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

Association between the rs2106261 polymorphism in the zinc finger homeobox 3 gene and risk of atrial fibrillation: Evidence from a PRISMA-compliant meta-analysis.

Medicine - 10 Dec 2021

Wei Yue, Wang Lingjie, Lin Changjian, Xie Yun, Bao Yangyang, Luo Qingzhi, Zhang Ning

Abstract excerpt

INTRODUCTION: Previous genome-wide studies have identified an association between the rs2106261 single-nucleotide polymorphism (SNP) in the zinc finger homeobox 3 (ZFHX3) gene and an increased risk of atrial fibrillation (AF). However, this association remains controversial, since conflicting results have been reported in previous studies. We aimed to investigate the association between the ZFHX3 rs2106261...

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 Atrial Fibrillation
Share to Genes, Homeobox
Share to Genetic Predisposition to Disease
Share to Homeodomain Proteins
Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 34889223
DOI: 10.1097/MD.0000000000027749
PMCID: PMC8663867

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between the rs2106261 polymorphism in the zinc finger homeobox 3 gene and risk of atrial fibrillation: Evidence from a PRISMA-compliant meta-analysis.PMID 34889223Read ↗

Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons.Semantic proximity Read ↗

Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.Semantic proximity Read ↗

Genetic polymorphisms in ZFHX3 are associated with atrial fibrillation in a Chinese Han population.Semantic proximity Read ↗

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.Semantic proximity Read ↗

Association of ZFHX3 gene variation with atrial fibrillation, cerebral infarction, and lung thromboembolism: An autopsy study.Semantic proximity Read ↗

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.Semantic proximity Read ↗

Association of atrial fibrillation susceptibility genes, atrial fibrillation phenotypes and response to catheter ablation: a gene-based analysis of GWAS data.Semantic proximity Read ↗

Association of Gene Polymorphism at Atrial Fibrillation in the Kazakh Population: Case – Control StudySemantic proximity Read ↗

Genetic polymorphisms confer risk of atrial fibrillation in patients with heart failure: a population-based study.Semantic proximity Read ↗

KCNN3 SNP rs13376333 on Chromosome 1q21 Confers Increased Risk of Atrial Fibrillation.Semantic proximity Read ↗

Predicting atrial fibrillation using a combination of genetic risk score and clinical risk factors.Semantic proximity Read ↗

Variant rs2200733 on chromosome 4q25 confers increased risk of atrial fibrillation: evidence from a meta-analysis.Semantic proximity Read ↗

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