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Showing results (151-160 of 287) with videos related to

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Diabetologia|February 7, 2022
Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetesVenexia M Walker, Marijana Vujkovic, Alice R Carter, et al.
Human Molecular Genetics|January 25, 2018
Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studiesRebecca B Lawn, Emma L Anderson, Matthew Suderman, et al.
Disease Markers|December 9, 2014
Influence of adiposity-related genetic markers in a population of saudi arabians where other variables influencing obesity may be reducedKhalid K Alharbi, Tom G Richardson, Imran Ali Khan, et al.
Development and Psychopathology|June 10, 2017
Neonatal DNA methylation and early-onset conduct problems: A genome-wide, prospective studyCharlotte A M Cecil, Esther Walton, Sara R Jaffee, et al.
Genetic Testing and Molecular Biomarkers|June 22, 2011
Population mutation scanning of human GHR by meltMADGE and identification of a paucimorphic variantKhalid K Alharbi, Guangwei Hou, Xiao-he Chen, et al.
Diabetes|February 11, 2016
DNA Methylation and BMI: Investigating Identified Methylation Sites at HIF3A in a Causal FrameworkRebecca C Richmond, Gemma C Sharp, Mary E Ward, et al.
Gigascience|August 31, 2018
PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statisticsJie Zheng, Tom G Richardson, Louise A C Millard, et al.
Circulation. Cardiovascular Genetics|April 27, 2016
Metabolic Characterization of a Rare Genetic Variation Within APOC3 and Its Lipoprotein Lipase-Independent EffectsFotios Drenos, George Davey Smith, Mika Ala-Korpela, et al.
Genes and Immunity|April 11, 2001
Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK familiesJ W Holloway, C Lonjou, B Beghé, et al.
Human Mutation|September 17, 2014
Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesiaMuslim M Alsaadi, A Mesut Erzurumluoglu, Santiago Rodriguez, et al.
Pageof 29

Showing results (151-160 of 287) with videos related to

Sort By:
Pageof 29
Diabetologia|February 7, 2022
Separating the direct effects of traits on atherosclerotic cardiovascular disease from those mediated by type 2 diabetesVenexia M Walker, Marijana Vujkovic, Alice R Carter, et al.
Human Molecular Genetics|January 25, 2018
Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studiesRebecca B Lawn, Emma L Anderson, Matthew Suderman, et al.
Disease Markers|December 9, 2014
Influence of adiposity-related genetic markers in a population of saudi arabians where other variables influencing obesity may be reducedKhalid K Alharbi, Tom G Richardson, Imran Ali Khan, et al.
Development and Psychopathology|June 10, 2017
Neonatal DNA methylation and early-onset conduct problems: A genome-wide, prospective studyCharlotte A M Cecil, Esther Walton, Sara R Jaffee, et al.
Genetic Testing and Molecular Biomarkers|June 22, 2011
Population mutation scanning of human GHR by meltMADGE and identification of a paucimorphic variantKhalid K Alharbi, Guangwei Hou, Xiao-he Chen, et al.
Diabetes|February 11, 2016
DNA Methylation and BMI: Investigating Identified Methylation Sites at HIF3A in a Causal FrameworkRebecca C Richmond, Gemma C Sharp, Mary E Ward, et al.
Gigascience|August 31, 2018
PhenoSpD: an integrated toolkit for phenotypic correlation estimation and multiple testing correction using GWAS summary statisticsJie Zheng, Tom G Richardson, Louise A C Millard, et al.
Circulation. Cardiovascular Genetics|April 27, 2016
Metabolic Characterization of a Rare Genetic Variation Within APOC3 and Its Lipoprotein Lipase-Independent EffectsFotios Drenos, George Davey Smith, Mika Ala-Korpela, et al.
Genes and Immunity|April 11, 2001
Linkage analysis of the 5q31-33 candidate region for asthma in 240 UK familiesJ W Holloway, C Lonjou, B Beghé, et al.
Human Mutation|September 17, 2014
Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesiaMuslim M Alsaadi, A Mesut Erzurumluoglu, Santiago Rodriguez, et al.
Pageof 29