Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
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A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao)Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variationAdvances in the epidemiology of heart failure and left ventricular remodelingGenome-wide association studies of late-onset cardiovascular diseaseWDR12, a Member of Nucleolar PeBoW-Complex, Is Up-Regulated in Failing Hearts and Causes Deterioration of Cardiac FunctionHypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.Genetic determinants of myocardial dysfunction.Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study.Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.The Genetic Challenges and Opportunities in Advanced Heart FailureSubtypes of Native American ancestry and leading causes of death: Mapuche ancestry-specific associations with gallbladder cancer risk in Chile.Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype.Genetic polymorphism G894T and the prognosis of heart failure outpatientsGenome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) studyCausal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study.A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genesPharmacogenetics of heart failure.Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk.Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study.RAAS and adrenergic genes in heart failure: Function, predisposition and survival implicationsGenomic 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.The genomic architecture of sporadic heart failureFunctional genomics applied to cardiovascular medicine.Genetics and heart failure: a concise guide for the clinicianGenome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes.Genetics of common forms of heart failure: challenges and potential solutions.Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.Common Variants for Heart Failure.Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease PathogenesisDiscovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.Genetic Dissection of Cardiac Remodeling in an Isoproterenol-Induced Heart Failure Mouse Model.Usefulness of desirable lifestyle factors to attenuate the risk of heart failure among offspring whose parents had myocardial infarction before age 55 years.RNAseq analysis of heart tissue from mice treated with atenolol and isoproterenol reveals a reciprocal transcriptional response.Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.Associations between metabolomic compounds and incident heart failure among African Americans: the ARIC Study.Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes.Ceruloplasmin and heart failure in the Atherosclerosis Risk in Communities study.Genetic insights into cardiometabolic risk factors
P2860
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P2860
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
description
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2010
@ast
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2010/06/01)
@nl
wissenschaftlicher Artikel
@de
наукова стаття, опублікована в червні 2010
@uk
مقالة علمية (نشرت في يونيو 2010)
@ar
name
Association of genome-wide var ...... idemiology (CHARGE) consortium
@ast
Association of genome-wide var ...... idemiology (CHARGE) consortium
@en
type
label
Association of genome-wide var ...... idemiology (CHARGE) consortium
@ast
Association of genome-wide var ...... idemiology (CHARGE) consortium
@en
prefLabel
Association of genome-wide var ...... idemiology (CHARGE) consortium
@ast
Association of genome-wide var ...... idemiology (CHARGE) consortium
@en
P2093
P2860
P50
P921
P3181
P1476
Association of genome-wide var ...... idemiology (CHARGE) consortium
@en
P2093
Alanna C. Morrison
Bruno H. Stricker
Christopher J. O'Donnell
Daniel Levy
David Couper
Ervin R. Fox
Jacqueline C. M. Witteman
James T. Willerson
Janine F. Felix
Jerome I. Rotter
P2860
P304
P3181
P356
10.1161/CIRCGENETICS.109.895763
P50
P577
2010-06-01T00:00:00Z