- Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia2015 | First Faculty of Medicine
- Exome sequencing for identification of disease genes for rare syndromes. Experiences from Hamburg2014 | Second Faculty of Medicine
- Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing2020 | Faculty of Medicine in Pilsen
- Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer2022 | Faculty of Medicine in Pilsen
- Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer2022 | Faculty of Medicine in Pilsen
- A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer2021 | Faculty of Medicine in Pilsen
- Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders2024 | Second Faculty of Medicine
- Prot2HG: a database of protein domains mapped to the human genome2020 | Second Faculty of Medicine
- Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer2021 | Faculty of Medicine in Pilsen