A. Cabello

1.1k total citations
37 papers, 735 citations indexed

About

A. Cabello is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, A. Cabello has authored 37 papers receiving a total of 735 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Rheumatology and 6 papers in Genetics. Recurrent topics in A. Cabello's work include Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). A. Cabello is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), Metabolism and Genetic Disorders (6 papers) and Glycogen Storage Diseases and Myoclonus (6 papers). A. Cabello collaborates with scholars based in Spain, United States and Austria. A. Cabello's co-authors include R.D. Lobato, Joaquı́n Arenas, José Ramón Ricoy, Yolanda Campos, Jesús S. Mora, Miguel A. Martı́n, J. Figols, Onofre Combarros, E. Lamas and J. Bautista and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

A. Cabello

37 papers receiving 707 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Cabello Spain 18 299 215 176 138 133 37 735
Guilhem Solé France 15 250 0.8× 176 0.8× 107 0.6× 152 1.1× 94 0.7× 62 731
He Lv China 17 396 1.3× 263 1.2× 147 0.8× 221 1.6× 92 0.7× 68 850
Donal Costigan Ireland 10 472 1.6× 183 0.9× 33 0.2× 131 0.9× 100 0.8× 16 901
Giovanna Stefania Colafati Italy 17 239 0.8× 277 1.3× 56 0.3× 83 0.6× 342 2.6× 90 836
A. Bornemann Germany 17 239 0.8× 286 1.3× 86 0.5× 143 1.0× 168 1.3× 42 755
G. W. Pearce United Kingdom 15 344 1.2× 161 0.7× 48 0.3× 157 1.1× 191 1.4× 25 766
Philippe Petiot France 13 159 0.5× 408 1.9× 55 0.3× 207 1.5× 45 0.3× 26 681
J. He China 14 222 0.7× 127 0.6× 52 0.3× 221 1.6× 88 0.7× 70 854
Emmanuel Ellie France 14 177 0.6× 312 1.5× 92 0.5× 160 1.2× 53 0.4× 36 682
Rumiko Izumi Japan 16 327 1.1× 142 0.7× 38 0.2× 68 0.5× 138 1.0× 50 609

Countries citing papers authored by A. Cabello

Since Specialization
Citations

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

Fields of papers citing papers by A. Cabello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Cabello

This figure shows the co-authorship network connecting the top 25 collaborators of A. Cabello. A scholar is included among the top collaborators of A. Cabello 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 A. Cabello. A. Cabello 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.
García‐Consuegra, Inés, Carlos Rubio-Terrés, Gisela Nogales‐Gadea, et al.. (2009). Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNA. Journal of Medical Genetics. 46(3). 198–202. 21 indexed citations
2.
Quintana, Ester, Johannes A. Mayr, Aida Font, et al.. (2009). PDH E1β deficiency with novel mutations in two patients with Leigh syndrome. Journal of Inherited Metabolic Disease. 32(S1). 339–343. 22 indexed citations
3.
Paradas, Carmen, Lidia González‐Quereda, Noemí de Luna, et al.. (2008). A new phenotype of dysferlinopathy with congenital onset. Neuromuscular Disorders. 19(1). 21–25. 49 indexed citations
4.
Kaen, Ariel, Ignacio Arrese, Alfonso Lagares, A. Cabello, & R.D. Lobato. (2007). Haemangiopericytoma presenting with acute intracerebral haemorrhage. Acta Neurochirurgica. 149(4). 415–418. 7 indexed citations
5.
Rueda, A., Sara Jiménez, Pilar del Hoyo, et al.. (2007). A novel mutation in the mitochondrial DNA tRNA Leu (UUR) gene associated with late-onset ocular myopathy. Neuromuscular Disorders. 17(5). 415–418. 3 indexed citations
6.
Miranda, P., R.D. Lobato, Pedro A. Gómez, A. Cabello, & Ana Martı́nez de Aragón. (2006). Complete surgical resection of high-grade astroblastoma with long time survival: case report and review of the literature. Neurocirugía. 17(1). 60–63. 19 indexed citations
7.
Blázquez, Alberto, Miguel A. Martı́n, Ramón Martí, et al.. (2005). Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIE. Neuromuscular Disorders. 15(11). 775–778. 14 indexed citations
8.
9.
Campos, Yolanda, Sara Jiménez, Carlos Rubio-Terrés, et al.. (2002). Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy. Muscle & Nerve. 25(2). 185–188. 13 indexed citations
10.
Lobato, R.D., et al.. (2000). Suprasellar chordoid glioma. Acta Neuropathologica. 99(6). 699–703. 41 indexed citations
11.
Calandre, L, et al.. (1998). Lysis rates with rt-PA vary between different human emboli in a rat model of cerebral embolism. Fibrinolysis & proteolysis. 12(2). 107–111. 4 indexed citations
12.
Campos, Yolanda, J. Bautista, Eduardo Gutiérrez‐Rivas, et al.. (1995). Clinical heterogeneity in two pedigrees with the 3243 bp tRNALeu(UUR)mutation of mitochondrial DNA. Acta Neurologica Scandinavica. 91(1). 62–65. 19 indexed citations
13.
Campos, Yolanda, Juan Carlos Gómez‐Esteban, A. Cabello, & Joaquı́n Arenas. (1994). Genetic analysis of one family with myoclonic epilepsy and ragged-red fibers (MERRF). PubMed. 17(10). 1229–31. 3 indexed citations
14.
Thomas, P. K., V.P. Misra, R. H. M. King, et al.. (1994). Autosomal recessive hereditary sensory neuropathy with spastic paraplegia. Brain. 117(4). 651–659. 17 indexed citations
15.
Cabello, A., et al.. (1991). Continuous muscle fiber activity, peripheral neuropathy, and thymoma. Annals of Neurology. 29(2). 215–218. 51 indexed citations
16.
Cabello, A., et al.. (1990). Myopathy with nemaline structures associated with HIV infection. Journal of Neurology. 237(1). 64–65. 17 indexed citations
17.
Cabello, A., et al.. (1987). Chromatolytic changes in the central nervous system of patients with the toxic oil syndrome. Acta Neuropathologica. 74(4). 354–361. 3 indexed citations
18.
Cabello, A., et al.. (1985). Hypotrophy of type I fibres with central nuclei: recovery 4 years after diagnosis.. Journal of Neurology Neurosurgery & Psychiatry. 48(2). 167–171. 7 indexed citations
19.
Ricoy, José Ramón & A. Cabello. (1981). Dysmaturative Myopathy Evolution of the Morphological Picture in Three Cases. PubMed. 7. 313–316. 9 indexed citations
20.
Lamas, E., et al.. (1978). Multiple intracranial arterial occlusions (moyamoya disease) in patients with neurofibromatosis one case report with autopsy. Acta Neurochirurgica. 45(1-2). 133–145. 38 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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