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Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates.
Zouk, Hana; Yu, Wanfeng; Oza, Andrea; Hawley, Megan; Vijay Kumar, Prathik K; Koch, Christopher; Mahanta, Lisa M; Harley, John B; Jarvik, Gail P; Karlson, Elizabeth W; Leppig, Kathleen A; Myers, Melanie F; Prows, Cynthia A; Williams, Marc S; Weiss, Scott T; Lebo, Matthew S; Rehm, Heidi L.
Afiliación
  • Zouk H; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA; Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
  • Yu W; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA.
  • Oza A; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA.
  • Hawley M; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA.
  • Vijay Kumar PK; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA.
  • Koch C; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA.
  • Mahanta LM; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA.
  • Harley JB; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; University of Cincinnati College of Medicine, Cincinnati, OH; US Department of Veteran Affairs Medical Center, Cincinnati, OH.
  • Jarvik GP; Departments of Medicine (Medical Genetics) and Genome Sciences, University of Washington School of Medicine, Seattle, WA.
  • Karlson EW; Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
  • Leppig KA; Genetic Services, Kaiser Permanente of Washington, Seattle, WA.
  • Myers MF; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; University of Cincinnati College of Medicine, Cincinnati, OH.
  • Prows CA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
  • Williams MS; Genomic Medicine Institute, Geisinger, Danville, PA.
  • Weiss ST; Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
  • Lebo MS; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA; Brigham and Women's Hospital, Harvard Medical School, Boston, MA; Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA.
  • Rehm HL; Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, Cambridge, MA; Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA; Brigham and Women's Hospital, Harvard Medical School, Boston, MA; Medical and Population Genetics, Broad Institut
Genet Med ; 24(2): 454-462, 2022 02.
Article en En | MEDLINE | ID: mdl-34906510
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Pruebas Genéticas Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Marruecos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Pruebas Genéticas Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Marruecos