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. 2010 World Congress on International Society for Biomedical Research on Alcoholism, Paris, France, 13-16 September 2010. Hoboken, NJ, U.S.A.: Wiley-Blackwell Publishing. doi: 10.1111/j.1530-0277.2010.01292_3.x
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. 6th World Congress for Hair Research, Cairns, QLD, Australia, 16-19 June 2010. Oxford, United Kingdom: Wiley-Blackwell. doi: 10.1111/j.1600-0625.2010.01097.x
Zhan, Liang, Leow, Alex D., Jahanshad, Neda, Lee, Agatha D., Barysheva, Marina, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2010). Genetic analysis of high angular resolution diffusion images (HARDI). MICCAI 2010 Workshop on Computational Diffusion MRI, Beijiing, China, 20-24 September 2010. Berlin, Germany: Springer.
Lee, Agatha D., Leporé, Natasha, de Leeuw, Jan, Brun, Caroline C., Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2010). Multivariate variance-components analysis in DTI. 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, Rotterdam, Netherlands, 14-17 April 2010. Piscataway, NJ, U.S.A.: I E E E. doi: 10.1109/ISBI.2010.5490199
Patel, V, Chiang, MC, Thompson, PM, McMahon, KL, de Zubicaray, GI, Martin, NG, Wright, MJ and Toga, AW (2010). Scalar connectivity measures from fast-marching tractography reveal heritability of white matter architecture. ISBI 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, Rotterdam, Netherlands, 14-17 April 2010. Piscataway, NJ, U.S.A.: Institute of Electrical and Electronic Engineers (IEEE). doi: 10.1109/ISBI.2010.5490187
Lepore, Natasha, Brun, Caroline, Descoteaux, Maxime, Lee, Agatha D., Barysheva, Marina, Chou, Yi-Yu, de Zubicaray, Greig, McMahon, Katie, Wright, Margaret J., Martin, Nicholas G., Gee, James C. and Thompson, Paul M. (2010). Multivariate group-wise genetic analysis of white matter integrity using orientation distribution functions. MICCAI Workshop on Computational Diffusion MRI, Beijiing, China, 20-24 September 2010.
Verweij, Kjh, Zietsch, BP, Lynskey, MT, Heath, AC and Martin, NG (2010). Examining the relationship between sexual orientation and depression: overlapping genetic and early environmental influences. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009.
Mosing, MA, Wright, MJ, Pedersen, Nancy L. and Martin, NG (2010). Genetic influences on optimism and its relationship to health. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009.
Blokland, G, McMahon, K, Thompson, P, Martin, N, de Zubicaray, G and Wright, MJ (2010). Heritability of FMRI response in young adult twins. 40th Annual Meeting of Behavior-Genetics-Association, Pennsylvania PA, MAY, 2009. NEW YORK: SPRINGER.
Mosing, Miriam A., Gordon, Scott D., Medland, Sarah E., Statham, Dixie J., Nelson, Elliot C., Heath, Andrew C., Martin, Nicholas G. and Wray, Naomi R. (2009). Genetic and Environmental Influences on the Co-morbidity Between Depression, Panic Disorder, Agoraphobia, and Social Phobia: A Twin Study. United States: John Wiley & Sons, Inc.. doi: 10.1002/da.20611
Valle, A. M., Radic, Z., Rana, B. K., Whitfield, J. B., O'Connor, D. T., Martin, N. G. and Taylor, P. (2008). The cholinesterases: Analysis by pharmacogenomics in man. 9th International Meeting on Cholinesterases, Suzhou Peoples R China, May 06-10, 2007. CLARE: ELSEVIER IRELAND LTD. doi: 10.1016/j.cbi.2008.04.042
Data Collection
Wright, Margaret Jane, Martin, Nicholas and Hickie, Ian (2017). Data for the psychometric analysis reported in "Validation and psychometric properties of the Somatic and Psychological HEalth REport (SPHERE) in a young Australian-based population sample using non-parametric Item Response Theory". The University of Queensland. (Dataset) doi: 10.14264/uql.2017.647