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Nature Genetics|March 8, 2011
A rare variant in MYH6 is associated with high risk of sick sinus syndromeHilma Holm, Daniel F Gudbjartsson, Patrick Sulem, et al.
Clinical and Translational Science|October 17, 2012
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOELaura J Rasmussen-Torvik, Jennifer A Pacheco, Russell A Wilke, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcareCecile Avery, Mojgan Babanejad, James Baker, et al.
Plos One|June 2, 2015
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin TherapySara L Van Driest, Tracy L McGregor, Digna R Velez Edwards, et al.
Circulation. Arrhythmia and Electrophysiology|December 15, 2023
Clinical Management of Brugada Syndrome: Commentary From the ExpertsMichael J Cutler, Lee L Eckhardt, Elizabeth S Kaufman, et al.
Human Genetics|August 25, 2017
A multi-stage genome-wide association study of uterine fibroids in African AmericansJacklyn N Hellwege, Janina M Jeff, Lauren A Wise, et al.
Human Genetics|October 5, 2017
Erratum to: A multi-stage genome-wide association study of uterine fibroids in African AmericansJacklyn N Hellwege, Janina M Jeff, Lauren A Wise, et al.
Scientific Reports|May 7, 2020
The polygenic architecture of left ventricular mass mirrors the clinical epidemiologyJonathan D Mosley, Rebecca T Levinson, Eric Farber-Eger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2022
Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohortJosephina A N Meester, Silke Peeters, Lotte Van Den Heuvel, et al.
Journal of the American Medical Informatics Association : JAMIA|September 6, 2015
Desiderata for computable representations of electronic health records-driven phenotype algorithmsHuan Mo, William K Thompson, Luke V Rasmussen, et al.
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