Jesús Esteban‐Pérez

3.8k total citations
38 papers, 951 citations indexed

About

Jesús Esteban‐Pérez is a scholar working on Neurology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jesús Esteban‐Pérez has authored 38 papers receiving a total of 951 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Neurology, 18 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jesús Esteban‐Pérez's work include Amyotrophic Lateral Sclerosis Research (19 papers), Neurogenetic and Muscular Disorders Research (18 papers) and Hereditary Neurological Disorders (6 papers). Jesús Esteban‐Pérez is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (19 papers), Neurogenetic and Muscular Disorders Research (18 papers) and Hereditary Neurological Disorders (6 papers). Jesús Esteban‐Pérez collaborates with scholars based in Spain, United States and United Kingdom. Jesús Esteban‐Pérez's co-authors include Diane McKenna‐Yasek, Robert H. Brown, H. Robert Horvitz, Peter C. Sapp, Alberto García‐Redondo, J. O'Regan, D.R. Rosen, J.J. Rivas, Carmen Paradas and Catalina Alarcón‐de‐la‐Lastra and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Jesús Esteban‐Pérez

38 papers receiving 936 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jesús Esteban‐Pérez Spain 19 490 327 281 214 213 38 951
Sarah Mustafa United Kingdom 11 158 0.3× 185 0.6× 286 1.0× 183 0.9× 156 0.7× 16 942
Sang Su Oh United States 14 235 0.5× 149 0.5× 371 1.3× 201 0.9× 75 0.4× 17 949
Franck Patin France 16 426 0.9× 204 0.6× 270 1.0× 76 0.4× 110 0.5× 25 721
Kon‐Ping Lin Taiwan 13 245 0.5× 89 0.3× 199 0.7× 168 0.8× 111 0.5× 40 634
Lauren Martins Valentim Brazil 15 77 0.2× 74 0.2× 342 1.2× 157 0.7× 90 0.4× 18 854
Sonja Körner Germany 19 722 1.5× 386 1.2× 272 1.0× 153 0.7× 128 0.6× 33 1.1k
Julian P. Tuazon United States 14 76 0.2× 92 0.3× 224 0.8× 76 0.4× 143 0.7× 18 553
Daud Lodin United States 6 304 0.6× 141 0.4× 140 0.5× 52 0.2× 62 0.3× 10 509
Fengyuan Che China 13 243 0.5× 48 0.1× 188 0.7× 67 0.3× 174 0.8× 49 685
Brian C. Kramer United States 16 163 0.3× 100 0.3× 199 0.7× 218 1.0× 125 0.6× 26 670

Countries citing papers authored by Jesús Esteban‐Pérez

Since Specialization
Citations

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

Fields of papers citing papers by Jesús Esteban‐Pérez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jesús Esteban‐Pérez. 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 Jesús Esteban‐Pérez. The network helps show where Jesús Esteban‐Pérez may publish in the future.

Co-authorship network of co-authors of Jesús Esteban‐Pérez

This figure shows the co-authorship network connecting the top 25 collaborators of Jesús Esteban‐Pérez. A scholar is included among the top collaborators of Jesús Esteban‐Pérez 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 Jesús Esteban‐Pérez. Jesús Esteban‐Pérez 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., Elena Aller, M.J. Colomina, et al.. (2024). Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish Population. Biomedicines. 12(2). 356–356. 7 indexed citations
2.
Lupo, Vincenzo, Laura Bermejo‐Guerrero, Aurelio Hernández‐Laín, et al.. (2023). Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3. Journal of Neurology. 271(2). 986–994. 3 indexed citations
3.
Serrano‐Lorenzo, Pablo, Jesús Esteban‐Pérez, Cristina Domínguez‐González, et al.. (2022). Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI). Genes. 13(10). 1835–1835. 5 indexed citations
4.
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
5.
Fernández‐Marmiesse, Ana, et al.. (2019). Bethlem myopathy: a series of 16 patients and description of seven new associated mutations. Journal of Neurology. 266(4). 934–941. 14 indexed citations
6.
Esteban‐Pérez, Jesús, et al.. (2017). Report by the Spanish Foundation for the Brain on the social impact of amyotrophic lateral sclerosis and other neuromuscular disorders. SHILAP Revista de lepidopterología. 33(1). 35–46. 12 indexed citations
7.
Mancuso, Renzo, Anna Martínez‐Muriana, David I. Gregorio, et al.. (2016). Neuregulin-1 promotes functional improvement by enhancing collateral sprouting in SOD1G93A ALS mice and after partial muscle denervation. Neurobiology of Disease. 95. 168–178. 45 indexed citations
8.
Esteban‐Pérez, Jesús, et al.. (2015). Informe de la Fundación Del Cerebro sobre el impacto social de la esclerosis lateral amiotrófica y las enfermedades neuromusculares. Neurología. 33(1). 35–46. 19 indexed citations
9.
Paredes, Igor, Jesús Esteban‐Pérez, Ana Ramos, Pedro González, & J.J. Rivas. (2013). A severe case of Hirayama disease successfully treated by anterior cervical fusion. Journal of Neurosurgery Spine. 20(2). 191–195. 27 indexed citations
10.
Esteban‐Pérez, Jesús. (2013). Poliomielitis paralítica. Nuevos problemas: el síndrome postpolio. Revista Española de Salud Pública. 87(5). 517–522. 10 indexed citations
11.
Galán, Lucía, César Augusto Restrepo Valencia, Paz de la Torre, et al.. (2012). SOD1-N196 mutation in a family with amyotrophic lateral sclerosis. SHILAP Revista de lepidopterología. 27(1). 11–15. 2 indexed citations
12.
Galán, Lucía, César Augusto Restrepo Valencia, Paz de la Torre, et al.. (2012). Mutación SOD1-N19S en una familia de esclerosis lateral amiotrófica. Neurología. 27(1). 11–15. 2 indexed citations
13.
Calvo, Ana Cristina, Raquel Manzano, Sara Oliván, et al.. (2012). Genetic Biomarkers for ALS Disease in Transgenic SOD1G93A Mice. PLoS ONE. 7(3). e32632–e32632. 48 indexed citations
14.
Beghi, Ettore, Adriano Chiò, Philippe Couratier, et al.. (2010). The epidemiology and treatment of ALS: Focus on the heterogeneity of the disease and critical appraisal of therapeutic trials. Amyotrophic Lateral Sclerosis. 12(1). 1–10. 106 indexed citations
15.
Esteban‐Pérez, Jesús, et al.. (2010). Spanish adaptation of the revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R). Amyotrophic Lateral Sclerosis. 11(5). 475–477. 28 indexed citations
16.
Salas, Teresa, et al.. (2008). Spanish adaptation of the Amyotrophic Lateral Sclerosis Questionnaire ALSAQ-40 for ALS patients. Amyotrophic Lateral Sclerosis. 9(3). 168–172. 14 indexed citations
17.
Bustos, F. de, Félix Javier Jiménez‐Jiménez, J. A. Molina, et al.. (1998). Cerebrospinal fluid levels of alpha-tocopherol in amyotrophic lateral sclerosis. Journal of Neural Transmission. 105(6-7). 703–708. 22 indexed citations
18.
Esteban‐Pérez, Jesús, et al.. (1996). Hypokalemic periodic paralysis mutations: Confirmation of mutation and analysis of founder effect. Neuromuscular Disorders. 6(1). 27–31. 40 indexed citations
19.
Sapp, Peter C., D.R. Rosen, Betsy A. Hosler, et al.. (1995). Identification of three novel mutations in the gene for superoxide dismutase in patients with familial amyotrophic lateral sclerosis. Neuromuscular Disorders. 5(5). 353–357. 48 indexed citations
20.
Esteban‐Pérez, Jesús, D.R. Rosen, Allen C. Bowling, et al.. (1994). Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis. Human Molecular Genetics. 3(6). 997–998. 65 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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