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Paper Details

Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing.
PLoS One
12
2019
SRM, SRM 3-, Statin, Statin-related myopathy, common genetic variants, creatine, creatine phosphokinase, muscle injury, people, rare coding variants, rare variants, rhabdomyolysis, statin, statin-related myopathy, statins
Author NameAffiliation
James S FloydUniversity of Washington
James S FloydUniversity of Washington
Jennifer A BrodyUniversity of Washington
Moneeza K SiddiquiDivision of Molecular and Clinical Medicine, University of Dundee
Xiaoming LiuUniversity of Texas Health Science Center
Joshua C BisUniversity of Washington
Patrik K E MagnussonKarolinska Institutet
Kerri L WigginsUniversity of Washington
Alanna C MorrisonSchool of Public Health, The University of Texas Health Science Center at Houston
Susan R HeckbertUniversity of Washington
Richard A GibbsBaylor College of Medicine
Russell P TracyLarner College of Medicine, University of Vermont
Eric BoerwinkleSchool of Public Health, The University of Texas Health Science Center at Houston
Eric BoerwinkleSchool of Public Health, The University of Texas Health Science Center at Houston
Daniel GaudetClinical Lipidology and Rare Lipid Disorders Unit, Universite de Montreal Community Gene Medicine Center, Lipid Clinic Chicoutimi Hospital and ECOGENE-21 Clinical and Translational Research Center
Kenneth RiceUniversity of Washington
Anke-Hilse Maitland-van der Zee
Andrew P MorrisUniversity of Liverpool
Andrew P MorrisUniversity of Liverpool
Colin N A PalmerDivision of Molecular and Clinical Medicine, University of Dundee
Colin N A PalmerDivision of Molecular and Clinical Medicine, University of Dundee
Bruce M PsatyUniversity of Washington
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