Publications
Book Chapters
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
Eaves, Lindon J., Hatemi, Peter K., Heath, Andrew C. and Martin, Nicholas G. (2013). Modeling the cultural and biological inheritance of social and political behavior in twins and nuclear families. Man is by nature a political animal. (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
Gillespie, N. A. and Martin, N. G. (2006). Neuroticism as a genetic marker for mood and anxiety. Biology of Personality & Individual Differences. (pp. 225-250) edited by T. Canli. New York, U.S.A.: Guilford Press.
Luciano, M., Wright, M. J., Smith, G. A., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2003). Genetic covariance between processing speed and IQ. Behavior genetics in the postgenomic era. (pp. 163-182) edited by Robert Plomin, John C. Defries, Ian W. Craig and Peter McGuffin. Washington, DC, USA: APA Books.
Boomsma, D. I. and Martin, N. G. (2002). Gene-environment interactions. Biological Psychiatry. (pp. 181-187) edited by H. D'haenen, J. A. den Boer and P. Willner. New York: John Wiley & Sons Ltd.
Dempsey, P. J., Townsend, G. C. and Martin, N. G. (1999). Insights into the genetic basis of human dental variation from statistical modelling analyses. Perspectives in Human Biology. (pp. 9-18) edited by Loren Knapp. Nedlands: The University of Western Australia.
Heath, A., Madden, P. A., Cloninger, C. R. and Martin, N. G. (1999). Genetic and environmental structure of personality. Personality and Psychopathology. (pp. 343-367) edited by C. Robert Cloninger. Washington, U.S.A.: American Psychiatric Press.
Eaves, Lindon J., Heath, A., Martin, Nicholas G., Neale, Michael C., Meyer, J. M., Silberg, J. L., Corey, Linda, Truett, Kimberley and Walters, Ellen (1999). Biological and cultural inheritance of stature and attitudes. Personality and Psychopathology. (pp. 269-308) edited by C. Robert Cloninger. Washington: American Psychiatric Press.
Martin, N. G. (1999). Gene-environment interaction and twin studies. Advances in Twin and Sib-pair Analysis. (pp. 143-150) edited by Tim D. Spector, Harold Snieder and Alex J. MacGregor. London: Greenwich Medical Media Ltd.
Journal Articles
García-Marín, Luis M., Campos, Adrián I., Kho, Pik-Fang, Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2021). Phenome-wide screening of GWAS data reveals the complex causal architecture of obesity. Human Genetics, 140 (8), 1253-1265. doi: 10.1007/s00439-021-02298-9
Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Martin, Nicholas G., Couvy-Duchesne, Baptiste, Hermens, Daniel F., Parker, Richard, Gillespie, Nathan A., Medland, Sarah E. and Hickie, Ian B. (2021). Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults. Translational Psychiatry, 11 (1) 285, 285. doi: 10.1038/s41398-021-01390-y
Lafontaine, Nicole, Campbell, Purdey J., Castillo-Fernandez, Juan E., Mullin, Shelby, Lim, Ee Mun, Kendrew, Phillip, Lewer, Michelle, Brown, Suzanne J., Huang, Rae-Chi, Melton, Phillip E., Mori, Trevor A., Beilin, Lawrence J., Dudbridge, Frank, Spector, Tim D., Wright, Margaret J., Martin, Nicholas G., McRae, Allan F., Panicker, Vijay, Zhu, Gu, Walsh, John P., Bell, Jordana T. and Wilson, Scott G. (2021). Epigenome-wide association study of thyroid function traits identifies novel associations of fT3 with KLF9 and DOT1L. The Journal of Clinical Endocrinology and Metabolism, 106 (5), e2191-e2202. doi: 10.1210/clinem/dgaa975
Campos, Adrian I., Thompson, Paul M., Veltman, Dick J., Pozzi, Elena, van Veltzen, Laura S., Jahanshad, Neda, Adams, Mark J., Baune, Bernhard T., Berger, Klaus, Brosch, Katharina, Bülow, Robin, Connolly, Colm G., Dannlowski, Udo, Davey, Christopher G., de Zubicaray, Greig I., Dima, Danai, Erwin-Grabner, Tracy, Evans, Jennifer W., Fu, Cynthia H.Y., Gotlib, Ian H., Goya-Maldonado, Roberto, Grabe, Hans J., Grotegerd, Dominik, Harris, Matthew A., Harrison, Ben J., Hatton, Sean N., Hermesdorf, Marco, Hickie, Ian B., Ho, Tiffany C. ... Rentería, Miguel E. (2021). Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts. Biological Psychiatry. doi: 10.1016/j.biopsych.2021.03.015
Simcoe, Mark, Valdes, Ana, Liu, Fan, Furlotte, Nicholas A., Evans, David M., Hemani, Gibran, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Vuckovic, Dragana, Girotto, Giorgia, Sala, Cinzia, Catamo, Eulalia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan, Hewitt, Alex, Wu, Wenting, Kraft, Peter, Hammond, Christopher J., Shi, Yuan, Chen, Yan ... the International Visible Trait Genetics Consortium (2021). Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Science Advances, 7 (11) abd1239, eabd1239. doi: 10.1126/sciadv.abd1239
Gharahkhani, Puya, NEIGHBORHOOD consortium, Jorgenson, Eric, Hysi, Pirro, Khawaja, Anthony P., Pendergrass, Sarah, Han, Xikun, Ong, Jue Sheng, Hewitt, Alex W., Segrè, Ayellet V., Rouhana, John M., Hamel, Andrew R., Igo, Robert P., Choquet, Helene, Qassim, Ayub, Josyula, Navya S., Cooke Bailey, Jessica N., Bonnemaijer, Pieter W. M., Iglesias, Adriana, Siggs, Owen M., Young, Terri L., Vitart, Veronique, Thiadens, Alberta A. H. J., Karjalainen, Juha, Uebe, Steffen, Melles, Ronald B., Nair, K. Saidas, Luben, Robert, Simcoe, Mark ... 23 and Me Research Team (2021). Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Nature Communications, 12 (1) 1258, 1-16. doi: 10.1038/s41467-020-20851-4
Laisk, Triin, Soares, Ana Luiza G., Ferreira, Teresa, Painter, Jodie N., Censin, Jenny C., Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y., Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S., Yang, Ling, Becker, Christian M., Børglum, Anders D., Gordon, Scott D., Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M., Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A., Metspalu, Andres ... Lindgren, Cecilia M. (2020). The genetic architecture of sporadic and multiple consecutive miscarriage. Nature Communications, 11 (1) 5980, 1-12. doi: 10.1038/s41467-020-19742-5
Cuellar-Partida, Gabriel, Tung, Joyce Y., Eriksson, Nicholas, Albrecht, Eva, Aliev, Fazil, Andreassen, Ole A., Barroso, Inês, Beckmann, Jacques S., Boks, Marco P., Boomsma, Dorret I., Boyd, Heather A., Breteler, Monique M. B., Campbell, Harry, Chasman, Daniel I., Cherkas, Lynn F., Davies, Gail, de Geus, Eco J. C., Deary, Ian J., Deloukas, Panos, Dick, Danielle M., Duffy, David L., Eriksson, Johan G., Esko, Tõnu, Feenstra, Bjarke, Geller, Frank, Gieger, Christian, Giegling, Ina, Gordon, Scott D., Han, Jiali ... Medland, Sarah E. (2020). Genome-wide association study identifies 48 common genetic variants associated with handedness. Nature Human Behaviour, 5 (1), 59-70. doi: 10.1038/s41562-020-00956-y
Pizzagalli, Fabrizio, Auzias, Guillaume, Yang, Qifan, Mathias, Samuel R., Faskowitz, Joshua, Boyd, Joshua D., Amini, Armand, Rivière, Denis, McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Mangin, Jean-François, Glahn, David C., Blangero, John, Wright, Margaret J., Thompson, Paul M., Kochunov, Peter and Jahanshad, Neda (2020). The reliability and heritability of cortical folds and their genetic correlations across hemispheres. Communications Biology, 3 (1) 510, 510. doi: 10.1038/s42003-020-01163-1
Hagenaars, Saskia P., Coleman, Jonathan R. I., Choi, Shing Wan, Gaspar, Héléna, Adams, Mark J., Howard, David M., Hodgson, Karen, Traylor, Matthew, Air, Tracy M., Andlauer, Till F. M., Arolt, Volker, Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H. R., Boomsma, Dorret I., Campbell, Archie, Cearns, Micah, Czamara, Darina, Dannlowski, Udo, Domschke, Katharina, de Geus, Eco J. C., Hamilton, Steven P., Hayward, Caroline, Hickie, Ian B., Hottenga, Jouke Jan, Ising, Marcus, Jones, Ian, Jones, Lisa, Kutalik, Zoltan ... Lewis, Cathryn M. (2020). Genetic comorbidity between major depression and cardio‐metabolic traits, stratified by age at onset of major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 183 (6) ajmg.b.32807, 309-330. doi: 10.1002/ajmg.b.32807
Karagiannis, Tanya T., Cleary, John P., Gok, Busra, Henderson, Andrew J., Martin, Nicholas G., Yajima, Masanao, Nelson, Elliot C. and Cheng, Christine S. (2020). Single cell transcriptomics reveals opioid usage evokes widespread suppression of antiviral gene program. Nature Communications, 11 (1) 2611, 2611. doi: 10.1038/s41467-020-16159-y
Landi, Maria Teresa, GenoMEL Consortium, Bishop, D. Timothy, MacGregor, Stuart, Machiela, Mitchell J., Stratigos, Alexander J., Ghiorzo, Paola, Brossard, Myriam, Calista, Donato, Choi, Jiyeon, Fargnoli, Maria Concetta, Zhang, Tongwu, Rodolfo, Monica, Trower, Adam J., Menin, Chiara, Martinez, Jacobo, Hadjisavvas, Andreas, Song, Lei, Stefanaki, Irene, Scolyer, Richard, Yang, Rose, Goldstein, Alisa M., Potrony, Miriam, Kypreou, Katerina P., Pastorino, Lorenza, Queirolo, Paola, Pellegrini, Cristina, Cattaneo, Laura, Zawistowski, Matthew ... MelaNostrum Consortium (2020). Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5), 494-504. doi: 10.1038/s41588-020-0611-8
Revez, Joana A, Lin, Tian, Qiao, Zhen, Xue, Angli, Holtz, Yan, Zhu, Zhihong, Zeng, Jian, Wang, Huanwei, Sidorenko, Julia, Kemper, Kathryn E., Vinkhuyzen, Anna A. E., Frater, Julanne, Eyles, Darryl, Burne, Thomas H. J., Mitchell, Brittany, Martin, Nicholas G, Zhu, Gu, Visscher, Peter M., Yang, Jian, Wray, Naomi R. and McGrath, John J. (2020). Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Nature Communications, 11 (1) 1647, 1-12. doi: 10.1038/s41467-020-15421-7
Campbell, Purdey J., Brown, Suzanne J., Kendrew, Phillip, Lewer, Michelle, Lim, Ee Mun, Joseph, John, Cross, Simone M., Wright, Margaret J., Martin, Nicholas G., Wilson, Scott G. and Walsh, John P. (2020). Changes in thyroid function across adolescence: a longitudinal study. The Journal of Clinical Endocrinology and Metabolism, 105 (4), e1162-e1170. doi: 10.1210/clinem/dgz331
Cai, Na, Revez, Joana A., Adams, Mark J., Andlauer, Till F. M., Breen, Gerome, Byrne, Enda M., Clarke, Toni-Kim, Forstner, Andreas J., Grabe, Hans J., Hamilton, Steven P., Levinson, Douglas F., Lewis, Cathryn M., Lewis, Glyn, Martin, Nicholas G., Milaneschi, Yuri, Mors, Ole, Müller-Myhsok, Bertram, Penninx, Brenda W. J. H., Perlis, Roy H., Pistis, Giorgio, Potash, James B., Preisig, Martin, Shi, Jianxin, Smoller, Jordan W., Streit, Fabien, Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Viktorin, Alexander ... Flint, Jonathan (2020). Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nature Genetics, 52 (4), 437-447. doi: 10.1038/s41588-020-0594-5
Fan, Qiao, Pozarickij, Alfred, Tan, Nicholas Y. Q., Guo, Xiaobo, Verhoeven, Virginie J. M., Vitart, Veronique, Guggenheim, Jeremy A., Miyake, Masahiro, Tideman, J. Willem L., Khawaja, Anthony P., Zhang, Liang, MacGregor, Stuart, Höhn, René, Chen, Peng, Biino, Ginevra, Wedenoja, Juho, Saffari, Seyed Ehsan, Tedja, Milly S., Xie, Jing, Lanca, Carla, Wang, Ya Xing, Sahebjada, Srujana, Mazur, Johanna, Mirshahi, Alireza, Martin, Nicholas G., Yazar, Seyhan, Pennell, Craig E., Yap, Maurice, Haarman, Annechien E. G. ... Evans, David M. (2020). Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Communications Biology, 3 (1) 133, 133. doi: 10.1038/s42003-020-0802-y
Ong, Jue-Sheng, Hwang, Liang-Dar, Zhong, Victor W., An, Jiyuan, Gharahkhani, Puya, Breslin, Paul A. S., Wright, Margaret J., Lawlor, Deborah A., Whitfield, John, MacGregor, Stuart, Martin, Nicholas G. and Corneli, Marilyn C. (2020). Author Correction: Understanding the role of bitter taste perception in coffee, tea and alcohol consumption through Mendelian randomization. Scientific Reports, 10 (1) 4778, 4778. doi: 10.1038/s41598-020-60488-3
Buchwald, Jadwiga, Chenoweth, Meghan J., Palviainen, Teemu, Zhu, Gu, Benner, Christian, Gordon, Scott, Korhonen, Tellervo, Ripatti, Samuli, Madden, Pamela A. F., Lehtimäki, Terho, Raitakari, Olli T., Salomaa, Veikko, Rose, Richard J., George, Tony P., Lerman, Caryn, Pirinen, Matti, Martin, Nicholas G., Kaprio, Jaakko, Loukola, Anu and Tyndale, Rachel F. (2020). Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Molecular Psychiatry. doi: 10.1038/s41380-020-0702-z
Polimanti, Renato, Walters, Raymond K., Johnson, Emma C., McClintick, Jeanette N., Adkins, Amy E., Adkins, Daniel E., Bacanu, Silviu-Alin, Bierut, Laura J., Bigdeli, Tim B., Brown, Sandra, Bucholz, Kathleen K., Copeland, William E., Costello, E. Jane, Degenhardt, Louisa, Farrer, Lindsay A, Foroud, Tatiana M., Fox, Louis, Goate, Alison M., Grucza, Richard, Hack, Laura M., Hancock, Dana B., Hartz, Sarah M., Heath, Andrew C., Hewitt, John K., Hopfer, Christian J., Johnson, Eric O., Kendler, Kenneth S., Kranzler, Henry R., Krauter, Kenneth ... Gelernter, Joel (2020). Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Molecular Psychiatry, 25 (8), 1673-1687. doi: 10.1038/s41380-020-0677-9
Campos, Adrián I., García-Marín, Luis M., Byrne, Enda M., Martin, Nicholas G., Cuéllar-Partida, Gabriel and Rentería, Miguel E. (2020). Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Nature Communications, 11 (1) 817, 817. doi: 10.1038/s41467-020-14625-1
Duffy, David L., Jagirdar, Kasturee, Lee, Katie J., McWhirter, Seamus R., McMeniman, Erin K., De’Ambrosis, Brian, Pflugfelder, Annette, Rayner, Jenna E., Whiteman, David C., Brown, Matthew A., Martin, N.G., Smithers, B.M., Schaider, Helmut, Soyer, H. Peter and Sturm, Richard A. (2020). Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls. Journal of Investigative Dermatology, 140 (2), 498-501.e17. doi: 10.1016/j.jid.2019.05.032
Cox, Jiayi W., Sherva, Richard M., Lunetta, Kathryn L., Johnson, Emma C., Martin, Nicholas G., Degenhardt, Louisa, Agrawal, Arpana, Nelson, Elliot C., Kranzler, Henry R., Gelernter, Joel and Farrer, Lindsay A. (2020). Genome-wide association study of opioid cessation. Journal of Clinical Medicine, 9 (1), 180. doi: 10.3390/jcm9010180
Kendler, Kenneth S., Gardner, Charles O., Neale, Michael C., Aggen, Steve, Heath, Andrew, Colodro-Conde, Lucía, Couvyduchesne, Baptiste, Byrne, Enda M., Martin, Nicholas G. and Gillespie, Nathan A. (2019). Shared and specific genetic risk factors for lifetime major depression, depressive symptoms and neuroticism in three population-based twin samples. Psychological Medicine, 49 (16), 2745-2753. doi: 10.1017/S003329171800377X
Xiong, Ziyi, Dankova, Gabriela, Howe, Laurence J., Lee, Myoung Keun, Hysi, Pirro G., de Jong, Markus A., Zhu, Gu, Adhikari, Kaustubh, Li, Dan, Li, Yi, Pan, Bo, Feingold, Eleanor, Marazita, Mary L., Shaffer, John R., McAloney, Kerrie, Xu, Shu-Hua, Jin, Li, Wang, Sijia, de Vrij, Femke Ms, Lendemeijer, Bas, Richmond, Stephen, Zhurov, Alexei, Lewis, Sarah, Sharp, Gemma C., Paternoster, Lavinia, Thompson, Holly, Gonzalez-Jose, Rolando, Bortolini, Maria Catira, Canizales-Quinteros, Samuel ... Kayser, Manfred (2019). Novel genetic loci affecting facial shape variation in humans. eLife, 8 e49898. doi: 10.7554/eLife.49898
Clark, David W., Okada, Yukinori, Moore, Kristjan H. S., Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Mattsson, Hannele, Barnes, Catriona L. K., Lin, Kuang, Zhao, Jing Hua, Deelen, Patrick, Rohde, Rebecca, Schurmann, Claudia, Guo, Xiuqing, Giulianini, Franco, Zhang, Weihua, Medina-Gomez, Carolina, Karlsson, Robert, Bao, Yanchun, Bartz, Traci M., Baumbach, Clemens, Biino, Ginevra, Bixley, Matthew J., Brumat, Marco, Chai, Jin-Fang, Corre, Tanguy, Cousminer, Diana L., Dekker, Annelot M., Eccles, David A. ... Wilson, James F. (2019). Associations of autozygosity with a broad range of human phenotypes. Nature Communications, 10 (1) 4957, 4957. doi: 10.1038/s41467-019-12283-6
Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A. ... Morton, C. C. (2019). Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Nature Communications, 10 (1) 4857, 4857. doi: 10.1038/s41467-019-12536-4
Satizabal, Claudia L., Adams, Hieab H. H., Hibar, Derrek P., White, Charles C., Knol, Maria J., Stein, Jason L., Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V., Smith, Albert V., Bis, Joshua C., Jian, Xueqiu, Luciano, Michelle, Hofer, Edith, Teumer, Alexander, van der Lee, Sven J., Yang, Jingyun, Yanek, Lisa R., Lee, Tom V., Li, Shuo, Hu, Yanhui, Koh, Jia Yu, Eicher, John D., Desrivières, Sylvane, Arias-Vasquez, Alejandro, Chauhan, Ganesh, Athanasiu, Lavinia, Rentería, Miguel E. ... Ikram, M. Arfan (2019). Genetic architecture of subcortical brain structures in 38,851 individuals. Nature Genetics, 51 (11), 1624-1636. doi: 10.1038/s41588-019-0511-y
Nievergelt, Caroline M., Maihofer, Adam X., Klengel, Torsten, Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R. I., Dalvie, Shareefa, Duncan, Laramie E., Gelernter, Joel, Levey, Daniel F., Logue, Mark W., Polimanti, Renato, Provost, Allison C., Ratanatharathorn, Andrew, Stein, Murray B., Torres, Katy, Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Søren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Babić, Dragan, Bækvad-Hansen, Marie, Baker, Dewleen G. ... Koenen, Karestan C. (2019). International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Nature Communications, 10 (1) 4558, 4558. doi: 10.1038/s41467-019-12576-w
Tin, Adrienne, Marten, Jonathan, Halperin Kuhns, Victoria L., Li, Yong, Wuttke, Matthias, Kirsten, Holger, Sieber, Karsten B., Qiu, Chengxiang, Gorski, Mathias, Yu, Zhi, Giri, Ayush, Sveinbjornsson, Gardar, Li, Man, Chu, Audrey Y., Hoppmann, Anselm, O’Connor, Luke J., Prins, Bram, Nutile, Teresa, Noce, Damia, Akiyama, Masato, Cocca, Massimiliano, Ghasemi, Sahar, van der Most, Peter J., Horn, Katrin, Xu, Yizhe, Fuchsberger, Christian, Sedaghat, Sanaz, Afaq, Saima, Amin, Najaf ... Köttgen, Anna (2019). Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Nature Genetics, 51 (10), 1459-1474. doi: 10.1038/s41588-019-0504-x
van Velzen, Laura S., Kelly, Sinead, Isaev, Dmitry, Aleman, Andre, Aftanas, Lyubomir I., Bauer, Jochen, Baune, Bernhard T., Brak, Ivan V., Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Danilenko, Konstantin V., Dannlowski, Udo, Enneking, Verena, Filimonova, Elena, Förster, Katharina, Frodl, Thomas, Gotlib, Ian H., Groenewold, Nynke A., Grotegerd, Dominik, Harris, Mathew A., Hatton, Sean N., Hawkins, Emma L., Hickie, Ian B., Ho, Tiffany C., Jansen, Andreas, Kircher, Tilo, Klimes-Dougan, Bonnie ... Schmaal, Lianne (2019). White matter disturbances in major depressive disorder: a coordinated analysis across 20 international cohorts in the ENIGMA MDD working group. Molecular Psychiatry, 25 (7), 1511-1525. doi: 10.1038/s41380-019-0477-2
Evangelou, Evangelos, Gao, He, Chu, Congying, Ntritsos, Georgios, Blakeley, Paul, Butts, Andrew R., Pazoki, Raha, Suzuki, Hideaki, Koskeridis, Fotios, Yiorkas, Andrianos M., Karaman, Ibrahim, Elliott, Joshua, Luo, Qiang, Aeschbacher, Stefanie, Bartz, Traci M., Baumeister, Sebastian E., Braund, Peter S., Brown, Michael R., Brody, Jennifer A., Clarke, Toni-Kim, Dimou, Niki, Faul, Jessica D., Homuth, Georg, Jackson, Anne U., Kentistou, Katherine A., Joshi, Peter K., Lemaitre, Rozenn N., Lind, Penelope A., Lyytikäinen, Leo-Pekka ... Elliott, Paul (2019). New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Nature Human Behaviour, 3 (9), 950-961. doi: 10.1038/s41562-019-0653-z
Gillespie, Nathan A., Bates, Timothy C., Hickie, Ian B., Medland, Sarah E., Verhulst, Brad, Kirkpatrick, Robert M., Kendler, Kenneth S., Martin, Nicholas G. and Benotsch, Eric G. (2019). Genetic and environmental risk factors in the non-medical use of over-the-counter or prescribed analgesics, and their relationship to major classes of licit and illicit substance use and misuse in a population-based sample of young adult twins. Addiction, 114 (12) add.14750, 2229-2240. doi: 10.1111/add.14750
Watson, Hunna J., Yilmaz, Zeynep, Thornton, Laura M., Hübel, Christopher, Coleman, Jonathan R. I., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Purves, Kirstin L., Adan, Roger A. H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Baker, Jessica H., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Perica, Vesna Boraska, Buehren, Katharina, Burghardt, Roland, Cassina, Matteo, Cichon, Sven ... Bulik, Cynthia M. (2019). Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Nature Genetics, 51 (8), 1207-1214. doi: 10.1038/s41588-019-0439-2
Hwang, Liang-Dar, Lin, Cailu, Gharahkhani, Puya, Cuellar-Partida, Gabriel, Ong, Jue-Sheng, An, Jiyuan, Gordon, Scott D., Zhu, Gu, MacGregor, Stuart, Lawlor, Deborah A., Breslin, Paul A. S., Wright, Margaret J., Martin, Nicholas G. and Reed, Danielle R. (2019). New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. The American Journal of Clinical Nutrition, 109 (6), 1724-1737. doi: 10.1093/ajcn/nqz043
Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B., Feitosa, Mary F., Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y., Hoppmann, Anselm, Kirsten, Holger, Giri, Ayush, Chai, Jin-Fang, Sveinbjornsson, Gardar, Tayo, Bamidele O., Nutile, Teresa, Fuchsberger, Christian, Marten, Jonathan, Cocca, Massimiliano, Ghasemi, Sahar, Xu, Yizhe, Horn, Katrin, Noce, Damia, van der Most, Peter J., Sedaghat, Sanaz, Yu, Zhi, Akiyama, Masato, Afaq, Saima, Ahluwalia, Tarunveer S. ... Pattaro, Cristian (2019). A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nature Genetics, 51 (6), 957-972. doi: 10.1038/s41588-019-0407-x
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