Your browser doesn't support javascript.
loading
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.
Haggerty, Christopher M; James, Cynthia A; Calkins, Hugh; Tichnell, Crystal; Leader, Joseph B; Hartzel, Dustin N; Nevius, Christopher D; Pendergrass, Sarah A; Person, Thomas N; Schwartz, Marci; Ritchie, Marylyn D; Carey, David J; Ledbetter, David H; Williams, Marc S; Dewey, Frederick E; Lopez, Alexander; Penn, John; Overton, John D; Reid, Jeffrey G; Lebo, Matthew; Mason-Suares, Heather; Austin-Tse, Christina; Rehm, Heidi L; Delisle, Brian P; Makowski, Daniel J; Mehra, Vishal C; Murray, Michael F; Fornwalt, Brandon K.
Afiliação
  • Haggerty CM; Department of Imaging Science and Innovation, Geisinger Health System, Danville, Pennsylvania, USA.
  • James CA; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Calkins H; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Tichnell C; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Leader JB; Biomedical and Translational Informatics Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Hartzel DN; Biomedical and Translational Informatics Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Nevius CD; Department of Imaging Science and Innovation, Geisinger Health System, Danville, Pennsylvania, USA.
  • Pendergrass SA; Biomedical and Translational Informatics Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Person TN; Biomedical and Translational Informatics Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Schwartz M; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Ritchie MD; Biomedical and Translational Informatics Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Carey DJ; Weis Center for Health Research, Geisinger Health System, Danville, Pennsylvania, USA.
  • Ledbetter DH; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Williams MS; Genomic Medicine Institute, Geisinger Health System, Danville, Pennsylvania, USA.
  • Dewey FE; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
  • Lopez A; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
  • Penn J; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
  • Overton JD; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
  • Reid JG; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
  • Lebo M; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts, USA.
  • Mason-Suares H; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Austin-Tse C; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts, USA.
  • Rehm HL; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Delisle BP; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts, USA.
  • Makowski DJ; Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine, Cambridge, Massachusetts, USA.
  • Mehra VC; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Murray MF; Department of Physiology, University of Kentucky, Lexington, Kentucky, USA.
  • Fornwalt BK; Division of Cardiology, Geisinger Health System, Danville, Pennsylvania, USA.
Genet Med ; 19(11): 1245-1252, 2017 11.
Article em En | MEDLINE | ID: mdl-28471438
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Análise de Sequência de DNA / Displasia Arritmogênica Ventricular Direita / Exoma Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Análise de Sequência de DNA / Displasia Arritmogênica Ventricular Direita / Exoma Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article