Rafael Sivera

1.1k total citations
26 papers, 572 citations indexed

About

Rafael Sivera is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology. According to data from OpenAlex, Rafael Sivera has authored 26 papers receiving a total of 572 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cellular and Molecular Neuroscience, 9 papers in Neurology and 8 papers in Neurology. Recurrent topics in Rafael Sivera's work include Hereditary Neurological Disorders (18 papers), Genetic Neurodegenerative Diseases (15 papers) and Neurological diseases and metabolism (8 papers). Rafael Sivera is often cited by papers focused on Hereditary Neurological Disorders (18 papers), Genetic Neurodegenerative Diseases (15 papers) and Neurological diseases and metabolism (8 papers). Rafael Sivera collaborates with scholars based in Spain, France and Italy. Rafael Sivera's co-authors include Teresa Sevilla, Carmen Espinós, Juan J. Vílchez, Francesc Palau, Ronald Brown, Philip J. Higgins, Dolores Martínez‐Rubio, Nuria Muelas, María José Chumillas and Vincenzo Lupo and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Rafael Sivera

25 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rafael Sivera Spain 11 374 166 154 140 69 26 572
Ingrid Bauer Germany 12 233 0.6× 190 1.1× 30 0.2× 123 0.9× 4 0.1× 48 602
Tomotada Ohtsuki Japan 20 14 0.0× 103 0.6× 35 0.2× 29 0.2× 19 0.3× 58 1.2k
Christopher S. Bjornsson United States 7 136 0.4× 234 1.4× 67 0.4× 28 0.2× 28 0.4× 9 533
Alessandro Geroldi Italy 13 285 0.8× 214 1.3× 94 0.6× 134 1.0× 90 1.3× 30 461
Araks Martirosyan Armenia 8 209 0.6× 292 1.8× 377 2.4× 67 0.5× 17 0.2× 13 694
Andrew J. Morris United States 9 30 0.1× 269 1.6× 14 0.1× 15 0.1× 30 0.4× 15 445
B. Kremer Netherlands 10 316 0.8× 298 1.8× 108 0.7× 124 0.9× 30 0.4× 15 484
Simona Capponi Italy 12 222 0.6× 211 1.3× 74 0.5× 92 0.7× 76 1.1× 16 405
R. Weber Switzerland 13 83 0.2× 104 0.6× 178 1.2× 46 0.3× 36 0.5× 29 658
Elizabeth J. Akin United States 13 236 0.6× 429 2.6× 21 0.1× 23 0.2× 138 2.0× 21 610

Countries citing papers authored by Rafael Sivera

Since Specialization
Citations

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

Fields of papers citing papers by Rafael Sivera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rafael Sivera

This figure shows the co-authorship network connecting the top 25 collaborators of Rafael Sivera. A scholar is included among the top collaborators of Rafael Sivera 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 Rafael Sivera. Rafael Sivera 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.
Muelas, Nuria, Pilar Martí, Inmaculada Azorı́n, et al.. (2025). Clinical features, mutation spectrum and factors related to reaching molecular diagnosis in a cohort of patients with distal myopathies. Journal of Neurology. 272(1). 97–97. 2 indexed citations
2.
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
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.
Azorı́n, Inmaculada, Pilar Martí, Nuria Muelas, et al.. (2024). Insights into phenotypic variability caused by GARS1 pathogenic variants. European Journal of Neurology. 31(10). e16416–e16416. 4 indexed citations
5.
Muelas, Nuria, Rafael Sivera, Irene Martínez‐Torres, et al.. (2023). Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain. Movement Disorders Clinical Practice. 10(6). 992–997. 3 indexed citations
6.
Mayordomo, Émpar, Eva González, Miguel Salavert, et al.. (2023). Disseminated toxoplasma infection after hematopoietic stem cell transplantation with myositis and encephalitis. Transplant Infectious Disease. 25(4). e14067–e14067. 2 indexed citations
7.
Thomas, Florian P., Mario Saporta, Shahram Attarian, et al.. (2022). Patient-Reported Symptom Burden of Charcot–Marie–Tooth Disease Type 1A: Findings From an Observational Digital Lifestyle Study. Journal of Clinical Neuromuscular Disease. 24(1). 7–17. 8 indexed citations
8.
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
9.
Frasquet, Marina, Ricard Rojas‐García, Juan F. Vázquez‐Costa, et al.. (2020). Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation. European Journal of Neurology. 28(4). 1334–1343. 42 indexed citations
10.
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
11.
Lupo, Vincenzo, Francisco García‐García, Antonia Albertí, et al.. (2016). Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy. Journal of Molecular Diagnostics. 18(2). 225–234. 35 indexed citations
12.
Sevilla, Teresa, Vincenzo Lupo, Dolores Martínez‐Rubio, et al.. (2015). Mutations in theMORC2gene cause axonal Charcot–Marie–Tooth disease. Brain. 139(1). 62–72. 58 indexed citations
13.
Pla‐Martín, David, Eduardo Calpena, Vincenzo Lupo, et al.. (2014). Junctophilin-1 is a modifier gene of GDAP1-related Charcot–Marie–Tooth disease. Human Molecular Genetics. 24(1). 213–229. 38 indexed citations
14.
Berciano, José, Teresa Sevilla, Carlos Casasnovas, et al.. (2012). Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease. SHILAP Revista de lepidopterología. 27(3). 169–178. 10 indexed citations
15.
Berciano, José, Teresa Sevilla, Carlos Casasnovas, et al.. (2011). Guía diagnóstica en el paciente con enfermedad de Charcot-Marie-Tooth. Neurología. 27(3). 169–178. 10 indexed citations
16.
Sevilla, Teresa, Vincenzo Lupo, Rafael Sivera, et al.. (2011). Congenital hypomyelinating neuropathy due to a novel MPZ mutation. Journal of the Peripheral Nervous System. 16(4). 347–352. 12 indexed citations
17.
Sivera, Rafael, N Martin, Isabel Boscá, et al.. (2011). Autoimmunity as a prognostic factor in sporadic adult onset cerebellar ataxia. Journal of Neurology. 259(5). 851–854. 7 indexed citations
18.
Brown, Ronald, Philip J. Higgins, & Rafael Sivera. (2011). Nonabelian Algebraic Topology. 51 indexed citations
19.
Brown, Ronald, et al.. (2011). Nonabelian Algebraic Topology: Filtered Spaces, Crossed Complexes, Cubical Homotopy Groupoids. Medical Entomology and Zoology. 40 indexed citations
20.
Sivera, Rafael, Carmen Espinós, Juan J. Vílchez, et al.. (2010). Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot‐Marie‐Tooth disease. Journal of the Peripheral Nervous System. 15(4). 334–344. 54 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 Ingrid Bauer Breakdown of academic impact, for papers by Tomotada Ohtsuki Breakdown of academic impact, for papers by Christopher S. Bjornsson Breakdown of academic impact, for papers by Alessandro Geroldi Breakdown of academic impact, for papers by Araks Martirosyan Breakdown of academic impact, for papers by Andrew J. Morris Breakdown of academic impact, for papers by B. Kremer Breakdown of academic impact, for papers by Simona Capponi Breakdown of academic impact, for papers by R. Weber Breakdown of academic impact, for papers by Elizabeth J. Akin
Rankless by CCL
2026