Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation - Wikidata - awgldk - TriplyDB

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

http://www.wikidata.org/entity/Q37146274

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Emerging directions in the genetics of atrial fibrillation Highlights of the year in JACC 2012 Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.Severity of obstructive sleep apnea influences the effect of genotype on response to anti-arrhythmic drug therapy for atrial fibrillation.PITX2-dependent gene regulation in atrial fibrillation and rhythm control.Common variants in KCNN3 are associated with lone atrial fibrillation.Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population Safety and efficacy of multipolar pulmonary vein ablation catheter vs. irrigated radiofrequency ablation for paroxysmal atrial fibrillation: a randomized multicentre trial.Pitx2 prevents susceptibility to atrial arrhythmias by inhibiting left-sided pacemaker specification Genome-wide association studies in cardiac electrophysiology: recent discoveries and implications for clinical practice Systematic analysis of gene expression differences between left and right atria in different mouse strains and in human atrial tissue Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans.Independent susceptibility markers for atrial fibrillation on chromosome 4q25.Genome-wide association studies of atrial fibrillation: past, present, and future.Genetics of atrial fibrillation: implications for future research directions and personalized medicine.Lack of replication in polymorphisms reported to be associated with atrial fibrillation Usefulness of single nucleotide polymorphism in chromosome 4q25 to predict in-hospital and long-term development of atrial fibrillation and survival in patients undergoing coronary artery bypass grafting Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias.Personalized medicine and the genotype-phenotype dilemma.Genetic and clinical risk prediction model for postoperative atrial fibrillation.Genetics of atrial fibrillation and possible implications for ischemic stroke.Atrial fibrillation: current knowledge and future directions in epidemiology and genomics.Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project.Comprehensive risk reduction in patients with atrial fibrillation: emerging diagnostic and therapeutic options--a report from the 3rd Atrial Fibrillation Competence NETwork/European Heart Rhythm Association consensus conference.Genetic risk for atrial fibrillation could motivate patient adherence to warfarin therapy: a cost effectiveness analysis.Meta-analysis identifies six new susceptibility loci for atrial fibrillation Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight?Cardiovascular pharmacogenomics: the future of cardiovascular therapeutics?Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation.Genetic mechanisms of atrial fibrillation: impact on response to treatment Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion Novel risk factors for atrial fibrillation: useful for risk prediction and clinical decision making?Almanac 2011: Cardiac Arrhythmias and Pacing. The National Society Journals Present Selected Research that has Driven Recent Advances in Clinical Cardiology.Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis Contemporary role of medical genetics in internal medicine.Molecular genetics of atrial fibrillation.

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Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation

http://www.wikidata.org/entity/Q37146274

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 13 January 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Large scale replication and me ...... iated with atrial fibrillation

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Large scale replication and me ...... ated with atrial fibrillation.

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Large scale replication and me ...... iated with atrial fibrillation

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Large scale replication and me ...... ated with atrial fibrillation.

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Large scale replication and me ...... iated with atrial fibrillation

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Large scale replication and me ...... ated with atrial fibrillation.

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European Heart Journal

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Large scale replication and me ...... iated with atrial fibrillation

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Annette Wacker

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Arne Pfeufer

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Brian S Donahue

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Britt M Beckmann

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Calum A MacRae

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Charlotte van Noord

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Dan M Roden

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Daniel Levy

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Gerhard Steinbeck

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H-Erich Wichmann

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P2860

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

KCNQ1 gain-of-function mutation in familial atrial fibrillation

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

A common allele on chromosome 9 associated with coronary heart disease

Meta-analysis in clinical trials

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

HTRA1 promoter polymorphism in wet age-related macular degeneration

The transcription factor Pitx2 mediates situs-specific morphogenesis in response to left-right asymmetric signals

Molecular pathway for the localized formation of the sinoatrial node

Dosage requirement of Pitx2 for development of multiple organs

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813-819

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scholarly article

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10.1093/EURHEARTJ/EHN578

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7

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30

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Thomas Meitinger

Christopher Newton-Cheh

Emelia J. Benjamin

André Uitterlinden

Martin G Larson

Kathryn L. Lunetta

Albert Schömig

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2009-01-13T00:00:00Z

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23785067

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19141561

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atrial fibrillation

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2663727

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