Wallid Deb

10PUBLICATIONS
206CO-AUTHORS
Genome structure and regulationMedical mycologyNeurogeneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (10)

|Sep 16, 2026
De novo variants in the poly(rC)-binding protein gene PCBP1 cause a neurodevelopmental disorder.

|Apr 21, 2026
Revisiting LSDMCA: male lethality escape and genotype-phenotype correlations.

|Dec 19, 2025
DE NOVO VARIANTS IN THE POLY(RC)-BINDING PROTEIN GENE PCBP1 CAUSE A NEURODEVELOPMENTAL DISORDER.

Wallid Deb, Thomas Besnard, Florence Desprez

|Nov 26, 2025
Investigating the neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.

Sébastien Küry, Janelle E Stanton, Geeske M van Woerden

|Nov 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

Ghayda M Mirzaa, Keqin Yan, Raissa Relator

|Sep 17, 2025
Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder.

Jeanne Jury, Thomas Besnard, Wallid Deb

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Frequent Collaborators

6 joint publications

Benjamin Cogné

5 joint publications

Frédéric Laumonnier

5 joint publications

Stéphane Bézieau

5 joint publications

Sébastien Küry