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Human Molecular Genetics|November 15, 2011
A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-AAurelie Carabalona, Shirley Beguin, Emilie Pallesi-Pocachard, et al.
Journal of Neuroinflammation|November 16, 2024
Cytomegalovirus infection of the fetal brain: intake of aspirin during pregnancy blunts neurodevelopmental pathogenesis in the offspringSarah Tarhini, Carla Crespo-Quiles, Emmanuelle Buhler, et al.
Neurobiology of Disease|June 9, 2024
FLNA regulates neuronal maturation by modulating RAC1-Cofilin activity in the developing cortexAntonio Falace, Lea Corbieres, Catia Palminha, et al.
Human Molecular Genetics|October 13, 2025
Mosaic expression of SLC35A2 pathogenetic variants impairs neuronal migration and dendritogenesis in the developing cortexAntonio Falace, Léa Corbières, Lucas Silvagnoli, et al.
Plos One|July 30, 2016
Cytomegalovirus Infection of the Rat Developing Brain In Utero Prominently Targets Immune Cells and Promotes Early Microglial ActivationRobin Cloarec, Sylvian Bauer, Hervé Luche, et al.
Frontiers in Cellular Neuroscience|March 22, 2018
In Utero Administration of Drugs Targeting Microglia Improves the Neurodevelopmental Outcome Following Cytomegalovirus Infection of the Rat Fetal BrainRobin Cloarec, Sylvian Bauer, Natacha Teissier, et al.
Journal of Visualized Experiments : Jove|December 30, 2017
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain MalformationsValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
Brain : a Journal of Neurology|September 24, 2013
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneValerio Conti, Aurelie Carabalona, Emilie Pallesi-Pocachard, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disabilityAnne-Laure Mosca-Boidron, Lucie Gueneau, Guillaume Huguet, et al.
Molecular Psychiatry|June 30, 2021
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neuronsKaren Runge, Rémi Mathieu, Stéphane Bugeon, et al.
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