- Effects of alkylating agents on lymphocytes from controls and from patients with Fanconi's anemia - Studies of sister chromatid exchanges, chromosome aberrations, and kinetics of cell division1979 | Second Faculty of Medicine
- Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children2016 | Second Faculty of Medicine
- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene - Case Report2016 | Second Faculty of Medicine
- Fanconi anemia in the Czech Republic: Role of HSCT and long-term follow-up2020 | Second Faculty of Medicine
- Hematopoietic stem cell transplantation in patients with Fanconi anemia for bone marrow failure in the Czech Republic and Slovakia (2005-2016)2020 | Second Faculty of Medicine
- CRISPR/Cas9-Mediated Correction of the FANCD1 Gene in Primary Patient Cells2017 | Second Faculty of Medicine
- Outcomes after related and unrelated umbilical cord blood transplantation for hereditary bone marrow failure syndromes other than Fanconi anemia2011 | Second Faculty of Medicine
- Hypersensitivity to chemoradiation in FANCA carrier with cervical carcinoma - A case report and review of the literature2015 | Faculty of Medicine in Hradec Králové
- Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic2015 | First Faculty of Medicine
- Model of abasic site DNA cross-link repair; from the architecture of NEIL3 DNA binding domains to the X-structure model2022 | Central Library of Charles University, Faculty of Science
- A Rare Truncating BRCA2 Variant and Genetic Susceptibility to Upper Aerodigestive Tract Cancer2015 | First Faculty of Medicine
- Bone Marrow Transplantation for Inherited Bone Marrow Failure Syndromes2010 | Second Faculty of Medicine
- Sequential cytogenetic study of patients after bone marrow transplantation1994 | Second Faculty of Medicine
- Premature chromosome condensation in humans associated with microcephaly and mental retardation: A novel autosomal recessive condition2002 | Central Library of Charles University
- Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients2016 | First Faculty of Medicine
- DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population2021 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Central Library of Charles University
- Hematopoietic stem cells of lower-risk MDS patients with rapid progression show quiescent-like cell state similar to that of higher-risk MDS cellsPublication without faculty affiliation
- DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations2021 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Central Library of Charles University