Your browser doesn't support javascript.
loading
Rare coding variants pinpoint genes that control human hematological traits.
Mousas, Abdou; Ntritsos, Georgios; Chen, Ming-Huei; Song, Ci; Huffman, Jennifer E; Tzoulaki, Ioanna; Elliott, Paul; Psaty, Bruce M; Auer, Paul L; Johnson, Andrew D; Evangelou, Evangelos; Lettre, Guillaume; Reiner, Alexander P.
Afiliação
  • Mousas A; Department of Medicine, Université de Montréal, Montréal, Québec, Canada.
  • Ntritsos G; Montreal Heart Institute, Montréal, Québec, Canada.
  • Chen MH; Department of Hygiene and Epidemiology, University of Ioannina Medical School, Ioannina, Greece.
  • Song C; Population Sciences Branch, National Heart Lung and Blood Institute, The Framingham Heart Study, Framingham, MA, United States of America.
  • Huffman JE; Population Sciences Branch, National Heart Lung and Blood Institute, The Framingham Heart Study, Framingham, MA, United States of America.
  • Tzoulaki I; Population Sciences Branch, National Heart Lung and Blood Institute, The Framingham Heart Study, Framingham, MA, United States of America.
  • Elliott P; Department of Hygiene and Epidemiology, University of Ioannina Medical School, Ioannina, Greece.
  • Psaty BM; Department of Epidemiology and Biostatistics, MRC-PHE Centre for Environment and Health, School of Public Health, Imperial College London, London, United Kingdom.
  • Auer PL; Cardiovascular Health Research Unit, Departments of Medicine, Epidemiology, and Health Services, University of Washington, Seattle, WA, United States of America.
  • Johnson AD; Kaiser Permanente Washington Health Research Institute, Seattle, WA, United States of America.
  • Lettre G; Zilber School of Public Health, University of Wisconsin-Milwaukee, Milwaukee, WI, United States of America.
  • Reiner AP; Population Sciences Branch, National Heart Lung and Blood Institute, The Framingham Heart Study, Framingham, MA, United States of America.
PLoS Genet ; 13(8): e1006925, 2017 Aug.
Article em En | MEDLINE | ID: mdl-28787443

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Genoma Humano / Polimorfismo de Nucleotídeo Único / Endometriose / Rinite Alérgica Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma / Genoma Humano / Polimorfismo de Nucleotídeo Único / Endometriose / Rinite Alérgica Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article