Kinga Hadzsiev

14PUBLICATIONS
38CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cell and nuclear divisionNeurology and neuromuscular diseasesCancer geneticsInfant and child health
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Publications (14)

|Dec 11, 2025
Heterogeneity of Orodental Features in a Family with Noonan Syndrome.

Gréta Antal, Laura Csabai, Anna Zsigmond

|Sep 27, 2025
Uncovering Rare Structural Chromosomal Rearrangements: Insights from Molecular Cytogenetics.

Márta Czakó, András Szabó, Ágnes Till

|Jan 25, 2025
Increased Phenotype Severity Associated with Splice-Site Variants in a Hungarian Pediatric Neurofibromatosis 1 Cohort: A Retrospective Study.

Klára Veres, Benedek Nagy, Zsófia Ember

|Nov 09, 2024
Molecular and Clinical Heterogeneity in Hungarian Patients with Treacher Collins Syndrome-Identification of Two Novel Mutations by Next-Generation Sequencing.

Gréta Antal, Anna Zsigmond, Ágnes Till

|Jun 19, 2024
NGS-Based Identification of Two Novel PCDH19 Mutations in Female Patients with Early-Onset Epilepsy.

Renata Szalai, Kinga Hadzsiev, Agnes Till

|Jun 19, 2024
Case Report of Suspected Gonadal Mosaicism in FOXP1-Related Neurodevelopmental Disorder.

Anna Zsigmond, Ágnes Till, Judit Bene

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Frequent Collaborators

10 joint publications

Judit Bene

2 joint publications

András Szabó

2 joint publications

Márta Czakó

2 joint publications

Anita Maász