- GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia2009 | Second Faculty of Medicine
- Spectrum of mutations in CX 26 gene in 142 patients with congenital nonsyndromic hearing loss2003 | Second Faculty of Medicine, Central Library of Charles University
- Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes2020 | Second Faculty of Medicine, Central Library of Charles University, First Faculty of Medicine
- Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene2019 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study2005 | Second Faculty of Medicine
- Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general gypsy population and individual subisolates2007 | Second Faculty of Medicine