V. des Portes

1.6k total citations
47 papers, 1.1k citations indexed

About

V. des Portes is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, V. des Portes has authored 47 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 9 papers in Molecular Biology. Recurrent topics in V. des Portes's work include Genetics and Neurodevelopmental Disorders (18 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Autism Spectrum Disorder Research (7 papers). V. des Portes is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Autism Spectrum Disorder Research (7 papers). V. des Portes collaborates with scholars based in France, United States and Italy. V. des Portes's co-authors include Laurent Guibaud, G Ponsot, C. Beldjord, Isabelle Desguerre, Olivier Dulac, J.-M. Pinard, J. Motte, Pierre Lebon, Bénédicte Héron and Fiona Francis and has published in prestigious journals such as NeuroImage, Neurology and Human Molecular Genetics.

In The Last Decade

V. des Portes

44 papers receiving 1.0k citations

Peers

Countries citing papers authored by V. des Portes

Since Specialization

Citations

This map shows the geographic impact of V. des Portes's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by V. des Portes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites V. des Portes more than expected).

Fields of papers citing papers by V. des Portes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by V. des Portes. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by V. des Portes. The network helps show where V. des Portes may publish in the future.

Co-authorship network of co-authors of V. des Portes

This figure shows the co-authorship network connecting the top 25 collaborators of V. des Portes. A scholar is included among the top collaborators of V. des Portes based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with V. des Portes. V. des Portes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes 2022 ·European Journal of Medical Genetics ·(unknown), (unknown), Alexis Arzimanoglou, Audrey Putoux, Nicolas Chatron, Gaëtan Lesca, V. des Portes	3
2	A french adaptation of the vineland adaptive behavior scales VABS-II 2021 ·European Psychiatry ·(unknown), Benjamin Riche, V. des Portes, (unknown), Ségolène Gaillard, Muriel Rabilloud, Behrouz Kassaï, Sandrine Sonié	5
3	Approche développementale des fonctions exécutives : du bébé à l’adolescence 2016 ·Archives de Pédiatrie ·Pierre Fourneret, V. des Portes	7
4	Le syndrome de Smith-Magenis, une association unique de troubles du comportement et du cycle veille/sommeil 2015 ·Archives de Pédiatrie ·Alice Poisson, A. Nicolas, Damien Sanlaville, Pierre Cochat, Hélène De Leersnyder, (unknown), Patricia Franco, V. des Portes, Patrick Edery, Caroline Demily	6
5	Fragile X syndrome: economic burden and health‐related quality of life of patients and caregivers in France 2015 ·Journal of Intellectual Disability Research ·Karine Chevreul, Karen Berg Brigham, Matthias Brunn, V. des Portes	20
6	Neurofibromatose de type 2 : différence inter-générationnelle d’expression génétique et clinique 2014 ·Archives de Pédiatrie ·A. Drouet, François Le Moigne, (unknown), (unknown), (unknown), V. des Portes, L. Guilloton, S. Pinson	2
7	Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification 2014 ·NeuroImage ·David Germanaud, Julien Lefèvre, Clara Fischer, (unknown), Aurore Curie, V. des Portes, Stéphan Eliez, Monique Elmaleh, (unknown), Sandrine Passemard, (unknown), Marie Schaer, Alain Verloès, Roberto Toro, Jean‐François Mangin, Lucie Hertz‐Pannier	24
8	Prenatal diagnosis of cerebellar cortical dysplasia associated with abnormalities of foliation 2012 ·Ultrasound in Obstetrics and Gynecology ·Mona Massoud, Jérôme Clerc, (unknown), Alexandre Vasiljevic, Jérôme Massardier, Muriel Doret, P. Gaucherand, V. des Portes, Laurent Guibaud	3
9	Stratégie d’exploration d’une déficience intellectuelle inexpliquée 2012 ·Archives de Pédiatrie ·Alain Verloès, D. Héron, Thierry Billette de Villemeur, (unknown), (unknown), Nadia Bahi‐Buisson, Perrine Charles, Anne Faudet, Aurélia Jacquette, Cyril Mignot, (unknown), Sandrine Passemard, Marlène Rio, Laurence Robel, Christelle Rougeot, Dorothée Ville, Lydie Bürglen, V. des Portes	6
10	Implicit procedural learning in fragile X and Down syndrome 2011 ·Journal of Intellectual Disability Research ·Gérald Bussy, (unknown), Brun Amandine, Aurore Curie, V. des Portes	24
11	The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated males 2010 ·Clinical Genetics ·David Germanaud, Massimiliano Rossi, Gérald Bussy, Daniel Gérard, Lucie Hertz‐Pannier, Patricia Blanchet, Hélène Dollfus, Fabienne Giuliano, (unknown), P. Sardá, Sabine Sigaudy, Aurore Curie, (unknown), Renaud Touraine, V. des Portes	36
12	La dyspraxie verbale: trouble spécifique complexe du neurodéveloppement 2010 ·(unknown), (unknown), (unknown), Gaëtan Lesca, Aurore Curie, V. des Portes, Christophe Rousselle	0
13	Abnormal Sylvian fissure on prenatal cerebral imaging: significance and correlation with neuropathological and postnatal data 2008 ·Ultrasound in Obstetrics and Gynecology ·Laurent Guibaud, Lise Selleret, Jeanne‐Claudie Larroche, Annie Buénerd, (unknown), P. Gaucherand, V. des Portes, J.P. Pracros	32
14	L'IRM morphométrique : un reflet du fonctionnement du cerveau 2006 ·Archives de Pédiatrie ·Aurore Curie, Laurent Guibaud, V. des Portes	0
15	Actualités sur la génétique des retards mentaux liés au chromosome X 2006 ·Revue Neurologique ·Nadia Bahi‐Buisson, Jamel Chelly, V. des Portes	1
16	Extracerebellar ectopic brain tissue in the posterior fossa 2005 ·Ultrasound in Obstetrics and Gynecology ·Laurent Guibaud, (unknown), V. des Portes, P.A. Ndoye Roth, P. Gaucherand, J.P. Pracros	3
17	Démarche diagnostique devant une déficience mentale de l’enfant en 2002 2002 ·Archives de Pédiatrie ·V. des Portes, Marie-Odile Livet, Louis Vallée	10
18	Retard mental et troubles de la corticogenèse 2000 ·Archives de Pédiatrie ·V. des Portes, Jean-Marc Pinard, Fiona Francis, C. Beldjord, G Ponsot, Jamel Chelly	1
19	Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation. 1998 ·PubMed ·Pierre Billuart, T. Bienvenu, Nathalie Ronce, V. des Portes, Marie Claude Vinet, Ramzi Zemni, Alain Carrié, C. Beldjord, A Kahn, (unknown), Jamel Chelly	33
20	X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter 1996 ·American Journal of Medical Genetics ·V. des Portes, L Bachner, Thomas Brüls, C. Beldjord, Pierre Billuart, Nadem Soufir, (unknown), Marie Claude Vinet, Elisabetta Malaspina, Valentina Marchiani, Enrico Bertini, A Kahn, Emilio Franzonı, Jamel Chelly	7

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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