Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic markers of repolarization and arrhythmic events after acute coronary syndromes.

American heart journal - 1 Apr 2015

Earle N J, Poppe K K, Pilbrow A P, Cameron V A, Troughton R W, Skinner J R, Love D R, Shelling A N, Whalley G A, Ellis C J, Richards A M, Doughty R N

Abstract excerpt

BACKGROUND: There is a genetic contribution to the risk of ventricular arrhythmias in survivors of acute coronary syndromes (ACS). We wished to explore the role of 33 candidate single nucleotide polymorphisms (SNPs) in prolonged repolarization and sudden death in patients surviving ACS. METHODS: A total of 2,139 patients (1680 white ethnicity) surviving an admission for ACS were enrolled in the prospective...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acute Coronary Syndrome
Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Arrhythmias, Cardiac

Share to Electrocardiography

Share to Follow-Up Studies

Share to Genetic Markers

Share to Risk Factors

Source

Identifiers

PMID: 25819866
DOI: 10.1016/j.ahj.2014.11.015

Genes

SCD
GPC5
KCNJ2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic markers of repolarization and arrhythmic events after acute coronary syndromes.PMID 25819866Read ↗

GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.Semantic proximity Read ↗

A common NOS1AP genetic polymorphism, rs12567209 G>A, is associated with sudden cardiac death in patients with chronic heart failure in the Chinese Han population.Semantic proximity Read ↗

Common variants in CASQ2, GPD1L, and NOS1AP are significantly associated with risk of sudden death in patients with coronary artery disease.Semantic proximity Read ↗

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.Semantic proximity Read ↗

NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Population-Based Analysis of Rare Genetic Variants in Sudden Cardiac Arrest.Semantic proximity Read ↗

Genetic Causes of Sudden Cardiac Arrest in the CommunitySemantic proximity Read ↗

Disorders of cardiac repolarization: long QT and short QT syndromes.Semantic proximity Read ↗

NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis.Semantic proximity Read ↗

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac ArrestSemantic proximity Read ↗

A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.Semantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.