Caroline Espil

411 total citations
10 papers, 91 citations indexed

About

Caroline Espil is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Caroline Espil has authored 10 papers receiving a total of 91 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Caroline Espil's work include Neurogenetic and Muscular Disorders Research (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital Anomalies and Fetal Surgery (3 papers). Caroline Espil is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital Anomalies and Fetal Surgery (3 papers). Caroline Espil collaborates with scholars based in France, Netherlands and Denmark. Caroline Espil's co-authors include Christine Barnérias, Christian Richelme, B. Chabrol, Julie Miro, Valérie Serre, Sylvie Tuffery‐Giraud, Karima Ghorab, Konstantina Fragaki, Sylviane Peudenier and Justine Lerat and has published in prestigious journals such as Journal of Medical Genetics, Journal of Neurology and European Journal of Neurology.

In The Last Decade

Caroline Espil

9 papers receiving 90 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 France 6 54 26 23 20 14 10 91
Eugenia Borgione Italy 8 81 1.5× 18 0.7× 13 0.6× 27 1.4× 5 0.4× 19 125
Abdulaziz Alsaman Saudi Arabia 7 93 1.7× 30 1.2× 30 1.3× 14 0.7× 12 0.9× 15 129
Maysoon Alsagob Saudi Arabia 6 62 1.1× 22 0.8× 8 0.3× 15 0.8× 4 0.3× 12 109
Ana Kosać Serbia 7 82 1.5× 9 0.3× 53 2.3× 12 0.6× 31 2.2× 15 120
V. Branković Serbia 5 50 0.9× 7 0.3× 26 1.1× 26 1.3× 14 1.0× 9 79
Nuria García Segarra Switzerland 7 78 1.4× 57 2.2× 8 0.3× 18 0.9× 7 0.5× 10 148
Mojgan Reza United Kingdom 7 165 3.1× 33 1.3× 16 0.7× 30 1.5× 16 1.1× 10 193
Spencer Goodman United States 5 61 1.1× 6 0.2× 6 0.3× 21 1.1× 5 0.4× 7 105
Agustí Rodríguez‐Palmero Spain 6 84 1.6× 7 0.3× 6 0.3× 19 0.9× 3 0.2× 11 118
Liena E. O. Elsayed Sudan 6 40 0.7× 13 0.5× 28 1.2× 53 2.6× 2 0.1× 14 108

Countries citing papers authored by Caroline Espil

Since Specialization
Citations

This map shows the geographic impact of Caroline Espil'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 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 more than expected).

Fields of papers citing papers by Caroline Espil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Espil

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

All Works

10 of 10 papers shown
1.
Ropars, Juliette, Pascale Saugier-Véber, I. Desguerre, et al.. (2025). Spectrum of Phenotypes in SMA Patients With 4 SMN2 Copies in the French Population. Neurology Genetics. 11(2). e200222–e200222.
2.
Attarian, Shahram, Sadia Beloribi‐Djefaflia, Rafaëlle Bernard, et al.. (2024). French National Protocol for diagnosis and care of facioscapulohumeral muscular dystrophy (FSHD). Journal of Neurology. 271(9). 5778–5803. 6 indexed citations
3.
Lebigot, Élise, Emmanuel Roze, Claude Cancés, et al.. (2022). Movement disorders in valine métabolism diseases caused by HIBCH and ECHS1 deficiencies. European Journal of Neurology. 29(11). 3229–3242. 11 indexed citations
4.
Grimaldi‐Bensouda, Lamiae, Jon Andoni Urtizberea, Anthony Béhin, et al.. (2021). SMA – OUTCOME MEASURES AND REGISTRIES. Neuromuscular Disorders. 31. S130–S131. 1 indexed citations
5.
Ropars, Juliette, et al.. (2020). Multidisciplinary approach and psychosocial management of spinal muscular atrophy (SMA). Archives de Pédiatrie. 27(7). 7S45–7S49. 12 indexed citations
6.
Cancès, C., Christian Richelme, Christine Barnérias, & Caroline Espil. (2020). Clinical features of spinal muscular atrophy (SMA) type 2. Archives de Pédiatrie. 27(7). 7S18–7S22. 7 indexed citations
7.
Lerat, Justine, Corinne Magdelaine, Caroline Espil, et al.. (2019). A novel pathogenic variant of NEFL responsible for deafness associated with peripheral neuropathy discovered through next‐generation sequencing and review of the literature. Journal of the Peripheral Nervous System. 24(1). 139–144. 14 indexed citations
8.
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
9.
10.
Rouzier, Cécile, Konstantina Fragaki, Valérie Serre, et al.. (2010). The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein. Journal of Medical Genetics. 47(10). 670–676. 37 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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Rankless by CCL
2026