Aurore Curie

Epigenetic Modification of the <i>FMR1</i> Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

Sébastien Jacquemont, Aurore Curie, Vincent des Portes et al. · Science Translational Medicine · 2011 · 611 citations

Life Sciences, Molecular Biology, Neuroscience +17

Expanding the phenotypic spectrum of Allan–Herndon–Dudley syndrome in patients with <i><scp>SLC</scp>16A2</i> mutations

Ganaëlle Remérand, Odile Boespflug‐Tanguy, Davide Tonduti et al. · Developmental Medicine & Child Neurology · 2019 · 89 citations · Full text

Life Sciences, Genetics, Neurology +16

Neural correlates of non-verbal social interactions: A dual-EEG study

Mathilde Ménoret, Léo Varnet, Raphaël Fargier et al. · Neuropsychologia · 2013 · 83 citations

Life Sciences, Neuroscience, Psychology +10

Outcome of isolated agenesis of the corpus callosum: A population-based prospective study

Vincent des Portes, Anne Rolland, Juan Velazquez-Dominguez et al. · European Journal of Paediatric Neurology · 2017 · 60 citations

Medicine, Neurology, Pediatrics +3

The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males

David Germanaud, Massimiliano Rossi, Gérald Bussy et al. · Clinical Genetics · 2010 · 50 citations

Life Sciences, Genetics, Molecular Genetics +9