Chris Cotsapas
Chris Cotsapas
Yale School of Medicine
Verified email at - Homepage
Cited by
Cited by
Systematic localization of common disease-associated variation in regulatory DNA
MT Maurano, R Humbert, E Rynes, RE Thurman, E Haugen, H Wang, ...
Science 337 (6099), 1190-1195, 2012
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Nature Genetics 45 (11), 1353-60, 2013
Pleiotropy in complex traits: challenges and strategies
N Solovieff, C Cotsapas, PH Lee, SM Purcell, JW Smoller
Nature Reviews Genetics 14 (7), 483-495, 2013
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
RM Plenge, C Cotsapas, L Davies, AL Price, PIW De Bakker, J Maller, ...
Nature genetics 39 (12), 1477-1482, 2007
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus
RR Graham, C Cotsapas, L Davies, R Hackett, CJ Lessard, JM Leon, ...
Nature genetics 40 (9), 1059-1061, 2008
Pervasive sharing of genetic effects in autoimmune disease
C Cotsapas, BF Voight, E Rossin, K Lage, BM Neale, C Wallace, ...
PLoS genetics 7 (8), e1002254, 2011
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
EJ Rossin, K Lage, S Raychaudhuri, RJ Xavier, D Tatar, Y Benita, ...
PLoS genetics 7 (1), e1001273, 2011
Class II HLA interactions modulate genetic risk for multiple sclerosis
Nature genetics 47 (10), 1107-1113, 2015
Genetic analysis of human traits in vitro: drug response and gene expression in lymphoblastoid cell lines
E Choy, R Yelensky, S Bonakdar, RM Plenge, R Saxena, PL De Jager, ...
PLoS genetics 4 (11), e1000287, 2008
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types
S Chun, A Casparino, NA Patsopoulos, DC Croteau-Chonka, BA Raby, ...
Nature genetics 49 (4), 600-605, 2017
Survey of variation in human transcription factors reveals prevalent DNA binding changes
LA Barrera, A Vedenko, JV Kurland, JM Rogers, SS Gisselbrecht, ...
Science 351 (6280), 1450-1454, 2016
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans
DL Morris, KE Taylor, MMA Fernando, J Nititham, ME Alarcón-Riquelme, ...
The American Journal of Human Genetics 91 (5), 778-793, 2012
Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls
SE Baranzini, P Khankhanian, NA Patsopoulos, M Li, J Stankovich, ...
The American Journal of Human Genetics 92 (6), 854-865, 2013
Common body mass index-associated variants confer risk of extreme obesity
C Cotsapas, EK Speliotes, IJ Hatoum, DM Greenawalt, R Dobrin, PY Lum, ...
Human molecular genetics 18 (18), 3502-3507, 2009
Low-frequency and rare-coding variation contributes to multiple sclerosis risk
M Mitrovič, NA Patsopoulos, AH Beecham, T Dankowski, A Goris, ...
Cell 175 (6), 1679-1687. e7, 2018
Immune-mediated disease genetics: the shared basis of pathogenesis
C Cotsapas, DA Hafler
Trends in immunology 34 (1), 22-26, 2013
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