- Gynecological lesions in hereditary cancer predisposition syndromes2021 | First Faculty of Medicine, Second Faculty of Medicine
- Genomics Driving Diagnosis and Treatment of Inborn Errors of Immunity with Cancer Predisposition2022 | Second Faculty of Medicine
- Cancer Predisposition Genes in Cancer-Free Families2020 | Faculty of Medicine in Pilsen
- CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate2020 | First Faculty of Medicine
- Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular Carcinoma2023 | First Faculty of Medicine, Central Library of Charles University, Faculty of Science
- Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium2023 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance2019 | First Faculty of Medicine
- Germline Variants of CYBA and TRPM4 Predispose to Familial Colorectal Cancer2022 | Faculty of Medicine in Pilsen
- 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
- Whole-body magnetic resonance imaging in pediatric oncology - recommendations by the Oncology Task Force of the ESPR2020 | Second Faculty of Medicine
- Somatic TP53 Mutation Mosaicism in a Patient With Li-Fraumeni Syndrome2009 | Second Faculty of Medicine
- The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases2020 | First Faculty of Medicine
- Possible mechanisms of subsequent neoplasia development in childhood cancer survivors: A review2021 | Second Faculty of Medicine
- Radiation-Induced Lymphopoenia and Treatment Outcome in Hereditary Breast Cancer Patients2023 | First Faculty of Medicine
- Germline mutations in RAD51C and RAD51D and hereditary predisposition to ovarian cancer2021 | First Faculty of Medicine
- Polygenic risk score (PRS) and its potential for breast cancer risk stratification2023 | First Faculty of Medicine
- Development of Soft Tissue Sarcomas in Ribosomal Proteins L5 and S24 Heterozygous Mice2016 | Central Library of Charles University
- Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer2015 | First Faculty of Medicine
- Increased sperm aneuploidy in two male carriers of germline TP53 mutations2011 | Second Faculty of Medicine
- Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTEN gene mutation in a patient with Cowden syndrome: Case report2011 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients2021 | 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
- Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTEN gene mutation in a patient with Cowden syndrome: Case report2011 | Second Faculty of Medicine
- Nibrin, a novel DNA double-strand break repair protein, is mutated in nijmegen breakage syndrome1998 | Second Faculty of Medicine
- Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents2016 | Second Faculty of Medicine
- Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia2007 | Second Faculty of Medicine
- Bone Marrow Transplantation for Inherited Bone Marrow Failure Syndromes2010 | Second Faculty of Medicine
- Li-Fraumeni Syndrome2003 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- The DNA methylome of cervical cells can predict the presence of ovarian cancer2022 | First Faculty of Medicine
- The TP53 gene promoter is not methylated in families suggestive of Li-Fraumeni syndrome with no germline TP53 mutations2009 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine