- Hereditary aetiology of cancer diseases and the importance of genetic counselling and testing in oncology2006 | Second Faculty of Medicine
- Unique characteristics of informed consent in clinical genetics and genetic counselling2019 | Second Faculty of Medicine, Faculty of Medicine in Pilsen
- Genetic counseling and fetal Medicíne2007 | First Faculty of Medicine
- Ethical and psychosocial problems in children with kidney disease2011 | Second Faculty of Medicine
- Risk Calculation in Genetic Counselling of Neuromuscular Disorders +12002 | Second Faculty of Medicine
- Ethical problems and genetic counselling2000 | First Faculty of Medicine
- Current ethical problems in genetic counseling1998 | Second Faculty of Medicine
- Genetic counselling and follow-up by patients and related with hereditable rick tumours GITPublication without faculty affiliation
- Cooperation between genetic counseling centers, cytogenetic laboratories and fertilization centers in the treatment of reproductive disorders2000 | First Faculty of Medicine
- Informing patients about their mutation tests: CDKN2A c.256G>A in melanoma as an example2020 | Faculty of Medicine in Pilsen
- Psychosocial Impact of Huntington's Disease and Incentives to Improve Care for Affected Families in the Underserved Region of the Slovak Republic2022 | First Faculty of Medicine, Third Faculty of Medicine
- Genetic Variants in Patients with Multiple Head and Neck Paragangliomas: Dilemma in Management2021 | First Faculty of Medicine, Third Faculty of Medicine
- European experts consensus: BRCA/homologous recombination deficiency testing in first-line ovarian cancerPublication without faculty affiliation
- Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations2005 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Localized mosaic neurofibromatosis type 12022 | Second Faculty of Medicine
- Genetics and ethics - past, present, and future +12005 | Publication without faculty affiliation
- Duchennes myopathy and its prenatal diagnostic2006 | First Faculty of Medicine
- Von Hippel-Lindau disease2009 | First Faculty of Medicine
- Molecular biology in medicine2007 | Second Faculty of Medicine
- Clinical and biochemical characterization of syndromes associated with defects of the insulin receptor1992 | Second 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
- Current Diagnostic Strategies and Overview of Preimplantation, Prenatal and Postnatal DNA Diagnostics of Cystic Fibrosis in the Czech Republic2008 | Second Faculty of Medicine, Third Faculty of Medicine
- Inborn Metabolic Diseases in Childhood2013 | First Faculty of Medicine
- Congenital muscular dystrophies +12012 | Second Faculty of Medicine
- Hereditary ichtyoses2014 | Second Faculty of Medicine
- X-linked Hypogammaglobulinaemia (Bruton´s Disease) - Three Case Studies and Molecular Genetic Studies in Their Families2004 | First Faculty of Medicine
- Female Reproductive System and Cancer2017 | Publication without faculty affiliation