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VP

Vincent des Portes

Université Claude Bernard Lyon 1 FR

173
Publications
8,423
Citations
43
H-Index
95
i10-Index
4.9
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex . OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

171 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

Mavoglurant in fragile X syndrome: Results of two randomized, double-blind, placebo-controlled trials

Elizabeth Berry‐Kravis, Vincent des Portes, Randi J. Hagerman, Sébastien Jacquemont, Perrine Charles et al. - Science Translational Medicine, 2016
Cited by 263 OpenAlex

PQBP1 Is a Proximal Sensor of the cGAS-Dependent Innate Response to HIV-1 PDF

Sunnie M. Yoh, Monika Schneider, Janna Seifried, Stephen Soonthornvacharin, Rana Elias Akleh et al. - Cell, 2015
Cited by 206 OpenAlex

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

Karine Poirier, Nicolas Lebrun, Loïc Broix, Guoling Tian, Yoann Saillour et al. - Nature Genetics, 2013
Cited by 493 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

The three stages of epilepsy in patients with <i>CDKL5</i> mutations

Nadia Bahi‐Buisson, Anna Kamińska, Nathalie Boddaert, Marlène Rio, Alexandra Afenjar et al. - Epilepsia, 2008
Cited by 188 OpenAlex

Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates PDF

Sébastien Jacquemont, Randi J. Hagerman, Maureen A. Leehey, Jim Grigsby, Lin Zhang et al. - The American Journal of Human Genetics, 2003
Cited by 764 OpenAlex

A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation

Ramzi Zemni, Thierry Bienvenu, Marie Claude Vinet, Aziz Sefiani, Alain Carrié et al. - Nature Genetics, 2000
Cited by 236 OpenAlex

A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome PDF

Vincent des Portes, Jean Marc Pinard, Pierre Billuart, Marie Claude Vinet, Annette Koulakoff et al. - Cell, 1998
Cited by 737 OpenAlex

Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation

Pierre Billuart, T Bienvenu, Nathalie Ronce, Vincent des Portes, Marie Claude Vinet et al. - Nature, 1998
Cited by 552 OpenAlex

Research Topics

Genetics and Neurodevelopmental Disorders (73) Genomic variations and chromosomal abnormalities (26) Genomics and Rare Diseases (25) Fetal and Pediatric Neurological Disorders (25) Epilepsy research and treatment (19)

Affiliations

Université Claude Bernard Lyon 1
FR 2025 - 2008
Hôpital Necker-Enfants Malades
FR 1994 - 1994
Centre National de la Recherche Scientifique
FR 2025 - 2008
Beth Israel Deaconess Medical Center
US 2017 - 2017
Harvard University
US 2017 - 2017

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