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

The Association Between Foxp3 Polymorphisms and Risk of Graves' Disease: A Systematic Review and Meta-Analysis of Observational Studies.

Frontiers in endocrinology - 1 Jan 2020

Li Han-Ning, Li Xing-Rui, Du Ya-Ying, Yang Zhi-Fang, Lv Zheng-Tao

Abstract excerpt

Purpose: This systematic review and meta-analysis was carried out with the aim of investigating the relationship between Foxp3 polymorphisms (rs3761547, r3761548, and rs3761549) and the risk of Graves' disease (GD). Methods: Four online database including PubMed, EMBASE, ISI Web of Science, and CNKI were searched to identify observational studies that evaluated the association between Foxp3 polymorphisms and risk...

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 Forkhead Transcription Factors
Share to Genetic Association Studies
Share to Genetic Predisposition to Disease
Share to Graves Disease
Share to Observational Studies as Topic
Share to Polymorphism, Single Nucleotide

Source

Open in PubMed Open full text

Identifiers

PMID: 32612577
DOI: 10.3389/fendo.2020.00392
PMCID: PMC7308555

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Association Between Foxp3 Polymorphisms and Risk of Graves' Disease: A Systematic Review and Meta-Analysis of Observational Studies.PMID 32612577Read ↗

Meta-analysis reveals significant association between FOXP3 polymorphisms and susceptibility to Graves' disease.Semantic proximity Read ↗

The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population.Semantic proximity Read ↗

Association of genetic variations in FoxP3 gene with Graves' disease in a Southwest Chinese Han population.Semantic proximity Read ↗

Foxp3 gene polymorphisms and haplotypes associate with susceptibility of Graves' disease in Chinese Han population.Semantic proximity Read ↗

Association of FoxP3 promoter polymorphisms with the risk of Graves' disease in ethnic Kashmiri population.Semantic proximity Read ↗

Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases.Semantic proximity Read ↗

Genetic study of early-onset Graves' disease in the Chinese Han population.Semantic proximity Read ↗

Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population.Semantic proximity Read ↗

The associations between the polymorphisms in the CTLA-4 gene and the risk of Graves' disease in the Chinese population.Semantic proximity Read ↗

Association between FOXP3 polymorphisms and susceptibility to autoimmune diseases: A meta-analysis.Semantic proximity Read ↗

Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease.Semantic proximity Read ↗

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.Semantic proximity Read ↗

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