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Wallid Deb

9PUBLICATIONS

203CO-AUTHORS

Medical mycologyNeurogeneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)

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Publications (9)

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|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 <i>PCBP1</i> 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 <i>GTF2I</i> at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder.

Jeanne Jury, Thomas Besnard, Wallid Deb

|Dec 12, 2024

Further delineation of the SCAF4-associated neurodevelopmental disorder.

Cosima M Schmid, Anne Gregor, Anna Ruiz

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Frequent Collaborators

6 joint publications

Benjamin Cogné

4 joint publications

Frédéric Laumonnier

4 joint publications

Stéphane Bézieau

4 joint publications

Frédéric Ebstein

4 joint publications

Sébastien Küry

3 joint publications

Tzung-Chien Hsieh

3 joint publications

Elke Hammer

3 joint publications

Victoria Most

3 joint publications

Geeske van Woerden

3 joint publications

Thomas Besnard

Frequent Collaborators

6 joint publications

Benjamin Cogné

4 joint publications

Frédéric Laumonnier

4 joint publications

Stéphane Bézieau

4 joint publications

Frédéric Ebstein

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