Aurore Curie

Université Claude Bernard Lyon 1 FR

0000-0001-7823-290X

Publications

1,734

Citations

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5.18

2yr Mean Cite

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Data combined from OpenAlex . OA = OpenAlex S2 = Semantic Scholar

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Publications

52 total

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome PDF

Elizabeth Berry‐Kravis, Lothar Lindemann, Aia Elise Jønch, George Apostol, Mark F. Bear et al. - Nature Reviews Drug Discovery, 2017

Cited by 344 OpenAlex

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, Maria Giulia Torrioli, Elizabeth Berry‐Kravis et al. - Science Translational Medicine, 2011

Cited by 611 OpenAlex

Research Topics

Genetics and Neurodevelopmental Disorders (18) Autism Spectrum Disorder Research (6) Genomics and Rare Diseases (6) Genomic variations and chromosomal abnormalities (5) Otitis Media and Relapsing Polychondritis (4)

Affiliations

Université Claude Bernard Lyon 1

FR 2025 - 2007

Centre National de la Recherche Scientifique

FR 2025 - 2006

Beth Israel Deaconess Medical Center

US 2017 - 2017

Harvard University

US 2017 - 2015

Inserm

FR 2025 - 2015

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Aurore Curie

Publication & Citation Trends

Publications

Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome PDF

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

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