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

Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population.

PloS one - 1 Jan 2016

Zhang Rongfeng, Tian Xiaochen, Gao Lianjun, Li Huihua, Yin Xiaomeng, Dong Yingxue, Yang Yanzong, Xia Yunlong

Abstract excerpt

BACKGROUND: PR interval variations have recently been associated with an increased risk of long-term atrial fibrillation (AF), heart block and all-cause mortality. Genome-wide association studies have linked the PR interval with several common variants in the TBX5 gene. Several variants in the TBX5 gene, including rs7312625 and rs883079, have been associated with AF. The purpose of this study was to determine the...

Read the complete abstract on PubMed

Topics

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Asian People

Share to Atrial Fibrillation

Share to Case-Control Studies

Share to Genetic Association Studies

Share to Odds Ratio

Share to T-Box Domain Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 27479212
DOI: 10.1371/journal.pone.0160467
PMCID: PMC4968840

Genes

TBX5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Common Variants in the TBX5 Gene Associated with Atrial Fibrillation in a Chinese Han Population.PMID 27479212Read ↗

SNP rs3825214 in TBX5 is associated with lone atrial fibrillation in Chinese Han population.Semantic proximity Read ↗

Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.Semantic proximity Read ↗

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.Semantic proximity Read ↗

TBX5 mutations contribute to early-onset atrial fibrillation in Chinese and Caucasians.Semantic proximity Read ↗

Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population.Semantic proximity Read ↗

A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation.Semantic proximity Read ↗

TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant.Semantic proximity Read ↗

Pitx2 modulates a Tbx5-dependent gene regulatory network to maintain atrial rhythm.Semantic proximity Read ↗

The role of transcription factors in atrial fibrillation.Semantic proximity Read ↗

A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valveSemantic proximity Read ↗

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.Semantic proximity Read ↗

Variants conferring risk of atrial fibrillation on chromosome 4q25.Semantic proximity Read ↗

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