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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 warfarin
Hua 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 recipients
Kelly A Birdwell, Ben Grady, Leena Choi, et al.
Clinical Pharmacology and Therapeutics
|
June 29, 2012
Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping
J 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 Analysis
Ya-Chen Lin, Siwei Zhang, Tess Vessels, et al.
Pharmacogenomics
|
October 8, 2019
A stepwise approach to implementing pharmacogenetic testing in the primary care setting
Kristin 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 variants
Anurag 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 Esophagitis
Bahram 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 Phenotypes
Ge 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 fibroid
Jacqueline 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 implementation
Alexis M Zebrowski, Darcy E Ellis, Frances K Barg, et al.
Page
of 48
Search research articles
Search
Showing results (331-340 of 480) with videos related to
Sort By:
Page
of 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 warfarin
Hua 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 recipients
Kelly A Birdwell, Ben Grady, Leena Choi, et al.
Clinical Pharmacology and Therapeutics
|
June 29, 2012
Optimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping
J 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 Analysis
Ya-Chen Lin, Siwei Zhang, Tess Vessels, et al.
Pharmacogenomics
|
October 8, 2019
A stepwise approach to implementing pharmacogenetic testing in the primary care setting
Kristin 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 variants
Anurag 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 Esophagitis
Bahram 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 Phenotypes
Ge 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 fibroid
Jacqueline 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 implementation
Alexis M Zebrowski, Darcy E Ellis, Frances K Barg, et al.
Page
of 48