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Paper Details

Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.
J Mol Diagn
13
2017
PGRNseq, participants, pharmacogenetic variants, rare
Author NameAffiliation
Laura J Rasmussen-TorvikNorthwestern University Feinberg School of Medicine
Laura J Rasmussen-TorvikNorthwestern University Feinberg School of Medicine
Berta AlmogueraCenter for Applied Genomics, Children's Hospital of Philadelphia
Kimberly F DohenyCenter for Inherited Disease Research, Institute of Genetic Medicine, Johns Hopkins University School of Medicine
Robert R FreimuthMayo Clinic
Adam S GordonUniversity of Washington
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia
Ammar HusamiCincinnati Children's Hospital Medical Center
Iftikhar J KulloMayo Clinic
Michael D LindermanMiddlebury College
Michael D LindermanMiddlebury College
Teri A ManolioNational Human Genome Research Institute
Teri A ManolioNational Human Genome Research Institute
Aniwaa Owusu ObengThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York Pharmacy Department, The Mount Sinai Hospital
Renata PellegrinoCenter for Applied Genomics, Children's Hospital of Philadelphia
Cynthia A ProwsCincinnati Children's Hospital Medical Center
Marylyn D Ritchie
Marylyn D Ritchie
Maureen E SmithCenter for Genetic Medicine, Northwestern University Feinberg School of Medicine
Sarah C StallingsVanderbilt Institute for Clinical and Translational Research
Wendy A WolfBoston Children's Hospital
Stuart A ScottIcahn School of Medicine at Mount Sinai
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