Publications
- Microsatellite Instability in Non-Endometrioid Ovarian Epithelial Tumors: A study of 400 cases Comparing Immunohistochemistry, PCR, and NGS Based Testing with Mutation Status of MMR Genes2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- Analysis of expression, epigenetic, and genetic changes of HNF1B in 130 kidney tumours2020 | First Faculty of Medicine
- Germline mutation in the TP53 gene in uveal melanoma2018 | Faculty of Physical Education and Sport, First Faculty of Medicine
- Somatic genomic and transcriptomic characterization of primary ovarian serous borderline tumors and low-grade serous carcinomas2024 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Third Faculty of Medicine
- A comprehensive molecular analysis of 113 primary ovarian clear cell carcinomas reveals common therapeutically significant aberrations2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- HER2 status as a potential predictive biomarker for ovarian clear cell carcinoma2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- Primary Mucinous Tumors of the Ovary: An Interobserver Reproducibility and Detailed Molecular Study Reveals Significant Overlap Between Diagnostic Categories2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- Refined criteria for p53 expression in ovarian mucinous tumours are highly concordant with TP53 mutation status, but p53 expression/TP53 status lack prognostic significance2023 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- Uterine cellular leiomyomas are characterized by common HMGA2 aberrations, followed by chromosome 1p deletion and MED12 mutation: morphological, molecular, and immunohistochemical study of 52 cases2022 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Gynecological lesions in hereditary cancer predisposition syndromes2021 | First Faculty of Medicine, Second Faculty of Medicine
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