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Paper Details

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
JAMA
130
2016
Author NameAffiliation
Sara L Van DriestVanderbilt University Medical Center
Quinn S WellsVanderbilt University Medical Center
Sarah C StallingsVanderbilt University Medical Center
William S BushVanderbilt University Medical Center, Tennessee2Case Western Reserve University
Adam S GordonUniversity of Washington
Deborah A NickersonUniversity of Washington
Deborah A NickersonUniversity of Washington
Jerry H KimUniversity of Washington
David R CrosslinUniversity of Washington
David R CrosslinUniversity of Washington
Gail P JarvikUniversity of Washington
Gail P JarvikUniversity of Washington
David S CarrellGroup Health Research Institute
James D RalstonGroup Health Research Institute
Eric B LarsonGroup Health Research Institute
Suzette J BielinskiMayo Clinic
Suzette J BielinskiMayo Clinic
Janet E OlsonMayo Clinic
Zi YeMayo Clinic
Iftikhar J KulloMayo Clinic
Noura S Abul-HusnIcahn School of Medicine at Mount Sinai
Noura S Abul-HusnIcahn School of Medicine at Mount Sinai
Stuart A ScottIcahn School of Medicine at Mount Sinai
Erwin P BottingerIcahn School of Medicine at Mount Sinai
Erwin P BottingerIcahn School of Medicine at Mount Sinai
Berta AlmogueraThe Children's Hospital of Philadelphia
John J ConnollyThe Children's Hospital of Philadelphia
Rosetta M ChiavacciThe Children's Hospital of Philadelphia
Hakon HakonarsonThe Children's Hospital of Philadelphia, Pennsylvania8Perelman School of Medicine, University of Pennsylvania
Hakon HakonarsonThe Children's Hospital of Philadelphia, Pennsylvania8Perelman School of Medicine, University of Pennsylvania
Laura J Rasmussen-TorvikNorthwestern University Feinberg School of Medicine
Laura J Rasmussen-TorvikNorthwestern University Feinberg School of Medicine
Vivian PanNorthwestern University Feinberg School of Medicine
Maureen A SmithNorthwestern University Feinberg School of Medicine
Rex L ChisholmNorthwestern University Feinberg School of Medicine
Terrie KitchnerMarshfield Clinic Research Foundation
Murray H BrilliantMarshfield Clinic Research Foundation
John R WallacePennsylvania State University, University Park.
Kimberly F DohenyJohns Hopkins School of Medicine
Moore Benjamin ShoemakerVanderbilt University Medical Center
Rongling LiNational Human Genome Research Institute, National Institutes of Health
Rongling LiNational Human Genome Research Institute, National Institutes of Health
Teri A ManolioNational Human Genome Research Institute, National Institutes of Health
Teri A ManolioNational Human Genome Research Institute, National Institutes of Health
Marc S Williams
David J Carey
David J Carey
Michael J AckermanMayo Clinic
Marylyn D RitchiePennsylvania State University, University Park16Geisinger Health System
Marylyn D RitchiePennsylvania State University, University Park16Geisinger Health System
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink