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 BRIP1 Variants among Korean Patients with BRCA1/2 Mutation-Negative High-Risk Breast Cancer.

Cancer research and treatment - 1 Jul 2016

Kim Haeyoung, Cho Dae-Yeon, Choi Doo Ho, Jung Gee Hue, Shin Inkyung, Park Won, Huh Seung Jae, Nam Seok Jin, Lee Jeong Eon, Gil Won Ho, Kim Seok Won

Abstract excerpt

PURPOSE: The aim of the current study is to assess the spectrum of genetic variation in the BRIP1 gene among Korean high-risk breast cancer patients who tested negative for the BRCA1/2 mutation. MATERIALS AND METHODS: Overall, 235 Korean patientswith BRCA1/2 mutation-negative high-risk breast cancerwere screened for BRIP1 mutations. The entire BRIP1 gene was analyzed using fluorescent-conformation sensitive gel...

Read the complete abstract on PubMed

Topics

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

Share to BRCA1 Protein
Share to BRCA2 Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fanconi Anemia Complementation Group Proteins

Share to Introns

Share to Protein Domains

Share to Republic of Korea

Share to RNA Helicases

Share to Silent Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 26790966
DOI: 10.4143/crt.2015.191
PMCID: PMC4946366

Genes

BRIP1
BRCA1

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

Analysis of BRIP1 Variants among Korean Patients with BRCA1/2 Mutation-Negative High-Risk Breast Cancer.PMID 26790966Read ↗

Further evidence for the contribution of the BRCA1-interacting protein-terminal helicase 1 (BRIP1) gene in breast cancer susceptibility.Semantic proximity Read ↗

Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer.Semantic proximity Read ↗

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.Semantic proximity Read ↗

Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families.Semantic proximity Read ↗

Rare BRIP1 Missense Alleles Confer Risk for Ovarian and Breast Cancer.Semantic proximity Read ↗

A novel breast cancer-associated BRIP1 (FANCJ/BACH1) germ-line mutation impairs protein stability and function.Semantic proximity Read ↗

Dominant-negative pathogenic variant BRIP1 c.1045G>C is a high-risk allele for non-mucinous epithelial ovarian cancer: A case-control study.Semantic proximity Read ↗

Mutation analysis of BRIP1 in male breast cancer cases: a population-based study in Central Italy.Semantic proximity Read ↗

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.Semantic proximity Read ↗

Protein-truncating variants in moderate-risk breast cancer susceptibility genes: a meta-analysis of high-risk case-control screening studies.Semantic proximity Read ↗

Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives.Semantic proximity Read ↗

Landscape of BRIP1 molecular lesions in gastrointestinal cancers from published genomic studies.Semantic proximity Read ↗

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