Colm O'Dushlaine

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Patrick F SullivanProfessor of Genetics, University of North Carolina; Professor, MEB, Karolinska InstitutetE-mail confirmado em med.unc.edu
Michael GillTrinity College DublinE-mail confirmado em tcd.ie
Shaun PurcellSleep & Neurogenetics Lab, Brigham & Women's Hospital, BostonE-mail confirmado em bwh.harvard.edu
Jordan SmollerMassachusetts General HospitalE-mail confirmado em broadinstitute.org
Prof. Aiden CorvinTrinity College DublinE-mail confirmado em tcd.ie
Michael O'DonovanCardiff UniversityE-mail confirmado em cardiff.ac.uk
Steven A McCarrollHarvard Medical School; Broad Institute of MIT and HarvardE-mail confirmado em genetics.med.harvard.edu
Elaine KennyTrinity College DublinE-mail confirmado em tcd.ie
Derek MorrisNational University of Ireland GalwayE-mail confirmado em nuigalway.ie
Christina HultmanKarolinska INstitutetE-mail confirmado em ki.se
Aris BarasRegeneron PharmaceuticalsE-mail confirmado em regeneron.com
Naomi WrayUniversity of QueenslandE-mail confirmado em uq.edu.au
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteE-mail confirmado em atgu.mgh.harvard.edu
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical SchoolE-mail confirmado em broadinstitute.org
Peter HolmansE-mail confirmado em cardiff.ac.uk
Jeffrey ReidRegeneron PharmaceuticalsE-mail confirmado em regeneron.com
Douglas RuderferAssociate Professor, Vanderbilt Genomics InstituteE-mail confirmado em vanderbilt.edu
Stephan RipkeDepartment of Psychiatry and Psychotherapy, Charité - Universitätsmedizin BerlinE-mail confirmado em charite.de
Phil Hyoun Lee, PhDAssociate Professor, Harvard Medical School, Massachusetts General HospitalE-mail confirmado em mgh.harvard.edu
Evan K. MaxwellRegeneron Genetics Center, Regeneron PharmaceuticalsE-mail confirmado em regeneron.com

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Colm O'Dushlaine

Head of Statistical Genetics, insitro

E-mail confirmado em insitro.com - Página inicial

genetics genomics bioinformatics statistical genetics


Título Ordenar por citações Ordenar por ano Ordenar por título	Citado por Citado por	Ano
Biological insights from 108 schizophrenia-associated genetic loci C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ... Nature 511 (7510), 421-427, 2014	7653	2014
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder International Schizophrenia Consortium Manuscript preparation Purcell Shaun ... Nature 460 (7256), 748-752, 2009	5339	2009
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013	2403	2013
Genome-wide association study identifies five new schizophrenia loci Nature genetics 43 (10), 969-976, 2011	2041	2011
Genome-wide association analysis identifies 13 new risk loci for schizophrenia S Ripke, C O'dushlaine, K Chambert, JL Moran, AK Kähler, S Akterin, ... Nature genetics 45 (10), 1150-1159, 2013	1801	2013
Rare chromosomal deletions and duplications increase risk of schizophrenia Cardiff University O’Donovan Michael C. 5 Kirov George K. 5 Craddock Nick J ... Nature 455 (7210), 237-241, 2008	1583	2008
A polygenic burden of rare disruptive mutations in schizophrenia SM Purcell, JL Moran, M Fromer, D Ruderfer, N Solovieff, P Roussos, ... Nature 506 (7487), 185-190, 2014	1580	2014
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature genetics 43 (10), 977-983, 2011	1519	2011
Modeling linkage disequilibrium increases accuracy of polygenic risk scores BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ... The american journal of human genetics 97 (4), 576-592, 2015	1423	2015
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ... Nature genetics 49 (1), 27-35, 2017	981	2017
Genetic and pharmacologic inactivation of ANGPTL3 and cardiovascular disease FE Dewey, V Gusarova, RL Dunbar, C O’Dushlaine, C Schurmann, ... New England Journal of Medicine 377 (3), 211-221, 2017	818	2017
Computationally efficient whole-genome regression for quantitative and binary traits J Mbatchou, L Barnard, J Backman, A Marcketta, JA Kosmicki, ... Nature genetics 53 (7), 1097-1103, 2021	810	2021
A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease NS Abul-Husn, X Cheng, AH Li, Y Xin, C Schurmann, P Stevis, Y Liu, ... New England Journal of Medicine 378 (12), 1096-1106, 2018	749	2018
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ... Nature genetics 50 (9), 1234-1239, 2018	699	2018
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ... The American Journal of Human Genetics 95 (5), 535-552, 2014	673	2014
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study FE Dewey, MF Murray, JD Overton, L Habegger, JB Leader, SN Fetterolf, ... Science 354 (6319), aaf6814, 2016	578	2016
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ... Cell 173 (7), 1705-1715. e16, 2018	559	2018
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature neuroscience 18 (2), 199-209, 2015	532	2015
Inactivating variants in ANGPTL4 and risk of coronary artery disease FE Dewey, V Gusarova, C O’Dushlaine, O Gottesman, J Trejos, C Hunt, ... New England Journal of Medicine 374 (12), 1123-1133, 2016	510	2016
Exome sequencing and characterization of 49,960 individuals in the UK Biobank CV Van Hout, I Tachmazidou, JD Backman, JD Hoffman, D Liu, ... Nature 586 (7831), 749-756, 2020	451	2020

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