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

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

Journal of cardiovascular electrophysiology - 1 Feb 2013

Mohanty Sanghamitra, Santangeli Pasquale, Bai Rong, Di Biase Luigi, Mohanty Prasant, Pump Agnes, Natale Andrea

Abstract excerpt

INTRODUCTION: Several genome-wide association studies have identified rs2200733, a single-nucleotide polymorphism (SNP) at 4q25 to be the most common chromosomal variant present in patients with atrial fibrillation (AF). We aimed to explore the association of rs2200733 with AF through a systematic review and meta-analysis. METHOD: An extensive literature search was performed on PubMed, and other databases using...

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 Delete account & data About Contact Helena Bioinformatics

Share to Atrial Fibrillation
Share to Chromosomes, Human, Pair 4
Share to Evidence-Based Medicine
Share to Genetic Predisposition to Disease
Share to Genetic Variation
Share to Polymorphism, Single Nucleotide
Share to Prevalence
Share to Risk Factors

Source

Identifiers

PMID: 23130627
DOI: 10.1111/jce.12017

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variant rs2200733 on chromosome 4q25 confers increased risk of atrial fibrillation: evidence from a meta-analysis.PMID 23130627Read ↗

Association of RS2200733 but not RS10033464 on 4q25 with atrial fibrillation based on the recessive model in a Taiwanese population.Semantic proximity Read ↗

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation.Semantic proximity Read ↗

Association Between rs2200733 Polymorphism on Chromosome 4q25 and Atrial Fibrillation in a Greek Population.Semantic proximity Read ↗

Association between rs2200733 and rs7193343 genetic variants and atrial fibrillation in a Spanish population, and meta-analysis of previous studies.Semantic proximity Read ↗

Independent susceptibility markers for atrial fibrillation on chromosome 4q25.Semantic proximity Read ↗

Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.Semantic proximity Read ↗

Association of rs17042171 with chromosome 4q25 with atrial fibrillation in Chinese Han populations.Semantic proximity Read ↗

Genetics of atrial fibrillation-an update of recent findings.Semantic proximity Read ↗

Common variants for atrial fibrillation: results from genome-wide association studies.Semantic proximity Read ↗

Genetics of atrial fibrillation: from families to genomes.Semantic proximity Read ↗

Genetics of atrial fibrillation.Semantic proximity Read ↗

Association of rs2200733 at 4q25 with atrial flutter/fibrillation diseases in an Italian population.Semantic proximity Read ↗

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