Publications
- Diagnosis of laminopathy with predominant cardiac involvement during pretransplant assessment-a case report with a review of risk stratification and disease management of laminopathies2022 | Second Faculty of Medicine, Central Library of Charles University
- Complex approach towards patients with hypertrophic cardiomyopathy and indications to genetic testing2020 | Second Faculty of Medicine, Central Library of Charles University
- 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
- Quantitative fluorescent polymerase chain reaction (QFPCR) in the prenatal and postnatal diagnosis of the most frequent aneuploide2003 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Medical genetics in reproductive medicine2002 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Increased frequency of deltaF508 mutation carriers in men with non-obstructive azoospermia1999 | Second Faculty of Medicine
- Complex cytogenetic and molecular genetic diagnostics of congenital heart defectsPublication without faculty affiliation
- Post-mortem genetic testing in sudden cardiac death and genetic screening of relatives at risk: lessons learned from a Czech pilot multidisciplinary study2023 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Hradec Králové, Faculty of Medicine in Pilsen
- Postmortem genetic testing in sudden cardiac death victims and genetic screening of relatives at risk in the Czech Republic2023 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Hradec Králové
- PRKAG2 syndrome as a highly arrhythmogenic eventuality in the differential diagnosis of hypertrophic cardiomyopathy - an example of two families with a confirmed causative DNA variant2023 | Second Faculty of Medicine, Central Library of Charles University
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