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

Genome-wide detection of allelic genetic variation to predict advanced-stage prostate cancer after radical prostatectomy using an exome SNP chip.

Urologic oncology - 1 Sept 2015

Oh Jong Jin, Park Seunghyun, Lee Sang Eun, Hong Sung Kyu, Lee Sangchul, Jo Jung Ki, Lee Jung Keun, Ho Jin-Nyoung, Yoon Sungroh, Byun Seok-Soo

Abstract excerpt

OBJECTIVES: Genetic variations among patients with prostate cancer (PCa) who underwent radical prostatectomies were evaluated to predict advanced stage above T3 using an exome single nucleotide polymorphism (SNP) chip array. MATERIALS AND METHODS: We collected data of genetic SNP variants from 820 patients with PCa who underwent radical prostatectomy (RP) using a custom HumanExome BeadChip v1.0 (Illumina Inc.)....

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers, Tumor
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to Neoplasm Staging

Share to Oligonucleotide Array Sequence Analysis

Share to Prostatectomy

Share to Prostatic Neoplasms

Source

Identifiers

PMID: 26087972
DOI: 10.1016/j.urolonc.2015.05.016

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide detection of allelic genetic variation to predict advanced-stage prostate cancer after radical prostatectomy using an exome SNP chip.PMID 26087972Read ↗

A clinicogenetic model to predict lymph node invasion by use of genome-based biomarkers from exome arrays in prostate cancer patients.Semantic proximity Read ↗

The use of exome genotyping to predict pathological Gleason score upgrade after radical prostatectomy in low-risk prostate cancer patients.Semantic proximity Read ↗

Genome-wide detection of allelic genetic variation to predict biochemical recurrence after radical prostatectomy among prostate cancer patients using an exome SNP chip.Semantic proximity Read ↗

Exome-based genome-wide association study and risk assessment using genetic risk score to prostate cancer in the Korean population.Semantic proximity Read ↗

Comprehensive resequence analysis of a 123-kb region of chromosome 11q13 associated with prostate cancer.Semantic proximity Read ↗

Associations of prostate cancer risk variants with disease aggressiveness: results of the NCI-SPORE Genetics Working Group analysis of 18,343 cases.Semantic proximity Read ↗

Genetic variants in epithelial-mesenchymal transition genes as predictors of clinical outcomes in localized prostate cancer.Semantic proximity Read ↗

Utility of incorporating genetic variants for the early detection of prostate cancer.Semantic proximity Read ↗

The prostate cancer susceptibility variant rs2735839 near KLK3 gene is associated with aggressive prostate cancer and can stratify gleason score 7 patients.Semantic proximity Read ↗

Individual and cumulative effect of prostate cancer risk-associated variants on clinicopathologic variables in 5,895 prostate cancer patients.Semantic proximity Read ↗

Genome-wide association study identifies a genetic variant associated with risk for more aggressive prostate cancer.Semantic proximity Read ↗

Prostate cancer susceptibility variants confer increased risk of disease progression.Semantic proximity Read ↗

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