- Examination ofthe Gene for Connexin 26 in Czech Patients with Congenital Autosomal Recessive Non-SyndromicHearing Loss2002 | Second Faculty of Medicine
- Connnexin 26 in children with cochlear implant2002 | Second Faculty of Medicine, Central Library of Charles University
- Spectrum of mutations in CX 26 gene in 142 patients with congenital nonsyndromic hearing loss2003 | Second Faculty of Medicine, Central Library of Charles University
- Spectrum of Mutations in the Connexin 26 Gene among 142 Patients with Congenital Deafness in Czech Republic.2003 | Second Faculty of Medicine
- Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness2004 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene2009 | Second Faculty of Medicine
- 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 and Degree of Hearing Loss: A Multicenter Study2005 | 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
- GJB2 Mutations in Patients with Nonsyndromic Hearing Loss from Croatia2009 | Second Faculty of Medicine
- Pendred syndrome in the Czech Republic2011 | Second Faculty of Medicine, First Faculty of Medicine
- Hearing Function in Heterozygous Carriers of a Pathogenic GJB2 Gene Mutation2013 | Second Faculty of Medicine