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Aurore Curie
Researcher at University of Lyon
Publications - 27
Citations - 1274
Aurore Curie is an academic researcher from University of Lyon. The author has contributed to research in topics: Intellectual disability & Fragile X syndrome. The author has an hindex of 12, co-authored 24 publications receiving 1090 citations. Previous affiliations of Aurore Curie include Centre national de la recherche scientifique & Claude Bernard University Lyon 1.
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Journal ArticleDOI
Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056
Sébastien Jacquemont,Aurore Curie,Vincent des Portes,Maria Giulia Torrioli,Elizabeth Berry-Kravis,Randi J Hagerman,Feliciano J. Ramos,Kim Cornish,Yunsheng He,Charles Paulding,Giovanni Neri,Fei Chen,Fei Chen,Nouchine Hadjikhani,Nouchine Hadjikhani,Danielle Martinet,Joanne M. Meyer,Jacques S. Beckmann,Karine Delange,Amandine Brun,Gérald Bussy,Fabrizio Gasparini,Talita Hilse,Annette Floesser,Janice Branson,Graeme Bilbe,Donald Johns,Baltazar Gomez-Mancilla +27 more
TL;DR: An antagonist for the metabotropic glutamate receptor may improve symptoms in patients with fragile X syndrome whose FMR1 promoters are fully methylated, a sign that gene expression is completely silenced, and provides the basis for a larger study to test whether methylation can serve as a predictor of a positive antagonist response in a population of patients with Fragile X syndrome.
Journal ArticleDOI
Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome
Elizabeth Berry-Kravis,Lothar Lindemann,Aia E. Jønch,Aia E. Jønch,George Apostol,Mark F. Bear,Randall L. Carpenter,Jacqueline N. Crawley,Aurore Curie,Vincent des Portes,Farah Hossain,Fabrizio Gasparini,Baltazar Gomez-Mancilla,Baltazar Gomez-Mancilla,David R Hessl,Eva Loth,Sebastian H. Scharf,Paul P. Wang,Florian Von Raison,Randi J Hagerman,Will Spooren,Sébastien Jacquemont,Sébastien Jacquemont,Sébastien Jacquemont +23 more
TL;DR: FXS is at the forefront of efforts to develop drugs for neurodevelopmental disorders, and lessons learned in the process will also be important for such disorders.
Journal ArticleDOI
Neural correlates of non-verbal social interactions: a dual-EEG study.
Mathilde Ménoret,Léo Varnet,Raphaël Fargier,Anne Cheylus,Aurore Curie,Vincent des Portes,Tatjana A. Nazir,Yves Paulignan +7 more
TL;DR: Acting in a social context induced analogous modulations of motor and sensorimotor regions in observer and actor and sharing a common goal during an interaction seems thus to evoke a common representation of the global action that includes both actor and observer movements.
Journal ArticleDOI
The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males
David Germanaud,Massimiliano Rossi,Gérald Bussy,D. Gérard,Lucie Hertz-Pannier,Patricia Blanchet,Hélène Dollfus,Fabienne Giuliano,V. Bennouna-Greene,Pierre Sarda,Sabine Sigaudy,Aurore Curie,Marie-Claire Vincent,R. Touraine,V. des Portes,V. des Portes +15 more
TL;DR: The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1‐mutated males is presented.
Journal ArticleDOI
Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutations.
Ganaelle Remerand,Odile Boespflug-Tanguy,Davide Tonduti,Renaud Touraine,Diana Rodriguez,Aurore Curie,Nathalie Perreton,Vincent des Portes,Catherine Sarret +8 more
TL;DR: The phenotypic spectrum of Allan–Herndon–Dudley syndrome is extended to a mild intellectual disability with hypotonia, which may be adversely affected by neuro‐orthopaedic, pulmonary, and epileptic complications.