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

Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review.

Cancer science - 1 May 2016

Deng Changkai, Dai Rong, Li Xuliang, Liu Feng

Abstract excerpt

Over the last few decades, numerous biomarkers in Wilms' tumor have been confirmed and shown variations in prevalence. Most of these studies were based on small sample sizes. We carried out a meta-analysis of the research published from 1992 to 2015 to obtain more precise and comprehensive outcomes for genetic tests. In the present study, 70 out of 5175 published reports were eligible for the meta-analysis, which...

Read the complete abstract on PubMed

Topics

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

Share to Early Detection of Cancer
Share to CTNNB1 gene
Share to Gene Frequency

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

Share to MYCN gene

Share to Genetic Variation

Share to Publication Bias

Share to Wilms Tumor

Source

Open in PubMed Open full text

Identifiers

PMID: 26892980
DOI: 10.1111/cas.12910
PMCID: PMC4970837

Genes

CTNNB1
DGCR8
DROSHA
MYCN

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation frequencies in Wilms' tumor: A meta-analysis and systematic review.PMID 26892980Read ↗

Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization.Semantic proximity Read ↗

Update on Surveillance Guidelines in Emerging Wilms Tumor Predisposition Syndromes.Semantic proximity Read ↗

Intra-tumor genetic heterogeneity in Wilms tumor samples.Semantic proximity Read ↗

The genetic factors contributing to the development of Wilm's tumor and their clinical utility in its diagnosis and prognosis.Semantic proximity Read ↗

Molecular genetics of Wilms tumor.Semantic proximity Read ↗

A genome-wide association study identifies susceptibility loci for Wilms tumor.Semantic proximity Read ↗

Genetic and Epigenetic Drivers of Wilms Tumor Predisposition in Russian Pediatric Patients: A Multicenter Study.Semantic proximity Read ↗

The contribution of WTAP gene variants to Wilms tumor susceptibility.Semantic proximity Read ↗

The Genetic and Epigenetic Features of Bilateral Wilms Tumor Predisposition: A Report from the Children's Oncology Group AREN18B5-Q StudySemantic proximity Read ↗

YTHDC1 gene polymorphisms and Wilms tumor susceptibility in Chinese children: A five-center case-control study.Semantic proximity Read ↗

METTL1 gene polymorphisms and Wilms tumor susceptibility in Chinese children: A five-center case-control study.Semantic proximity Read ↗

Genetic and chromosomal alterations in Kenyan Wilms Tumor.Semantic proximity Read ↗

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