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Christopher Newton

Showing results (191-200 of 249) with videos related to

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Nature Genetics|October 8, 2013
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetesJason Flannick, Nicola L Beer, Alexander G Bick, et al.
Circulation. Genomic and Precision Medicine|March 16, 2018
Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human SubjectsRay Hu, Michael P Morley, Jeffrey Brandimarto, et al.
Plos One|July 10, 2009
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studiesIlja M Nolte, Chris Wallace, Stephen J Newhouse, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Human Molecular Genetics|March 23, 2011
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortiumXiaofeng Zhu, J H Young, Ervin Fox, et al.
Circulation. Cardiovascular Genetics|August 18, 2011
Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) projectRenate B Schnabel, Kathleen F Kerr, Steven A Lubitz, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Nature Communications|March 8, 2018
Genome-wide analysis yields new loci associating with aortic valve stenosisAnna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al.
BMC Medical Genetics|October 2, 2007
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reportsL Adrienne Cupples, Heather T Arruda, Emelia J Benjamin, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
Candidate gene association resource (CARe): design, methods, and proof of conceptKiran Musunuru, Guillaume Lettre, Taylor Young, et al.
Pageof 25

Showing results (191-200 of 249) with videos related to

Sort By:
Pageof 25
Nature Genetics|October 8, 2013
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetesJason Flannick, Nicola L Beer, Alexander G Bick, et al.
Circulation. Genomic and Precision Medicine|March 16, 2018
Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human SubjectsRay Hu, Michael P Morley, Jeffrey Brandimarto, et al.
Plos One|July 10, 2009
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studiesIlja M Nolte, Chris Wallace, Stephen J Newhouse, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) ConsortiumJared W Magnani, Jennifer A Brody, Bram P Prins, et al.
Human Molecular Genetics|March 23, 2011
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortiumXiaofeng Zhu, J H Young, Ervin Fox, et al.
Circulation. Cardiovascular Genetics|August 18, 2011
Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) projectRenate B Schnabel, Kathleen F Kerr, Steven A Lubitz, et al.
Circulation. Cardiovascular Genetics|December 15, 2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskBing Yu, Sara L Pulit, Shih-Jen Hwang, et al.
Nature Communications|March 8, 2018
Genome-wide analysis yields new loci associating with aortic valve stenosisAnna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al.
BMC Medical Genetics|October 2, 2007
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reportsL Adrienne Cupples, Heather T Arruda, Emelia J Benjamin, et al.
Circulation. Cardiovascular Genetics|April 20, 2010
Candidate gene association resource (CARe): design, methods, and proof of conceptKiran Musunuru, Guillaume Lettre, Taylor Young, et al.
Pageof 25