- 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
- Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer2022 | Faculty of Medicine in Pilsen
- CHEK2 Germline Variants in Cancer Predisposition: Stalemate Rather than Checkmate2020 | First Faculty of Medicine
- Rare deleterious germline variants and risk of lung cancer2021 | Second Faculty of Medicine
- Characterization of rare germline variants in familial multiple myeloma2021 | Faculty of Medicine in Pilsen
- Germline Variants of CYBA and TRPM4 Predispose to Familial Colorectal Cancer2022 | Faculty of Medicine in Pilsen
- A novel c. 204 Ile68Met germline variant in exon 2 of the mutL homolog 1 gene in a colorectal cancer patient2015 | First Faculty of Medicine
- Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer2009 | Second Faculty of Medicine
- Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium2023 | First Faculty of Medicine, 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
- Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer2021 | 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
- Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing2020 | Faculty of Medicine in Pilsen
- Genetic insights into biological mechanisms governing human ovarian ageing2021 | Faculty of Science
- JAK2 p.G571S in B-cell precursor acute lymphoblastic leukemia: a synergizing germline susceptibility2019 | Second Faculty of Medicine
- Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors2014 | First Faculty of Medicine
- Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases2019 | Second Faculty of Medicine
- Recommendations for whole genome sequencing in diagnostics for rare diseases2022 | Second Faculty of Medicine
- Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular Carcinoma2023 | First Faculty of Medicine, Faculty of Science, Central Library of Charles University
- Germline and somatic genetic variability of oxysterol-related genes in breast cancer patients with early disease of the luminal subtype2022 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Medicine in Pilsen
- Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma2023 | Faculty of Medicine in Pilsen
- Pharmacogenomics to Predict Tumor Therapy Response: A Focus on ATP-Binding Cassette Transporters and Cytochromes P4502020 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder2022 | Second Faculty of Medicine
- DNA Mismatch Repair Gene Variants in Sporadic Solid Cancers2020 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Science, Central Library of Charles University
- Role of Genetic Variation in ABC Transporters in Breast Cancer Prognosis and Therapy Response2020 | Faculty of Medicine in Pilsen
- Role of Genetic Variation in Cytochromes P450 in Breast Cancer Prognosis and Therapy Response2021 | Faculty of Medicine in Pilsen
- Germline SUCLG2 Variants in Patients With Pheochromocytoma and Paraganglioma2022 | Faculty of Science, Central Library of Charles University
- Newly designed 11-gene panel reveals first case of hereditary amyloidosis captured by massive parallel sequencing2018 | Second Faculty of Medicine
- Somatic genetic alterations in a large cohort of pediatric thyroid nodules2019 | Second Faculty of Medicine