Publications
- The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases2020 | First Faculty of Medicine
- Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer2019 | First Faculty of Medicine
- Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance2019 | First Faculty of Medicine
- Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients2016 | First Faculty of Medicine
- RE: frameshift variant FANCL*c.1096_1099dupATTA is not associated with high breast cancer risk2016 | First Faculty of Medicine
- Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic2016 | First Faculty of Medicine
- Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic2015 | First Faculty of Medicine
- Expression of human BRCA1 Delta 17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage response2013 | First Faculty of Medicine, Third Faculty of Medicine
- The PALB2 Gene Is a Strong Candidate for Clinical Testing in BRCA1- and BRCA2-Negative Hereditary Breast Cancer2013 | First Faculty of Medicine
- Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.2010 | First Faculty of Medicine
Loading network view...