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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2012
Mapping the incidentalome: estimating incidental findings generated through clinical pharmacogenomics testingMatthew J Westbrook, M Frances Wright, Sara L Van Driest, et al.Pharmacogenetics and Genomics|July 11, 2013
Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedemaGuillaume Pare, Michiaki Kubo, James B Byrd, et al.Human Genetics|January 30, 2010
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibilityRebecca L Zuvich, Jacob L McCauley, Jorge R Oksenberg, et al.Human Molecular Genetics|June 10, 2011
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complexRebecca L Zuvich, William S Bush, Jacob L McCauley, et al.American Journal of Epidemiology|June 5, 2010
Variation within DNA repair pathway genes and risk of multiple sclerosisFarren B S Briggs, Benjamin A Goldstein, Jacob L McCauley, et al.Human Molecular Genetics|March 10, 2010
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosisPaola G Bronson, Stacy Caillier, Patricia P Ramsay, et al.Human Molecular Genetics|August 12, 2010
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individualsFarren B S Briggs, Selena E Bartlett, Benjamin A Goldstein, et al.Pharmacogenomics|February 15, 2012
Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health recordAndrea H Ramirez, Yaping Shi, Jonathan S Schildcrout, et al.Current Protocols in Human Genetics|January 15, 2011
Quality control procedures for genome-wide association studiesStephen Turner, Loren L Armstrong, Yuki Bradford, 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.Pageof 2