Claudio Peter D'Incal

10PUBLICATIONS
14CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Nanoelectromechanical systemsDevelopmental genetics (incl. sex determination)Molecular targets
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Publications (10)

|Jan 28, 2026
A Systematic Review Illustrates the Expanding Clinical and Molecular Landscape of Helsmoortel-Van der Aa Syndrome.

Lusine Harutyunyan, Claudio P D'Incal, Anna C Jansen

|Nov 01, 2025
ADNP Exhibits Methyltransferase Activity in Overexpression Systems and Modulates DNA and Histone Methylation.

Claudio Peter D'Incal, Kirsten Esther Van Rossem, Elisa Cappuyns

|Oct 21, 2025
A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.

Claudio Peter D'Incal, Bram Dierckx, Claudia Vingerhoets

|Apr 18, 2024
ADNP dysregulates methylation and mitochondrial gene expression in the cerebellum of a Helsmoortel-Van der Aa syndrome autopsy case.

Claudio D'Incal, Anke Van Dijck, Joe Ibrahim

|Feb 29, 2024
Loss-of-function of activity-dependent neuroprotective protein (ADNP) by a splice-acceptor site mutation causes Helsmoortel-Van der Aa syndrome.

Claudio Peter D'Incal, Dale John Annear, Ellen Elinck

|Jan 25, 2024
Identification of a DLG3 stop mutation in the MRX20 family.

Jolien Huyghebaert, Ligia Mateiu, Ellen Elinck

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