Quantitative assessment of the influence of common variation rs16892766 at 8q23.3 with colorectal adenoma and cancer susceptibility.

doi:10.1007/s00438-014-0928-z

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

Quantitative assessment of the influence of common variation rs16892766 at 8q23.3 with colorectal adenoma and cancer susceptibility.

Molecular genetics and genomics : MGG - 1 Apr 2015

Li Ming, Gu Yahong

Abstract excerpt

Epidemiological studies indicate a genetic contribution to colorectal cancer (CRC) and colorectal adenoma (CRA) risk, but specific genetic variants remain unknown. Recently, genome-wide association studies have identified 8q23.3-rs16892766 as a new CRC susceptibility locus in populations of European descent. Since then, the relationship between 8q23.3-rs16892766 and CRC/CRA has been reported in various ethnic...

Read the complete abstract on PubMed

Topics

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Adenoma

Share to Chromosomes, Human, Pair 8

Share to Colorectal Neoplasms

Share to Genetic Association Studies

Share to Genetic Predisposition to Disease

Share to Polymorphism, Single Nucleotide

Share to Risk

Source

Open in PubMed

Identifiers

PMID: 25293934
DOI: 10.1007/s00438-014-0928-z

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

Quantitative assessment of the influence of common variation rs16892766 at 8q23.3 with colorectal adenoma and cancer susceptibility.PMID 25293934Read ↗

Common variation rs6983267 at 8q24.1 and risk of colorectal adenoma and cancer: evidence based on 31 studies.Semantic proximity Read ↗

Analyzing large-scale samples confirms the association between rs16892766 polymorphism and colorectal cancer susceptibility.Semantic proximity Read ↗

Common genetic variants (rs4779584 and rs10318) at 15q13.3 contributes to colorectal adenoma and colorectal cancer susceptibility: evidence based on 22 studies.Semantic proximity Read ↗

The SNP rs961253 in 20p12.3 is associated with colorectal cancer risk: a case-control study and a meta-analysis of the published literature.Semantic proximity Read ↗

Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese.Semantic proximity Read ↗

Genetic variants on chromosome 8q24 and colorectal neoplasia risk: a case-control study in China and a meta-analysis of the published literature.Semantic proximity Read ↗

Association of 8q24.21 loci with the risk of colorectal cancer: a systematic review and meta-analysis.Semantic proximity Read ↗

A comprehensive meta-analysis of genetic associations between five key SNPs and colorectal cancer risk.Semantic proximity Read ↗

Pooled analysis of genetic variation at chromosome 8q24 and colorectal neoplasia risk.Semantic proximity Read ↗

Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype.Semantic proximity Read ↗

Risk of genome-wide association study-identified genetic variants for colorectal cancer in a Chinese population.Semantic proximity Read ↗

Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.Semantic proximity Read ↗

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