Skip to Main Content

Paper Details

Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.
Nat Commun
3
2021
cardiovascular diseases, patients, pleiotropic SNPs
Author NameAffiliation
Ruowang LiUniversity of Pennsylvania
Rui DuanHarvard T.H. Chan School of Public Health
Thomas LumleyUniversity of Auckland
Sarah A PendergrassBiomedical and Translational Informatics Institute
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia
David S CarrellKaiser Permanente Washington Health Research Institute
Jordan W SmollerCenter for Genomic Medicine, Massachusetts General Hospital
Jordan W SmollerCenter for Genomic Medicine, Massachusetts General Hospital
Wei-Qi WeiVanderbilt University Medical Centre
Robert J CarrollVanderbilt University Medical Centre
Digna R Velez EdwardsClinical and Translational Hereditary Cancer Program, Vanderbilt-Ingram Cancer Center, Vanderbilt University
Georgia L WiesnerClinical and Translational Hereditary Cancer Program, Vanderbilt-Ingram Cancer Center, Vanderbilt University
Patrick M A SleimanCenter for Applied Genomics, Children's Hospital of Philadelphia
Patrick M A SleimanCenter for Applied Genomics, Children's Hospital of Philadelphia
Joshua C DennyVanderbilt University Medical Centre
Jonathan D MosleyVanderbilt University Medical Centre
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Yong ChenUniversity of Pennsylvania
Jason H MooreUniversity of Pennsylvania
  • 1 - 21

Datasets