Publications by authors named "M G Heulin"

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De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.
Samuel M Bradbrook, Gail Graham, Melissa T Carter, Maria Kibaek, Christina Fagerberg, Mathilde Heulin

Am J Med Genet A· January 2026

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Systematic analysis of snRNA genes reveals frequent variants in dominant and recessive developmental and epileptic encephalopathies.
Elsa Leitão, Amandine Santini, Benjamin Cogne, Myriam Essid, Maria Athanasiadou, Mathilde Heulin

medRxiv· September 2025

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NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder.
J Lévy, S Grotto, C Mignot, A Maruani, A Delahaye-Duriez, M Heulin

Clin Genet· August 2018

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[Association between the presence of antiphospholipid antibodies and the occurrence of autism spectrum disorder in childhood].
F Lageix, P Nicaise-Roland, M Houlier, P Zylberberg, M Dubrel, M Heulin

Arch Pediatr· November 2015

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[Complications of autism].
L de Pontual, M Heulin, E Charles, B Héron, P Zylberberg

Arch Pediatr· May 2015

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