Chris Cotsapas

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Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteZweryfikowany adres z atgu.mgh.harvard.edu
Philip L. De JagerWeil-Granat Professor of Neurology at Columbia UniversityZweryfikowany adres z cumc.columbia.edu
David HaflerProfessor of Neurology and Immunobiology, Yale UniversityZweryfikowany adres z yale.edu
John D. RiouxProfessor of Medicine, Université de Montréal and the Montreal Heart InstituteZweryfikowany adres z umontreal.ca
Peter K. GregersenHead, Robert S. Boas Center for Genomics and Human GeneticsZweryfikowany adres z nshs.edu
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical SchoolZweryfikowany adres z broadinstitute.org
Elizabeth J. RossinMass Eye and EarZweryfikowany adres z meei.harvard.edu
Benjamin F. VoightAssociate Professor, Dept. of Systems Pharmacology and Translational Therapeutics, Dept. of GeneticsZweryfikowany adres z pennmedicine.upenn.edu
Robert PlengeZweryfikowany adres z partners.org
Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theZweryfikowany adres z umcg.nl
Manuel A. RivasAssistant Professor, Department of Biomedical Data Science, Stanford UniversityZweryfikowany adres z stanford.edu
Shaun PurcellSleep & Neurogenetics Lab, Brigham & Women's Hospital, BostonZweryfikowany adres z bwh.harvard.edu
Soumya RaychaudhuriHarvard Medical School; Brigham and Women's Hospital, Broad InstituteZweryfikowany adres z broadinstitute.org
Eva ChanNSW Health PathologyZweryfikowany adres z health.nsw.gov.au
Goncalo AbecasisUniversity of Michigan School of Public HealthZweryfikowany adres z umich.edu
Chris WallaceUniversity of CambridgeZweryfikowany adres z cam.ac.uk
Prof David A van HeelQueen Mary University of London & Barts Health NHS TrustZweryfikowany adres z qmul.ac.uk
Jeffrey BarrettNightingale HealthZweryfikowany adres z nightingalehealth.com
Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann ArborZweryfikowany adres z umich.edu
Eleazar EskinUniversity of California, Los AngelesZweryfikowany adres z cs.ucla.edu

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Chris Cotsapas

Yale School of Medicine

Zweryfikowany adres z broadinstitute.org - Strona główna

Genetics of neurological and inflammatory disease pleiotropy


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
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	4127	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	2339	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	1498	2018
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis WTCCC WTCCC2) Nature Genetics 45 (11), 1353-60, 2013	1387	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	1189	2013
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility International Multiple Sclerosis Genetics Consortium*†, ANZgene, ... Science 365 (6460), eaav7188, 2019	1084	2019
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), 2018	707	2018
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	682	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	674	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	645	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	518	2011
Class II HLA interactions modulate genetic risk for multiple sclerosis Nature genetics 47 (10), 1107-1113, 2015	440	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	289	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	270	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	248	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	208	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	186	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	169	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	154	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	148	2018

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