Cyril Gitiaux

3.6k total citations
84 papers, 1.4k citations indexed

About

Cyril Gitiaux is a scholar working on Molecular Biology, Epidemiology and Rheumatology. According to data from OpenAlex, Cyril Gitiaux has authored 84 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 28 papers in Epidemiology and 19 papers in Rheumatology. Recurrent topics in Cyril Gitiaux's work include Inflammatory Myopathies and Dermatomyositis (23 papers), Muscle Physiology and Disorders (15 papers) and Eosinophilic Disorders and Syndromes (14 papers). Cyril Gitiaux is often cited by papers focused on Inflammatory Myopathies and Dermatomyositis (23 papers), Muscle Physiology and Disorders (15 papers) and Eosinophilic Disorders and Syndromes (14 papers). Cyril Gitiaux collaborates with scholars based in France, United Kingdom and Canada. Cyril Gitiaux's co-authors include Isabelle Desguerre, Bénédicte Chazaud, Claire Latroche, Rémi Mounier, Fabrice Chrétien, Christine Barnérias, Brigitte Bader‐Meunier, Michèle Weiss‐Gayet, Nathalie Boddaert and François‐Jérôme Authier and has published in prestigious journals such as The Lancet, Neurology and PEDIATRICS.

In The Last Decade

Cyril Gitiaux

76 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cyril Gitiaux France 20 559 328 256 254 213 84 1.4k
Meenakshi B. Bhattacharjee United States 19 662 1.2× 131 0.4× 241 0.9× 144 0.6× 100 0.5× 59 1.4k
Christopher Eckstein United States 24 412 0.7× 158 0.5× 232 0.9× 267 1.1× 251 1.2× 46 2.0k
Jonathan B. Strober United States 24 444 0.8× 136 0.4× 677 2.6× 119 0.5× 204 1.0× 43 1.9k
Jun Shimizu Japan 22 477 0.9× 421 1.3× 686 2.7× 91 0.4× 251 1.2× 101 1.7k
Ian Sutton Australia 20 352 0.6× 206 0.6× 814 3.2× 224 0.9× 164 0.8× 43 2.0k
J. F. Pellissier France 30 1.0k 1.8× 386 1.2× 456 1.8× 137 0.5× 274 1.3× 91 2.2k
Francesca Andreetta Italy 28 1.6k 2.8× 283 0.9× 885 3.5× 158 0.6× 139 0.7× 78 2.7k
Juan J. Vílchez Spain 32 1.5k 2.6× 209 0.6× 894 3.5× 197 0.8× 177 0.8× 130 3.0k
Jin‐Hong Shin South Korea 27 1.5k 2.6× 165 0.5× 199 0.8× 685 2.7× 96 0.5× 121 2.1k
Brith Otterud United States 23 865 1.5× 119 0.4× 197 0.8× 421 1.7× 107 0.5× 41 2.1k

Countries citing papers authored by Cyril Gitiaux

Since Specialization
Citations

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

Fields of papers citing papers by Cyril Gitiaux

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cyril Gitiaux

This figure shows the co-authorship network connecting the top 25 collaborators of Cyril Gitiaux. A scholar is included among the top collaborators of Cyril Gitiaux 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 Cyril Gitiaux. Cyril Gitiaux 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.
Gitiaux, Cyril, et al.. (2025). BAG3-related myofibrillar myopathy: focus on its cardiac involvement. Frontiers in Genetics. 16. 1636999–1636999.
2.
Bader‐Meunier, Brigitte, T. Moreau, Florence A. Aeschlimann, et al.. (2025). Myositis-specific autoantibody subtypes are associated with response to Janus kinase inhibitors in patients with juvenile dermatomyositis. Lara D. Veeken. 64(10). 5487–5492. 1 indexed citations
3.
Fournier, Benjamin, Jamie Sugrue, Thomas Moreau, et al.. (2025). Dazukibart for the treatment of severe TIF1γ ‐positive juvenile dermatomyositis. Journal of the European Academy of Dermatology and Venereology. 40(4). e189–e192.
4.
Semeraro, Michaëla, Fabienne Marquant, Laurence Robel, et al.. (2025). Allopurinol Treatment Improves Cognitive Skills, Adaptive Behavior, and Biochemical Markers in Young Patients With Adenylosuccinate Lyase Deficiency. Journal of Inherited Metabolic Disease. 48(6). e70092–e70092. 1 indexed citations
5.
Barcia, Giulia, Marlène Rio, Cyril Gitiaux, et al.. (2024). Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisal. European Journal of Medical Genetics. 72. 104979–104979.
6.
Barrois, Rémi, Lucie Griffon, Christine Barnérias, et al.. (2024). Polysomnography findings and respiratory muscle function in infants with early onset spinal muscular atrophy after gene replacement as monotherapy: A prospective study. Sleep Medicine. 119. 335–341. 1 indexed citations
7.
Mansour‐Hendili, Lamisse, Cyril Gitiaux, Céline Latouche, et al.. (2024). Recurrent “outsider” intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb. Frontiers in Genetics. 15. 1352006–1352006. 1 indexed citations
8.
Roux, Charles‐Joris, Marie Hully, Agnès Rötig, et al.. (2024). Polyradiculoneuritis on MRI. Neurology. 102(11). e209356–e209356.
9.
Roux, Charles‐Joris, Rémi Barrois, Apolline Imbard, et al.. (2024). Vitamin deficiencies in children: Lessons from clinical and neuroimaging findings. European Journal of Paediatric Neurology. 50. 6–15. 3 indexed citations
10.
Bader‐Meunier, Brigitte, Sylvain Breton, Darragh Duffy, et al.. (2023). Osteonecrosis in patients with juvenile dermatomyositis: is it associated with anti-MDA5 autoantibody?. Lara D. Veeken. 62(8). e242–e245. 1 indexed citations
11.
Barrois, Rémi, et al.. (2023). Correlations between clinical motor scores and CMAP in patients with type 2 spinal muscular amyotrophy treated with nusinersen. Archives de Pédiatrie. 31(1). 26–31. 3 indexed citations
12.
Rodero, Mathieu P., Florence A. Aeschlimann, François‐Jérôme Authier, et al.. (2022). Efficacy and tolerance of corticosteroids and methotrexate in patients with juvenile dermatomyositis: a retrospective cohort study. Lara D. Veeken. 61(11). 4514–4520. 3 indexed citations
13.
Rossi, Massimo, et al.. (2022). Infant botulism: Report of a misleading case and important key messages. Archives de Pédiatrie. 29(5). 395–397. 1 indexed citations
14.
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
15.
Gitiaux, Cyril, Mélanie Magnan, Sylvain Cuvellier, et al.. (2020). Derivation and Characterization of Immortalized Human Muscle Satellite Cell Clones from Muscular Dystrophy Patients and Healthy Individuals. Cells. 9(8). 1780–1780. 20 indexed citations
16.
Barnérias, Christine, Christine Bodemer, Isabelle Desguerre, et al.. (2020). From Diagnosis to Prognosis: Revisiting the Meaning of Muscle ISG15 Overexpression in Juvenile Inflammatory Myopathies. Arthritis & Rheumatology. 73(6). 1044–1052. 14 indexed citations
17.
Aeschlimann, Florence A., Marie‐Louise Frémond, Darragh Duffy, et al.. (2018). A child with severe juvenile dermatomyositis treated with ruxolitinib. Journal of Financial Econometrics. 5 indexed citations
18.
Latroche, Claire, Michèle Weiss‐Gayet, Laurent Muller, et al.. (2017). Coupling between Myogenesis and Angiogenesis during Skeletal Muscle Regeneration Is Stimulated by Restorative Macrophages. Stem Cell Reports. 9(6). 2018–2033. 164 indexed citations
19.
Cavallin, Mara, A. Millischer, Despina Moshous, et al.. (2017). Prenatal and postnatal presentations of corpus callosum agenesis with polymicrogyria caused by EGP5 mutation. American Journal of Medical Genetics Part A. 173(3). 706–711. 10 indexed citations
20.
Ζεκερίδου, Αναστασία, Aurélien Viaccoz, François Ducray, et al.. (2015). Treatment and outcome of children and adolescents with N-methyl-d-aspartate receptor encephalitis. Journal of Neurology. 262(8). 1859–1866. 95 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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