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Nicholas J Wareham

Showing results (741-750 of 867) with videos related to

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Nature Genetics|October 10, 2018
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsAnubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2011
CUBN is a gene locus for albuminuriaCarsten A Böger, Ming-Huei Chen, Adrienne Tin, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2011
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumptionGunter Schumann, Lachlan J Coin, Anbarasu Lourdusamy, et al.
Nature Genetics|June 28, 2011
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profileTuomas O Kilpeläinen, M Carola Zillikens, Alena Stančákova, et al.
Nature Human Behaviour|March 2, 2023
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locusIain Mathieson, Felix R Day, Nicola Barban, et al.
Nature Genetics|June 8, 2023
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptakeAlice Williamson, Dougall M Norris, Xianyong Yin, et al.
Human Molecular Genetics|August 9, 2014
FTO genetic variants, dietary intake and body mass index: insights from 177,330 individualsQibin Qi, Tuomas O Kilpeläinen, Mary K Downer, et al.
Diabetes|December 4, 2015
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in DiabetesAlexander Teumer, Adrienne Tin, Rossella Sorice, et al.
Human Molecular Genetics|July 31, 2012
Genome-wide meta-analysis of common variant differences between men and womenVesna Boraska, Ana Jerončić, Vincenza Colonna, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
Pageof 87

Showing results (741-750 of 867) with videos related to

Sort By:
Pageof 87
Nature Genetics|October 10, 2018
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsAnubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2011
CUBN is a gene locus for albuminuriaCarsten A Böger, Ming-Huei Chen, Adrienne Tin, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2011
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumptionGunter Schumann, Lachlan J Coin, Anbarasu Lourdusamy, et al.
Nature Genetics|June 28, 2011
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profileTuomas O Kilpeläinen, M Carola Zillikens, Alena Stančákova, et al.
Nature Human Behaviour|March 2, 2023
Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locusIain Mathieson, Felix R Day, Nicola Barban, et al.
Nature Genetics|June 8, 2023
Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptakeAlice Williamson, Dougall M Norris, Xianyong Yin, et al.
Human Molecular Genetics|August 9, 2014
FTO genetic variants, dietary intake and body mass index: insights from 177,330 individualsQibin Qi, Tuomas O Kilpeläinen, Mary K Downer, et al.
Diabetes|December 4, 2015
Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in DiabetesAlexander Teumer, Adrienne Tin, Rossella Sorice, et al.
Human Molecular Genetics|July 31, 2012
Genome-wide meta-analysis of common variant differences between men and womenVesna Boraska, Ana Jerončić, Vincenza Colonna, et al.
The New England Journal of Medicine|March 3, 2016
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease, Nathan O Stitziel, Kathleen E Stirrups, et al.
Pageof 87