Viktor Stranecky

11PUBLICATIONS
155CO-AUTHORS
Cell and nuclear divisionEpidemiological modellingMedical molecular engineering of nucleic acids and proteinsGene expression (incl. microarray and other genome-wide approaches)Optical technology
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Publications (11)

|Aug 20, 2026
Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

|Jul 01, 2026
De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity.

|Apr 10, 2026
Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Alena Vrbacká, Anna Přistoupilová, Kendrah O Kidd

|Feb 27, 2026
Analyses of ATP7B mRNA in Nasopharyngeal Swab Samples Increase Yields of Wilson Disease Molecular Genetic Diagnostics.

Lenka Steiner Mrázová, Alena Vrbacká, Filip Majer

|Apr 14, 2025
Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy.

Lubica Dudakova, Lenka Noskova, Stanislav Kmoch

|Jun 29, 2024
Sodium-glucose cotransporter 2 inhibitors induce anti-inflammatory and anti-ferroptotic shift in epicardial adipose tissue of subjects with severe heart failure.

Barbora Judita Kasperova, Milos Mraz, Petr Svoboda

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Frequent Collaborators

4 joint publications

Hana Hartmannová

4 joint publications

Lenka Steiner-Mrázová

4 joint publications

Lenka Nosková

4 joint publications

Stanislav Kmoch