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

Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example.

Scientific reports - 21 May 2015

Klonowska Katarzyna, Ratajska Magdalena, Czubak Karol, Kuzniacka Alina, Brozek Izabela, Koczkowska Magdalena, Sniadecki Marcin, Debniak Jaroslaw, Wydra Dariusz, Balut Magdalena, Stukan Maciej, Zmienko Agnieszka, Nowakowska Beata, Irminger-Finger Irmgard, Limon Janusz, Kozlowski Piotr

Abstract excerpt

Only approximately 50% of all familial breast cancers can be explained by known genetic factors, including mutations in BRCA1 and BRCA2. One of the most extensively studied candidates for breast and/or ovarian cancer susceptibility is BARD1. Although it was suggested that large mutations may cont...

Read the complete abstract on PubMed

Topics

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

Share to Breast Neoplasms
Share to Multiplex Polymerase Chain Reaction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation, Missense

Share to Ovarian Neoplasms

Share to Poland

Share to Tumor Suppressor Proteins

Share to Ubiquitin-Protein Ligases

Share to White People

Source

Open in PubMed Open full text

Identifiers

PMID: 25994375
DOI: 10.1038/srep10424
PMCID: PMC4439969

Genes

BARD1
BRCA1
BRCA2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25994375-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example.PMID 25994375Read ↗

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

Apparent regional differences in the spectrum of BARD1 pathogenic variants in Spanish population and importance of copy number variants.Semantic proximity Read ↗

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

Mutational analysis of BARD1 in familial breast cancer patients in Japan.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 ↗

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

Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms.Semantic proximity Read ↗

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

Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families.Semantic proximity Read ↗

BARD1 and Breast Cancer: The Possibility of Creating Screening Tests and New Preventive and Therapeutic Pathways for Predisposed WomenSemantic proximity Read ↗

BARD1 and Breast Cancer: the Possibility of Creating Screening Tests and New Preventive and Therapeutic Pathways for Predisposed WomenSemantic proximity Read ↗

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