Genome-wide association studies of the PR interval in African Americans - Wikidata - wikimedia - TriplyDB

Genome-wide association studies of the PR interval in African Americans

Genome-wide association studies of the PR interval in African Americans

http://www.wikidata.org/entity/Q30433126

about

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome Dissection of a quantitative trait locus for PR interval duration identifies Tnni3k as a novel modulator of cardiac conduction Emerging directions in the genetics of atrial fibrillation Cardiovascular genomics Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.Impact of ancestry and common genetic variants on QT interval in African Americans.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 identification of expression quantitative trait loci (eQTLs) in human heart OccuPeak: ChIP-Seq peak calling based on internal background modelling Genetic determinants of P wave duration and PR segment Genetic 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.Evidence of heterogeneity by race/ethnicity in genetic determinants of QT interval.Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.TBX5 drives Scn5a expression to regulate cardiac conduction system function Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population.Sequential Binding of MEIS1 and NKX2-5 on the Popdc2 Gene: A Mechanism for Spatiotemporal Regulation of Enhancers during Cardiogenesis Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples Loss of the transcription factor Meis1 prevents sympathetic neurons target-field innervation and increases susceptibility to sudden cardiac death Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis.Playing with heart and soul…and genomes: sports implications and applications of personal genomics Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans Reference ranges of PR duration and P-wave indices in individuals free of cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA).A SCN10A SNP biases human pain sensitivity.Attitudes toward Genetic Testing for Hypertension among African American Women and Girls.Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes Genetic Variants Associated With Atrial Fibrillation and PR Interval Following Cardiac Surgery.A common genetic variant within SCN10A modulates cardiac SCN5A expression Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation.Recent genetic discoveries implicating ion channels in human cardiovascular diseases First-degree AV block-an entirely benign finding or a potentially curable cause of cardiac disease?Genetics of sudden cardiac death caused by ventricular arrhythmias.Genetic variation in T-box binding element functionally affects SCN5A/SCN10A enhancer.Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.Animal models of RLS phenotypes.Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes.Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.

P2860

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P2860

Genome-wide association studies of the PR interval in African Americans

http://www.wikidata.org/entity/Q30433126

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Genome-wide association studies of the PR interval in African Americans

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Genome-wide association studies of the PR interval in African Americans

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Genome-wide association studies of the PR interval in African Americans

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Genome-wide association studies of the PR interval in African Americans

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Genome-wide association studies of the PR interval in African Americans

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Genome-wide association studies of the PR interval in African Americans

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JOURNAL.PGEN.1001304

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Genome-wide association studies of the PR interval in African Americans

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Arne Pfeufer

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Cameron Palmer

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Candidate-gene Association Resource (CARe) Consortium

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Daniel S Evans

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Dina N Paltoo

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Elsayed Z Soliman

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Ervin R Fox

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J Gustav Smith

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Jared W Magnani

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Kathleen F Kerr

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P2860

Sensitive detection of chromosomal segments of distinct ancestry in admixed populations

The genetic structure and history of Africans and African Americans

Methods for high-density admixture mapping of disease genes

Genetic variation in SCN10A influences cardiac conduction

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

PLINK: a tool set for whole-genome association and population-based linkage analyses

A haplotype map of the human genome

Principal components analysis corrects for stratification in genome-wide association studies

Genetic analysis of African populations: human evolution and complex disease

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e1001304

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10.1371/JOURNAL.PGEN.1001304

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2

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7

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Alan B. Zonderman

Michele K. Evans

Susan R Heckbert

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2011-02-10T00:00:00Z

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49967957

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21347284

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genome-wide association study

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