Genome-wide association study-identified novel genetic loci for QT interval in Taiwan: implications for population-specific arrhythmia risk.

doi:10.1093/europace/euag055

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

Community

Back to search

Article

Genome-wide association study-identified novel genetic loci for QT interval in Taiwan: implications for population-specific arrhythmia risk.

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology - 30 Mar 2026

Huang Pang-Shuo, Li Guan-Wei, Cheng Jen-Fang, Chen Jien-Jiun, Ho Li-Ting, Lin Ting-Tse, Chiu Fu-Chun, Wu Cho-Kai, Chang Sheng-Nan, Chuang Eric Y, Wang Yi-Chih, Tsai Chia-Ti

Abstract excerpt

AIMS: Prolonged QT interval is a well-established marker for malignant ventricular arrhythmias and sudden cardiac death (SCD). Although previous genome-wide association studies (GWASs) have identified multiple QT-associated loci, most were conducted in European cohorts, limiting generalizability to East Asian populations. This study aimed to identify genetic determinants of QTc interval in a Taiwanese population....

Read the complete abstract on PubMed

Topics

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

Share to Arrhythmias, Cardiac

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexin 43

Share to Death, Sudden, Cardiac

Share to East Asian People

Share to ERG1 Potassium Channel

Share to KCNQ1 Potassium Channel

Share to Long QT Syndrome

Share to Potassium Channels, Voltage-Gated

Source

Open in PubMed Open full text

Identifiers

PMID: 41954913
DOI: 10.1093/europace/euag055
PMCID: PMC13122361

Genes

CD46
GJA1
SCD
KCNH2
KCNQ1
NOS1AP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide association study-identified novel genetic loci for QT interval in Taiwan: implications for population-specific arrhythmia risk.PMID 41954913Read ↗

Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations.Semantic proximity Read ↗

Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations.Semantic proximity Read ↗

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.Semantic proximity Read ↗

Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders.Semantic proximity Read ↗

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathwaysSemantic proximity Read ↗

Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarizationSemantic proximity Read ↗

Fine-mapping and initial characterization of QT interval loci in African Americans.Semantic proximity Read ↗

Genome-Wide Association Study for Resting Electrocardiogram in the Qatari Population Identifies 6 Novel Genes and Validates Novel Polygenic Risk Scores.Semantic proximity Read ↗

A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.Semantic proximity Read ↗

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.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 ↗

Common genetic variants, QT interval, and sudden cardiac death in a Finnish population-based study.Semantic proximity Read ↗

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