Associated Papers
Risk of ovarian cancer in women with a pathogenic or likely pathogenic variant in NBN: a systematic review and meta-analysis.
Ganesan S et al.
American Journal of Obstetrics and Gynecology, 2026
The Spectrum of Disease-Associated Alleles in Countries with a Predominantly Slavic Population.
Yanus GA et al.
International Journal of Molecular Sciences, 2024
39273284 (PubMed )
Supplement: ijms-25-09335-s001.zip › ijms-3137350-supplementary.pdf
Current status of inherited pancreatic cancer.
Olakowski M et al.
Hereditary Cancer in Clinical Practice, 2022
Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation.
Kim H et al.
Familial Cancer, 2015
Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients.
Sokolenko AP et al.
Cancer Letters, 2015
High prevalence of GPRC5A germline mutations in BRCA1-mutant breast cancer patients.
Sokolenko AP et al.
International Journal of Cancer, 2014
Fibroblast-based radiosensitivity assays as a clinically valuable tool for (severe) combined immunodeficiency syndromes.
Beyls E et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis, 0
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