Jonathan Levy

29PUBLICATIONS
368CO-AUTHORS
Child and adolescent developmentNeurogeneticsNeurology and neuromuscular diseasesMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)
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Publications (29)

|Sep 09, 2026
Clinical and Genetic Factors Associated With Regression in Children With Autism Spectrum Disorders.

|Jul 27, 2026
Further characterization of the BRSK2-associated neurodevelopmental disorder.

|Jul 24, 2026
Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

|May 30, 2026
COXFA4L2 upregulation preserves residual cytochrome c oxidase activity in COXFA4-related Leigh-like encephalopathy.

|Apr 09, 2026
Identification of an episignature for CHD3-related Snijders Blok-Campeau syndrome reveals heterogeneity in the CHARGE syndrome episignature: towards a better characterisation of chromatinopathies.

Amandine Santini, Angelo Tognon, Anne-Claire Richard

|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

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Frequent Collaborators

12 joint publications

Alain Verloes

8 joint publications

Anne-Sophie Denommé-Pichon

7 joint publications

Marlène Rio

6 joint publications

Anne-Claude Tabet