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Josh C Denny

Showing results (11-20 of 34) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|April 17, 2018
Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine DisordersKathryn M Dahir, Daniel R Tilden, Jeremy L Warner, et al.
Journal of Thrombosis and Thrombolysis|October 9, 2015
Evaluation of the F2R IVS-14A/T PAR1 polymorphism with subsequent cardiovascular events and bleeding in patients who have undergone percutaneous coronary interventionEitan A Friedman, Luisa Texeira, Jessica Delaney, 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.
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.
Nature Communications|January 9, 2021
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statisticsRuowang Li, Rui Duan, Xinyuan Zhang, et al.
The Journal of Allergy and Clinical Immunology|June 16, 2015
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studiesMichael J McGeachie, Ann C Wu, Sze Man Tse, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2026
Shared trans-ancestry architecture of HLA-mediated disease risk in the <i>All of Us</i> Research ProgramKwangmi Ahn, John S House, Adam Burkholder, et al.
Circulation. Cardiovascular Genetics|October 27, 2016
Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical DataJonathan D Mosley, Sara L van Driest, Quinn S Wells, et al.
Scientific Reports|April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE networkJacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.
Circulation. Cardiovascular Genetics|April 19, 2017
Investigating the Genetic Architecture of the PR Interval Using Clinical PhenotypesJonathan D Mosley, M Benjamin Shoemaker, Quinn S Wells, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
The Journal of Clinical Endocrinology and Metabolism|April 17, 2018
Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine DisordersKathryn M Dahir, Daniel R Tilden, Jeremy L Warner, et al.
Journal of Thrombosis and Thrombolysis|October 9, 2015
Evaluation of the F2R IVS-14A/T PAR1 polymorphism with subsequent cardiovascular events and bleeding in patients who have undergone percutaneous coronary interventionEitan A Friedman, Luisa Texeira, Jessica Delaney, 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.
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.
Nature Communications|January 9, 2021
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statisticsRuowang Li, Rui Duan, Xinyuan Zhang, et al.
The Journal of Allergy and Clinical Immunology|June 16, 2015
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studiesMichael J McGeachie, Ann C Wu, Sze Man Tse, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2026
Shared trans-ancestry architecture of HLA-mediated disease risk in the <i>All of Us</i> Research ProgramKwangmi Ahn, John S House, Adam Burkholder, et al.
Circulation. Cardiovascular Genetics|October 27, 2016
Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical DataJonathan D Mosley, Sara L van Driest, Quinn S Wells, et al.
Scientific Reports|April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE networkJacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.
Circulation. Cardiovascular Genetics|April 19, 2017
Investigating the Genetic Architecture of the PR Interval Using Clinical PhenotypesJonathan D Mosley, M Benjamin Shoemaker, Quinn S Wells, et al.
Pageof 4