Cyril Goizet

13.6k total citations
133 papers, 4.0k citations indexed

About

Cyril Goizet is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Cyril Goizet has authored 133 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 46 papers in Cellular and Molecular Neuroscience and 23 papers in Neurology. Recurrent topics in Cyril Goizet's work include Genetic Neurodegenerative Diseases (27 papers), Hereditary Neurological Disorders (27 papers) and Mitochondrial Function and Pathology (23 papers). Cyril Goizet is often cited by papers focused on Genetic Neurodegenerative Diseases (27 papers), Hereditary Neurological Disorders (27 papers) and Mitochondrial Function and Pathology (23 papers). Cyril Goizet collaborates with scholars based in France, United States and Germany. Cyril Goizet's co-authors include Didier Lacombe, Demetrio Raldúa, Stéphane Mathis, Patrick J. Babin, Jean‐Michel Vallat, Alexandra Dürr, Benoı̂t Arveiler, Gaëtan Lesca, Gwendal Le Masson and Isabelle Coupry and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Cyril Goizet

128 papers receiving 3.9k 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 Goizet France 35 1.7k 1.1k 762 735 539 133 4.0k
Ubaldo Del Carro Italy 31 1.5k 0.9× 1.2k 1.1× 584 0.8× 613 0.8× 310 0.6× 81 3.9k
Gaëtan Lesca France 33 1.2k 0.7× 610 0.5× 382 0.5× 920 1.3× 1.0k 1.9× 160 3.4k
Nobutaka Kawahara Japan 32 1.2k 0.7× 1.1k 0.9× 1.0k 1.3× 654 0.9× 95 0.2× 87 4.4k
David W. Stockton United States 32 3.3k 1.9× 1.3k 1.1× 483 0.6× 413 0.6× 1.3k 2.5× 70 4.9k
Erik‐Jan Kamsteeg Netherlands 32 2.2k 1.3× 704 0.6× 258 0.3× 206 0.3× 470 0.9× 124 3.2k
O. Dubourg France 33 985 0.6× 910 0.8× 668 0.9× 385 0.5× 121 0.2× 70 3.0k
Rashmi Bansal United States 45 3.0k 1.7× 1.5k 1.3× 244 0.3× 274 0.4× 354 0.7× 95 5.6k
Chao Zhao United Kingdom 43 3.3k 1.9× 1.9k 1.7× 412 0.5× 461 0.6× 359 0.7× 94 8.4k
Annie Laquerrière France 32 1.4k 0.8× 502 0.4× 248 0.3× 300 0.4× 584 1.1× 109 3.3k
Franco Taroni Italy 44 3.2k 1.9× 2.3k 2.1× 1.3k 1.7× 488 0.7× 367 0.7× 156 5.2k

Countries citing papers authored by Cyril Goizet

Since Specialization
Citations

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

Fields of papers citing papers by Cyril Goizet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cyril Goizet

This figure shows the co-authorship network connecting the top 25 collaborators of Cyril Goizet. A scholar is included among the top collaborators of Cyril Goizet 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 Goizet. Cyril Goizet 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.
Aupy, Jérôme, Laurent Villard, Nathalie Villeneuve, et al.. (2025). GABRA2‐related encephalopathy: Identification of two phenotypes with distinctive electroclinical features. Epilepsia. 66(8).
2.
Ewenczyk, Claire, Mathieu Anheim, Alexandra Dürr, et al.. (2025). French guidelines for the diagnosis and management of pure hereditary spastic paraplegia. Revue Neurologique. 181(6). 471–482.
3.
Fergelot, Patricia, Caroline Rooryck, Dominique P. Germain, et al.. (2024). Prevalence of Fabry disease in patients with chronic pain: Lessons from the DOUFAB and DOUFABIS studies. European Journal of Pain. 29(1). e4708–e4708.
4.
Barnérias, Christine, Mehrdad A. Estiar, Claire Ewenczyk, et al.. (2024). From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants. European Journal of Neurology. 32(1). e70025–e70025. 2 indexed citations
5.
Trimouille, Aurélien, Cyril Goizet, Guilhem Solé, et al.. (2022). Renal involvement is frequent in adults with primary mitochondrial disorders: an observational study. Clinical Kidney Journal. 16(1). 100–110. 5 indexed citations
6.
Masingue, Marion, Timothée Lenglet, Cyril Goizet, et al.. (2020). Natural History of Adult Patients with GM2 Gangliosidosis. Annals of Neurology. 87(4). 609–617. 41 indexed citations
7.
Mazza, Davide, Franca Codazzi, Tyler Mark Pierson, et al.. (2019). Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation. Journal of Medical Genetics. 56(8). 499–511. 19 indexed citations
8.
Trimouille, Aurélien, Cyril Goizet, Romain Boulestreau, et al.. (2019). Adult onset tubulo‐interstitial nephropathy in MT‐ND5‐related phenotypes. Clinical Genetics. 97(4). 628–633. 14 indexed citations
9.
Balayn, Nathalie, Larissa Lordier, Francesco Baschieri, et al.. (2019). Disrupted filamin A/αIIbβ3 interaction induces macrothrombocytopenia by increasing RhoA activity. Blood. 133(16). 1778–1788. 25 indexed citations
10.
Moutton, Sébastien, Ange‐Line Bruel, Mirna Assoum, et al.. (2018). Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features. Clinical Genetics. 93(6). 1172–1178. 17 indexed citations
11.
Servais, Aude, Cyril Goizet, Aurélia Bertholet‐Thomas, et al.. (2015). La cystinose chez l’adulte : une maladie systémique. Néphrologie & Thérapeutique. 11(3). 152–159. 6 indexed citations
12.
Moutton, Sébastien, Caroline Rooryck, Jérôme Toutain, et al.. (2012). Dysmorphic features in subtelomeric 20p13 deletion excluding JAG1: A recognizable microdeletion phenotype?. European Journal of Medical Genetics. 55(2). 151–155. 4 indexed citations
13.
Lüdecke, Hermann‐Josef, Igor Sibon, Christophe Richez, et al.. (2011). Rheumatologic and neurological events in an elderly patient with tricho-rhino-phalangeal syndrome type I. European Journal of Medical Genetics. 54(4). e405–e408. 6 indexed citations
14.
Rooryck, Caroline, Dorothée Cailley, Julie Bouron, et al.. (2010). Array‐CGH analysis of a cohort of 86 patients with oculoauriculovertebral spectrum. American Journal of Medical Genetics Part A. 152A(8). 1984–1989. 44 indexed citations
15.
Rouanet, François, Igor Sibon, Cyril Goizet, Peter Renou, & William A. Meissner. (2009). [Etiological assessment of cerebral infarct in the young. Proposals from the working group of the French Neuro-vascular Society (December 2008)].. PubMed. 165 Spec No 4. F283–8. 6 indexed citations
16.
Chevrollier, Arnaud, Virginie Guillet, Dominique Loiseau, et al.. (2008). Hereditary optic neuropathies share a common mitochondrial coupling defect. Annals of Neurology. 63(6). 794–798. 94 indexed citations
17.
Hanein, Sylvain, Elodie Martin, Amir Boukhris, et al.. (2008). Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome. The American Journal of Human Genetics. 82(4). 992–1002. 148 indexed citations
18.
Goizet, Cyril, Amir Boukhris, Emeline Mundwiller, et al.. (2008). Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10. Human Mutation. 30(2). E376–E385. 95 indexed citations
19.
Lesca, Gaëtan, Carla Olivieri, Nelly Burnichon, et al.. (2007). Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: Data from the French-Italian HHT network. Genetics in Medicine. 9(1). 14–22. 157 indexed citations
20.
Barat, Pascal, et al.. (2004). Phenotypic heterogeneity in AAAS gene mutation. Acta Paediatrica. 93(9). 1257–1259. 4 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ubaldo Del Carro Breakdown of academic impact, for papers by Gaëtan Lesca Breakdown of academic impact, for papers by Nobutaka Kawahara Breakdown of academic impact, for papers by David W. Stockton Breakdown of academic impact, for papers by Erik‐Jan Kamsteeg Breakdown of academic impact, for papers by O. Dubourg Breakdown of academic impact, for papers by Rashmi Bansal Breakdown of academic impact, for papers by Chao Zhao Breakdown of academic impact, for papers by Annie Laquerrière Breakdown of academic impact, for papers by Franco Taroni
Rankless by CCL
2026