Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.
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Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population.Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands.Increased left ventricular mass as a predictor of sudden cardiac death: is it time to put it to the test?Common CD36 SNPs reduce protein expression and may contribute to a protective atherogenic profileGenomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.Hypertension and genetic variation in endothelial-specific genesIncreased left ventricular mass and decreased left ventricular systolic function have independent pathways to ventricular arrhythmogenesis in coronary artery disease.Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study.CD36 genetics and the metabolic complications of obesity.Whole-exome sequencing and an iPSC-derived cardiomyocyte model provides a powerful platform for gene discovery in left ventricular hypertrophyGenome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population.Association of KCNB1 polymorphisms with lipid metabolisms and insulin resistance: a case-control design of population-based cross-sectional study in Chinese Han populationCD36 genotype associated with ischemic stroke in Chinese Han.Association of CD36 gene polymorphisms with echo- and electrocardiographic parameters in patients with early onset coronary artery diseaseAdaptive genetic variation and heart disease risk.Genetic risk factors and Mendelian randomization in cardiovascular disease.Contextualizing Genetics for Regional Heart Failure CareThe utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): rationale, potential and challengesLack of association between common endothelial nitric oxide synthase gene haplotypes and left ventricular hypertrophy in hypertensionSequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families.Three-dimensional cardiovascular imaging-genetics: a mass univariate framework.Genetic variants implicated in telomere length associated with left ventricular function in patients with hypertension and cardiac organ damage.
P2860
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P2860
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.
description
2009 nî lūn-bûn
@nan
2009 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genome-wide association study ...... in humans: the HyperGEN Study.
@ast
Genome-wide association study ...... in humans: the HyperGEN Study.
@en
type
label
Genome-wide association study ...... in humans: the HyperGEN Study.
@ast
Genome-wide association study ...... in humans: the HyperGEN Study.
@en
prefLabel
Genome-wide association study ...... in humans: the HyperGEN Study.
@ast
Genome-wide association study ...... in humans: the HyperGEN Study.
@en
P2093
P2860
P50
P356
P1433
P1476
Genome-wide association study ...... in humans: the HyperGEN Study
@en
P2093
Dabeeru C Rao
Rachel Kraemer
Ulrich Broeckel
Weihong Tang
P2860
P2888
P356
10.1186/1471-2350-10-43
P577
2009-05-19T00:00:00Z
P5875
P6179
1034904829