Teresa Sevilla

4.0k total citations
102 papers, 2.3k citations indexed

About

Teresa Sevilla is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Teresa Sevilla has authored 102 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Cellular and Molecular Neuroscience, 41 papers in Neurology and 37 papers in Molecular Biology. Recurrent topics in Teresa Sevilla's work include Hereditary Neurological Disorders (49 papers), Genetic Neurodegenerative Diseases (29 papers) and Neurological diseases and metabolism (19 papers). Teresa Sevilla is often cited by papers focused on Hereditary Neurological Disorders (49 papers), Genetic Neurodegenerative Diseases (29 papers) and Neurological diseases and metabolism (19 papers). Teresa Sevilla collaborates with scholars based in Spain, France and United States. Teresa Sevilla's co-authors include Juan J. Vílchez, Francesc Palau, Carmen Espinós, María José Chumillas, F. Mayordomo, Juan F. Vázquez‐Costa, Nuria Muelas, Luís Bataller, Dolores Martínez‐Rubio and Rafael Sivera and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Teresa Sevilla

96 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Teresa Sevilla Spain 27 1.2k 846 759 526 343 102 2.3k
Juan J. Vílchez Spain 32 1.5k 1.2× 894 1.1× 1.5k 1.9× 435 0.8× 261 0.8× 130 3.0k
Alessandro Malandrini Italy 26 591 0.5× 577 0.7× 973 1.3× 546 1.0× 184 0.5× 95 2.2k
Julia Wanschitz Austria 26 594 0.5× 715 0.8× 741 1.0× 321 0.6× 297 0.9× 78 1.9k
Yeşim Parman Türkiye 23 482 0.4× 637 0.8× 580 0.8× 200 0.4× 196 0.6× 98 1.6k
Velina Guergueltcheva Bulgaria 23 561 0.5× 408 0.5× 899 1.2× 213 0.4× 133 0.4× 52 1.6k
Pedro Mancías United States 15 809 0.7× 380 0.4× 750 1.0× 280 0.5× 121 0.4× 37 1.7k
Yoshihisa Takiyama Japan 30 1.6k 1.3× 693 0.8× 1.7k 2.3× 524 1.0× 140 0.4× 139 2.4k
Michael C. Kruer United States 25 449 0.4× 901 1.1× 746 1.0× 501 1.0× 145 0.4× 74 2.2k
A.A.W.M. Gabreëls‐Festen Netherlands 26 1.3k 1.1× 743 0.9× 439 0.6× 564 1.1× 123 0.4× 54 2.0k
Ricard Rojas‐García Spain 29 802 0.6× 2.1k 2.5× 857 1.1× 183 0.3× 600 1.7× 67 3.1k

Countries citing papers authored by Teresa Sevilla

Since Specialization
Citations

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

Fields of papers citing papers by Teresa Sevilla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teresa Sevilla

This figure shows the co-authorship network connecting the top 25 collaborators of Teresa Sevilla. A scholar is included among the top collaborators of Teresa Sevilla 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 Teresa Sevilla. Teresa Sevilla 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.
Vázquez‐Costa, Juan F., et al.. (2026). Muscle MRI Contributes to the Differential Diagnosis Between Distal Myopathies and Distal Hereditary Motor Neuropathies. European Journal of Neurology. 33(1). e70456–e70456.
2.
Sevilla, Teresa & Lucía Galán Dávila. (2025). Neuropatías de fibra pequeña. Medicina Clínica. 165(3). 106950–106950.
3.
Vílchez, Juan J., Inmaculada Azorı́n, Pilar Martí, et al.. (2024). ITPR3‐associated neuropathy: Report of a further family with adult onset intermediate Charcot–Marie–Tooth disease. European Journal of Neurology. 31(12). e16485–e16485. 1 indexed citations
4.
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
5.
Dávila, Lucía Galán, et al.. (2024). A description of variant transthyretin amyloidosis (ATTRv) stage 1 patients and asymptomatic carriers in Spain: the EMPATIa study. Orphanet Journal of Rare Diseases. 19(1). 323–323. 1 indexed citations
6.
Pérez‐Martínez, Pablo, et al.. (2024). Impact of SARS‐CoV‐2 infection and COVID‐19 pandemic on the morbidity and mortality of amyotrophic lateral sclerosis patients in Valencia, Spain. European Journal of Neurology. 31(12). e16465–e16465. 1 indexed citations
7.
López, Inés Losada, et al.. (2024). Management of Hereditary Transthyretin Amyloidosis (ATTRv) Patients and Asymptomatic Carriers in Spain: The EMPATIa Study. Journal of Clinical Medicine. 13(24). 7587–7587.
8.
Antozzi, Carlo, Jeffrey T. Guptill, Vera Bril, et al.. (2023). Safety and Efficacy of Nipocalimab in Patients With Generalized Myasthenia Gravis. Neurology. 102(2). e207937–e207937. 30 indexed citations
9.
Vázquez‐Costa, Juan F., Mónica Povedano, S. Kapetanovic García, et al.. (2022). Nusinersen in adult patients with 5q spinal muscular atrophy: A multicenter observational cohorts' study. European Journal of Neurology. 29(11). 3337–3346. 20 indexed citations
10.
Vázquez‐Costa, Juan F., Mónica Povedano, S. Kapetanovic García, et al.. (2022). Validation of motor and functional scales for the evaluation of adult patients with 5q spinal muscular atrophy. European Journal of Neurology. 29(12). 3666–3675. 26 indexed citations
11.
Vázquez‐Costa, Juan F., Carmen Paradas, Ricardo Rojas-García, et al.. (2022). Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease. European Journal of Neurology. 30(4). 861–871. 3 indexed citations
12.
Frutos, Fernando de, Juan Pablo Ochoa, David Reyes‐Leiva, et al.. (2022). Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain. Amyloid. 30(2). 199–207. 6 indexed citations
13.
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
14.
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
15.
Cortés‐Vicente, Elena, Ricard Rojas‐García, Jordi Díaz‐Manera, et al.. (2018). The impact of rituximab infusion protocol on the long‐term outcome in anti‐MuSK myasthenia gravis. Annals of Clinical and Translational Neurology. 5(6). 710–716. 36 indexed citations
16.
Vázquez‐Costa, Juan F., Jacinto Javier Martínez Payá, José Ignacio Tembl, et al.. (2018). New insights into the pathophysiology of fasciculations in amyotrophic lateral sclerosis: An ultrasound study. Clinical Neurophysiology. 129(12). 2650–2657. 26 indexed citations
17.
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
18.
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
19.
Claramunt, Reyes, Teresa Sevilla, Vincenzo Lupo, et al.. (2007). The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot–Marie–Tooth disease type 4. Clinical Genetics. 71(4). 343–349. 34 indexed citations
20.

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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