- First report for SLC26A4 gene for czech patients with non-syndromic hearing lossPublication without faculty affiliation
- Spectrum and Frequency of SLC26A4 Mutations Among Czech Patients with Early Hearing Loss with and without Enlarged Vestibular Aqueduct (EVA)2010 | Second Faculty of Medicine, Central Library of Charles University
- Pendred syndrome in the Czech Republic2011 | Second Faculty of Medicine, First Faculty of Medicine
- Pendrin and its role in the pathogenesis of congenital hypothyroidism and other diseases2006 | Second Faculty of Medicine, Third Faculty of Medicine
- Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing2020 | Second Faculty of Medicine, First Faculty of Medicine
