- Introduction of molecular genetic diagnosis in syndromes with a hearing defect1998 | Second Faculty of Medicine
- Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young2008 | Second Faculty of Medicine
- Molecular genetic diagnosis of polycystic kidney disease and autosomal dominant type2002 | Publication without faculty affiliation
- Current possibilities of prenatal and postnatal molecular genetic diagnosis of cystic fibrosis in the Czech and Slovak Republics1997 | Central Library of Charles University, Second Faculty of Medicine
- Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders - updated European recommendations2009 | Second Faculty of Medicine
- Molecular genetic diagnosis of congenital contracture arachnodactyly and complex treatment of a Czech girl: a case study2023 | First Faculty of Medicine
- New options of expensive pneumo-oncological therapy for advanced non-small-cell lung carcinoma (NSCLC) in the first line based on morphological and molecular genetic diagnosis in the Czech Republic2012 | Central Library of Charles University, Faculty of Medicine in Pilsen, First Faculty of Medicine
- New emerging entities: renal tumors described after WHO Classification 20162020 | Faculty of Medicine in Pilsen
- Contemporary State of the Diagnosis of Cystic Fibrosis1999 | Second Faculty of Medicine
- Alports's Syndrome and Benign Familial Haematuria1999 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Microdeletions of the Y Chromosome in Czech Males with Serious Reproductive Disorders2003 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Stay in touch with the medicine and on maternity leave2008 | Second Faculty of Medicine
- Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom2015 | Second Faculty of Medicine
- Czech Association for Preventive Cardiology Expert Consensus Statement on the State of Genetic Testing for Inherited Cardiovascular Diseases2023 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Current and Future Therapeutical Options in Alport Syndrome2023 | First Faculty of Medicine
- DNA diagnostics of Friedrich's ataxia1997 | Second Faculty of Medicine
- Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia2012 | Faculty of Medicine in Pilsen