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

BARD1 homozygous deletion, a possible alternative to BRCA1 mutation in basal breast cancer.

Genes, chromosomes & cancer - 1 Dec 2010

Sabatier Renaud, Adélaïde José, Finetti Pascal, Ferrari Anthony, Huiart Laetitia, Sobol Hagay, Chaffanet Max, Birnbaum Daniel, Bertucci François

Abstract excerpt

Hereditary breast cancers (BCs) are incompletely explained by BRCA genes abnormalities, as ∼70% of them are not associated with known genetic alterations. Array-based comparative genomic hybridization (aCGH) of tumors provides an opportunity for identifying new BC susceptibility genes. By analyzing our database of high-resolution aCGH profiles of 330 BCs, we identified a case with homozygous deletion of the...

Read the complete abstract on PubMed

Topics

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

Share to Comparative Genomic Hybridization
Share to Gene Deletion

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

Share to Genes, BRCA1

Share to Genes, Tumor Suppressor

Share to Oligonucleotide Array Sequence Analysis

Share to Sequence Deletion

Share to Tumor Suppressor Proteins

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 20842729
DOI: 10.1002/gcc.20822

Genes

BARD1
BRCA1
CHEK1
FANCA
PARP1
RAD51

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

BARD1 homozygous deletion, a possible alternative to BRCA1 mutation in basal breast cancer.PMID 20842729Read ↗

Contribution of BARD1 gene to male breast cancer- report of a family with different types of cancer.Semantic proximity Read ↗

Summary of BARD1 Mutations and Precise Estimation of Breast and Ovarian Cancer Risks Associated with the Mutations.Semantic proximity Read ↗

Literature Review of BARD1 as a Cancer Predisposing Gene with a Focus on Breast and Ovarian Cancers.Semantic proximity Read ↗

BARD1 mystery: tumor suppressors are cancer susceptibility genesSemantic proximity Read ↗

BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort.Semantic proximity Read ↗

Mutations in exon region of BRCA1-related RING domain 1 gene and risk of breast cancer.Semantic proximity Read ↗

The Effects of Genetic and Epigenetic Alterations of BARD1 on the Development of Non-Breast and Non-Gynecological Cancers.Semantic proximity Read ↗

Frequent incidence of BARD1-truncating mutations in germline DNA from triple-negative breast cancer patients.Semantic proximity Read ↗

Cancer predisposing BARD1 mutations in breast-ovarian cancer families.Semantic proximity Read ↗

Is there more to BARD1 than BRCA1?Semantic proximity Read ↗

Multimodal analysis of rare BARD1 missense variant suggests its pathogenicity is conditionalSemantic proximity Read ↗

New concepts on BARD1: Regulator of BRCA pathways and beyond.Semantic proximity Read ↗

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