Publications
- Germline mutations 657del5 and 643C > T (R215W) in NBN are not likely to be associated with increased risk of breast cancer in Czech women2012 | First Faculty of Medicine
- The clinical importance of a genetic analysis of moderate-risk cancer susceptibility genes in breast and other cancer patients from the Czech Republic2012 | First Faculty of Medicine
- Prerequisites for preimplantation genetic diagnosis (PGD in carriers of mutations responsible for hereditary cancers2009 | First Faculty of Medicine, Third Faculty of Medicine
- Low Frequency of Cancer-Predisposition Gene Mutations in Liver Transplant Candidates with Hepatocellular Carcinoma2023 | First Faculty of Medicine, Central Library of Charles University, Faculty of Science
- Germline multigene panel testing of patients with endometrial cancer2023 | First Faculty of Medicine, Faculty of Medicine in Pilsen, Faculty of Science
- Importance of Germline and Somatic Alterations in Human MRE11, RAD50, and NBN Genes Coding for MRN Complex2023 | First Faculty of Medicine, Faculty of Science
- ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk2023 | First Faculty of Medicine, Central Library of Charles University
- Classification of germline variants identified in cancer predisposition genetic testing - consensus of the CZECANCA consortium2023 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- Polygenic risk score (PRS) and its potential for breast cancer risk stratification2023 | First Faculty of Medicine
- Early-Onset Ovarian Cancer <30 Years: What Do We Know about Its Genetic Predisposition?2023 | First Faculty of Medicine
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