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 modifier of the QTc interval associated with early-onset atrial fibrillation.

The Canadian journal of cardiology - 1 Oct 2013

Andreasen Laura, Nielsen Jonas B, Christophersen Ingrid E, Holst Anders Gaarsdal, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten S

Abstract excerpt

BACKGROUND: Both shortening and prolongation of the QTc interval have been associated with atrial fibrillation (AF). We investigated whether 8 single nucleotide polymorphisms (SNPs) at loci previously shown to affect QTc interval duration were associated with lone AF. METHODS: We included 358 pat...

Read the complete abstract on PubMed

Topics

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

Share to Age of Onset
Share to Atrial Fibrillation
Share to Confidence Intervals

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Denmark

Share to Electrocardiography

Share to ERG1 Potassium Channel

Share to Ether-A-Go-Go Potassium Channels

Share to Incidence

Source

Identifiers

PMID: 24074973
DOI: 10.1016/j.cjca.2013.06.009

Genes

KCNH2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24074973-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic modifier of the QTc interval associated with early-onset atrial fibrillation.PMID 24074973Read ↗

Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years.Semantic proximity Read ↗

Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.Semantic proximity Read ↗

Common variants in KCNN3 are associated with lone atrial fibrillation.Semantic proximity Read ↗

Genetic aspects of lone atrial fibrillation: what do we know?Semantic proximity Read ↗

Association of rs2200733 at 4q25 with early onset of lone atrial fibrillation in young patients.Semantic proximity Read ↗

Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.Semantic proximity Read ↗

Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation.Semantic proximity Read ↗

Uncovering an intermediate phenotype associated with rs2200733 at 4q25 in lone atrial fibrillation.Semantic proximity Read ↗

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.Semantic proximity Read ↗

Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance.Semantic proximity Read ↗

Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.Semantic proximity Read ↗

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.Semantic proximity Read ↗

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