Associated Papers
Functional analysis of BRCA1 and BRCA2 splicing variants using a minigene assay.
Yim H et al.
Human Genomics, 2025
Ethnic-specificity, evolution origin and deleteriousness of Asian BRCA variation revealed by over 7500 BRCA variants derived from Asian population.
Qin Z et al.
International Journal of Cancer, 2023
36385461 (PubMed )
Supplement: IJC-152-1159-s002.xlsx › BRCA2
Reclassification of variants of tumor suppressor genes based on Sanger RNA sequencing without NMD inhibition.
Ha C et al.
Frontiers in Genetics, 2023
Rates of Variants of Uncertain Significance Among Patients With Breast Cancer Undergoing Genetic Testing: Regional Perspectives.
Abdel-Razeq H et al.
Frontiers in Oncology, 2022
Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients.
Torres D et al.
Scientific Reports, 2017
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