Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.

doi:10.1093/carcin/bgs117

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

Community

Back to search

Article

Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.

Carcinogenesis - 1 May 2012

Song Xiao, Zhou Keke, Zhao Yingjie, Huai Cong, Zhao Yao, Yu Hongjie, Chen Yuanyuan, Chen Gong, Chen Hongyan, Fan Weiwei, Mao Ying, Lu Daru

Abstract excerpt

Genome-wide association studies have identified the susceptibility single nucleotide polymorphisms (SNPs) of glioma at chromosome 20q13.33, and the replication study conducted among Chinese Han population also confirmed the susceptibility locus rs6010620 is located in this region. To identify other genetic variants in 20q13.33, we genotyped 13 common tagging SNPs and imputed 86 additional SNPs in a region ∼100 kb...

Read the complete abstract on PubMed

Topics

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

Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Brain Neoplasms

Share to Case-Control Studies

Share to Chromosomes, Human, Pair 20

Share to Genetic Loci

Share to Genome-Wide Association Study

Share to Glioma

Share to Odds Ratio

Source

Open in PubMed

Identifiers

PMID: 22387365
DOI: 10.1093/carcin/bgs117

Genes

RTEL1
ZBTB46
ZGPAT

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

Fine mapping analysis of a region of 20q13.33 identified five independent susceptibility loci for glioma in a Chinese Han population.PMID 22387365Read ↗

Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population.Semantic proximity Read ↗

Genome-wide association study identifies five susceptibility loci for glioma.Semantic proximity Read ↗

Genome-wide association study of glioma and meta-analysis.Semantic proximity Read ↗

Genome-wide association study identifies multiple susceptibility loci for glioma.Semantic proximity Read ↗

Deciphering the 8q24.21 association for glioma.Semantic proximity Read ↗

RTEL1 tagging SNPs and haplotypes were associated with glioma development.Semantic proximity Read ↗

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.Semantic proximity Read ↗

An Updated and Comprehensive Meta-Analysis of Association Between Seven Hot Loci Polymorphisms from Eight GWAS and Glioma Risk.Semantic proximity Read ↗

Fine-mapping of a region of chromosome 5p15.33 (TERT-CLPTM1L) suggests a novel locus in TERT and a CLPTM1L haplotype are associated with glioma susceptibility in a Chinese population.Semantic proximity Read ↗

Australian genome-wide association study confirms higher female risk for adult glioma associated with variants in the region of CCDC26.Semantic proximity Read ↗

Genetic advances in glioma: susceptibility genes and networks.Semantic proximity Read ↗

A functional variant on 20q13.33 related to glioma risk alters enhancer activity and modulates expression of multiple genes.Semantic proximity Read ↗

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