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

Genomic Copy Number Variations in the Genomes of Leukocytes Predict Prostate Cancer Clinical Outcomes.

PloS one - 1 Jan 2015

Yu Yan P, Liu Silvia, Huo Zhiguang, Martin Amantha, Nelson Joel B, Tseng George C, Luo Jian-Hua

Abstract excerpt

Accurate prediction of prostate cancer clinical courses remains elusive. In this study, we performed whole genome copy number analysis on leukocytes of 273 prostate cancer patients using Affymetrix SNP6.0 chip. Copy number variations (CNV) were found across all chromosomes of the human genome. An average of 152 CNV fragments per genome was identified in the leukocytes from prostate cancer patients. The size...

Read the complete abstract on PubMed

Topics

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

Share to DNA Copy Number Variations
Share to Leukocytes, Mononuclear

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Neoplasm Recurrence, Local

Share to Nomograms

Share to Oncogene Proteins, Fusion

Share to Prostate-Specific Antigen

Share to Prostatic Neoplasms

Share to Survival Analysis

Source

Open in PubMed Open full text

Identifiers

PMID: 26295840
DOI: 10.1371/journal.pone.0135982
PMCID: PMC4546524

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genomic Copy Number Variations in the Genomes of Leukocytes Predict Prostate Cancer Clinical Outcomes.PMID 26295840Read ↗

Genome abnormalities precede prostate cancer and predict clinical relapse.Semantic proximity Read ↗

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 analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.Semantic proximity Read ↗

Genome-wide association study of germline copy number variations reveals an association with prostate cancer aggressiveness.Semantic proximity Read ↗

Comprehensive assessment of DNA copy number alterations in human prostate cancers using Affymetrix 100K SNP mapping arraySemantic proximity Read ↗

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

Simultaneously detection of genomic and expression alterations in prostate cancer using cDNA microarray.Semantic proximity Read ↗

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

High-Resolution Analysis of Gene Copy Number Alterations in Human Prostate Cancer Using CGH on cDNA Microarrays: Impact of Copy Number on Gene ExpressionSemantic proximity Read ↗

Integrated Analysis of CNV, Gene Expression and Disease State Data in Prostate CancerSemantic proximity Read ↗

High-Resolution Analysis of Gene Copy Number Alterations in Human Prostate Cancer Using CGH on cDNA Microarrays: Impact of Copy Number on Gene ExpressionSemantic proximity Read ↗

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