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Christopher G Bell

Showing results (31-40 of 57) with videos related to

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Clinical Epigenetics|March 29, 2026
An epigenomic investigation of atrial fibrillation in a matched left and right atrial human cohortAdrian Rodriguez, Stephanie Frost, Alison M Thomas, et al.
Genome Biology|September 25, 2016
Novel regional age-associated DNA methylation changes within human common disease-associated lociChristopher G Bell, Yudong Xia, Wei Yuan, et al.
Epigenetics|August 27, 2019
Deep proteomic analysis of Dnmt1 mutant/hypomorphic colorectal cancer cells reveals dysregulation of epithelial-mesenchymal transition and subcellular re-localization of Beta-CateninEmily H Bowler, Alex Smith-Vidal, Alex Lester, et al.
Epigenetics|October 17, 2025
Identification of blood-derived DNA methylation biomarkers of glaucoma and intraocular pressure measurements in three European ancestry cohorts including the Canadian longitudinal study on agingXiaofan Jiang, Omar A Mahroo, Anthony P Khawaja, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2016
Contribution of Heritability and Epigenetic Factors to Skeletal Muscle Mass Variation in United Kingdom TwinsGregory Livshits, Fei Gao, Ida Malkin, et al.
Diabetes|June 29, 2004
Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19qChristopher G Bell, Michael Benzinou, Afshan Siddiq, et al.
American Journal of Human Genetics|September 8, 2023
Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertensionStefan van Duijvenboden, Julia Ramírez, William J Young, et al.
Human Genetics|July 5, 2024
Fine mapping of candidate effector genes for heart rateJulia Ramírez, Stefan van Duijvenboden, William J Young, et al.
Nature Communications|January 4, 2018
Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated lociChristopher G Bell, Fei Gao, Wei Yuan, et al.
European Journal of Human Genetics : EJHG|December 14, 2006
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseasesChristopher G Bell, David Meyre, Enrico Petretto, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Clinical Epigenetics|March 29, 2026
An epigenomic investigation of atrial fibrillation in a matched left and right atrial human cohortAdrian Rodriguez, Stephanie Frost, Alison M Thomas, et al.
Genome Biology|September 25, 2016
Novel regional age-associated DNA methylation changes within human common disease-associated lociChristopher G Bell, Yudong Xia, Wei Yuan, et al.
Epigenetics|August 27, 2019
Deep proteomic analysis of Dnmt1 mutant/hypomorphic colorectal cancer cells reveals dysregulation of epithelial-mesenchymal transition and subcellular re-localization of Beta-CateninEmily H Bowler, Alex Smith-Vidal, Alex Lester, et al.
Epigenetics|October 17, 2025
Identification of blood-derived DNA methylation biomarkers of glaucoma and intraocular pressure measurements in three European ancestry cohorts including the Canadian longitudinal study on agingXiaofan Jiang, Omar A Mahroo, Anthony P Khawaja, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2016
Contribution of Heritability and Epigenetic Factors to Skeletal Muscle Mass Variation in United Kingdom TwinsGregory Livshits, Fei Gao, Ida Malkin, et al.
Diabetes|June 29, 2004
Genome-wide linkage analysis for severe obesity in french caucasians finds significant susceptibility locus on chromosome 19qChristopher G Bell, Michael Benzinou, Afshan Siddiq, et al.
American Journal of Human Genetics|September 8, 2023
Integration of genetic fine-mapping and multi-omics data reveals candidate effector genes for hypertensionStefan van Duijvenboden, Julia Ramírez, William J Young, et al.
Human Genetics|July 5, 2024
Fine mapping of candidate effector genes for heart rateJulia Ramírez, Stefan van Duijvenboden, William J Young, et al.
Nature Communications|January 4, 2018
Obligatory and facilitative allelic variation in the DNA methylome within common disease-associated lociChristopher G Bell, Fei Gao, Wei Yuan, et al.
European Journal of Human Genetics : EJHG|December 14, 2006
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseasesChristopher G Bell, David Meyre, Enrico Petretto, et al.
Pageof 6