Arnaud Isapof

1.4k total citations
21 papers, 288 citations indexed

About

Arnaud Isapof is a scholar working on Neurology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arnaud Isapof has authored 21 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Neurology, 5 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Arnaud Isapof's work include Myasthenia Gravis and Thymoma (3 papers), Hereditary Neurological Disorders (3 papers) and Neurological diseases and metabolism (2 papers). Arnaud Isapof is often cited by papers focused on Myasthenia Gravis and Thymoma (3 papers), Hereditary Neurological Disorders (3 papers) and Neurological diseases and metabolism (2 papers). Arnaud Isapof collaborates with scholars based in France, United Kingdom and United States. Arnaud Isapof's co-authors include Thierry Billette de Villemeur, Marie‐Laure Moutard, Virginie Kieffer, A. Gélot, F. Lewin, Cyril Gitiaux, C. Adamsbaum, Jean‐Luc Charuel, Pierre Quartier and Josué Feingold and has published in prestigious journals such as Neurology, Scientific Reports and Nephrology Dialysis Transplantation.

In The Last Decade

Arnaud Isapof

20 papers receiving 282 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arnaud Isapof France 9 105 86 71 45 36 21 288
Syed Wasim Canada 9 66 0.6× 80 0.9× 42 0.6× 23 0.5× 101 2.8× 16 427
Octavian Munteanu Romania 11 99 0.9× 56 0.7× 31 0.4× 24 0.5× 60 1.7× 76 398
P Tron France 10 54 0.5× 73 0.8× 27 0.4× 84 1.9× 87 2.4× 27 363
Iason S. Mantagos United States 13 73 0.7× 79 0.9× 46 0.6× 64 1.4× 22 0.6× 43 498
Aatish Mahajan India 9 69 0.7× 16 0.2× 64 0.9× 52 1.2× 121 3.4× 17 280
Eva Bueltmann Germany 11 21 0.2× 82 1.0× 67 0.9× 113 2.5× 20 0.6× 17 338
Isa Menezes Lyra Brazil 13 69 0.7× 17 0.2× 46 0.6× 9 0.2× 44 1.2× 42 440
Teresa Olivé Spain 9 86 0.8× 19 0.2× 11 0.2× 32 0.7× 64 1.8× 16 301
Preeti Patil Chhablani India 10 32 0.3× 50 0.6× 19 0.3× 96 2.1× 27 0.8× 26 311
Takashi Soga Japan 8 25 0.2× 45 0.5× 23 0.3× 9 0.2× 55 1.5× 25 202

Countries citing papers authored by Arnaud Isapof

Since Specialization
Citations

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

Fields of papers citing papers by Arnaud Isapof

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnaud Isapof

This figure shows the co-authorship network connecting the top 25 collaborators of Arnaud Isapof. A scholar is included among the top collaborators of Arnaud Isapof 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 Arnaud Isapof. Arnaud Isapof 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.
Isapof, Arnaud, Alix de Becdelièvre, Marina Konyukh, et al.. (2024). A previously unreported NARS1 variant causes dominant distal hereditary motor neuropathy in a French family. Journal of the Peripheral Nervous System. 29(2). 275–278. 1 indexed citations
2.
Zaki, Maha S., Mahmoud Y. Issa, Boris Keren, et al.. (2024). Biallelic variants in ERLIN1: a series of 13 individuals with spastic paraparesis. Human Genetics. 143(11). 1353–1362. 1 indexed citations
3.
Wolff, Nicolas, Damien Sternberg, Anthony Béhin, et al.. (2023). New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome. Scientific Reports. 13(1). 14054–14054. 2 indexed citations
4.
Beloribi‐Djefaflia, Sadia, Raúl Juntas Morales, Farzad Fatehi, et al.. (2023). Clinical and genetic features of patients suffering from CMT4J. Journal of Neurology. 271(3). 1355–1365. 6 indexed citations
5.
Stalens, Caroline, Isabelle Desguerre, Christine Barnérias, et al.. (2022). Parents' dilemma: A therapeutic decision for children with spinal muscular atrophy (SMA) type 1. Frontiers in Pediatrics. 10. 1062390–1062390. 2 indexed citations
6.
Gedda, Michel, Capucine de Lattre, Arnaud Isapof, et al.. (2022). Evidence-Based, Implementable Motor Rehabilitation Guidelines for Individuals With Cerebral Palsy. Neurology. 99(7). 283–297. 22 indexed citations
7.
Gitiaux, Cyril, Christine Barnérias, Frédérique Audic, et al.. (2022). Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis. Neurology. 98(23). 14 indexed citations
8.
Voyer, Tom Le, Cyril Gitiaux, François‐Jérôme Authier, et al.. (2021). JAK inhibitors are effective in a subset of patients with juvenile dermatomyositis: a monocentric retrospective study. Lara D. Veeken. 60(12). 5801–5808. 54 indexed citations
9.
Giabicani, Éloïse, et al.. (2020). Paroxysmal strabismus and stridor acquired in childhood: Do not overlook calcemia!. Archives de Pédiatrie. 27(2). 104–106. 1 indexed citations
10.
Doummar, Diane, Sandra Whalen, Boris Keren, et al.. (2020). Congenital immobility and stiffness related to biallelic ATAD1 variants. Neurology Genetics. 6(6). e520–e520. 4 indexed citations
11.
Aouizerate, Jessie, Marie De Antonio, Brigitte Bader‐Meunier, et al.. (2018). Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis. Lara D. Veeken. 57(5). 873–879. 43 indexed citations
12.
Moutard, Marie‐Laure, Virginie Kieffer, Josué Feingold, et al.. (2012). Isolated corpus callosum agenesis: a ten‐year follow‐up after prenatal diagnosis (How are the children without corpus callosum at 10 years of age?). Prenatal Diagnosis. 32(3). 277–283. 66 indexed citations
13.
Villemeur, Thierry Billette de, et al.. (2012). Comment la loi Leonetti s’applique-t-elle à l’enfant polyhandicapé ?. 15(1). 34–37. 5 indexed citations
14.
Milcent, Karen, et al.. (2010). Hernie hiatale paraœsophagienne primitive. Archives de Pédiatrie. 18(1). 76–78.
15.
Leroy, Sandrine, Arnaud Isapof, Sonia Fargue, et al.. (2010). Tacrolimus nephrotoxicity: beware of the association of diarrhea, drug interaction and pharmacogenetics. Pediatric Nephrology. 25(5). 965–969. 29 indexed citations
16.
Isapof, Arnaud, Virginie Kieffer, Silvia Sacco, et al.. (2010). Impact du dépistage anténatal des agénésies du corps calleux sur le devenir des grossesses. Étude de 155 dossiers de 2000 à 2006. Archives de Pédiatrie. 17(3). 226–232. 10 indexed citations
17.
Isapof, Arnaud, et al.. (2010). Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type Ib. Journal of Inherited Metabolic Disease. 33(S3). 477–480. 2 indexed citations
18.
19.
Minard‐Colin, Véronique, et al.. (2006). Tumeurs solides malignes néonatales: à propos de 71 cas. Archives de Pédiatrie. 13(12). 1486–1494. 8 indexed citations
20.
Isapof, Arnaud, Hanna Dêbiec, M Pressac, et al.. (2006). Gross proteinuria post transplant in a child with nephrotic syndrome of the Finnish type--mechanical vs immunological pathogenesis. Nephrology Dialysis Transplantation. 21(12). 3579–3582. 1 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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