| Polarity complex proteins E Assémat, E Bazellières, E Pallesi-Pocachard, A Le Bivic, ... Biochimica et Biophysica Acta (BBA)-Biomembranes 1778 (3), 614-630, 2008 | 580 | 2008 |
| Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14. 3-q15 deletion C Cardoso, A Boys, E Parrini, C Mignon-Ravix, JM Mcmahon, S Khantane, ... Neurology 72 (9), 784-792, 2009 | 142 | 2009 |
| Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model N Lozovaya, S Gataullina, T Tsintsadze, V Tsintsadze, ... Nature communications 5 (1), 4563, 2014 | 108 | 2014 |
| TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway A Falace, E Buhler, M Fadda, F Watrin, P Lippiello, E Pallesi-Pocachard, ... Proceedings of the National Academy of Sciences 111 (6), 2337-2342, 2014 | 102 | 2014 |
| Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene V Conti, A Carabalona, E Pallesi-Pocachard, E Parrini, RJ Leventer, ... Brain 136 (11), 3378-3394, 2013 | 100 | 2013 |
| A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A A Carabalona, S Beguin, E Pallesi-Pocachard, E Buhler, C Pellegrino, ... Human molecular genetics 21 (5), 1004-1017, 2012 | 76 | 2012 |
| Hook2 is involved in the morphogenesis of the primary cilium CL Baron Gaillard, E Pallesi-Pocachard, D Massey-Harroche, F Richard, ... Molecular biology of the cell 22 (23), 4549-4562, 2011 | 60 | 2011 |
| An epilepsy-related ARX polyalanine expansion modifies glutamatergic neurons excitability and morphology without affecting GABAergic neurons development S Beguin, V Crépel, L Aniksztejn, H Becq, B Pelosi, E Pallesi-Pocachard, ... Cerebral cortex 23 (6), 1484-1494, 2013 | 49 | 2013 |
| A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability AL Mosca-Boidron, L Gueneau, G Huguet, A Goldenberg, C Henry, ... European Journal of Human Genetics 24 (6), 838-843, 2016 | 45 | 2016 |
| Cytomegalovirus Infection of the Rat Developing Brain In Utero Prominently Targets Immune Cells and Promotes Early Microglial Activation R Cloarec, S Bauer, H Luche, E Buhler, E Pallesi-Pocachard, M Salmi, ... PLoS One 11 (7), e0160176, 2016 | 24 | 2016 |
| Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons K Runge, R Mathieu, S Bugeon, S Lafi, C Beurrier, S Sahu, F Schaller, ... Molecular psychiatry 26 (11), 6125-6148, 2021 | 19 | 2021 |
| Hook2, a microtubule-binding protein, interacts with Par6α and controls centrosome orientation during polarized cell migration E Pallesi-Pocachard, E Bazellieres, A Viallat-Lieutaud, MH Delgrossi, ... Scientific Reports 6 (1), 33259, 2016 | 15 | 2016 |
| Early life oxytocin treatment improves thermo-sensory reactivity and maternal behavior in neonates lacking the autism-associated gene Magel2 LC Da Prato, U Zayan, D Abdallah, V Point, F Schaller, ... Neuropsychopharmacology 47 (11), 1901-1912, 2022 | 14 | 2022 |
| Time‐limited alterations in cortical activity of a knock‐in mouse model of KCNQ2‐related developmental and epileptic encephalopathy N Biba‐Maazou, H Becq, E Pallesi‐Pocachard, S Sarno, S Granjeaud, ... The Journal of Physiology 600 (10), 2429-2460, 2022 | 10 | 2022 |
| In Utero Administration of Drugs Targeting Microglia Improves the Neurodevelopmental Outcome Following Cytomegalovirus Infection of the Rat Fetal Brain R Cloarec, S Bauer, N Teissier, F Schaller, H Luche, S Courtens, M Salmi, ... Frontiers in Cellular Neuroscience 12, 55, 2018 | 9 | 2018 |
| Disruption of the transcription factor NEUROD2 causes an autism syndrome via cell-autonomous defects in cortical projection neurons K Runge, R Mathieu, S Bugeon, S Lafi, C Beurrier, S Sahu, F Schaller, ... BioRxiv, 296889, 2018 | 5 | 2018 |
| Quantification of NMDAR Subunit Genes Expression by qRT-PCR. pallesi-pocachard | 1 | 2017 |
| Correction: Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons K Runge, R Mathieu, S Bugeon, S Lafi, C Beurrier, S Sahu, F Schaller, ... Molecular psychiatry 26 (12), 7852-7852, 2021 | | 2021 |
| Characterization and rescue by oxytocin of an atypical thermo-sensory reactivity in neonatal mice lacking the autism-associated gene Magel2 LCD Prato, D Abdallah, V Point, F Schaller, E Pallesi-Pocachard, ... bioRxiv, 869487, 2019 | | 2019 |
| A novel strategy combining array-CGH, whole-exome sequencing and in utero electroporation in rodents to identify causative genes for brain malformations V Conti, A Carabalona, E Pallesi-Pocachard, RJ Leventer, F Schaller, ... JoVE (Journal of Visualized Experiments), e53570, 2017 | | 2017 |
Antonio FalaceLaboratory of Neurobiology, Child Neurology Unit, Children’s Hospital A. MeyerBestätigte E-Mail-Adresse bei meyer.it
