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2020 Journal Article Comparison of genome-wide association scans for quantitative and observational measures of human hair curvatureHo, Yvonne Y. W., Mina-Vargas, Angela, Zhu, Gu, Brims, Mark, Mcnevin, Dennis, Montgomery, Grant W., Martin, Nicholas G., Medland, Sarah E. and Painter, Jodie N. (2020). Comparison of genome-wide association scans for quantitative and observational measures of human hair curvature. Twin Research and Human Genetics, 23 (5) PII S183242742000078X, 271-277. doi: 10.1017/thg.2020.78 |
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2020 Journal Article Genome-wide association study identifies 48 common genetic variants associated with handednessCuellar-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 |
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2020 Journal Article Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adultsHofer, 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 |
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2020 Journal Article Septic shock: a genomewide association study and polygenic risk score analysisD'Urso, Shannon, Rajbhandari, Dorrilyn, Peach, Elizabeth, De Guzman, Erika, Li, Qiang, Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Ligthart, Symen, Brown, Matthew A., Powell, Joseph, McArthur, Colin, Rhodes, Andrew, Meyer, Jason, Finfer, Simon, Myburgh, John, Blumenthal, Antje, Cohen, Jeremy, Venkatesh, Balasubramanian, Cuellar-Partida, Gabriel and Evans, David M. (2020). Septic shock: a genomewide association study and polygenic risk score analysis. Twin Research and Human Genetics, 23 (4) PII S1832427420000602, 204-213. doi: 10.1017/thg.2020.60 |
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2020 Journal Article Cohort profile: the Australian genetics of depression studyByrne, Enda M., Kirk, Katherine M., Medland, Sarah E., McGrath, John J., Colodro-Conde, Lucia, Parker, Richard, Cross, Simone, Sullivan, Lenore, Statham, Dixie J., Levinson, Douglas F., Licinio, Julio, Wray, Naomi R, Hickie, Ian B. and Martin, Nicholas G. (2020). Cohort profile: the Australian genetics of depression study. BMJ Open, 10 (5) e032580, e032580. doi: 10.1136/bmjopen-2019-032580 |
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2020 Journal Article Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working groupHan, Laura K. M., Dinga, Richard, Hahn, Tim, Ching, Christopher R. K., Eyler, Lisa T., Aftanas, Lyubomir, Aghajani, Moji, Aleman, André, Baune, Bernhard T., Berger, Klaus, Brak, Ivan, Filho, Geraldo Busatto, Carballedo, Angela, Connolly, Colm G., Couvy-Duchesne, Baptiste, Cullen, Kathryn R., Dannlowski, Udo, Davey, Christopher G., Dima, Danai, Duran, Fabio L. S., Enneking, Verena, Filimonova, Elena, Frenzel, Stefan, Frodl, Thomas, Fu, Cynthia H. Y., Godlewska, Beata R., Gotlib, Ian H., Grabe, Hans J., Groenewold, Nynke A. ... Schmaal, Lianne (2020). Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group. Molecular Psychiatry, 26 (9), 5124-5139. doi: 10.1038/s41380-020-0754-0 |
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2020 Journal Article Mapping brain asymmetry in health and disease through the ENIGMA consortiumKong, 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, 43 (1) hbm.25033, 167-181. doi: 10.1002/hbm.25033 |
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2020 Journal Article Educational attainment polygenic scores are associated with cortical total surface area and regions important for language and memoryMitchell, 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 |
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2020 Journal Article Curly questionsMedland, Sarah E. (2020). Curly questions. Twin Research and Human Genetics, 23 (2), 98-99. doi: 10.1017/thg.2020.23 |
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2020 Journal Article EditorialEvans, David, Medland, Sarah E. and Gillespie, Nathan (2020). Editorial. Twin Research and Human Genetics, 23 (2), 67-67. doi: 10.1017/thg.2020.45 |
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2020 Journal Article ENIGMA and global neuroscience: a decade of large-scale studies of the brain in health and disease across more than 40 countriesThompson, 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 |
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2020 Journal Article The genetic architecture of the human cerebral cortexGrasby, 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, 1-17. doi: 10.1126/science.aay6690 |
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2020 Journal Article Genome-wide association analysis in humans links nucleotide metabolism to Leukocyte Telomere LengthLi, 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 |
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2020 Journal Article Shared genetic risk between eating disorder- and substance-use-related phenotypes: evidence from genome-wide association studiesMunn-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 |
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2020 Journal Article Rethinking Measurement of Parenting Stress in ADHD-Affected Families: A Principal Components Analysis of the Disruptive Behaviour Stress InventoryMaclean, 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 |
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2020 Journal Article 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 adultsScott, 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 |
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2019 Journal Article 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 BiobankSalminen, 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 |
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2019 Journal Article The CODATwins Project: the current status and recent findings of COllaborative Project of Development of Anthropometrical Measures in TwinsSilventoinen, 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) PII S1832427419000355, 1-9. doi: 10.1017/thg.2019.35 |
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2019 Journal Article Full exploitation of high dimensionality in brain imaging: The JPND working group statement and findingsAdams, 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 |
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2019 Journal Article Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitryMufford, 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 |
