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American Journal of Medical Genetics. Part A|April 17, 2008
Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardationAline Dubos, Solange Pannetier, André Hanauer
Current Opinion in Neurobiology|April 24, 2010
Signaling mechanisms regulating synapse formation and function in mental retardationBernadett Boda, Aline Dubos, Dominique Muller
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 13, 2012
Alteration of synaptic network dynamics by the intellectual disability protein PAK3Aline Dubos, Gaelle Combeau, Yann Bernardinelli, et al.
Scientific Reports|December 24, 2017
Integrated transcriptional analysis unveils the dynamics of cellular differentiation in the developing mouse hippocampusGiovanni Iacono, Marco Benevento, Aline Dubos, et al.
Human Mutation|April 10, 2026
Cellular Functional Analyses of ARX Variants Reveal New Insights Into Genotype-Phenotype Correlations in Neurodevelopmental Disorders Among Male and Female PatientsRasha Faraj, Audrey Farrugia, Anna C E Hurst, et al.
Biomedicines|December 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse ModelsHamid Meziane, Marie-Christine Birling, Olivia Wendling, et al.
Molecular Psychiatry|July 9, 2025
Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesisMaria Victoria Hinckelmann, Aline Dubos, Victorine Artot, et al.
Nucleic Acids Research|March 20, 2018
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndromeGiovanni Iacono, Aline Dubos, Hamid Méziane, et al.
Human Molecular Genetics|April 17, 2018
A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterationsAline Dubos, Hamid Meziane, Giovanni Iacono, et al.
Scientific Reports|August 31, 2017
Atp6ap2 ablation in adult mice impairs viability through multiple organ deficienciesOlivia Wendling, Marie-France Champy, Solène Jaubert, et al.
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