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Todd L Edwards

Showing results (111-120 of 203) with videos related to

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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.
Plos Genetics|March 28, 2017
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressureKaren Y He, Heming Wang, Brian E Cade, et al.
Annals of Human Genetics|January 15, 2010
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseaseTodd L Edwards, William K Scott, Cherylyn Almonte, et al.
Journal of the American Medical Informatics Association : JAMIA|August 8, 2016
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individualsPedro L Teixeira, Wei-Qi Wei, Robert M Cronin, et al.
Nature Communications|December 14, 2022
Genetic architecture of heart failure with preserved versus reduced ejection fractionJacob Joseph, Chang Liu, Qin Hui, et al.
Plos One|September 2, 2009
Apoptotic engulfment pathway and schizophreniaXiangning Chen, Cuie Sun, Qi Chen, et al.
American Journal of Epidemiology|November 23, 2011
HTR1B, ADIPOR1, PPARGC1A, and CYP19A1 and obesity in a cohort of Caucasians and African Americans: an evaluation of gene-environment interactions and candidate genesTodd L Edwards, Digna R Velez Edwards, Raquel Villegas, et al.
Genetic Epidemiology|November 30, 2007
Discussing gene-gene interaction: warning--translating equations to English may result in jabberwockyChristopher W Bartlett, Veronica J Vieland, Jacquelaine Bartlett, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 15, 2021
Association Between Genetic Variation in Blood Pressure and Increased Lifetime Risk of Peripheral Artery DiseaseMichael G Levin, Derek Klarin, Venexia M Walker, et al.
Plos One|March 3, 2012
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphismsDigna R Velez Edwards, Alessandra Tacconelli, Christian Wejse, et al.
Pageof 21

Showing results (111-120 of 203) with videos related to

Sort By:
Pageof 21
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.
Plos Genetics|March 28, 2017
Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressureKaren Y He, Heming Wang, Brian E Cade, et al.
Annals of Human Genetics|January 15, 2010
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseaseTodd L Edwards, William K Scott, Cherylyn Almonte, et al.
Journal of the American Medical Informatics Association : JAMIA|August 8, 2016
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individualsPedro L Teixeira, Wei-Qi Wei, Robert M Cronin, et al.
Nature Communications|December 14, 2022
Genetic architecture of heart failure with preserved versus reduced ejection fractionJacob Joseph, Chang Liu, Qin Hui, et al.
Plos One|September 2, 2009
Apoptotic engulfment pathway and schizophreniaXiangning Chen, Cuie Sun, Qi Chen, et al.
American Journal of Epidemiology|November 23, 2011
HTR1B, ADIPOR1, PPARGC1A, and CYP19A1 and obesity in a cohort of Caucasians and African Americans: an evaluation of gene-environment interactions and candidate genesTodd L Edwards, Digna R Velez Edwards, Raquel Villegas, et al.
Genetic Epidemiology|November 30, 2007
Discussing gene-gene interaction: warning--translating equations to English may result in jabberwockyChristopher W Bartlett, Veronica J Vieland, Jacquelaine Bartlett, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|April 15, 2021
Association Between Genetic Variation in Blood Pressure and Increased Lifetime Risk of Peripheral Artery DiseaseMichael G Levin, Derek Klarin, Venexia M Walker, et al.
Plos One|March 3, 2012
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphismsDigna R Velez Edwards, Alessandra Tacconelli, Christian Wejse, et al.
Pageof 21