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Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals.
Verma, Anurag; Bang, Lisa; Miller, Jason E; Zhang, Yanfei; Lee, Ming Ta Michael; Zhang, Yu; Byrska-Bishop, Marta; Carey, David J; Ritchie, Marylyn D; Pendergrass, Sarah A; Kim, Dokyoon.
Afiliação
  • Verma A; Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA; The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
  • Bang L; Biomedical and Translational Informatics Institute, Geisinger, Danville, PA 17821, USA.
  • Miller JE; Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Zhang Y; Genomic Medicine Institute, Geisinger, Danville, PA 17821, USA.
  • Lee MTM; Genomic Medicine Institute, Geisinger, Danville, PA 17821, USA.
  • Zhang Y; Department of Statistics, The Pennsylvania State University, University Park, PA 16802, USA.
  • Byrska-Bishop M; Biomedical and Translational Informatics Institute, Geisinger, Danville, PA 17821, USA.
  • Carey DJ; Weis Center for Research, Geisinger, Danville, PA 17821, USA.
  • Ritchie MD; Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA; The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
  • Pendergrass SA; Biomedical and Translational Informatics Institute, Geisinger, Danville, PA 17821, USA.
  • Kim D; The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA; Biomedical and Translational Informatics Institute, Geisinger, Danville, PA 17821, USA. Electronic address: dkim@geisinger.edu.
Am J Hum Genet ; 104(1): 55-64, 2019 01 03.
Article em En | MEDLINE | ID: mdl-30598166
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Doença / Polimorfismo de Nucleotídeo Único / Registros Eletrônicos de Saúde / Estudos de Associação Genética Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Doença / Polimorfismo de Nucleotídeo Único / Registros Eletrônicos de Saúde / Estudos de Associação Genética Idioma: En Ano de publicação: 2019 Tipo de documento: Article