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Harold Snieder

Showing results (331-340 of 495) with videos related to

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Nature Genetics|October 7, 2024
Genetic architecture reconciles linkage and association studies of complex traitsJulia Sidorenko, Baptiste Couvy-Duchesne, Kathryn E Kemper, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 2022
Variants in the <i>GPR146</i> Gene Are Associated With a Favorable Cardiometabolic Risk ProfileAntoine Rimbert, Ming W Yeung, Nawar Dalila, et al.
Diabetologia|February 16, 2022
Epigenome-wide association study of incident type 2 diabetes: a meta-analysis of five prospective European cohortsEliza Fraszczyk, Annemieke M W Spijkerman, Yan Zhang, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2018
<i>NPHP1</i> (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRDRozemarijn Snoek, Jessica van Setten, Brendan J Keating, et al.
Diabetologia|June 18, 2014
GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescenceKaren M Eny, Helen L Lutgers, John Maynard, et al.
Cell Reports. Medicine|February 21, 2024
Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferationValeria Lo Faro, Arjun Bhattacharya, Wei Zhou, 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.
Human Molecular Genetics|June 16, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
American Journal of Human Genetics|September 2, 2022
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapiesCharli E Harlow, Josan Gandawijaya, Rosemary A Bamford, et al.
Pageof 50

Showing results (331-340 of 495) with videos related to

Sort By:
Pageof 50
Nature Genetics|October 7, 2024
Genetic architecture reconciles linkage and association studies of complex traitsJulia Sidorenko, Baptiste Couvy-Duchesne, Kathryn E Kemper, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 1, 2022
Variants in the <i>GPR146</i> Gene Are Associated With a Favorable Cardiometabolic Risk ProfileAntoine Rimbert, Ming W Yeung, Nawar Dalila, et al.
Diabetologia|February 16, 2022
Epigenome-wide association study of incident type 2 diabetes: a meta-analysis of five prospective European cohortsEliza Fraszczyk, Annemieke M W Spijkerman, Yan Zhang, et al.
Journal of the American Society of Nephrology : JASN|April 15, 2018
<i>NPHP1</i> (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRDRozemarijn Snoek, Jessica van Setten, Brendan J Keating, et al.
Diabetologia|June 18, 2014
GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescenceKaren M Eny, Helen L Lutgers, John Maynard, et al.
Cell Reports. Medicine|February 21, 2024
Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferationValeria Lo Faro, Arjun Bhattacharya, Wei Zhou, 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.
Human Molecular Genetics|June 16, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
Medrxiv : the Preprint Server for Health Sciences|January 23, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
American Journal of Human Genetics|September 2, 2022
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapiesCharli E Harlow, Josan Gandawijaya, Rosemary A Bamford, et al.
Pageof 50