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

Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer.

International journal of cancer - 15 Oct 2011

Andersen Claus Lindbjerg, Lamy Philippe, Thorsen Kasper, Kjeldsen Eigil, Wikman Friedrik, Villesen Palle, Øster Bodil, Laurberg Søren, Ørntoft Torben Falck

Abstract excerpt

Genomic alterations play important roles in colorectal cancer (CRC) carcinogenesis. Here, we aimed to identify and characterize recurrent copy-number alterations (CNAs) associated with clinical outcome of CRC by the use of single nucleotide polymorphism arrays, genomic quantitative PCR (qPCR) and...

Read the complete abstract on PubMed

Topics

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

Share to Adenoma
Share to Carcinoma
Share to Cell Line, Tumor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 16

Share to Colorectal Neoplasms

Share to Disease-Free Survival

Share to DNA Copy Number Variations

Share to Oligonucleotide Array Sequence Analysis

Source

Identifiers

PMID: 21154748
DOI: 10.1002/ijc.25841

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21154748-2026-09-02.2. 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

Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer.PMID 21154748Read ↗

Association of survival and disease progression with chromosomal instability: a genomic exploration of colorectal cancer.Semantic proximity Read ↗

Chromosome copy number analysis in screening for prognosis-related genomic regions in colorectal carcinoma.Semantic proximity Read ↗

Tumor-associated chromosomal instability drives progression of colorectal adenoma to adenocarcinoma: evidence from 17-year follow-up after adenoma diagnosisSemantic proximity Read ↗

Gene expression profiles of CMS2-epithelial/canonical colorectal cancers are largely driven by DNA copy number gainsSemantic proximity Read ↗

High Prevalence and Clinical Relevance of Genes Affected by Chromosomal Breaks in Colorectal Cancer.Semantic proximity Read ↗

A Comprehensive Characterization of Genome-Wide Copy Number Aberrations in Colorectal Cancer Reveals Novel Oncogenes and Patterns of AlterationsSemantic proximity Read ↗

Comprehensive analysis of copy number aberrations in microsatellite stable colon cancer in view of stromal component.Semantic proximity Read ↗

A genome-wide study of cytogenetic changes in colorectal cancer using SNP microarrays: opportunities for future personalized treatment.Semantic proximity Read ↗

Distinct Genetic Alterations in Colorectal CancerSemantic proximity Read ↗

DNA copy number alterations, gene expression changes and disease-free survival in patients with colorectal cancer: a 10 year follow-upSemantic proximity Read ↗

Integrated analysis of genome-wide copy number alterations and gene expression in microsatellite stable, CpG island methylator phenotype-negative colon cancer.Semantic proximity Read ↗

The order of genetic events associated with colorectal cancer progression inferred from meta‐analysis of copy number changesSemantic proximity Read ↗

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