- Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation2016 | Second Faculty of Medicine
- European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe2022 | Second Faculty of Medicine
- Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey2022 | Second Faculty of Medicine
- A restricted spectrum of NRAS mutations causes Noonan syndrome2010 | Second Faculty of Medicine
- Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 12021 | Second Faculty of Medicine
- Prenatal phenotype of RASopathies2020 | Publication without faculty affiliation
- The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered2021 | Second Faculty of Medicine
- Alterations in key signaling pathways in sinonasal tract melanoma. A molecular genetics and immunohistochemical study of 90 cases and comprehensive review of the literature2022 | Faculty of Medicine in Pilsen