Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
about
A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao)Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndromeRING finger protein RNF207, a novel regulator of cardiac excitationTbx20 regulates a genetic program essential to adult mouse cardiomyocyte functionGene regulatory networks in cardiac conduction system developmentInherited bradyarrhythmia: A diverse genetic backgroundNav1.7 and other voltage-gated sodium channels as drug targets for pain reliefCommon variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathPrioritizing causal disease genes using unbiased genomic featuresGenetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationSequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Systematic localization of common disease-associated variation in regulatory DNAA common SCN5A variant is associated with PR interval and atrial fibrillation among African AmericansNovel loci associated with PR interval in a genome-wide association study of 10 African American cohortsDeleterious protein-altering mutations in the SCN10A voltage-gated sodium channel gene are associated with prolonged QT.Pitx2, an atrial fibrillation predisposition gene, directly regulates ion transport and intercalated disc genes.Genome-wide identification of expression quantitative trait loci (eQTLs) in human heartOccuPeak: ChIP-Seq peak calling based on internal background modellingLarge-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.Enhanced risk profiling of implanted defibrillator shocks with circulating SCN5A mRNA splicing variants: a pilot trial.Is experimentally induced pain associated with socioeconomic status? Do poor people hurt more?Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.Gene-based tests of associationAn enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolatesProtein phosphatase 2a (PP2A) binds within the oligomerization domain of striatin and regulates the phosphorylation and activation of the mammalian Ste20-Like kinase Mst3.A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect.Dual transcriptional activator and repressor roles of TBX20 regulate adult cardiac structure and functionGenetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study.Fine-mapping and initial characterization of QT interval loci in African Americans.Brugada syndrome risk loci seem protective against atrial fibrillation.Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease.Genome-wide meta-analysis of systolic blood pressure in children with sickle cell diseaseGenetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.Strategic approaches to unraveling genetic causes of cardiovascular diseases.Personalized medicine and the genotype-phenotype dilemma.A draft de novo genome assembly for the northern bobwhite (Colinus virginianus) reveals evidence for a rapid decline in effective population size beginning in the Late PleistoceneThe Rotterdam Study: 2012 objectives and design update.Prolonged QRS duration on the resting ECG is associated with sudden death risk in coronary disease, independent of prolonged ventricular repolarizationVentricular conduction and long-term heart failure outcomes and mortality in African Americans: insights from the Jackson Heart Study.
P2860
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P2860
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Common variants in 22 loci are ...... ardiac ventricular conduction.
@ast
Common variants in 22 loci are ...... ardiac ventricular conduction.
@en
Common variants in 22 loci are ...... ardiac ventricular conduction.
@nl
type
label
Common variants in 22 loci are ...... ardiac ventricular conduction.
@ast
Common variants in 22 loci are ...... ardiac ventricular conduction.
@en
Common variants in 22 loci are ...... ardiac ventricular conduction.
@nl
prefLabel
Common variants in 22 loci are ...... ardiac ventricular conduction.
@ast
Common variants in 22 loci are ...... ardiac ventricular conduction.
@en
Common variants in 22 loci are ...... ardiac ventricular conduction.
@nl
P2093
P2860
P50
P356
P1433
P1476
Common variants in 22 loci are ...... ardiac ventricular conduction.
@en
P2093
Aaron Isaacs
Alan F Wright
Aravinda Chakravarti
Arne Pfeufer
Astrid Petersmann
Ben A Oostra
Bruno H Ch Stricker
Christine Schwienbacher
Christopher J O'Donnell
Claudia Beu Volpato
P2860
P2888
P304
P356
10.1038/NG.716
P407
P50
P577
2010-11-14T00:00:00Z