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

copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.

PloS one - 1 Jan 2013

Kuusisto Kirsi M, Akinrinade Oyediran, Vihinen Mauno, Kankuri-Tammilehto Minna, Laasanen Satu-Leena, Schleutker Johanna

Abstract excerpt

BACKGROUND: Inherited factors predisposing individuals to breast and ovarian cancer are largely unidentified in a majority of families with hereditary breast and ovarian cancer (HBOC). We aimed to identify germline copy number variations (CNVs) contributing to HBOC susceptibility in the Finnish population. METHODS: A cohort of 84 HBOC individuals (negative for BRCA1/2-founder mutations and pre-screened for the...

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 Finland

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

Share to Gene Duplication

Share to Genes, BRCA1

Share to Genes, BRCA2

Share to Germ-Line Mutation

Share to Hereditary Breast and Ovarian Cancer Syndrome

Share to Reproducibility of Results

Source

Open in PubMed Open full text

Identifiers

PMID: 23967248
DOI: 10.1371/journal.pone.0071802
PMCID: PMC3742470

Genes

BRCA1
EPHA3
CSMD1

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

copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer.PMID 23967248Read ↗

Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia.Semantic proximity Read ↗

Rare copy number variants (CNVs) and breast cancer riskSemantic proximity Read ↗

Copy number variants in BRCA1 and BRCA2 genes in Polish patients with breast and ovarian cancer.Semantic proximity Read ↗

Rare Copy Number Variants (CNVs) and Breast Cancer RiskSemantic proximity Read ↗

Copy number variants in BRCA1 and BRCA2 genes in Polish patients with breast and ovarian cancerSemantic proximity Read ↗

Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families.Semantic proximity Read ↗

Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility.Semantic proximity Read ↗

Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.Semantic proximity Read ↗

Targeted sequencing for hereditary breast and ovarian cancer in BRCA1/2-negative families reveals complex genetic architecture and phenocopies.Semantic proximity Read ↗

Germline BRCA1/2 Variants in Polish Patients with Family History of Breast and Ovarian Cancer: Prevalence, CNV Detection, and Identification of a Novel Loss-of-Function Mutation.Semantic proximity Read ↗

Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC).Semantic proximity Read ↗

Germline copy number variation analysis in Finnish families with hereditary prostate cancer.Semantic proximity Read ↗

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