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Number of items: 20.


Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer
et al (show 561 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313-+.


de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L, Ota, Vanessa K, Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J, Patel, Hamel
et al (show 362 more authors) (2018) Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. COMMUNICATIONS BIOLOGY, 1 (1). 163-.


Walton, E, Hibar, D, Yilmaz, Z, Jahanshad, N, Cheung, J, Batury, V-L, Seitz, J, Bulik, CM, Thompson, PM, Ehrlich, Stefan
et al (show 500 more authors) (2019) Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. MOLECULAR NEUROBIOLOGY, 56 (7). pp. 5146-5156.


Mullins, Niamh, Bigdeli, Tim B, Borglum, Anders D, Coleman, Jonathan RI, Demontis, Ditte, Mehta, Divya, Power, Robert A, Ripke, Stephan, Stahl, Eli A, Starnawska, Anna
et al (show 108 more authors) (2019) GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. American Journal of Psychiatry, 176 (8). pp. 651-660.


Huckins, Laura M, Dobbyn, Amanda, Ruderfer, Douglas M, Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F, Rajagopal, Veera M, Als, Thomas D, Nguyen, Hoang T, Girdhar, Kiran
et al (show 346 more authors) (2019) Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. NATURE GENETICS, 51 (4). 659-+.


Satizabal, Claudia L, Adams, Hieab HH, Hibar, Derrek P, White, Charles C, Knol, Maria J, Stein, Jason L, Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V
et al (show 279 more authors) (2019) Genetic architecture of subcortical brain structures in 38,851 individuals. NATURE GENETICS, 51 (11). 1624-+.


Hofer, Edith, Roshchupkin, Gennady V ORCID: 0000-0002-3403-2313, Adams, Hieab HH ORCID: 0000-0003-3687-2508, Knol, Maria J ORCID: 0000-0002-3597-1531, Lin, Honghuang ORCID: 0000-0003-3043-3942, Li, Shuo ORCID: 0000-0003-2331-2448, Zare, Habil, Ahmad, Shahzad ORCID: 0000-0002-8658-3790, Armstrong, Nicola J, Satizabal, Claudia L
et al (show 90 more authors) (2020) Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Nature communications, 11 (1). 4796-.


Stahl, Eli A, Breen, Gerome, Forstner, Andreas J, McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan RI, Gaspar, Helena A
et al (show 267 more authors) (2019) Genome-wide association study identifies 30 loci associated with bipolar disorder. NATURE GENETICS, 51 (5). 793-+.


Mullins, Niamh, Forstner, Andreas J, O'Connell, Kevin S, Coombes, Brandon, Coleman, Jonathan RI, Qiao, Zhen, Als, Thomas D, Bigdeli, Tim B, Borte, Sigrid, Bryois, Julien
et al (show 305 more authors) (2021) Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. NATURE GENETICS, 53 (6). 817-+.


Ruderfer, Douglas M, Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A, Pavlides, Jennifer M Whitehead, Mullins, Niamh, Charney, Alexander W, Ori, Anil PS, Loohuis, Loes M Olde
et al (show 534 more authors) (2018) Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. CELL, 173 (7). pp. 1705-1715.


Lee, Phil H, Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A, Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M, Nivard, Michel G, Grotzinger, Andrew D, Posthuma, Danielle
et al (show 592 more authors) (2019) Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. CELL, 179 (7). 1469-+.


Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard
et al (show 266 more authors) (2019) Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51 (3). 431-+.


Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli
et al (show 260 more authors) (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12). pp. 1091-1102.


Hibar, Derrek P, Adams, Hieab HH, Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L, Hofer, Edith, Renteria, Miguel E, Bis, Joshua C, Arias-Vasquez, Alejandro, Ikram, M Kamran
et al (show 322 more authors) (2017) Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS, 8 (1). 13624-.


Harold, Denise, Connolly, Siobhan, Riley, Brien P, Kendler, Kenneth S, McCarthy, Shane E, McCombie, William R, Richards, Alex, Owen, Michael J, O'Donovan, Michael C, Walters, James
et al (show 350 more authors) (2019) Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (3). pp. 223-231.


Blokland, Gabriella AM, Grove, Jakob, Chen, Chia-Yen, Cotsapas, Chris, Tobet, Stuart, Handa, Robert, St Clair, David, Lencz, Todd, Mowry, Bryan J, Periyasamy, Sathish
et al (show 119 more authors) (2022) Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. BIOLOGICAL PSYCHIATRY, 91 (1). pp. 102-117.


Munn-Chernoff, Melissa A, Johnson, Emma C, Chou, Yi-Ling, Coleman, Jonathan RI, Thornton, Laura M, Walters, Raymond K, Yilmaz, Zeynep, Baker, Jessica H, Hubel, Christopher, Gordon, Scott
et al (show 342 more authors) (2021) Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. ADDICTION BIOLOGY, 26 (1). e12880-.


Winsvold, Bendik S ORCID: 0000-0003-4171-8919, Bettella, Francesco, Witoelar, Aree, Anttila, Verneri, Gormley, Padhraig ORCID: 0000-0002-8908-6968, Kurth, Tobias ORCID: 0000-0001-7169-2620, Terwindt, Gisela M, Freilinger, Tobias M, Frei, Oleksander, Shadrin, Alexey
et al (show 9 more authors) (2017) Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. PloS one, 12 (9). e0185663-.


LeBlanc, Marissa ORCID: 0000-0003-2148-2814, Zuber, Verena ORCID: 0000-0001-9827-1877, Thompson, Wesley K, Andreassen, Ole A, Schizophrenia and Bipolar Disorder Working Groups of the Psychia, , Frigessi, Arnoldo ORCID: 0000-0001-7103-7589 and Andreassen, Bettina Kulle
(2018) A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework. BMC genomics, 19 (1). 494-.


Grasby, Katrina L, Jahanshad, Neda, Painter, Jodie N, Colodro-Conde, Lucia, Bralten, Janita, Hibar, Derrek P, Lind, Penelope A, Pizzagalli, Fabrizio, Ching, Christopher RK, McMahon, Mary Agnes B
et al (show 350 more authors) (2020) The genetic architecture of the human cerebral cortex. SCIENCE, 367 (6484). 1340-+.

This list was generated on Sat Feb 24 12:45:23 2024 GMT.