Marketa Wayhelova

5PUBLICATIONS
0CO-AUTHORS
Genetic immunologyNeonatologyNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

|Oct 23, 2025
Intragenic TTN Deletions in a Single Family with Dilated Cardiomyopathy.

Marketa Wayhelova, Petra Peldova, Alice Krebsova

|Feb 06, 2024
Exome sequencing improves the molecular diagnostics of paediatric unexplained neurodevelopmental disorders.

Marketa Wayhelova, Vladimira Vallova, Petr Broz

|Nov 25, 2021
Novel de novo pathogenic variant in the GNAI1 gene as a cause of severe disorders of intellectual development.

Marketa Wayhelova, Vladimira Vallova, Petr Broz

|Jun 22, 2020
Novel familial IQSEC2 pathogenic sequence variant associated with neurodevelopmental disorders and epilepsy.

Marketa Wayhelova, Michal Ryzí, Jan Oppelt

|Jul 25, 2019
The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.

Marketa Wayhelova, Jan Smetana, Vladimira Vallova

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