ScholarIQanswers from OpenAlex & ORCID
Vincent des Portes
ResearcherPublications, citations & collaboration network
Vincent des Portes is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Vincent des Portes have?
ScholarIQindexed works
Vincent des Portes has 180 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Vincent des Portes have?
ScholarIQcitation count
Vincent des Portes has 8,563 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Vincent des Portes?
ScholarIQh-index
Vincent des Portes has an h-index of 44 in OpenAlex.
What is the i10-index of Vincent des Portes?
ScholarIQi10-index
Vincent des Portes has an i10-index of 98 in OpenAlex.
What is the OpenAlex record for Vincent des Portes?
ScholarIQopenalex
The OpenAlex for Vincent des Portes is on the source record.
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
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
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
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
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