Carmen Espinós

3.2k total citations
95 papers, 1.9k citations indexed

About

Carmen Espinós is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Carmen Espinós has authored 95 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cellular and Molecular Neuroscience, 44 papers in Molecular Biology and 26 papers in Neurology. Recurrent topics in Carmen Espinós's work include Hereditary Neurological Disorders (36 papers), Neurological diseases and metabolism (25 papers) and Genetic Neurodegenerative Diseases (25 papers). Carmen Espinós is often cited by papers focused on Hereditary Neurological Disorders (36 papers), Neurological diseases and metabolism (25 papers) and Genetic Neurodegenerative Diseases (25 papers). Carmen Espinós collaborates with scholars based in Spain, Czechia and United States. Carmen Espinós's co-authors include Francesc Palau, Teresa Sevilla, Vincenzo Lupo, Dolores Martínez‐Rubio, Juan J. Vílchez, José M. Millán, Rafael Sivera, María José Chumillas, Nuria Muelas and Carmén Nájera and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Carmen Espinós

93 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carmen Espinós Spain 26 1.1k 831 426 249 215 95 1.9k
Satoko Miyatake Japan 29 1.5k 1.4× 508 0.6× 131 0.3× 195 0.8× 201 0.9× 146 2.4k
Masako M. Bilak United States 20 664 0.6× 377 0.5× 215 0.5× 198 0.8× 152 0.7× 26 1.3k
Daniele Ghezzi Italy 33 2.6k 2.5× 408 0.5× 189 0.4× 337 1.4× 131 0.6× 91 3.2k
Srinivasa Subramaniam United States 27 1.3k 1.3× 942 1.1× 173 0.4× 332 1.3× 266 1.2× 44 2.2k
Jesse D. Sengillo United States 21 1.1k 1.0× 284 0.3× 842 2.0× 456 1.8× 102 0.5× 74 2.4k
Jacqueline L. Vanderluit Canada 25 1.2k 1.1× 366 0.4× 143 0.3× 126 0.5× 207 1.0× 33 1.8k
Andreas Eilers Germany 14 1.1k 1.0× 601 0.7× 88 0.2× 86 0.3× 171 0.8× 23 1.9k
Linda Moran United Kingdom 19 574 0.5× 713 0.9× 558 1.3× 810 3.3× 133 0.6× 39 1.8k
Heike Rebholz United States 18 1.2k 1.1× 203 0.2× 125 0.3× 98 0.4× 113 0.5× 27 1.6k
Hiroyuki Ishiura Japan 25 844 0.8× 633 0.8× 383 0.9× 627 2.5× 177 0.8× 146 1.8k

Countries citing papers authored by Carmen Espinós

Since Specialization
Citations

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

Fields of papers citing papers by Carmen Espinós

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmen Espinós

This figure shows the co-authorship network connecting the top 25 collaborators of Carmen Espinós. A scholar is included among the top collaborators of Carmen Espinós 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 Carmen Espinós. Carmen Espinós 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.
Sivera, Rafael, Ana L. Pelayo‐Negro, Ivonne Jericó, et al.. (2024). Expanding the Clinical Spectrum of DRP2 -Associated Charcot-Marie-Tooth Disease. Neurology. 102(7). e209174–e209174. 2 indexed citations
2.
Penning, Louis C., Marina Berenguer, Anna Członkowska, et al.. (2023). A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and Treatment. Biomedicines. 11(2). 420–420. 6 indexed citations
3.
Martínez‐Rubio, Dolores, Clara Marco‐Marín, Vincenzo Lupo, et al.. (2023). Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy. International Journal of Molecular Sciences. 24(22). 16400–16400. 3 indexed citations
4.
Jesús, Silvia, Fátima Carrillo, Dolores Martínez‐Rubio, et al.. (2021). NR4A2 Mutations Can Cause Intellectual Disability and Language Impairment With Persistent Dystonia-Parkinsonism. Neurology Genetics. 7(1). e543–e543. 12 indexed citations
5.
Sivera, Rafael, Vincenzo Lupo, Marina Frasquet, et al.. (2021). Charcot–Marie–Tooth disease due to MORC2 mutations in Spain. European Journal of Neurology. 28(9). 3001–3011. 10 indexed citations
6.
Martínez‐Torres, Irene, et al.. (2020). Genetics of Wilson disease and Wilson‐like phenotype in a clinical series from eastern Spain. Clinical Genetics. 97(5). 758–763. 19 indexed citations
7.
Lupo, Vincenzo, Marina Frasquet, Ana L. Pelayo‐Negro, et al.. (2018). Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations. Journal of Medical Genetics. 55(12). 814–823. 15 indexed citations
8.
Frasquet, Marina, Vincenzo Lupo, María José Chumillas, et al.. (2018). Phenotypical features of two patients diagnosed with PHARC syndrome and carriers of a new homozygous mutation in the ABHD12 gene. Journal of the Neurological Sciences. 387. 134–138. 17 indexed citations
9.
Sevilla, Teresa, et al.. (2017). Audiological Findings in Charcot–Marie–Tooth Disease Type 4C. The Journal of International Advanced Otology. 13(1). 93–99. 8 indexed citations
10.
Soldevilla, Beatriz, Clara Ibáñez, Fulvio Santacatterina, et al.. (2017). Plasma metabolome and skin proteins in Charcot-Marie-Tooth 1A patients. PLoS ONE. 12(6). e0178376–e0178376. 13 indexed citations
11.
Calpena, Eduardo, Víctor López Del Amo, Beatriz Llamusí, et al.. (2017). The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway. Disease Models & Mechanisms. 11(1). 14 indexed citations
12.
Lupo, Vincenzo, Eduardo Calpena, Luca Bartesaghi, et al.. (2013). Sh3tc2 deficiency affects neuregulin‐1/ErbB signaling. Glia. 61(7). 1041–1051. 36 indexed citations
13.
Sevilla, Teresa, Dolores Martínez‐Rubio, Catalina Márquez-Vega, et al.. (2012). Genetics of the Charcot‐Marie‐Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy‐Russe in depth. Clinical Genetics. 83(6). 565–570. 25 indexed citations
14.
Lupo, Vincenzo, Máximo Ibo Galindo, Dolores Martínez‐Rubio, et al.. (2009). Missense mutations in the SH3TC2 protein causing Charcot-Marie-Tooth disease type 4C affect its localization in the plasma membrane and endocytic pathway. Human Molecular Genetics. 18(23). 4603–4614. 47 indexed citations
15.
Palau, Francesc, et al.. (2008). Gene symbol: SH3TC2. Disease: Charcot-Marie-Tooth type 4C.. PubMed. 124(3). 320–320. 1 indexed citations
16.
Artuch, Rafael, Gloria Brea‐Calvo, Paz Briones, et al.. (2006). Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation. Journal of the Neurological Sciences. 246(1-2). 153–158. 74 indexed citations
17.
Garcı́a-Planells, Javier, J A Burguera, José M. Millán, et al.. (2005). Ancient origin of the CAG expansion causing Huntington disease in a Spanish population. Human Mutation. 25(5). 453–459. 17 indexed citations
18.
Espinós, Carmen, et al.. (2004). Polymorphism of Alcohol Dehydrogenase Genes in Alcoholic and Nonalcoholic Individuals from Valencia (Spain). Hereditas. 126(3). 247–253. 14 indexed citations
19.
Casaña, Pilar, Francisco Martı́nez, Saturnino Haya, Carmen Espinós, & José A. Aznar. (2001). Significant linkage and non‐linkage of type 1 von Willebrand disease to the von Willebrand factor gene. British Journal of Haematology. 115(3). 692–700. 25 indexed citations
20.
Casaña, Pilar, Francisco Martı́nez, Saturnino Haya, et al.. (2000). Q1311X: a novel nonsense mutation of putative ancient origin in the von Willebrand factor gene. SHORT REPORT. British Journal of Haematology. 111(2). 552–555. 8 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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