Roel A. Ophoff
Roel A. Ophoff
Professor of Psychiatry and Human Genetics, University of California Los Angeles
Adresse e-mail validée de ucla.edu
Titre
Citée par
Citée par
Année
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
RA Ophoff, GM Terwindt, MN Vergouwe, R Van Eijk, PJ Oefner, ...
Cell 87 (3), 543-552, 1996
25531996
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
Cross-Disorder Group of the Psychiatric Genomics Consortium
The Lancet 381 (9875), 1371-1379, 2013
21472013
Large recurrent microdeletions associated with schizophrenia
H Stefansson, D Rujescu, S Cichon, OPH Pietiläinen, A Ingason, ...
nature 455 (7210), 232, 2008
17792008
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
BK Bulik-Sullivan, PR Loh, HK Finucane, S Ripke, J Yang, N Patterson, ...
Nature genetics 47 (3), 291-295, 2015
16482015
Common variants conferring risk of schizophrenia
H Stefansson, RA Ophoff, S Steinberg, OA Andreassen, S Cichon, ...
Nature 460 (7256), 744-747, 2009
16442009
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984, 2013
16382013
Genome-wide association study identifies five new schizophrenia loci
S Ripke, AR Sanders, KS Kendler, DF Levinson, P Sklar, PA Holmans, ...
Nature genetics 43 (10), 969, 2011
15652011
Biological insights from 108 schizophrenia-associated genetic loci
S Ripke, BM Neale, A Corvin, JTR Walters, KH Farh, PA Holmans, P Lee, ...
Nature 511 (7510), 421-427, 2014
13722014
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, 2013
13272013
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
CA Anderson, G Boucher, CW Lees, A Franke, M D'Amato, KD Taylor, ...
Nature genetics 43 (3), 246-252, 2011
13242011
Schizophrenia risk from complex variation of complement component 4
A Sekar, AR Bialas, H de Rivera, A Davis, TR Hammond, N Kamitaki, ...
Nature 530 (7589), 177-183, 2016
12132016
Partitioning heritability by functional annotation using genome-wide association summary statistics
HK Finucane, B Bulik-Sullivan, A Gusev, G Trynka, Y Reshef, PR Loh, ...
Nature genetics 47 (11), 1228, 2015
9222015
Multiple common variants for celiac disease influencing immune gene expression
PCA Dubois, G Trynka, L Franke, KA Hunt, J Romanos, A Curtotti, ...
Nature genetics 42 (4), 295-302, 2010
9012010
Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium
TGM van Erp, DP Hibar, JM Rasmussen, DC Glahn, GD Pearlson, ...
Molecular psychiatry 21 (4), 547-553, 2016
5732016
Identification of common variants associated with human hippocampal and intracranial volumes
JL Stein, SE Medland, AA Vasquez, DP Hibar, RE Senstad, AM Winkler, ...
Nature genetics 44 (5), 552-561, 2012
5722012
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ...
Nature 520 (7546), 224-229, 2015
5702015
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
SH Lee, TR DeCandia, S Ripke, J Yang, PF Sullivan, ME Goddard, ...
Nature genetics 44 (3), 247-250, 2012
5532012
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
5202009
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
4972018
Disruption of the neurexin 1 gene is associated with schizophrenia
D Rujescu, A Ingason, S Cichon, OPH Pietiläinen, MR Barnes, ...
Human molecular genetics 18 (5), 988-996, 2009
4962009
Le système ne peut pas réaliser cette opération maintenant. Veuillez réessayer plus tard.
Articles 1–20