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Providing Access to Genomic Variant Knowledge in a Healthcare Setting: A Vision for the ClinGen Electronic Health Records Workgroup.
Overby, C L; Heale, B; Aronson, S; Cherry, J M; Dwight, S; Milosavljevic, A; Nelson, T; Niehaus, A; Weaver, M A; Ramos, E M; Williams, M S.
Afiliação
  • Overby CL; Program for Personalized and Genomic Medicine & Center for Health-related Informatics and Bioimaging, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Heale B; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Aronson S; University of Utah, Salt Lake City, Utah, USA.
  • Cherry JM; Partners HealthCare Personalized Medicine, Cambridge, Massachusetts, USA.
  • Dwight S; Stanford University, School of Medicine, Stanford, California, USA.
  • Milosavljevic A; Stanford University, School of Medicine, Stanford, California, USA.
  • Nelson T; Baylor College of Medicine, Houston, Texas, USA.
  • Niehaus A; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Weaver MA; National Human Genome Research Institute, National Institutes of Health, Rockville, Maryland, USA.
  • Ramos EM; American College of Medical Genetics and Genomics, Bethesda, Maryland, USA.
  • Williams MS; National Human Genome Research Institute, National Institutes of Health, Rockville, Maryland, USA.
Clin Pharmacol Ther ; 99(2): 157-60, 2016 Feb.
Article em En | MEDLINE | ID: mdl-26418054
The Clinical Genome Resource (ClinGen) is a National Institutes of Health (NIH)-funded collaborative program that brings together a variety of projects designed to provide high-quality, curated information on clinically relevant genes and variants. ClinGen's EHR (Electronic Health Record) Workgroup aims to ensure that ClinGen is accessible to providers and patients through EHR and related systems. This article describes the current scope of these efforts and progress to date. The ClinGen public portal can be accessed at www.clinicalgenome.org.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacogenética / Registros Eletrônicos de Saúde Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacogenética / Registros Eletrônicos de Saúde Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Clin Pharmacol Ther Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos