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Article

A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.

PloS one - 1 Jan 2017

Jabbari Reza, Glinge Charlotte, Jabbari Javad, Risgaard Bjarke, Winkel Bo Gregers, Terkelsen Christian Juhl, Tilsted Hans-Henrik, Jensen Lisette Okkels, Hougaard Mikkel, Haunsø Stig, Engstrøm Thomas, Albert Christine M, Tfelt-Hansen Jacob

Abstract excerpt

BACKGROUND: Several common genetic variants have been associated with either ventricular fibrillation (VF) or sudden cardiac death (SCD). However, replication efforts have been limited. Therefore, we aimed to analyze whether such variants may contribute to VF caused by first ST-elevation myocardial infarction (STEMI). METHODS: We analyzed 27 single nucleotide polymorphisms (SNP) previously associated with SCD/VF...

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Identifiers

PMID: 28085969
DOI: 10.1371/journal.pone.0170193
PMCID: PMC5234807

Genes

SCD
HEY2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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