PDF) The Breast Cancer Information Core: Database design, structure, and scope
![PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/131c15db5c7b7fa8885fd4f7cce9c40d0e09dbb2/11-Table1-1.png "PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar")
PDF] Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control | Semantic Scholar
BRCA2 Deleterious Mutations BIC database, Breast Cancer Information... | Download Table
Abbreviation: BIC, Breast Cancer Information Core database. a GenBank... | Download Scientific Diagram
BIC - Breast Cancer Information Core
BRCA1 And BRCA2 analysis of Argentinean breast/ovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin – topic of research paper in Biological
A characterization of genetic haplotypes in BRCA1 identifies linkage ...
BRCA1 and BRCA2 genes mutations among high risk breast cancer patients in Jordan | Scientific Reports
Prevalence and characterization of BRCA1 and BRCA2 germline mutations in Chinese women with familial breast cancer - Document - Gale OneFile: Health and Medicine
Mutational analysis of BRCA1 and BRCA2 genes in Peruvian families with hereditary breast and ovarian cancer - Buleje - 2017 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic - Annals of Oncology
PDF) The Breast Cancer Information Core: Database design, structure, and scope
BIC - Breast Cancer Information Core
Frameshift mutations detected in BRCA genes | Download Table
BRCA2 Deleterious Mutations BIC database, Breast Cancer Information... | Download Table
Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases | Journal of Translational Medicine | Full Text
BRCA2 c.8827C>T pathogenic mutation in a consanguineous Chinese family with hereditary breast cancer - Wang - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Germline sequence variants contributing to cancer susceptibility in South African breast cancer patients of African ancestry | Scientific Reports
Table 1 from BRCA1 and BRCA2 germline mutations in Korean ovarian cancer patients | Semantic Scholar
Concordance of Genomic Variants in Matched Primary Breast Cancer, Metastatic Tumor, and Circulating Tumor DNA: The MIRROR Study | JCO Precision Oncology
BRCA1/2 testing: therapeutic implications for breast cancer management | British Journal of Cancer
Cancers | Free Full-Text | The Genetic Analyses of French Canadians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and/or Ovarian Cancer Syndrome Families | HTML
BRCA1 mutations occur at the highest rates in the RING domain, exons... | Download Scientific Diagram
Research Projects
PDF) Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1 | Lawrence Brody - Academia.edu
Novel loss‑of‑function mutation in BRCA2 gene identified in a Chinese female with a family history of ovarian cancer: A case report
The Breast Information Core (BIC) Website Features. Overview and map of... | Download Scientific Diagram
Comparative oncogenomics identifies combinations of driver genes and drug targets in BRCA1-mutated breast cancer | Nature Communications
