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Eric Boerwinkle

Showing results (531-540 of 1,213) with videos related to

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Research in Autism Spectrum Disorders|April 2, 2019
Interaction between manganese and <i>GSTP1</i> in relation to autism spectrum disorder while controlling for exposure to mixture of lead, mercury, arsenic, and cadmiumMohammad H Rahbar, Maureen Samms-Vaughan, MinJae Lee, et al.
JAMA Cardiology|July 28, 2020
Molecular Signature of Multisystem Cardiometabolic Stress and Its Association With PrognosisVenkatesh L Murthy, Bing Yu, Wenshuang Wang, et al.
Circulation. Cardiovascular Genetics|October 23, 2012
Hypertension susceptibility loci and blood pressure response to antihypertensives: results from the pharmacogenomic evaluation of antihypertensive responses studyYan Gong, Caitrin W McDonough, Zhiying Wang, et al.
Circulation Research|November 15, 2012
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studiesKhanh-Dung H Nguyen, Vasyl Pihur, Santhi K Ganesh, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyJoshua C Bis, Charles C White, Nora Franceschini, et al.
Circulation. Cardiovascular Genetics|January 2, 2015
Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American familiesPriya B Shetty, Hua Tang, Tao Feng, et al.
Plos Genetics|September 26, 2019
Unraveling the functional role of the orphan solute carrier, SLC22A24 in the transport of steroid conjugates through metabolomic and genome-wide association studiesSook Wah Yee, Adrian Stecula, Huan-Chieh Chien, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 13, 2007
Five common gene variants identify elevated genetic risk for coronary heart diseaseLance A Bare, Alanna C Morrison, Charles M Rowland, et al.
Genome Medicine|July 22, 2015
Secondary findings and carrier test frequencies in a large multiethnic sampleTomasz Gambin, Shalini N Jhangiani, Jennifer E Below, et al.
The American Journal of Clinical Nutrition|May 30, 2020
Serum sphingolipids and incident diabetes in a US population with high diabetes burden: the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)Guo-Chong Chen, Jin Choul Chai, Bing Yu, et al.
Pageof 122

Showing results (531-540 of 1,213) with videos related to

Sort By:
Pageof 122
Research in Autism Spectrum Disorders|April 2, 2019
Interaction between manganese and <i>GSTP1</i> in relation to autism spectrum disorder while controlling for exposure to mixture of lead, mercury, arsenic, and cadmiumMohammad H Rahbar, Maureen Samms-Vaughan, MinJae Lee, et al.
JAMA Cardiology|July 28, 2020
Molecular Signature of Multisystem Cardiometabolic Stress and Its Association With PrognosisVenkatesh L Murthy, Bing Yu, Wenshuang Wang, et al.
Circulation. Cardiovascular Genetics|October 23, 2012
Hypertension susceptibility loci and blood pressure response to antihypertensives: results from the pharmacogenomic evaluation of antihypertensive responses studyYan Gong, Caitrin W McDonough, Zhiying Wang, et al.
Circulation Research|November 15, 2012
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studiesKhanh-Dung H Nguyen, Vasyl Pihur, Santhi K Ganesh, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyJoshua C Bis, Charles C White, Nora Franceschini, et al.
Circulation. Cardiovascular Genetics|January 2, 2015
Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American familiesPriya B Shetty, Hua Tang, Tao Feng, et al.
Plos Genetics|September 26, 2019
Unraveling the functional role of the orphan solute carrier, SLC22A24 in the transport of steroid conjugates through metabolomic and genome-wide association studiesSook Wah Yee, Adrian Stecula, Huan-Chieh Chien, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 13, 2007
Five common gene variants identify elevated genetic risk for coronary heart diseaseLance A Bare, Alanna C Morrison, Charles M Rowland, et al.
Genome Medicine|July 22, 2015
Secondary findings and carrier test frequencies in a large multiethnic sampleTomasz Gambin, Shalini N Jhangiani, Jennifer E Below, et al.
The American Journal of Clinical Nutrition|May 30, 2020
Serum sphingolipids and incident diabetes in a US population with high diabetes burden: the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)Guo-Chong Chen, Jin Choul Chai, Bing Yu, et al.
Pageof 122