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Vincent des Portes
ResearcherPublications, citations & collaboration network
Vincent des Portes is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 180 works, 8,563 citations, an h-index of 44 and an i10-index of 98.
180
Works
8,563
Citations
44
h-index
98
i10-index
IDs:OpenAlex
How has Vincent des Portes's publication output changed over time?
ScholarIQpublication output · 1998–2024
Output declined50% over the shown period — from 2 works in 1998 to 1 in 2024.
2
1
1
1
1
1
1
1
1
1
1998200020032008201120132015201620172024
What are the most-cited papers on Vincent des Portes?
ScholarIQmost cited works
Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates
Sébastien Jacquemont, Randi J. Hagerman, Maureen A. Leehey, Jim Grigsby, Lin Zhang, James A. Brunberg, Claudia Greco, Vincent des Portes, Tristan Jardini, Richard A. Levine, Elizabeth Berry‐Kravis, W. Ted Brown, S. Schaeffer, John T. Kissel, Flora Tassone, Paul J. Hagerman
S134425043. 2003765 CitationsOPEN ACCESS
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
Vincent des Portes, Jean Marc Pinard, Pierre Billuart, Marie Claude Vinet, Annette Koulakoff, Alain Carrié, A. Gélot, Elisabeth Dupuis, Jacques Motté, Yoheved Berwald‐Netter, Martin Catala, Axel Kahn, Chérif Beldjord, Jamel Chelly
S110447773. 1998738 CitationsOPEN ACCESS
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, Randi J. Hagerman, Feliciano J. Ramos, Kim Cornish, Yunsheng He, Charles Paulding, Giovanni Neri, Fei Chen, Nouchine Hadjikhani, Danielle Martinet, Joanne Meyer, J. Beckmann, Delange Karine, Brun Amandine, Gérald Bussy, F. Gasparini, Talita Hilse, Annette Floesser, Janice Branson, Graeme Bilbe, Donald R. Johns, Baltazar Gomez‐Mancilla
S24207032. 2011611 CitationsOPEN ACCESS
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
Pierre Billuart, T Bienvenu, Nathalie Ronce, Vincent des Portes, Marie Claude Vinet, Ramzi Zemni, Hugues Roest Crollius, Alain Carrié, Fabien Fauchereau, Michele Cherry, Sylvain Briault, Ben C.J. Hamel, Jean‐Pierre Fryns, Chérif Beldjord, Axel Kahn, Claude Moraine, Jamel Chelly
Nature. 1998557 Citations
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Karine Poirier, Nicolas Lebrun, Loïc Broix, Guoling Tian, Yoann Saillour, Cécile Boscheron, Elena Parrini, Stéphanie Valence, Benjamin Saint Pierre, Madison Oger, Didier Lacombe, David Geneviève, Elena Fontana, Francesca Darra, Claude Cancès, Magalie Barth, Dominique Bonneau, Bernardo Dalla Bernadina, Sylvie Nguyen, Cyril Gitiaux, Philippe Parent, Vincent des Portes, Jean Michel Pedespan, Victoire Legrez, Laetitia Castelnau-Ptakine, Patrick Nitschké, Thierry Hieu, Cécile Masson, Diana Zélénika, Annie Andrieux, Fiona Francis, Renzo Guerrini, Nicholas J. Cowan, Nadia Bahi‐Buisson, Jamel Chelly
S137905309. 2013499 Citations
Related on ScholarIQ
Lyon 1 Université
Institution
Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates
Paper
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
Paper
Epigenetic Modification of the <i>FMR1</i> Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056
Paper
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
Paper
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Paper