- Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene - Case Report2016 | Second Faculty of Medicine
- CRISPR/Cas9-Mediated Correction of the FANCD1 Gene in Primary Patient Cells2017 | 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 in the Czech Republic: Role of HSCT and long-term follow-up2020 | Second Faculty of Medicine