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

Screening of SNPs at 18 positional candidate genes, located within the GD-1 locus on chromosome 14q23-q32, for susceptibility to Graves' disease: a TDT study.

Molecular genetics and metabolism - 1 Nov 2004

Chistiakov D A, Savost'anov K V, Turakulov R I

Abstract excerpt

Graves' disease (GD) is a complex autoimmune thyroid disorder with a strong genetic component. Genome-wide screens resolved several susceptibility loci that contribute to the development of GD. One of the susceptibility loci (GD-1 locus) was mapped on chromosome 14q31. However, a susceptibility gene located within the GD-1 locus remains undefined. Here we screen eighteen single nucleotide polymorphisms (SNPs),...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 14
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Graves Disease

Share to Iodide Peroxidase

Share to Iodothyronine Deiodinase Type II

Share to Linkage Disequilibrium

Share to Receptors, Thyrotropin

Share to Russia

Source

Identifiers

PMID: 15542398
DOI: 10.1016/j.ymgme.2004.07.011

Genes

DIO2
TSHR

Variants

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening of SNPs at 18 positional candidate genes, located within the GD-1 locus on chromosome 14q23-q32, for susceptibility to Graves' disease: a TDT study.PMID 15542398Read ↗

Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.Semantic proximity Read ↗

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

The genetics of Graves' disease.Semantic proximity Read ↗

Dissecting the Genetic Susceptibility to Graves’ Disease in a Cohort of Patients of Italian OriginSemantic proximity Read ↗

rs3827440, a nonsynonymous single nucleotide polymorphism within GPR174 gene in X chromosome, is associated with Graves' disease in Polish Caucasian population.Semantic proximity Read ↗

A dense mapping study of six European AITD susceptibility regions in a large Chinese Han Cohort of Graves' disease.Semantic proximity Read ↗

The replication of the association of the rs6832151 within chromosomal band 4p14 with Graves' disease in a Polish Caucasian population.Semantic proximity Read ↗

Genetic associations of the thyroid stimulating hormone receptor gene with Graves diseases and Graves ophthalmopathy: A meta-analysis.Semantic proximity Read ↗

The variants in PTPRB, TRAF3IP3, and DISC1 genes were associated with Graves' disease in the Chinese population.Semantic proximity Read ↗

Association of 4p14 and 6q27 variation with Graves disease: a case-control study and a meta-analysis of available evidence.Semantic proximity Read ↗

Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population.Semantic proximity Read ↗

Association of polymorphisms of rs179247 and rs12101255 in thyroid stimulating hormone receptor intron 1 with an increased risk of Graves' disease: A meta-analysis.Semantic proximity Read ↗

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