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

Mutation screening of the BARD1 gene: evidence for involvement of the Cys557Ser allele in hereditary susceptibility to breast cancer.

Journal of medical genetics - 1 Sept 2004

Karppinen S-M, Heikkinen K, Rapakko K, Winqvist R

Abstract excerpt

No abstract is available from the source.

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 Cysteine
Share to Finland
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ovarian Neoplasms

Share to Serine

Share to Tumor Suppressor Proteins

Share to Ubiquitin-Protein Ligases

Source

Open in PubMed Open full text

Identifiers

PMID: 15342711
DOI: 10.1136/jmg.2004.020669
PMCID: PMC1735890

Genes

BARD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutation screening of the BARD1 gene: evidence for involvement of the Cys557Ser allele in hereditary susceptibility to breast cancer.PMID 15342711Read ↗

BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition.Semantic proximity Read ↗

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies.Semantic proximity Read ↗

Lack of association between BARD1 Cys557Ser variant and breast cancer risk: a meta-analysis of 11,870 cases and 7,687 controls.Semantic proximity Read ↗

The BARD1 Cys557Ser variant and risk of familial breast cancer in a South-American population.Semantic proximity Read ↗

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

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

The BARD1 Cys557Ser variant and breast cancer risk in Iceland.Semantic proximity Read ↗

Identification of functional SNPs in BARD1 gene and in silico analysis of damaging SNPs: based on data procured from dbSNP database.Semantic proximity Read ↗

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

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

Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers.Semantic proximity Read ↗

A cross-sectional study of associations between nonsynonymous mutations of the BARD1 gene and breast cancer in Han Chinese women.Semantic proximity Read ↗

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