- Both 17q12 duplication and deletion detected in the patient with normal phenotype and their segregation in family with variably affected members2020 | Second Faculty of Medicine
- The role of retrotransposons in gene family expansions: insights from the mouse Abp gene family2013 | Faculty of Science
- On the Limits of Fundamental Rights in the Czech Republic2018 | Faculty of Law
- Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability2010 | Second Faculty of Medicine