Genome-wide association analysis identifies multiple loci related to resting heart rate - Test2 - elhamkhani - TriplyDB

Genome-wide association analysis identifies multiple loci related to resting heart rate

Genome-wide association analysis identifies multiple loci related to resting heart rate

http://www.wikidata.org/entity/Q24624928

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The anatomical distribution of genetic associations.Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death A rare variant in MYH6 is associated with high risk of sick sinus syndrome Fear and C-reactive protein cosynergize annual pulse increases in healthy adults Mapping genetic variants associated with beta-adrenergic responses in inbred mice Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c.Detection of pleiotropy through a Phenome-wide association study (PheWAS) of epidemiologic data as part of the Environmental Architecture for Genes Linked to Environment (EAGLE) study.Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart Discovery of novel heart rate-associated loci using the Exome Chip.Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.Genetic copy number variants in myocardial infarction patients with hyperlipidemia.Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.Factor structure underlying components of allostatic load Genetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies.Associations of daytime, nighttime, and 24-hour heart rate with four distinct markers of inflammation in hypertensive patients: the Styrian Hypertension Study.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 Pleistocene The Rotterdam Study: 2012 objectives and design update.Cumulative effects of common genetic variants on risk of sudden cardiac death.Epidemiology and genetics of sudden cardiac death Markers of endogenous desaturase activity and risk of coronary heart disease in the CAREMA cohort study Autonomic dysfunction determines stress-induced cardiovascular and immune complications in mice.Genetic locus on mouse chromosome 7 controls elevated heart rate Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population.The genetics of sudden cardiac death.A novel FADS1 isoform potentiates FADS2-mediated production of eicosanoid precursor fatty acids.Desaturase and elongase-limiting endogenous long-chain polyunsaturated fatty acid biosynthesis.SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this condition.Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders Silencing of the Drosophila ortholog of SOX5 in heart leads to cardiac dysfunction as detected by optical coherence tomography Genome-wide compendium and functional assessment of in vivo heart enhancers.Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.A genome-wide association study of the human metabolome in a community-based cohort Genetics of sudden cardiac death caused by ventricular arrhythmias.Genetic contribution to the variance of blood pressure and heart rate: a systematic review and meta-regression of twin studies.Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.Endophenotype best practices.

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P2860

Genome-wide association analysis identifies multiple loci related to resting heart rate

http://www.wikidata.org/entity/Q24624928

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին 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 analysis identifies multiple loci related to resting heart rate

@ast

Genome-wide association analysis identifies multiple loci related to resting heart rate

@en

Genome-wide association analysis identifies multiple loci related to resting heart rate

@nl

type

label

Genome-wide association analysis identifies multiple loci related to resting heart rate

@ast

Genome-wide association analysis identifies multiple loci related to resting heart rate

@en

Genome-wide association analysis identifies multiple loci related to resting heart rate

@nl

prefLabel

Genome-wide association analysis identifies multiple loci related to resting heart rate

@ast

Genome-wide association analysis identifies multiple loci related to resting heart rate

@en

Genome-wide association analysis identifies multiple loci related to resting heart rate

@nl

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Human Molecular Genetics

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Genome-wide association analysis identifies multiple loci related to resting heart rate

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Aaron Isaacs

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Alan F Wright

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Ben A Oostra

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Bruno H Ch Stricker

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Carmilla M Licht

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Christopher J O'Donnell

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Dan E Arking

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Ervin R Fox

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Florian Ernst

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P2860

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

Titin mutations as the molecular basis for dilated cardiomyopathy

Mutation in myosin heavy chain 6 causes atrial septal defect

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

Cloning and characterization of SOX5, a new member of the human SOX gene family

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

Common variants at 30 loci contribute to polygenic dyslipidemia

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10.1093/HMG/DDQ303

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19

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19

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Heinz Erich Wichmann

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