| Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056 S Jacquemont, A Curie, V Des Portes, MG Torrioli, E Berry-Kravis, ... Science translational medicine 3 (64), 64ra1-64ra1, 2011 | 424 | 2011 |
| Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome EM Berry-Kravis, L Lindemann, AE Jønch, G Apostol, MF Bear, ... Nature reviews Drug discovery 17 (4), 280-299, 2018 | 274 | 2018 |
| Neural correlates of non-verbal social interactions: a dual-EEG study M Ménoret, L Varnet, R Fargier, A Cheylus, A Curie, V Des Portes, ... Neuropsychologia 55, 85-97, 2014 | 85 | 2014 |
| Expanding the phenotypic spectrum of Allan–Herndon–Dudley syndrome in patients with SLC16A2 mutations G Remerand, O Boespflug‐Tanguy, D Tonduti, R Touraine, D Rodriguez, ... Developmental Medicine & Child Neurology 61 (12), 1439-1447, 2019 | 65 | 2019 |
| Outcome of isolated agenesis of the corpus callosum: A population-based prospective study V Des Portes, A Rolland, J Velazquez-Dominguez, E Peyric, MP Cordier, ... European Journal of Paediatric Neurology 22 (1), 82-92, 2018 | 56 | 2018 |
| The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1‐mutated males D Germanaud, M Rossi, G Bussy, D Gérard, L Hertz‐Pannier, P Blanchet, ... Clinical genetics 79 (3), 225-235, 2011 | 55 | 2011 |
| Placebo responses in genetically determined intellectual disability: a meta-analysis A Curie, K Yang, I Kirsch, RL Gollub, V Des Portes, TJ Kaptchuk, ... PloS one 10 (7), e0133316, 2015 | 48 | 2015 |
| Implicit procedural learning in fragile X and Down syndrome G Bussy, E Charrin, A Brun, A Curie, V Des Portes Journal of Intellectual Disability Research 55 (5), 521-528, 2011 | 47 | 2011 |
| Long-term follow-up in 12 children with pulmonary arteriovenous malformations: confirmation of hereditary hemorrhagic telangiectasia in all cases A Curie, G Lesca, V Cottin, P Edery, G Bellon, ME Faughnan, H Plauchu The journal of pediatrics 151 (3), 299-306, 2007 | 40 | 2007 |
| Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification D Germanaud, J Lefèvre, C Fischer, M Bintner, A Curie, V Des Portes, ... NeuroImage 102, 317-331, 2014 | 38 | 2014 |
| Syntax at hand: common syntactic structures for actions and language AC Roy, A Curie, T Nazir, Y Paulignan, V Des Portes, P Fourneret, ... PloS One 8 (8), e72677, 2013 | 28 | 2013 |
| Stroke by carotid artery complete occlusion in Kawasaki disease: case report and review of literature I Sabatier, S Chabrier, A Brun, L Hees, A Cheylus, R Gollub, N Hadjikhani, ... Pediatric Neurology 49 (6), 469-473, 2013 | 26 | 2013 |
| A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome A Masurel‐Paulet, A Piton, S Chancenotte, C Redin, C Thauvin‐Robinet, ... American Journal of Medical Genetics Part A 170 (8), 2103-2110, 2016 | 22 | 2016 |
| Certainty of genuine treatment increases drug responses among intellectually disabled patients KB Jensen, I Kirsch, M Pontén, A Rosén, K Yang, RL Gollub, V des Portes, ... Neurology 88 (20), 1912-1918, 2017 | 21 | 2017 |
| Asperger syndrome and early-onset schizophrenia associated with a novel MECP2 deleterious missense variant A Curie, G Lesca, G Bussy, S Manificat, V Arnaud, S Gonzalez, O Revol, ... Psychiatric Genetics 27 (3), 105-109, 2017 | 19 | 2017 |
| A novel analog reasoning paradigm: new insights in intellectually disabled patients A Curie, A Brun, A Cheylus, A Reboul, T Nazir, G Bussy, K Delange, ... PloS one 11 (2), e0149717, 2016 | 19 | 2016 |
| Deciphering the natural history of SCA7 in children MG Bah, D Rodriguez, C Cazeneuve, F Mochel, D Devos, A Suppiej, ... European Journal of Neurology 27 (11), 2267-2276, 2020 | 18 | 2020 |
| A new mouse model of ARX dup24 recapitulates the patients’ behavioral and fine motor alterations A Dubos, H Meziane, G Iacono, A Curie, F Riet, C Martin, N Loaëc, ... Human molecular genetics 27 (12), 2138-2153, 2018 | 18 | 2018 |
| The c. 429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia A Curie, T Nazir, A Brun, Y Paulignan, A Reboul, K Delange, A Cheylus, ... Orphanet journal of rare diseases 9 (1), 1-16, 2014 | 15 | 2014 |
| Simultaneous action execution and observation optimise grasping actions M Ménoret, A Curie, V Des Portes, TA Nazir, Y Paulignan Experimental brain research 227 (3), 407-419, 2013 | 14 | 2013 |
