Chris Cotsapas

Alıntı yapanlar

	Hepsi	2020 yılından bugüne
Alıntılar	19908	9883
h-endeksi	43	36
i10-endeksi	63	57

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200820092010201120122013201420152016201720182019202020212022202320242025144 353 350 387 488 667 959 1106 1203 1221 1350 1605 1885 1983 1918 1850 1873 368

Genel erişim

Tümünü görüntüle

59 makale

2 makale

genel erişime açık olanlar

genel erişime açık olmayanlar

Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad Instituteatgu.mgh.harvard.edu üzerinde doğrulanmış e-posta adresine sahip
Philip L. De JagerWeil-Granat Professor of Neurology at Columbia Universitycumc.columbia.edu üzerinde doğrulanmış e-posta adresine sahip
David HaflerProfessor of Neurology and Immunobiology, Yale Universityyale.edu üzerinde doğrulanmış e-posta adresine sahip
John D. RiouxProfessor of Medicine, Université de Montréal and the Montreal Heart Instituteumontreal.ca üzerinde doğrulanmış e-posta adresine sahip
Peter K. GregersenHead, Robert S. Boas Center for Genomics and Human Geneticsnshs.edu üzerinde doğrulanmış e-posta adresine sahip
Benjamin NealeMassachusetts General Hospital; Broad Institute; Harvard Medical Schoolbroadinstitute.org üzerinde doğrulanmış e-posta adresine sahip
Elizabeth J. RossinMass Eye and Earmeei.harvard.edu üzerinde doğrulanmış e-posta adresine sahip
Benjamin F. VoightAssociate Professor, Dept. of Systems Pharmacology and Translational Therapeutics, Dept. of Geneticspennmedicine.upenn.edu üzerinde doğrulanmış e-posta adresine sahip
Robert Plengepartners.org üzerinde doğrulanmış e-posta adresine sahip
Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theumcg.nl üzerinde doğrulanmış e-posta adresine sahip
Manuel A. RivasAssistant Professor, Department of Biomedical Data Science, Stanford Universitystanford.edu üzerinde doğrulanmış e-posta adresine sahip
Shaun PurcellSleep & Neurogenetics Lab, Brigham & Women's Hospital, Bostonbwh.harvard.edu üzerinde doğrulanmış e-posta adresine sahip
Soumya RaychaudhuriHarvard Medical School; Brigham and Women's Hospital, Broad Institutebroadinstitute.org üzerinde doğrulanmış e-posta adresine sahip
Eva ChanNSW Health Pathologyhealth.nsw.gov.au üzerinde doğrulanmış e-posta adresine sahip
Goncalo AbecasisUniversity of Michigan School of Public Healthumich.edu üzerinde doğrulanmış e-posta adresine sahip
Chris WallaceUniversity of Cambridgecam.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Prof David A van HeelQueen Mary University of London & Barts Health NHS Trustqmul.ac.uk üzerinde doğrulanmış e-posta adresine sahip
Jeffrey BarrettNightingale Healthnightingalehealth.com üzerinde doğrulanmış e-posta adresine sahip
Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann Arborumich.edu üzerinde doğrulanmış e-posta adresine sahip
Eleazar EskinUniversity of California, Los Angelescs.ucla.edu üzerinde doğrulanmış e-posta adresine sahip

Takip et

Chris Cotsapas

Yale School of Medicine

broadinstitute.org üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

Genetics of neurological and inflammatory disease pleiotropy


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
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	4142	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	2327	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	1557	2018
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis WTCCC WTCCC2) Nature Genetics 45 (11), 1353-60, 2013	1407	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	1197	2013
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility International Multiple Sclerosis Genetics Consortium*†, ANZgene, ... Science 365 (6460), eaav7188, 2019	1166*	2019
Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), eaap8757, 2018	720	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	686	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	673	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	639	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	521	2011
Class II HLA interactions modulate genetic risk for multiple sclerosis Nature genetics 47 (10), 1107-1113, 2015	445	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	285	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	274	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	252	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	165	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	156	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

Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.

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