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C Denny

Showing results (331-340 of 480) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|June 16, 2011
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarinHua Xu, Min Jiang, Matt Oetjens, et al.
Pharmacogenetics and Genomics|November 24, 2011
The use of a DNA biobank linked to electronic medical records to characterize pharmacogenomic predictors of tacrolimus dose requirement in kidney transplant recipientsKelly A Birdwell, Ben Grady, Leena Choi, et al.
Clinical Pharmacology and Therapeutics|June 29, 2012
Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotypingJ S Schildcrout, J C Denny, E Bowton, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Overcome the Limitation of Phenome-Wide Association Studies (PheWAS): Extension of PheWAS to Efficient and Robust Large-Scale ICD Codes AnalysisYa-Chen Lin, Siwei Zhang, Tess Vessels, et al.
Pharmacogenomics|October 8, 2019
A stepwise approach to implementing pharmacogenetic testing in the primary care settingKristin Wiisanen Weitzel, Benjamin Q Duong, Meghan J Arwood, et al.
BMC Medical Genomics|August 19, 2016
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variantsAnurag Verma, Shefali S Verma, Sarah A Pendergrass, et al.
Frontiers in Genetics|December 6, 2014
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic EsophagitisBahram Namjou, Keith Marsolo, Robert J Caroll, et al.
JAMA Network Open|June 7, 2021
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease PhenotypesGe Liu, Mingjian Shi, Jonathan D Mosley, et al.
Human Genetics|February 28, 2022
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroidJacqueline A Piekos, Jacklyn N Hellwege, Yanfei Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 24, 2018
Qualitative study of system-level factors related to genomic implementationAlexis M Zebrowski, Darcy E Ellis, Frances K Barg, et al.
Pageof 48

Showing results (331-340 of 480) with videos related to

Sort By:
Pageof 48
Journal of the American Medical Informatics Association : JAMIA|June 16, 2011
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarinHua Xu, Min Jiang, Matt Oetjens, et al.
Pharmacogenetics and Genomics|November 24, 2011
The use of a DNA biobank linked to electronic medical records to characterize pharmacogenomic predictors of tacrolimus dose requirement in kidney transplant recipientsKelly A Birdwell, Ben Grady, Leena Choi, et al.
Clinical Pharmacology and Therapeutics|June 29, 2012
Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotypingJ S Schildcrout, J C Denny, E Bowton, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Overcome the Limitation of Phenome-Wide Association Studies (PheWAS): Extension of PheWAS to Efficient and Robust Large-Scale ICD Codes AnalysisYa-Chen Lin, Siwei Zhang, Tess Vessels, et al.
Pharmacogenomics|October 8, 2019
A stepwise approach to implementing pharmacogenetic testing in the primary care settingKristin Wiisanen Weitzel, Benjamin Q Duong, Meghan J Arwood, et al.
BMC Medical Genomics|August 19, 2016
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variantsAnurag Verma, Shefali S Verma, Sarah A Pendergrass, et al.
Frontiers in Genetics|December 6, 2014
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic EsophagitisBahram Namjou, Keith Marsolo, Robert J Caroll, et al.
JAMA Network Open|June 7, 2021
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease PhenotypesGe Liu, Mingjian Shi, Jonathan D Mosley, et al.
Human Genetics|February 28, 2022
Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroidJacqueline A Piekos, Jacklyn N Hellwege, Yanfei Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 24, 2018
Qualitative study of system-level factors related to genomic implementationAlexis M Zebrowski, Darcy E Ellis, Frances K Barg, et al.
Pageof 48