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The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.
Popejoy, Alice B; Ritter, Deborah I; Crooks, Kristy; Currey, Erin; Fullerton, Stephanie M; Hindorff, Lucia A; Koenig, Barbara; Ramos, Erin M; Sorokin, Elena P; Wand, Hannah; Wright, Mathew W; Zou, James; Gignoux, Christopher R; Bonham, Vence L; Plon, Sharon E; Bustamante, Carlos D.
Afiliação
  • Popejoy AB; Department of Biomedical Data Science, Stanford University, Standford, California.
  • Ritter DI; Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
  • Crooks K; Department of Pathology, University of Colorado, Anschutz Medical Campus, Aurora, Colorado.
  • Currey E; Department of Medicine, Division of Bioinformatics and Personalized Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Fullerton SM; Division of Genomics and Society, National Human Genome Research Institute (NHGRI), Bethesda, Maryland.
  • Hindorff LA; Department of Bioethics & Humanities, University of Washington, Seattle, Washington.
  • Koenig B; Division of Genomics and Society, National Human Genome Research Institute (NHGRI), Bethesda, Maryland.
  • Ramos EM; Department of Anthropology, History, and Social Medicine, University of California, San Francisco.
  • Sorokin EP; Division of Genomics and Society, National Human Genome Research Institute (NHGRI), Bethesda, Maryland.
  • Wand H; Department of Biomedical Data Science, Stanford University, Standford, California.
  • Wright MW; Department of Biomedical Data Science, Stanford University, Standford, California.
  • Zou J; Department of Biomedical Data Science, Stanford University, Standford, California.
  • Gignoux CR; Department of Biomedical Data Science, Stanford University, Standford, California.
  • Bonham VL; Department of Medicine, Division of Bioinformatics and Personalized Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
  • Plon SE; Social and Behavioral Research Branch, National Human Genome Research Institute (NHGRI), Bethesda, Maryland.
  • Bustamante CD; Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
Hum Mutat ; 39(11): 1713-1720, 2018 11.
Article em En | MEDLINE | ID: mdl-30311373
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Aspecto: Determinantes_sociais_saude Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética Tipo de estudo: Guideline / Prognostic_studies / Qualitative_research Aspecto: Determinantes_sociais_saude Limite: Humans Idioma: En Revista: Hum Mutat Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de publicação: Estados Unidos