Spectrum and frequencies of non <scp> <i>GJB2</i> </scp> gene mutations in Czech patients with early non‐syndromic hearing loss detected by gene panel NGS and whole‐exome sequencingDana Šafka Brožková, Pavel Seeman, Simona Poisson Marková et al.|Clinical Genetics|2020Cited by 35
<i>STRC</i> Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech PopulationSimona Poisson Marková, Pavel Seeman, Dana Šafka Brožková et al.|Genetic Testing and Molecular Biomarkers|2018Cited by 26
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—A Comprehensive Study of the GJB2/DFNB1 RegionDana Šafka Brožková, Pavel Seeman, Anna Uhrová Mészárosová et al.|Genes|2021Cited by 21
Mutations in eight small DFNB genes are not a frequent cause of non-syndromic hereditary hearing loss in Czech patientsSimona Poisson Marková, Pavel Seeman, Jana Neupauerová et al.|International Journal of Pediatric Otorhinolaryngology|2016Cited by 17
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variantDana Šafka Brožková, Pavel Seeman, Lukáš Varga et al.|Orphanet Journal of Rare Diseases|2020Cited by 15