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Colm O'Dushlaine
Colm O'Dushlaine
Head of Statistical Genetics, insitro
Verified email at insitro.com - Homepage
Title
Cited by
Cited by
Year
Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
75842014
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
International Schizophrenia Consortium Manuscript preparation Purcell Shaun ...
Nature 460 (7256), 748-752, 2009
53142009
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
23892013
Genome-wide association study identifies five new schizophrenia loci
Nature genetics 43 (10), 969-976, 2011
20292011
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
17922013
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
15802008
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
15752014
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
Nature genetics 43 (10), 977-983, 2011
15152011
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
14002015
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
9722017
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
8092017
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
7462021
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
7332018
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
6722018
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
6682014
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
5702016
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
5522018
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
5272015
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
5062016
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
4382020
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