Publications
- Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes2020 | First Faculty of Medicine, Central Library of Charles University
- The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases2020 | First Faculty of Medicine
- Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families2020 | First Faculty of Medicine
- Multigene Panel Germline Testing of 1333 Czech Patients with Ovarian Cancer2020 | First Faculty of Medicine
- Genetic analysis of subsequent second primary malignant neoplasms in long-term pancreatic cancer survivors suggests new potential hereditary genetic alterations2019 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Estrogen Receptor Status Oppositely Modifies Breast Cancer Prognosis in BRCA1/BRCA2 Mutation Carriers Versus Non-Carriers2019 | First Faculty of Medicine, Third Faculty of Medicine
- Homologous recombination DNA repair defects in PALB2-associated breast cancers2019 | 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
- Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes2018 | First Faculty of Medicine
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