A genome-wide association study on medulloblastoma.

doi:10.1007/s11060-020-03424-9

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

A genome-wide association study on medulloblastoma.

Journal of neuro-oncology - 1 Apr 2020

Dahlin Anna M, Wibom Carl, Andersson Ulrika, Bybjerg-Grauholm Jonas, Deltour Isabelle, Hougaard David M, Scheurer Michael E, Lau Ching C, McKean-Cowdin Roberta, Kennedy Rebekah J, Hung Long T, Yee Janis, Margol Ashley S, Barrington-Trimis Jessica, Gauderman W James, Feychting Maria, Schüz Joachim, Röösli Martin, Kjaerheim Kristina, Januszkiewicz-Lewandowska Danuta, Fichna Marta, Nowak Jerzy, Searles Nielsen Susan, Asgharzadeh Shahab, Mirabello Lisa, Hjalmars Ulf, Melin Beatrice

Abstract excerpt

INTRODUCTION: Medulloblastoma is a malignant embryonal tumor of the cerebellum that occurs predominantly in children. To find germline genetic variants associated with medulloblastoma risk, we conducted a genome-wide association study (GWAS) including 244 medulloblastoma cases and 247 control subjects from Sweden and Denmark. METHODS: Genotyping was performed using Illumina BeadChips, and untyped variants were...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers, Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Cerebellar Neoplasms

Share to Cohort Studies

Share to Genome-Wide Association Study

Share to Medulloblastoma

Share to Polymorphism, Single Nucleotide

Share to Prognosis

Source

Open in PubMed Open full text

Identifiers

PMID: 32056145
DOI: 10.1007/s11060-020-03424-9
PMCID: PMC7136185

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

A genome-wide association study on medulloblastoma.PMID 32056145Read ↗

Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.Semantic proximity Read ↗

Genetic screening algorithm for children with medulloblastoma: a scoring system for stratifying the risk of hereditary variantsSemantic proximity Read ↗

Medulloblastoma: WHO 2021 and BeyondSemantic proximity Read ↗

Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus.Semantic proximity Read ↗

OpenPBTA: An Open Pediatric Brain Tumor AtlasSemantic proximity Read ↗

The whole-genome landscape of medulloblastoma subtypes.Semantic proximity Read ↗

LncRNA CDKN2BAS rs2157719 genetic variant contributes to medulloblastoma predisposition.Semantic proximity Read ↗

Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci.Semantic proximity Read ↗

Molecular variants and mutations in medulloblastomaSemantic proximity Read ↗

Genetic predisposition to medulloblastomas: just follow the tumour genome.Semantic proximity Read ↗

CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma.Semantic proximity Read ↗

Comprehensive high-resolution genomic profiling and cytogenetics of two pediatric and one adult medulloblastoma.Semantic proximity Read ↗

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