Genome-wide association study of PR interval. - Wikidata - awgldk - TriplyDB

Genome-wide association study of PR interval.

Genome-wide association study of PR interval.

http://www.wikidata.org/entity/Q33772170

about

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome A connexin40 mutation associated with a malignant variant of progressive familial heart block type I Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science Genome-wide association analysis identifies multiple loci related to resting heart rate Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance Emerging directions in the genetics of atrial fibrillation Gene regulatory networks in cardiac conduction system development Late Sodium Current in Human Atrial Cardiomyocytes from Patients in Sinus Rhythm and Atrial Fibrillation Canonical wnt signaling regulates atrioventricular junction programming and electrophysiological properties.The cardiac conduction system Nav1.7 and other voltage-gated sodium channels as drug targets for pain relief Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death Mapping genetic variants associated with beta-adrenergic responses in inbred mice Lethal arrhythmias in Tbx3-deficient mice reveal extreme dosage sensitivity of cardiac conduction system function and homeostasis Prioritizing causal disease genes using unbiased genomic features Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts Genome-wide association studies of the PR interval in African Americans Pitx2, an atrial fibrillation predisposition gene, directly regulates ion transport and intercalated disc genes.Post-operative atrial fibrillation examined using whole-genome RNA sequencing in human left atrial tissue.Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart eMERGEing progress in genomics-the first seven years.OccuPeak: ChIP-Seq peak calling based on internal background modelling Pitx2-microRNA pathway that delimits sinoatrial node development and inhibits predisposition to atrial fibrillation A follow-up study for left ventricular mass on chromosome 12p11 identifies potential candidate genes Gene-based tests of association A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice Lack of association between rs3807989 in cav1 and atrial fibrillation.Genetic determinants of P wave duration and PR segment Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients.Baf250a orchestrates an epigenetic pathway to repress the Nkx2.5-directed contractile cardiomyocyte program in the sinoatrial node.Genetic loci associated with atrial fibrillation: relation to left atrial structure in the Framingham Heart Study.Independent susceptibility markers for atrial fibrillation on chromosome 4q25.Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.

P2860

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P2860

Genome-wide association study of PR interval.

http://www.wikidata.org/entity/Q33772170

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին 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

Genome-wide association study of PR interval.

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Genome-wide association study of PR interval.

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Genome-wide association study of PR interval.

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type

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Genome-wide association study of PR interval.

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Genome-wide association study of PR interval.

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Genome-wide association study of PR interval.

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prefLabel

Genome-wide association study of PR interval.

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Genome-wide association study of PR interval.

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Genome-wide association study of PR interval.

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P1433

Nature Genetics

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Genome-wide association study of PR interval.

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Aravinda Chakravarti

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Arne Pfeufer

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Britt M Beckmann

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Bruno H C Stricker

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Charlotte van Noord

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Dan E Arking

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Daniel Levy

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David R Van Wagoner

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Elsayed Z Soliman

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Georg B Ehret

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P2860

A tetrodotoxin-resistant voltage-gated sodium channel from human dorsal root ganglia, hPN3/SCN10A

A vascular cell-restricted RhoGAP, p73RhoGAP, is a key regulator of angiogenesis

A haplotype map of the human genome

Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria

Caveolae and caveolins in the cardiovascular system

Defects in caveolin-1 cause dilated cardiomyopathy and pulmonary hypertension in knockout mice

Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis

A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development

Tbx3 is required for outflow tract development

Genomic control for association studies

P2888

P304

153-159

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scholarly article

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10.1038/NG.517

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P433

2

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P478

42

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P50

Gonçalo Abecasis

Thomas Meitinger

Christian Gieger

David Schlessinger

Christopher Newton-Cheh

Fernando Rivadeneira

Vilmundur Gudnason

Eric Boerwinkle

P577

2010-01-10T00:00:00Z

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P5875

40899759

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P698

20062060

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P921

genome-wide association study

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2850197

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