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

Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients.

The Prostate - 1 Apr 2008

Sun Jielin, Lange Ethan M, Isaacs Sarah D, Liu Wennuan, Wiley Kathleen E, Lange Leslie, Gronberg Henrik, Duggan David, Carpten John D, Walsh Patrick C, Xu Jianfeng, Chang Bao-Li, Isaacs William B, Zheng S Lilly

Abstract excerpt

BACKGROUND: Multiple variants in three regions at 8q24 are consistently found to be associated with prostate cancer (PCa) risk in population-based association studies. The role that these variants may play in familial prostate cancer risk has not been extensively investigated. METHODS: We evaluat...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Aged, 80 and over
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 8

Share to Gene Frequency

Share to Haplotypes

Share to Prostatic Neoplasms

Share to Risk Factors

Source

Identifiers

PMID: 18213635
DOI: 10.1002/pros.20695

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18213635-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chromosome 8q24 risk variants in hereditary and non-hereditary prostate cancer patients.PMID 18213635Read ↗

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).Semantic proximity Read ↗

8q24 genetic variation and comprehensive haplotypes altering familial risk of prostate cancer.Semantic proximity Read ↗

Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans.Semantic proximity Read ↗

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.Semantic proximity Read ↗

Multiple loci on 8q24 associated with prostate cancer susceptibility.Semantic proximity Read ↗

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.Semantic proximity Read ↗

Two common chromosome 8q24 variants are associated with increased risk for prostate cancer.Semantic proximity Read ↗

Association of three 8q24 polymorphisms with prostate cancer susceptibility: evidence from a meta-analysis with 50,854 subjects.Semantic proximity Read ↗

Multiple regions within 8q24 independently affect risk for prostate cancer.Semantic proximity Read ↗

Association between genetic variations at 8q24 and prostate cancer risk in Mexican Men.Semantic proximity Read ↗

Confirmation of a positive association between prostate cancer risk and a locus at chromosome 8q24.Semantic proximity Read ↗

Systematic confirmation study of reported prostate cancer risk-associated single nucleotide polymorphisms in Chinese men.Semantic proximity Read ↗

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