Jean‐Michel Pedespan

1.1k total citations
34 papers, 536 citations indexed

About

Jean‐Michel Pedespan is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Jean‐Michel Pedespan has authored 34 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Pediatrics, Perinatology and Child Health and 7 papers in Genetics. Recurrent topics in Jean‐Michel Pedespan's work include Metabolism and Genetic Disorders (5 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Epilepsy research and treatment (4 papers). Jean‐Michel Pedespan is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Epilepsy research and treatment (4 papers). Jean‐Michel Pedespan collaborates with scholars based in France, Lebanon and United States. Jean‐Michel Pedespan's co-authors include D Fontan, Jean‐François Chateil, Didier Lacombe, Delphine Denis, Muriel Brun, Alain Rougier, Olivier Brissaud, A. Vital, Cécile Marchal and J Rivel and has published in prestigious journals such as Neurology, Epilepsia and Acta Neuropathologica.

In The Last Decade

Jean‐Michel Pedespan

31 papers receiving 518 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jean‐Michel Pedespan France 15 197 145 136 121 84 34 536
Christine Reyes United States 13 142 0.7× 165 1.1× 49 0.4× 100 0.8× 57 0.7× 22 586
Guido Lancman United States 15 82 0.4× 168 1.2× 146 1.1× 39 0.3× 74 0.9× 44 693
Mariko Taniguchi‐Ikeda Japan 15 144 0.7× 430 3.0× 38 0.3× 150 1.2× 58 0.7× 60 760
Agata Polizzi Italy 15 63 0.3× 183 1.3× 87 0.6× 190 1.6× 68 0.8× 36 590
Rachael Cohen United States 14 50 0.3× 122 0.8× 46 0.3× 79 0.7× 79 0.9× 54 624
Michael Nork United Arab Emirates 14 100 0.5× 120 0.8× 50 0.4× 99 0.8× 47 0.6× 26 405
R. Bauer Germany 11 56 0.3× 78 0.5× 126 0.9× 44 0.4× 68 0.8× 33 443
J. I. Manson Australia 13 146 0.7× 118 0.8× 164 1.2× 23 0.2× 69 0.8× 20 415
N P Cavanagh United Kingdom 14 73 0.4× 212 1.5× 41 0.3× 211 1.7× 68 0.8× 29 737
Gholamreza Zamani Iran 11 53 0.3× 129 0.9× 96 0.7× 31 0.3× 44 0.5× 50 387

Countries citing papers authored by Jean‐Michel Pedespan

Since Specialization
Citations

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

Fields of papers citing papers by Jean‐Michel Pedespan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Michel Pedespan. 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 Jean‐Michel Pedespan. The network helps show where Jean‐Michel Pedespan may publish in the future.

Co-authorship network of co-authors of Jean‐Michel Pedespan

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

All Works

20 of 20 papers shown
1.
Lacombe, Didier, Julien Van‐Gils, Marine Lebrun, et al.. (2022). Hemidystonia with polymicrogyria is part of ATP1A3-related disorders. Brain and Development. 44(8). 567–570.
2.
Crombé, Amandine, Vincent Jecko, P. Bessou, et al.. (2020). Magnetic resonance imaging diagnosis of subependymal giant cell astrocytomas in follow-up of children with tuberous sclerosis complex: should we always use contrast enhancement?. Pediatric Radiology. 50(10). 1397–1408. 5 indexed citations
3.
Fiévet, Alice, Dorine Bellanger, Laïla Zahed, et al.. (2019). DNA repair functional analyses of NBN hypomorphic variants associated with NBN‐related infertility. Human Mutation. 41(3). 608–618. 8 indexed citations
4.
Tarrano, Clément, Nicolas Wattiez, Cécile Delorme, et al.. (2019). Visual Sensory Processing is Altered in Myoclonus Dystonia. Movement Disorders. 35(1). 151–160. 6 indexed citations
5.
Fiévet, Alice, Dorine Bellanger, Stéphanie Valence, et al.. (2019). Three new cases of ataxia‐telangiectasia‐like disorder: No impairment of the ATM pathway, but S‐phase checkpoint defect. Human Mutation. 40(10). 1690–1699. 18 indexed citations
6.
Joubert, Bastien, Géraldine Picard, Véronique Rogemond, et al.. (2017). Initial clinical presentation of young children with N-methyl- d -aspartate receptor encephalitis. European Journal of Paediatric Neurology. 22(3). 404–411. 20 indexed citations
7.
Villega, Frédéric, et al.. (2017). Neuropathie héréditaire par hypersensibilité à la pression : à propos de 3 observations chez l’enfant. Archives de Pédiatrie. 24(3). 260–262. 2 indexed citations
8.
Bessou, P., et al.. (2014). Syndrome de Gradenigo au cours d’une apicite chez un enfant. Archives de Pédiatrie. 22(3). 283–286. 3 indexed citations
9.
Dureau‐Pournin, C., Jean‐Michel Pedespan, C. Droz‐Perroteau, et al.. (2013). Continuation rates of levetiracetam in children from the EULEVp cohort study. European Journal of Paediatric Neurology. 18(1). 19–24. 4 indexed citations
10.
Vézain, Myriam, Pascale Saugier-Véber, Judith Melki, et al.. (2007). A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy. European Journal of Human Genetics. 15(10). 1054–1062. 32 indexed citations
11.
Witte, S., Caroline Espil‐Taris, S. Brun, et al.. (2005). Syndrome d'Angelman et anévrisme intracrânien : association fortuite ou prédisposition génétique commune ?. Archives de Pédiatrie. 12(4). 431–433. 5 indexed citations
12.
Denis, Delphine, B. Maugey‐Laulom, Dominique Carles, et al.. (2001). Prenatal Diagnosis of Schizencephaly by Fetal Magnetic Resonance Imaging. Fetal Diagnosis and Therapy. 16(6). 354–359. 29 indexed citations
13.
Denis, Delphine, Jean‐François Chateil, Muriel Brun, et al.. (2001). Schizencephaly: clinical and imaging features in 30 infantile cases. Brain Dev. 9 indexed citations
14.
Denis, Delphine, Jean‐François Chateil, Muriel Brun, et al.. (2000). Schizencephaly: clinical and imaging features in 30 infantile cases. Brain and Development. 22(8). 475–483. 92 indexed citations
15.
Pedespan, Jean‐Michel, Laurence S. Jouaville, Claude Cancés, et al.. (1999). Menkes disease: study of the mitochondrial respiratory chain in three cases. European Journal of Paediatric Neurology. 3(4). 167–170. 21 indexed citations
16.
Pedespan, Jean‐Michel, et al.. (1998). Myopathie facio-scapulohumérale et mosaïque germinale. Archives de Pédiatrie. 5(8). 880–883. 1 indexed citations
17.
Bragado‐Nilsson, Elisabeth, et al.. (1997). Deletion of 11 Amino Acids in Tuberin Associated with Severe Tuberous Sclerosis Phenotypes: Evidence for a New Essential Domain in the First Third of the Protein. European Journal of Human Genetics. 5(5). 280–287. 5 indexed citations
18.
Pedespan, Jean‐Michel, et al.. (1996). Thromboses du sinus longitudinal supérieur chez l'enfant au cours de la première année de vie: aspects cliniques, imagerie etévolution. Archives de Pédiatrie. 3(6). 561–565. 7 indexed citations
19.
Vital, A., Cécile Marchal, Alain Rougier, et al.. (1994). Glial and neuronoglial malformative lesions associated with medically intractable epilepsy. Acta Neuropathologica. 87(2). 196–201. 28 indexed citations
20.
Chateil, Jean‐François, et al.. (1994). [Agyria-pachygyria and pachygyria in children. Contribution of imaging].. PubMed. 1(6). 551–60. 2 indexed citations

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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