Dana Safka-Brozkova

6PUBLICATIONS
9CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Medical infection agents (incl. prions)NeurogeneticsNeurology and neuromuscular diseases
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Publications (6)

|Jun 30, 2025
Reanalysis of Next-Generation Sequencing Data to Detect Tandem Repeat Expansions in 1,106 Czech Probands With Neurologic Disease.

Alena Musilova, Petra Lassuthova, Anna Uhrova Meszarosova

|Jan 23, 2023
A progressive KY myopathy could be caused by a missense pathogenic variant.

Anna Uhrova-Meszarosova, Marketa Vlckova, Ladislava Rennerova

|Jun 02, 2021
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes-A Comprehensive Study of the GJB2/DFNB1 Region.

Dana Safka Brozkova, Anna Uhrova Meszarosova, Petra Lassuthova

|Aug 30, 2020
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 sequencing.

Dana Safka Brozkova, Simona Poisson Marková, Anna Uhrová Mészárosová

|Aug 28, 2020
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 variant.

Dana Safka Brozkova, Lukas Varga, Anna Uhrova Meszarosova

|Aug 07, 2020
Demyelinating Charcot-Marie-Tooth neuropathy associated with FBLN5 mutations.

D Safka Brozkova, T Stojkovic, J Haberlová

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Frequent Collaborators

3 joint publications

Anna Uhrova-Meszarosova

1 joint publications

M Auer-Grumbach

1 joint publications

Daniela Gašperíková

1 joint publications

Alena Musilova