- FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism2010 | First Faculty of Medicine
- Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR11995 | Second Faculty of Medicine
- Concomitancy of mutation in FRDA gene and FMR1 premutation in 58 year-old woman2005 | Second Faculty of Medicine
- Genetic Study of Twenty Patients with Autism Spectrum Disorders2002 | Second Faculty of Medicine
- Syndrome of the fragile x chromosome with Tremor/Ataxia (FXTAS): a pilot study in a group of patients with ataxia of unknown aetiology2007 | Second Faculty of Medicine
- FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism2010 | Second Faculty of Medicine
- Different Manifestations of the Fragile X Chromosome Syndrome and Their Causes2007 | Second Faculty of Medicine
- Syndrome of the fragile X Chromosome with tremor/ataxia (FXTAS): a pilot study in a group of patients with ataxia of unknown aetiology2007 | First Faculty of Medicine
- Expanded DMPK repeats in dizygotic twins referred for diagnosis of autism versus absence of expanded DMPK repeats at screening of 330 children with autism2016 | Second Faculty of Medicine
- Genetic insights into biological mechanisms governing human ovarian ageing2021 | Faculty of Science
- Genomic Structure of Hstx2 Modifier of Prdm9-Dependent Hybrid Male Sterility in Mice2019 | Second Faculty of Medicine, Faculty of Science, Central Library of Charles University
