Dorota Wicher

7PUBLICATIONS
25CO-AUTHORS
NeonatologyEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Adolescent health
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Publications (7)

|Jul 28, 2026
PURA-Related Neurodevelopmental Disorder: Insight from Eight New Cases.

|Mar 28, 2026
Epilepsy as a Component of the Dysmorphic-Neurodevelopmental Phenotype in Pediatric Patients with Recurrent Copy Number Variants.

Marlena Młynek, Dorota Wicher, Agata Cieślikowska

|Feb 27, 2026
Molecular Profiling of Polish Pediatric Patients with Epilepsy: A Single-Center Diagnostic Experience Using Next-Generation Sequencing.

Beata Chałupczyńska, Elżbieta Ciara, Paulina Halat-Wolska

|Oct 29, 2025
Rubinstein-Taybi Syndrome: A Comprehensive Analysis of a Polish Cohort with Most Cases Due to Novel CREBBP and EP300 Variants.

Agata Cieślikowska, Agnieszka Madej-Pilarczyk, Piotr Iwanowski

|Feb 26, 2025
Molecular Review of Suspected Alport Syndrome Patients-A Single-Centre Experience.

Paulina Halat-Wolska, Elżbieta Ciara, Michał Pac

|Apr 30, 2020
Breakpoint Mapping of Symptomatic Balanced Translocations Links the EPHA6, KLF13 and UBR3 Genes to Novel Disease Phenotype.

Victor Murcia Pienkowski, Marzena Kucharczyk, Małgorzata Rydzanicz

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Frequent Collaborators

5 joint publications

Krystyna Chrzanowska

4 joint publications

Paulina Halat-Wolska

4 joint publications

Elżbieta Ciara

4 joint publications

Agnieszka Madej-Pilarczyk