Publications
- A rare large duplication of MLH1 identified in Lynch syndrome2021 | Faculty of Medicine in Pilsen
- Characterization of rare germline variants in familial multiple myeloma2021 | Faculty of Medicine in Pilsen
- Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer2021 | Faculty of Medicine in Pilsen
- Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer2021 | 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
- Family History of Head and Neck Cancers2021 | Faculty of Medicine in Pilsen
- Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer2021 | Faculty of Medicine in Pilsen
- Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing2020 | Faculty of Medicine in Pilsen
- Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example2020 | Faculty of Medicine in Pilsen
- A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer2020 | Faculty of Medicine in Pilsen
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