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 copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.

Urologic oncology - 1 Sept 2017

Poniah Prevathe, Mohd Zain Shamsul, Abdul Razack Azad Hassan, Kuppusamy Shanggar, Karuppayah Shankar, Sian Eng Hooi, Mohamed Zahurin

Abstract excerpt

BACKGROUND: Two key issues in prostate cancer (PCa) that demand attention currently are the need for a more precise and minimally invasive screening test owing to the inaccuracy of prostate-specific antigen and differential diagnosis to distinguish advanced vs. indolent cancers. This continues to pose a tremendous challenge in diagnosis and prognosis of PCa and could potentially lead to overdiagnosis and...

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

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

Share to DNA Copy Number Variations

Share to DDC gene

Share to Genetic Loci

Share to Genetic Predisposition to Disease

Share to Genome-Wide Association Study

Share to Prostatic Neoplasms

Source

Identifiers

PMID: 28527622
DOI: 10.1016/j.urolonc.2017.04.017

Genes

ARNT
DDC
SFRP1
THBS1

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

Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.PMID 28527622Read ↗

Detection of prostate cancer related copy number variations with SNP genotyping array.Semantic proximity Read ↗

Multi-omics approach for identifying CNV-associated lncRNA signatures with prognostic value in prostate cancerSemantic proximity Read ↗

Genome-wide copy-number variation analysis identifies common genetic variants at 20p13 associated with aggressiveness of prostate cancer.Semantic proximity Read ↗

Genetic variants in cell cycle control pathway confer susceptibility to aggressive prostate carcinoma.Semantic proximity Read ↗

Sequence variants at 22q13 are associated with prostate cancer risk.Semantic proximity Read ↗

Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.Semantic proximity Read ↗

Identification of functionally active, low frequency copy number variants at 15q21.3 and 12q21.31 associated with prostate cancer risk.Semantic proximity Read ↗

Characterization of germline copy number variation in high-risk African American families with prostate cancer.Semantic proximity Read ↗

Association of prostate cancer risk variants with gene expression in normal and tumor tissue.Semantic proximity Read ↗

Genomic Copy Number Variations in the Genomes of Leukocytes Predict Prostate Cancer Clinical Outcomes.Semantic proximity Read ↗

Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate TissuesSemantic proximity Read ↗

Copy number alterations in prostate tumors and disease aggressiveness.Semantic proximity Read ↗

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