Professor Sarah Medland
Honorary Professor
The University of Queensland Diamantina Institute
Book Chapters
Jahanshad, Neda, Roshchupkin, Gennady, Faskowitz, Joshua, Hibar, Derrek P., Gutman, Boris A., Adams, Hieab H. H., Niessen, Wiro J., Vernooij, Meike W., Ikram, M. Arfan, Zwiers, Marcel P., Arias-Vasquez, Alejandro, Franke, Barbara, Ing, Alex, Desrivieres, Sylvane, Schumann, Gunter, de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E., Wright, Margaret J. and Thompson, Paul M. (2018). Multisite metaanalysis of image-wide genome-wide associations with morphometry. Imaging genetics. (pp. 1-23) edited by Adrian Dalca, Kayhan Batmanghelich, Mert Sabuncu and Li Shen. London, United Kingdom: Academic Press. doi: 10.1016/B978-0-12-813968-4.00001-8
Hibar, Derrek P., Jahanshad, Neda, Medland, Sarah E. and Thompson, Paul M. (2017). Continuous inflation analysis: a threshold-free method to estimate genetic overlap and boost power in imaging genetics. Imaging Genetics. (pp. 147-162) Kidlington, Oxford, United Kingdom: Elsevier Inc.. doi: 10.1016/B978-0-12-813968-4.00009-2
Grasby, Katrina L., Verweij, Karin J. H., Mosing, Miriam A., Zietsch, Brendan P. and Medland, Sarah E. (2017). Estimating heritability from twin studies. In Robert C. Elston (Ed.), Statistical human genetics: methods and protocols 2nd ed. (pp. 171-194) New York, NY, United States: Humana Press. doi:10.1007/978-1-4939-7274-6_9
Journal Articles
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
Hwang, Liang-Dar, Mitchell, Brittany L., Medland, Sarah E., Martin, Nicholas G., Neale, Michael C. and Evans, David M. (2021). The augmented Classical Twin Design: incorporating genome‐wide identity by descent sharing into twin studies in order to model violations of the equal environments assumption. Behavior Genetics. doi: 10.1007/s10519-021-10044-0
Mitchell, Brittany L., Kirk, Katherine M., McAloney, Kerrie, Wright, Margaret J., Davenport, Tracey A., Hermens, Daniel F., Scott, James G., McGrath, John J., Gillespie, Nathan A., Carpenter, Joanne S., O’Callaghan, Victoria S., Medland, Sarah, Christensen, Helen, Martin, Nicholas G., Burns, Jane M. and Hickie, Ian B. (2021). 16Up: Outline of a study investigating wellbeing and information and communication technology use in adolescent twins. Twin Research and Human Genetics, 23 (6), 1-13. doi: 10.1017/thg.2020.83
Scott, Jan, Byrne, Enda, Medland, Sarah and Hickie, Ian (2020). Short communication: Self-reported sleep-wake disturbances preceding onset of full-threshold mood and/or psychotic syndromes in community residing adolescents and young adults. Journal of Affective Disorders, 277, 592-595. doi: 10.1016/j.jad.2020.08.083
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
Hofer, Edith, Roshchupkin, Gennady V., Adams, Hieab H. H., Knol, Maria J., Lin, Honghuang, Li, Shuo, Zare, Habil, Ahmad, Shahzad, Armstrong, Nicola J., Satizabal, Claudia L., Bernard, Manon, Bis, Joshua C., Gillespie, Nathan A., Luciano, Michelle, Mishra, Aniket, Scholz, Markus, Teumer, Alexander, Xia, Rui, Jian, Xueqiu, Mosley, Thomas H., Saba, Yasaman, Pirpamer, Lukas, Seiler, Stephan, Becker, James T., Carmichael, Owen, Rotter, Jerome I., Psaty, Bruce M., Lopez, Oscar L., Amin, Najaf ... Hansell, Narelle K. (2020). Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature Communications, 11 (1) 4796, 4796. doi: 10.1038/s41467-020-18367-y
Kong, Xiang-Zhen, Postema, Merel C., Guadalupe, Tulio, de Kovel, Carolien, Boedhoe, Premika S. W., Hoogman, Martine, Mathias, Samuel R., van Rooij, Daan, Schijven, Dick, Glahn, David C., Medland, Sarah E., Jahanshad, Neda, Thomopoulos, Sophia I., Turner, Jessica A., Buitelaar, Jan, van Erp, Theo G. M., Franke, Barbara, Fisher, Simon E., van den Heuvel, Odile A., Schmaal, Lianne, Thompson, Paul M. and Francks, Clyde (2020). Mapping brain asymmetry in health and disease through the ENIGMA consortium. Human Brain Mapping. doi: 10.1002/hbm.25033
Mitchell, Brittany L., Cuéllar-Partida, Gabriel, Grasby, Katrina L., Campos, Adrian I., Strike, Lachlan T., Hwang, Liang-Dar, Okbay, Aysu, Thompson, Paul M., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J. and Rentería, Miguel E. (2020). Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memory. NeuroImage, 212 116691, 116691. doi: 10.1016/j.neuroimage.2020.116691
Medland, Sarah E. (2020). Curly questions. Twin Research and Human Genetics, 23 (2), 98-99. doi: 10.1017/thg.2020.23
Evans, David, Medland, Sarah E. and Gillespie, Nathan (2020). Editorial. Twin Research and Human Genetics, 23 (2), 67-67. doi: 10.1017/thg.2020.45
Grasby, Katrina L., Jahanshad, Neda, Painter, Jodie N., Colodro-Conde, Lucía, Bralten, Janita, Hibar, Derrek P., Lind, Penelope A., Pizzagalli, Fabrizio, Ching, Christopher R. K., McMahon, Mary Agnes B., Shatokhina, Natalia, Zsembik, Leo C. P., Thomopoulos, Sophia I., Zhu, Alyssa H., Strike, Lachlan T., Agartz, Ingrid, Alhusaini, Saud, Almeida, Marcio A. A., Alnæs, Dag, Amlien, Inge K., Andersson, Micael, Ard, Tyler, Armstrong, Nicola J., Ashley-Koch, Allison, Atkins, Joshua R., Bernard, Manon, Brouwer, Rachel M., Buimer, Elizabeth E. L., Bülow, Robin ... Medland, Sarah E. (2020). The genetic architecture of the human cerebral cortex. Science, 367 (6484) aay6690, eaay6690-+. doi: 10.1126/science.aay6690
Thompson, Paul M., Jahanshad, Neda, Ching, Christopher R. K., Salminen, Lauren E., Thomopoulos, Sophia I., Bright, Joanna, Baune, Bernhard T., Bertolín, Sara, Bralten, Janita, Bruin, Willem B., Bülow, Robin, Chen, Jian, Chye, Yann, Dannlowski, Udo, de Kovel, Carolien G. F., Donohoe, Gary, Eyler, Lisa T., Faraone, Stephen V., Favre, Pauline, Filippi, Courtney A., Frodl, Thomas, Garijo, Daniel, Gil, Yolanda, Grabe, Hans J., Grasby, Katrina L., Hajek, Tomas, Han, Laura K. M., Hatton, Sean N., Hilbert, Kevin ... Zelman, Vladimir (2020). ENIGMA and global neuroscience: a decade of large-scale studies of the brain in health and disease across more than 40 countries. Translational psychiatry, 10 (1) 100, 100. doi: 10.1038/s41398-020-0705-1
Li, Chen, Stoma, Svetlana, Lotta, Luca A., Warner, Sophie, Albrecht, Eva, Allione, Alessandra, Arp, Pascal P., Broer, Linda, Buxton, Jessica L., Da Silva Couto Alves, Alexessander, Deelen, Joris, Fedko, Iryna O., Gordon, Scott D., Jiang, Tao, Karlsson, Robert, Kerrison, Nicola, Loe, Taylor K., Mangino, Massimo, Milaneschi, Yuri, Miraglio, Benjamin, Pervjakova, Natalia, Russo, Alessia, Surakka, Ida, van der Spek, Ashley, Verhoeven, Josine E., Amin, Najaf, Beekman, Marian, Blakemore, Alexandra I., Canzian, Federico ... Codd, Veryan (2020). Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere Length. American Journal of Human Genetics, 106 (3), 389-404. doi: 10.1016/j.ajhg.2020.02.006
Scott, Jan, Martin, Nicholas G., Parker, Richard, Couvy-Duchesne, Baptiste, Medland, Sarah E. and Hickie, Ian (2020). Prevalence of self-reported subthreshold phenotypes of major mental disorders and their association with functional impairment, treatment and full-threshold syndromes in a community-residing cohort of young adults. Early Intervention in Psychiatry, 15 (2) eip.12942, 306-313. doi: 10.1111/eip.12942
Maclean, Emmalie I., Andrew, Brooke, Lind, Penelope A. and Medland, Sarah E. (2020). Rethinking Measurement of Parenting Stress in ADHD-Affected Families: A Principal Components Analysis of the Disruptive Behaviour Stress Inventory. Journal of Child and Family Studies, 29 (11), 3253-3264. doi: 10.1007/s10826-020-01799-x
Munn-Chernoff, Melissa A., Johnson, Emma C., Chou, Yi-Ling, Coleman, Jonathan R.I., Thornton, Laura M., Walters, Raymond K., Yilmaz, Zeynep, Baker, Jessica H., Hübel, Christopher, Gordon, Scott, Medland, Sarah E., Watson, Hunna J., Gaspar, Héléna A., Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Ripke, Stephan, Yao, Shuyang, Giusti-Rodríguez, Paola, Hanscombe, Ken B., Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Andreassen, Ole A., Berrettini, Wade H., Boehm, Ilka, Boni, Claudette, Boraska Perica, Vesna ... Agrawal, Arpana (2020). Shared genetic risk between eating disorder- and substance-use-related phenotypes: evidence from genome-wide association studies. Addiction Biology, 26 (1) e12880, e12880. doi: 10.1111/adb.12880
Salminen, Lauren E., Wilcox, Rand R., Zhu, Alyssa H., Riedel, Brandalyn C., Ching, Christopher R K, Rashid, Faisal, Thomopoulos, Sophia I., Saremi, Arvin, Harrison, Marc B., Ragothaman, Anjanibhargavi, Knight, Victoria, Boyle, Christina P., Medland, Sarah E., Thompson, Paul M. and Jahanshad, Neda (2019). Altered cortical brain structure and increased risk for disease seen decades after perinatal exposure to maternal smoking: a study of 9000 adults in the UK Biobank. Cerebral Cortex, 29 (12), 5217-5233. doi: 10.1093/cercor/bhz060
Adams, Hieab H.H., Roshchupkin, Gennady V., DeCarli, Charles, Franke, Barbara, Grabe, Hans J., Habes, Mohamad, Jahanshad, Neda, Medland, Sarah E., Niessen, Wiro, Satizabal, Claudia L., Schmidt, Reinhold, Seshadri, Sudha, Teumer, Alexander, Thompson, Paul M., Vernooij, Meike W., Wittfeld, Katharina and Ikram, M. Arfan (2019). Full exploitation of high dimensionality in brain imaging: The JPND working group statement and findings. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring, 11 (C), 286-290. doi: 10.1016/j.dadm.2019.02.003
Silventoinen, K., Jelenkovic, A., Yokoyama, Y., Sund, R., Sugawara, M., Tanaka, M., Matsumoto, S., Bogl, L. H., Freitas, D. L., Maia, J. A., Hjelmborg, J. V.B., Aaltonen, S., Piirtola, M., Latvala, A., Calais-Ferreira, L., Oliveira, V. C., Ferreira, P. H., Ji, F., Ning, F., Pang, Z., Ordoñana, J. R., Sánchez-Romera, J. F., Colodro-Conde, L., Burt, S. A., Klump, K. L., Martin, N. G., Medland, S. E., Montgomery, G. W., Kandler, C. ... Kaprio, J. (2019). The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in Twins. Twin Research and Human Genetics, 22 (6), 1-9. doi: 10.1017/thg.2019.35
Mufford, Mary, Cheung, Josh, Jahanshad, Neda, van der Merwe, Celia, Ding, Linda, Groenewold, Nynke, Koen, Nastassja, Chimusa, Emile R., Dalvie, Shareefa, Ramesar, Raj, Knowles, James A., Lochner, Christine, Hibar, Derrek P., Paschou, Peristera, van den Heuvel, Odile A., Medland, Sarah E., Scharf, Jeremiah M., Mathews, Carol A., Thompson, Paul M., Stein, Dan J. and Psychiatric Genomics Consortium - Tourette Syndrome working group (2019). Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Translational Psychiatry, 9 (1) 120. doi: 10.1038/s41398-019-0452-3
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
Postema, Merel C., van Rooij, Daan, Anagnostou, Evdokia, Arango, Celso, Auzias, Guillaume, Behrmann, Marlene, Filho, Geraldo Busatto, Calderoni, Sara, Calvo, Rosa, Daly, Eileen, Deruelle, Christine, Di Martino, Adriana, Dinstein, Ilan, Duran, Fabio Luis S., Durston, Sarah, Ecker, Christine, Ehrlich, Stefan, Fair, Damien, Fedor, Jennifer, Feng, Xin, Fitzgerald, Jackie, Floris, Dorothea L., Freitag, Christine M., Gallagher, Louise, Glahn, David C., Gori, Ilaria, Haar, Shlomi, Hoekstra, Liesbeth, Jahanshad, Neda ... Francks, Clyde (2019). Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets. Nature Communications, 10 (1) 4958, 4958. doi: 10.1038/s41467-019-13005-8
Van Der Meer, Dennis, Sønderby, Ida E., Kaufmann, Tobias, Walters, G. Bragi, Abdellaoui, Abdel, Ames, David, Amunts, Katrin, Andersson, Micael, Armstrong, Nicola J., Bernard, Manon, Blackburn, Nicholas B., Blangero, John, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Bülow, Robin, Cahn, Wiepke, Calhoun, Vince D., Caspers, Svenja, Cavalleri, Gianpiero L., Ching, Christopher R. K., Cichon, Sven, Ciufolini, Simone, Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Dalvie, Shareefa, Dazzan, Paola, De Geus, Eco J. C. ... Andreassen, Ole A. (2019). Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry, 77 (4), 1-11. doi: 10.1001/jamapsychiatry.2019.3779
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
Morosoli, J. J., Colodro-Conde, L., Barlow, F. K. and Medland, S. E. (2019). Public understanding of behavioral genetics: Integrating heuristic thinking, motivated reasoning and planned social change theories for better communication strategies. Behavior Genetics, 49 (5), 469-477. doi: 10.1007/s10519-019-09964-9
Van der Spek, Ashley, Broer, Linda, Draisma, Harmen H. M., Pool, René, Albrecht, Eva, Beekman, Marian, Mangino, Massimo, Raag, Mait, Nyholt, Dale R., Dharuri, Harish K., Codd, Veryan, Amin, Najaf, de Geus, Eco J. C., Deelen, Joris, Demirkan, Ayse, Yet, Idil, Fischer, Krista, Haller, Toomas, Henders, Anjali K., Isaacs, Aaron, Medland, Sarah E., Montgomery, Grant W., Mooijaart, Simon P., Strauch, Konstantin, Suchiman, H. Eka D., Vaarhorst, Anika A. M., van Heemst, Diana, Wang-Sattler, Rui, Whitfield, John B. ... Gieger, Christian (2019). Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium. Scientific Reports, 9 (1) 11623, 11623. doi: 10.1038/s41598-019-47282-6
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
Peng, Fuduan, Zhu, Gu, Hysi, Pirro G., Eller, Ryan J., Chen, Yan, Li, Yi, Hamer, Merel A., Zeng, Changqing, Hopkins, Racquel L., Jacobus, Case L., Wallace, Paige L., Uitterlinden, André G., Ikram, M. Arfan, Nijsten, Tamar, Duffy, David L., Medland, Sarah E., Spector, Timothy D., Walsh, Susan, Martin, Nicholas G., Liu, Fan and Kayser, Manfred (2019). Genome-Wide Association Studies Identify Multiple Genetic Loci Influencing Eyebrow Color Variation in Europeans. Journal of Investigative Dermatology, 139 (7), 1601-1605. doi: 10.1016/j.jid.2018.12.029
Bray, Nicola, Grasby, Katrina L., Lind, Penelope A., Painter, Jodie N., Colodro-Conde, Lucía and Medland, Sarah E. (2019). The psychosocial impact of nausea and vomiting during pregnancy as a predictor of postpartum depression. Journal of Health Psychology, 135910531985904. doi: 10.1177/1359105319859048
Hysi, Pirro G., Valdes, Ana M., Liu, Fan, Furlotte, Nicholas A., Evans, David M., Bataille, Veronique, Visconti, Alessia, Hemani, Gibran, McMahon, George, Ring, Susan M., Smith, George Davey, Duffy, David L., Zhu, Gu, Gordon, Scott D., Medland, Sarah E., Lin, Bochao D., Willemsen, Gonneke, Jan Hottenga, Jouke, Vuckovic, Dragana, Girotto, Giorgia, Gandin, Ilaria, Sala, Cinzia, Concas, Maria Pina, Brumat, Marco, Gasparini, Paolo, Toniolo, Daniela, Cocca, Massimiliano, Robino, Antonietta, Yazar, Seyhan ... Spector, Timothy D. (2019). Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Nature Genetics, 51 (7), 1190-1190. doi: 10.1038/s41588-019-0446-3
Warrington, Nicole M., Beaumont, Robin N., Horikoshi, Momoko, Day, Felix R., Helgeland, Øyvind, Laurin, Charles, Bacelis, Jonas, Peng, Shouneng, Hao, Ke, Feenstra, Bjarke, Wood, Andrew R., Mahajan, Anubha, Tyrrell, Jessica, Robertson, Neil R., Rayner, N. William, Qiao, Zhen, Moen, Gunn-Helen, Vaudel, Marc, Marsit, Carmen J., Chen, Jia, Nodzenski, Michael, Schnurr, Theresia M., Zafarmand, Mohammad H., Bradfield, Jonathan P., Grarup, Niels, Kooijman, Marjolein N., Li-Gao, Ruifang, Geller, Frank, Paternoster, Lavinia ... Freathy, Rachel M. (2019). Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nature Genetics, 51 (5), 804-814. doi: 10.1038/s41588-019-0403-1
Stahl, Eli A., Breen, Gerome, Forstner, Andreas J., McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan R. I., Gaspar, Héléna A., de Leeuw, Christiaan A., Steinberg, Stacy, Pavlides, Jennifer M. Whitehead, Trzaskowski, Maciej, Byrne, Enda M., Pers, Tune H., Holmans, Peter A., Richards, Alexander L., Abbott, Liam, Agerbo, Esben, Akil, Huda, Albani, Diego, Alliey-Rodriguez, Ney, Als, Thomas D., Anjorin, Adebayo, Antilla, Verneri, Awasthi, Swapnil, Badner, Judith A., Bækvad-Hansen, Marie ... Sklar, Pamela (2019). Genome-wide association study identifies 30 loci associated with bipolar disorder. Nature Genetics, 51 (5), 793-803. doi: 10.1038/s41588-019-0397-8
Kong, Xiang-Zhen, Boedhoe, Premika S.W., Abe, Yoshinari, Alonso, Pino, Ameis, Stephanie H., Arnold, Paul D., Assogna, Francesca, Baker, Justin T., Batistuzzo, Marcelo C., Benedetti, Francesco, Beucke, Jan C., Bollettini, Irene, Bose, Anushree, Brem, Silvia, Brennan, Brian P., Buitelaar, Jan, Calvo, Rosa, Cheng, Yuqi, Cho, Kang Ik K., Dallaspezia, Sara, Denys, Damiaan, Ely, Benjamin A., Feusner, Jamie, Fitzgerald, Kate D., Fouche, Jean-Paul, Fridgeirsson, Egill A., Glahn, David C., Gruner, Patricia, Gürsel, Deniz A. ... Francks, Clyde (2019). Mapping cortical and subcortical asymmetry in obsessive-compulsive disorder: Findings from the ENIGMA Consortium. Biological Psychiatry, 87 (12), 1022-1034. doi: 10.1016/j.biopsych.2019.04.022
Choi, Karmel W., Chen, Chia-Yen, Stein, Murray B., Klimentidis, Yann C., Wang, Min-Jung, Koenen, Karestan C., Smoller, Jordan W., Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, TracyM., Andlauer, Till F. M., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan T. F., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas H. R., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Hvarregaard, Jane ... Sullivan, Patrick F. (2019). Assessment of bidirectional relationships between physical activity and depression among adults A 2-Sample mendelian randomization study. JAMA Psychiatry, 76 (4), 399-408. doi: 10.1001/jamapsychiatry.2018.4175
Klein, Marieke, Walters, Raymond K., Demontis, Ditte, Stein, Jason L., Hibar, Derrek P., Adams, Hieab H., Bralten, Janita, Mota, Nina Roth, Schachar, Russell, Sonuga-Barke, Edmund, Mattheisen, Manuel, Neale, Benjamin M., Thompson, Paul M., Medland, Sarah E., Børglum, Anders D., Faraone, Stephen V., Arias-Vasquez, Alejandro and Franke, Barbara (2019). Genetic markers of ADHD-related variations in intracranial volume. American Journal of Psychiatry, 176 (3), 228-238. doi: 10.1176/appi.ajp.2018.18020149
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