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The New England Journal of Medicine|May 23, 2014
Null mutation in hormone-sensitive lipase gene and risk of type 2 diabetesJessica S Albert, Laura M Yerges-Armstrong, Richard B Horenstein, et al.
The Pharmacogenomics Journal|September 22, 2018
Genome-wide association analysis of common genetic variants of resistant hypertensionNihal El Rouby, Caitrin W McDonough, Yan Gong, et al.
Archives of Internal Medicine|November 10, 2010
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amishHaiqing Shen, Coleen M Damcott, Evadnie Rampersaud, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Implementation of pharmacogenetics: the University of Maryland Personalized Anti-platelet Pharmacogenetics ProgramAlan R Shuldiner, Kathleen Palmer, Ruth E Pakyz, et al.
Circulation. Cardiovascular Genetics|February 9, 2013
Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomesJoshua P Lewis, Kathleen Ryan, Jeffrey R O'Connell, et al.
The New England Journal of Medicine|November 21, 2013
A pharmacogenetic versus a clinical algorithm for warfarin dosingStephen E Kimmel, Benjamin French, Scott E Kasner, et al.
JACC. Cardiovascular Interventions|November 6, 2017
Multisite Investigation of Outcomes With Implementation of CYP2C19 Genotype-Guided Antiplatelet Therapy After Percutaneous Coronary InterventionLarisa H Cavallari, Craig R Lee, Amber L Beitelshees, et al.
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