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Showing results (621-630 of 1,250) with videos related to

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Human Molecular Genetics|June 29, 2022
Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence dataWonji Kim, Julian Hecker, R Graham Barr, et al.
American Journal of Human Genetics|May 3, 2022
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence dataLe Huang, Jonathan D Rosen, Quan Sun, et al.
Nature Genetics|July 13, 2004
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetesDehuang Guo, Manyu Li, Yan Zhang, et al.
Nature Genetics|March 24, 2009
Common variants at ten loci influence QT interval duration in the QTGEN StudyChristopher Newton-Cheh, Mark Eijgelsheim, Kenneth M Rice, et al.
Circulation. Genomic and Precision Medicine|October 10, 2022
Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery DiseaseAmit V Khera, Minxian Wang, Mark Chaffin, et al.
Cell Genomics|August 21, 2023
Multiset correlation and factor analysis enables exploration of multi-omics dataBrielin C Brown, Collin Wang, Silva Kasela, et al.
Diabetes|August 23, 2022
Nontargeted and Targeted Metabolomic Profiling Reveals Novel Metabolite Biomarkers of Incident Diabetes in African AmericansZsu-Zsu Chen, Julian Avila Pacheco, Yan Gao, et al.
Nature Genetics|April 17, 2007
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisJohn D Rioux, Ramnik J Xavier, Kent D Taylor, et al.
The European Respiratory Journal|May 18, 2023
Incidence of interstitial lung abnormalities: the MESA Lung StudyClaire F McGroder, Spencer Hansen, Karen Hinckley Stukovsky, et al.
Journal of the American College of Cardiology|November 16, 2019
Rare Genetic Variants Associated With Sudden Cardiac Death in AdultsAmit V Khera, Heather Mason-Suares, Deanna Brockman, et al.
Pageof 125

Showing results (621-630 of 1,250) with videos related to

Sort By:
Pageof 125
Human Molecular Genetics|June 29, 2022
Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence dataWonji Kim, Julian Hecker, R Graham Barr, et al.
American Journal of Human Genetics|May 3, 2022
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence dataLe Huang, Jonathan D Rosen, Quan Sun, et al.
Nature Genetics|July 13, 2004
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetesDehuang Guo, Manyu Li, Yan Zhang, et al.
Nature Genetics|March 24, 2009
Common variants at ten loci influence QT interval duration in the QTGEN StudyChristopher Newton-Cheh, Mark Eijgelsheim, Kenneth M Rice, et al.
Circulation. Genomic and Precision Medicine|October 10, 2022
Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery DiseaseAmit V Khera, Minxian Wang, Mark Chaffin, et al.
Cell Genomics|August 21, 2023
Multiset correlation and factor analysis enables exploration of multi-omics dataBrielin C Brown, Collin Wang, Silva Kasela, et al.
Diabetes|August 23, 2022
Nontargeted and Targeted Metabolomic Profiling Reveals Novel Metabolite Biomarkers of Incident Diabetes in African AmericansZsu-Zsu Chen, Julian Avila Pacheco, Yan Gao, et al.
Nature Genetics|April 17, 2007
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesisJohn D Rioux, Ramnik J Xavier, Kent D Taylor, et al.
The European Respiratory Journal|May 18, 2023
Incidence of interstitial lung abnormalities: the MESA Lung StudyClaire F McGroder, Spencer Hansen, Karen Hinckley Stukovsky, et al.
Journal of the American College of Cardiology|November 16, 2019
Rare Genetic Variants Associated With Sudden Cardiac Death in AdultsAmit V Khera, Heather Mason-Suares, Deanna Brockman, et al.
Pageof 125