Raphael Helaers

8PUBLICATIONS
52CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsOptical properties of materialsOptical technologyAboriginal and Torres Strait Islander not-for-profit social enterprises
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Publications (8)

|Nov 06, 2024
Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC).

Peyman Ranji, Eleonore Pairet, Raphael Helaers

|Feb 07, 2024
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants.

Martina De Bortoli, Marta Ivars, Nicole Revencu

|Nov 06, 2023
Molecular investigation in individuals with orofacial clefts and microphthalmia-anophthalmia-coloboma spectrum.

Milena Atique Tacla, Matheus de Mello Copelli, Eleonore Pairet

|Apr 28, 2023
SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review.

Matheus de Mello Copelli, Eleonore Pairet, Milena Atique-Tacla

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