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

Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor.

PloS one - 1 Jan 2016

Dahlin Anna M, Wibom Carl, Ghasimi Soma, Brännström Thomas, Andersson Ulrika, Melin Beatrice

Abstract excerpt

Genome-wide association studies and candidate gene studies have identified several genetic variants that increase glioma risk. The majority of these variants are non-coding and the mechanisms behind the increased risk in carriers are not known. In this study, we hypothesize that some of the established glioma risk variants induce aberrant DNA methylation in the developing tumor, either locally (gene-specific) or...

Read the complete abstract on PubMed

Topics

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

Share to Brain Neoplasms
Share to CpG Islands
Share to Glioblastoma

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glioma

Share to Oligodendroglioma

Share to Pilot Projects

Share to RNA, Long Noncoding

Share to Telomerase

Source

Open in PubMed Open full text

Identifiers

PMID: 27780202
DOI: 10.1371/journal.pone.0163067
PMCID: PMC5079592

Genes

TERT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Relation between Established Glioma Risk Variants and DNA Methylation in the Tumor.PMID 27780202Read ↗

New insights into susceptibility to glioma.Semantic proximity Read ↗

Genetic risk profiles identify different molecular etiologies for glioma.Semantic proximity Read ↗

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

Genetics in glioma: lessons learned from genome-wide association studies.Semantic proximity Read ↗

Genetic causes of glioma: new leads in the labyrinth.Semantic proximity Read ↗

Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk loci.Semantic proximity Read ↗

Methylation-driven Cancer Genes and Methylation Profiling in Glioma: A Comparative Study between East Asian and non-Hispanic White PopulationsSemantic proximity Read ↗

TERT promoter mutations in gliomas, genetic associations and clinico-pathological correlations.Semantic proximity Read ↗

Cancer susceptibility variants and the risk of adult glioma in a US case-control study.Semantic proximity Read ↗

Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologies.Semantic proximity Read ↗

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

1p19q co-deletion is an independent prognostic factor in glioma with TERT promoter mutationsSemantic proximity Read ↗

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