Caroline Espil‐Taris

689 total citations
20 papers, 211 citations indexed

About

Caroline Espil‐Taris is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Caroline Espil‐Taris has authored 20 papers receiving a total of 211 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Neurology and 5 papers in Genetics. Recurrent topics in Caroline Espil‐Taris's work include Mitochondrial Function and Pathology (6 papers), Myasthenia Gravis and Thymoma (4 papers) and Muscle Physiology and Disorders (4 papers). Caroline Espil‐Taris is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Myasthenia Gravis and Thymoma (4 papers) and Muscle Physiology and Disorders (4 papers). Caroline Espil‐Taris collaborates with scholars based in France, Belgium and Switzerland. Caroline Espil‐Taris's co-authors include Pascal Laforêt, France Piétri‐Rouxel, I. Pénisson-Besnier, Rabah Ben Yaou, Luis Garcı́a, Thomas Voït, France Leturcq, Christel Gentil, Claude Cancés and Myriam Jugie and has published in prestigious journals such as Neurology, Human Molecular Genetics and Antioxidants and Redox Signaling.

In The Last Decade

Caroline Espil‐Taris

20 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caroline Espil‐Taris France 10 113 66 35 31 31 20 211
Marjorie Illingworth United Kingdom 5 142 1.3× 57 0.9× 65 1.9× 93 3.0× 7 0.2× 8 239
Yaqian Duan United States 6 76 0.7× 14 0.2× 29 0.8× 29 0.9× 29 0.9× 11 189
Ratna Bhavaraju‐Sanka United States 5 120 1.1× 62 0.9× 44 1.3× 13 0.4× 32 1.0× 10 206
Acary Sousa Bulle Oliveira Brazil 8 40 0.4× 56 0.8× 27 0.8× 27 0.9× 11 0.4× 14 161
Sho Katayama Japan 7 44 0.4× 36 0.5× 14 0.4× 43 1.4× 35 1.1× 29 203
Jurģis Strautmanis Latvia 7 53 0.5× 121 1.8× 6 0.2× 12 0.4× 11 0.4× 15 240
Marsela Qesari Italy 5 157 1.4× 19 0.3× 77 2.2× 16 0.5× 61 2.0× 5 339
Taro Kitamura Japan 10 49 0.4× 34 0.5× 55 1.6× 3 0.1× 12 0.4× 19 247
Erik Andersen Australia 7 86 0.8× 18 0.3× 15 0.4× 13 0.4× 5 0.2× 22 213
Alicia Alonso‐Jiménez Spain 8 47 0.4× 28 0.4× 17 0.5× 19 0.6× 36 1.2× 15 152

Countries citing papers authored by Caroline Espil‐Taris

Since Specialization
Citations

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

Fields of papers citing papers by Caroline Espil‐Taris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Caroline Espil‐Taris. 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 Caroline Espil‐Taris. The network helps show where Caroline Espil‐Taris may publish in the future.

Co-authorship network of co-authors of Caroline Espil‐Taris

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline Espil‐Taris. A scholar is included among the top collaborators of Caroline Espil‐Taris 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 Caroline Espil‐Taris. Caroline Espil‐Taris 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.
Ehlinger, Virginie, Maëlle Biotteau, Ulrike Walther‐Louvier, et al.. (2023). Confirmatory validation of the french version of the Duchenne Muscular Dystrophy module of the pediatric quality of life inventory (PedsQLTM3.0DMDfv). BMC Pediatrics. 23(1). 563–563. 1 indexed citations
2.
Barrois, Rémi, Christine Barnérias, Frédérique Audic, et al.. (2023). A new score combining compound muscle action potential (CMAP) amplitudes and motor score is predictive of motor outcome after AVXS-101 (Onasemnogene Abeparvovec) SMA therapy. Neuromuscular Disorders. 33(4). 309–314. 12 indexed citations
3.
Gitiaux, Cyril, Christine Barnérias, Frédérique Audic, et al.. (2022). Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis. Neurology. 98(23). 14 indexed citations
4.
Gitiaux, Cyril, Christine Barnérias, Frédérique Audic, et al.. (2022). Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis: The French Experience.. PubMed. 98(23). e2368–e2376. 9 indexed citations
5.
Trimouille, Aurélien, Benoı̂t Arveiler, Caroline Espil‐Taris, et al.. (2021). CHN1 and duane retraction syndrome: Expanding the phenotype to cranial nerves development disease. European Journal of Medical Genetics. 64(4). 104188–104188. 4 indexed citations
6.
Walther‐Louvier, Ulrike, Caroline Espil‐Taris, François Rivier, et al.. (2021). Evaluating next-generation sequencing in neuromuscular diseases with neonatal respiratory distress. European Journal of Paediatric Neurology. 31. 78–87. 9 indexed citations
7.
Baudou, Éloïse, Ulrike Walther‐Louvier, Caroline Espil‐Taris, et al.. (2021). Clinical Phenotype in an Early-Onset French Pediatric Population: Charcot–Marie–Tooth's Disease Type 2A. Neuropediatrics. 52(5). 351–357. 1 indexed citations
8.
Thibaud, Marie, Nathalie Aladjidi, P. Bessou, et al.. (2020). Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA. Neuropediatrics. 51(4). 245–250. 2 indexed citations
9.
Fontaine, Monique, Anne‐Frédérique Dessein, Karine Mention-Mulliez, et al.. (2018). Fluxomic assay-assisted diagnosis orientation in a cohort of 11 patients with myopathic form of CPT2 deficiency. Molecular Genetics and Metabolism. 123(4). 441–448. 11 indexed citations
10.
Wallach, Edward E., et al.. (2018). Arthrogryposis in children: Etiological assessments and preparation of a protocol for etiological investigations. Archives de Pédiatrie. 25(5). 322–326. 10 indexed citations
11.
Gentil, Christel, France Leturcq, Rabah Ben Yaou, et al.. (2012). Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation. Human Molecular Genetics. 21(15). 3449–3460. 39 indexed citations
12.
Bénard, Giovanni, Thomas Trian, Nadège Bellancé, et al.. (2012). Adaptative Capacity of Mitochondrial Biogenesis and of Mitochondrial Dynamics in Response to Pathogenic Respiratory Chain Dysfunction. Antioxidants and Redox Signaling. 19(4). 350–365. 20 indexed citations
13.
Gentil, Christel, France Leturcq, Rabah Ben Yaou, et al.. (2012). G.P.75 Variable phenotype of del45–55 Becker patients correlated to nNOSμ mislocalization and RYR1 hypernitrosylation. Neuromuscular Disorders. 22(9-10). 834–834. 19 indexed citations
14.
Joussain, Charles, Delphine Lamireau, Caroline Espil‐Taris, et al.. (2011). A 10-year-old boy with dark urine and acute kidney injury: question. Pediatric Nephrology. 26(8). 1229–1230. 2 indexed citations
15.
Villega, Frédéric, Caroline Espil‐Taris, Marie Husson, et al.. (2011). Polymorphisme d’expression de l’atteinte épileptique et cognitive du syndrome du chromosome 20 en anneau. Archives de Pédiatrie. 18(4). 394–396. 2 indexed citations
16.
Villega, Frédéric, Fabienne Picard, Caroline Espil‐Taris, et al.. (2010). Benign nocturnal alternating hemiplegia of childhood: Two cases with positive evolution. Brain and Development. 33(6). 525–529. 10 indexed citations
17.
Béhin, Anthony, M. Mayer, Myriam Jugie, et al.. (2008). Severe neonatal myasthenia due to maternal anti-MuSK antibodies. Neuromuscular Disorders. 18(6). 443–446. 35 indexed citations
18.
Béhin, Anthony, M. Mayer, Lucienne Chatenoud, et al.. (2006). G.P.3 09 Severe neonatal myasthenia due to maternal anti-MuSK antibodies. Neuromuscular Disorders. 16(9-10). 661–662. 1 indexed citations
19.
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
20.
Goizet, Cyril, Caroline Espil‐Taris, Marie Husson, et al.. (2003). A patient with hydranencephaly and PEHO-like dysmorphic features. Annales de Génétique. 46(1). 25–28. 5 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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