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Number of items: 7.


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-+.


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-+.


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.


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-+.


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.

This list was generated on Sun Mar 3 15:51:35 2024 GMT.