Common genetic variants associated with sudden cardiac death: the FinSCDgen study. - Wikidata - awgldk - TriplyDB

Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

http://www.wikidata.org/entity/Q36109680

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Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction KCNN2 polymorphisms and cardiac tachyarrhythmias.Risk factors and their combined effects on the incidence rate of subarachnoid hemorrhage--a population-based cohort study.Cumulative effects of common genetic variants on risk of sudden cardiac death.A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction Cause-specific mortality of 1-year survivors of subarachnoid hemorrhage Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.RyR2 QQ2958 Genotype and Risk of Malignant Ventricular Arrhythmias Atrial Fibrillation Genetics: Is There a Practical Clinical Value Now or in the Future?The 9p21 polymorphism is linked with atrial fibrillation during acute phase of ST-segment elevation myocardial infarction.Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction.Tobacco smoking and the risk of sudden cardiac death: a systematic review and meta-analysis of prospective studies.Body mass index, abdominal fatness, and the risk of sudden cardiac death: a systematic review and dose-response meta-analysis of prospective studies.Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

http://www.wikidata.org/entity/Q36109680

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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type

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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Annukka M Lahtinen

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Johannes Kettunen

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Kimmo Kontula

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Pekka J Karhunen

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Peter A Noseworthy

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P2860

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects

Quantifying heterogeneity in a meta-analysis

The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases

Molecular pathway for the localized formation of the sinoatrial node

The genome-wide patterns of variation expose significant substructure in a founder population

A common variant on chromosome 9p21 affects the risk of myocardial infarction

The validity of the Finnish Hospital Discharge Register and Causes of Death Register data on coronary heart disease.

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Christopher Newton-Cheh

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