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European Journal of Human Genetics : EJHG|May 8, 2003
Measured haplotype analysis of the aldosterone synthase gene and heart sizeBongani M Mayosi, Bernard Keavney, Hugh Watkins, et al.
Circulation. Genomic and Precision Medicine|April 22, 2026
Biobank-Scale Plasma Proteomics Identifies Novel Biomarkers in Hypertrophic CardiomyopathyJonathan H Chan, Christopher Grace, Mohsen Mazidi, et al.
European Heart Journal|February 16, 2008
Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertensionBongani M Mayosi, Peter J Avery, Martin Farrall, et al.
Nature Genetics|January 26, 2021
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivityAndrew R Harper, Anuj Goel, Christopher Grace, et al.
Journal of Medical Genetics|August 1, 2020
Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathyAdam Waring, Andrew Harper, Silvia Salatino, et al.
Human Molecular Genetics|December 1, 2007
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9pHelen M Broadbent, John F Peden, Stefan Lorkowski, et al.
Open Heart|May 2, 2018
Plasma cytokines and risk of coronary heart disease in the PROCARDIS studyRobert Clarke, Elsa Valdes-Marquez, Michael Hill, et al.
Human Molecular Genetics|January 13, 2021
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidomeKathryn A McGurk, Simon G Williams, Hui Guo, et al.
Human Molecular Genetics|February 14, 2004
Quantitative genetic variation: a post-modern viewMartin Farrall
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