Vincent Desportes

551 total citations
15 papers, 323 citations indexed

About

Vincent Desportes is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Vincent Desportes has authored 15 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Vincent Desportes's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (2 papers) and Competitive and Knowledge Intelligence (2 papers). Vincent Desportes is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (2 papers) and Competitive and Knowledge Intelligence (2 papers). Vincent Desportes collaborates with scholars based in France, Germany and Switzerland. Vincent Desportes's co-authors include Romain Marignier, Álvaro Cobo‐Calvo, Maryline Carneiro, Sandra Vukusic, Anne Ruiz, Françoise Durand‐Dubief, Anne‐Lise Poulat, Kumaran Deiva, Baltazar Gomez‐Mancilla and F. Gasparini and has published in prestigious journals such as The Journal of Clinical Psychiatry, Developmental Medicine & Child Neurology and Journal of Neurology.

In The Last Decade

Vincent Desportes

15 papers receiving 319 citations

Peers

Countries citing papers authored by Vincent Desportes

Since Specialization

Citations

This map shows the geographic impact of Vincent Desportes'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 Vincent Desportes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vincent Desportes more than expected).

Fields of papers citing papers by Vincent Desportes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent Desportes. 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 Vincent Desportes. The network helps show where Vincent Desportes may publish in the future.

Co-authorship network of co-authors of Vincent Desportes

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Desportes. A scholar is included among the top collaborators of Vincent Desportes 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 Vincent Desportes. Vincent Desportes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Cognitive and academic outcomes in children with myelin oligodendrocyte glycoprotein antibody‐associated disease 2024 ·Developmental Medicine & Child Neurology ·(unknown), Julie Pique, Vincent Desportes, Kumaran Deiva, Anne‐Lise Poulat, Romain Marignier	1
2	Entrer en stratégie 2020 ·Vincent Desportes, (unknown)	1
3	MOG antibody-related disorders: common features and uncommon presentations 2017 ·Journal of Neurology ·Álvaro Cobo‐Calvo, Anne Ruiz, (unknown), Anne‐Lise Poulat, Maryline Carneiro, (unknown), Françoise Durand‐Dubief, Kumaran Deiva, Sandra Vukusic, Vincent Desportes, Romain Marignier	95
4	Effect of desipramine on patients with breathing disorders in RETT syndrome 2017 ·Annals of Clinical and Translational Neurology ·Josette Mancini, J.‐C. Dubus, Élisabeth Jouve, Jean‐Christophe Roux, Patricia Franco, Emmanuelle Lagrue, Pierre Castelnau, Claude Cancès, Yves Chaix, (unknown), Catherine Cornu, Vincent Desportes, Louis Vallée, Nadia Bahi‐Buisson, Romain Truillet, Laurence Attolini, Laurent Villard, Olivier Blin, Joëlle Micallef	17
5	Attention and Executive Disorders in Neurofibromatosis 1: Comparison Between NF1 With ADHD Symptomatology (NF1 + ADHD) and ADHD Per Se 2017 ·Journal of Attention Disorders ·Laurence Lion‐François, Vania Herbillon, (unknown), Catherine Mercier, Daniel Gérard, Tiphanie Ginhoux, (unknown), Isabelle Kemlin, Behrouz Kassaï, Vincent Desportes, George A. Michael	11
6	Strategy in Theory 2014 ·Vincent Desportes	2
7	Translating Molecular Advances in Fragile X Syndrome Into Therapy 2014 ·The Journal of Clinical Psychiatry ·Randi J. Hagerman, Vincent Desportes, F. Gasparini, Sébastien Jacquemont, Baltazar Gomez‐Mancilla	40
8	La stratégie en théories 2014 ·Politique étrangère ·Vincent Desportes	2
9	Expanding the clinical phenotype of patients with a ZDHHC9 mutation 2013 ·American Journal of Medical Genetics Part A ·Alice Masurel‐Paulet, Vera M. Kalscheuer, Nicolas Lebrun, Hao Hu, (unknown), Christel Thauvin‐Robinet, Véronique Darmency‐Stamboul, Salima El Chehadeh, Julien Thévenon, (unknown), (unknown), (unknown), Jean‐Michel Pinoit, Frédéric Huet, Vincent Desportes, Jamel Chelly, Laurence Faivre	28
10	Prenatal unilateral cerebellar hypoplasia in a series of 26 cases: significance and implications for prenatal diagnosis 2013 ·Ultrasound in Obstetrics and Gynecology ·Mona Massoud, (unknown), Cathérine Garel, N. Varene, M.L. Moutard, T. Billette, A. Bénézit, Christelle Rougeot, Jean‐Marie Jouannic, Jérôme Massardier, P. Gaucherand, Vincent Desportes, Laurent Guibaud	37
11	Armées : « technologisme » ou « juste technologie » ? 2009 ·Politique étrangère ·Vincent Desportes	2
12	ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X‐inactivation pattern 2006 ·American Journal of Medical Genetics Part A ·Catherine Badens, Nathalie Martini, Sébastien Courrier, Vincent Desportes, Renaud Touraine, Nicolas Lévy, Patrick Edery	19
13	Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis 2005 ·Neurogenetics ·Karine Poirier, Didier Lacombe, Brigitte Gilbert‐Dussardier, Martine Raynaud, Vincent Desportes, Arjan P.M. de Brouwer, Claude Moraine, J P Fryns, Hans‐Hilger Ropers, C. Beldjord, Jamel Chelly, Thierry Bienvenu	32
14	MECP2 gene mutations in non‐syndromic X‐linked mental retardation: Phenotype–genotype correlation 2003 ·American Journal of Medical Genetics Part A ·Marie Gomot, Chantal Gendrot, Alain Verloès, Martine Raynaud, Albert David, Helger G. Yntema, (unknown), Vera M. Kalscheuer, Suzanna G.M. Frints, Philippe Couvert, Sylvain Briault, Sophie Blesson, Annick Toutain, Jamel Chelly, Vincent Desportes, Claude Moraine	30
15	Neuro-cognitive and behavioural aspects in non-specific mental retardation. A proposal for phenotyping new XLMR genes. 2002 ·PubMed ·Martine Borghgraef, Simona Sacco, Marie Gomot, (unknown), Arthur M. Jacobs, (unknown), Vincent Desportes	6

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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