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Paper Details

Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.
Genet Med
37
2017
ARVC, DSC2, DSG2, DSP, JUP, PKP2, TGF3, TMEM43, VUSs, arrhythmogenic right ventricular cardiomyopathy, electrophysiologic abnormalities, inherited heart disease, nonischemic cardiomyopathies, pLOF, pLOF variants, patients
Author NameAffiliation
Cynthia A JamesJohns Hopkins University
Joseph B LeaderBiomedical and Translational Informatics Institute
Sarah A PendergrassBiomedical and Translational Informatics Institute
Marylyn D RitchieBiomedical and Translational Informatics Institute
Marylyn D RitchieBiomedical and Translational Informatics Institute
David J CareyWeis Center for Health Research
David J CareyWeis Center for Health Research
David H LedbetterGenomic Medicine Institute
David H LedbetterGenomic Medicine Institute
Marc S WilliamsGenomic Medicine Institute
Frederick E DeweyRegeneron Pharmaceuticals
Alexander LopezRegeneron Pharmaceuticals
John PennRegeneron Pharmaceuticals
John D OvertonRegeneron Pharmaceuticals
John D OvertonRegeneron Pharmaceuticals
Jeffrey G ReidRegeneron Pharmaceuticals
Jeffrey G ReidRegeneron Pharmaceuticals
Matthew S LeboBrigham and Women's Hospital, Harvard Medical School
Matthew S Lebo
Heidi L Rehm
Heidi L RehmBrigham and Women's Hospital, Harvard Medical School
Heidi L Rehm
Heidi L RehmBrigham and Women's Hospital, Harvard Medical School
Michael F MurrayGenomic Medicine Institute
Michael F MurrayGenomic Medicine Institute
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