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Showing results (381-390 of 480) with videos related to

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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|March 14, 2019
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE networkXinyuan Zhang, Yogasudha Veturi, Shefali Verma, 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.
Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics. Evobio (Conference)|January 16, 2015
Replication of <i>SCN5A</i> Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic StudiesJanina M Jeff, Kristin Brown-Gentry, Robert Goodloe, et al.
BMC Medical Genomics|May 24, 2017
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) networkNina R Sperber, Janet S Carpenter, Larisa H Cavallari, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, 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.
JAMA Cardiology|January 24, 2019
Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysisJoe-Elie Salem, M Benjamin Shoemaker, Lisa Bastarache, et al.
Journal of the American Medical Informatics Association : JAMIA|November 22, 2011
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association studyAbel N Kho, M Geoffrey Hayes, Laura Rasmussen-Torvik, et al.
Molecular Vision|October 30, 2014
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility lociMarylyn D Ritchie, Shefali S Verma, Molly A Hall, 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 48

Showing results (381-390 of 480) with videos related to

Sort By:
Pageof 48
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|March 14, 2019
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE networkXinyuan Zhang, Yogasudha Veturi, Shefali Verma, 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.
Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics. Evobio (Conference)|January 16, 2015
Replication of <i>SCN5A</i> Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic StudiesJanina M Jeff, Kristin Brown-Gentry, Robert Goodloe, et al.
BMC Medical Genomics|May 24, 2017
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) networkNina R Sperber, Janet S Carpenter, Larisa H Cavallari, et al.
BMC Medical Genomics|January 7, 2021
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohortElisabeth A Rosenthal, David R Crosslin, Adam S Gordon, 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.
JAMA Cardiology|January 24, 2019
Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysisJoe-Elie Salem, M Benjamin Shoemaker, Lisa Bastarache, et al.
Journal of the American Medical Informatics Association : JAMIA|November 22, 2011
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association studyAbel N Kho, M Geoffrey Hayes, Laura Rasmussen-Torvik, et al.
Molecular Vision|October 30, 2014
Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility lociMarylyn D Ritchie, Shefali S Verma, Molly A Hall, 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 48