- Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population2005 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia2009 | Second Faculty of Medicine
- EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus2013 | Second Faculty of Medicine
- High prevalence of the IVS 1+1 G to A/GJB2 mutation among Czech hearing impaired patients with monoallelic mutation in the coding region of GJB22006 | Second Faculty of Medicine