Abelardo Solano

557 total citations
14 papers, 407 citations indexed

About

Abelardo Solano is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Abelardo Solano has authored 14 papers receiving a total of 407 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Abelardo Solano's work include Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (9 papers) and ATP Synthase and ATPases Research (4 papers). Abelardo Solano is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), Metabolism and Genetic Disorders (9 papers) and ATP Synthase and ATPases Research (4 papers). Abelardo Solano collaborates with scholars based in Spain, Mexico and Italy. Abelardo Solano's co-authors include Julio Montoya, Paz Briones, Antoni L. Andreu, Ester López‐Gallardo, Rafael Artuch, Manuel J. López‐Pérez, Lourdes Ibáñez, María Dolores Herrero, Merçè Pineda and Aída Ormazábal and has published in prestigious journals such as Annals of Neurology, Biochemical and Biophysical Research Communications and FEBS Letters.

In The Last Decade

Abelardo Solano

14 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Abelardo Solano Spain 11 265 159 62 52 46 14 407
Silvio Ferraris Italy 12 262 1.0× 198 1.2× 27 0.4× 42 0.8× 43 0.9× 12 370
Khalid Al‐Thihli Oman 13 219 0.8× 135 0.8× 50 0.8× 116 2.2× 66 1.4× 50 456
Lisbeth Dahl Schroeder Denmark 6 381 1.4× 265 1.7× 36 0.6× 51 1.0× 81 1.8× 11 514
Patricia Galvin‐Parton United States 11 192 0.7× 93 0.6× 36 0.6× 84 1.6× 47 1.0× 13 313
Paul de Laat Netherlands 15 391 1.5× 228 1.4× 99 1.6× 44 0.8× 47 1.0× 21 554
Femke C. C. Klouwer Netherlands 13 401 1.5× 182 1.1× 20 0.3× 67 1.3× 102 2.2× 26 521
Natalie Hauser United States 13 293 1.1× 111 0.7× 43 0.7× 228 4.4× 32 0.7× 26 562
BN Harding United Kingdom 9 178 0.7× 120 0.8× 58 0.9× 14 0.3× 59 1.3× 12 402
Nihal Demircan Türkiye 12 140 0.5× 62 0.4× 41 0.7× 39 0.8× 23 0.5× 30 622
Sarah Macklin United States 9 176 0.7× 121 0.8× 39 0.6× 183 3.5× 54 1.2× 21 423

Countries citing papers authored by Abelardo Solano

Since Specialization
Citations

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

Fields of papers citing papers by Abelardo Solano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abelardo Solano

This figure shows the co-authorship network connecting the top 25 collaborators of Abelardo Solano. A scholar is included among the top collaborators of Abelardo Solano 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 Abelardo Solano. Abelardo Solano is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

14 of 14 papers shown
1.
López‐Gallardo, Ester, Sonia Emperador, Abelardo Solano, et al.. (2014). Expanding the clinical phenotypes of MT-ATP6 mutations. Human Molecular Genetics. 23(23). 6191–6200. 32 indexed citations
2.
Lara‐Astiaso, David, Juan Camilo Estrada, Carmen Albó, et al.. (2012). Complement anaphylatoxins C3a and C5a induce a failing regenerative program in cardiac resident cells. Evidence of a role for cardiac resident stem cells other than cardiomyocyte renewal. SpringerPlus. 1(1). 63–63. 26 indexed citations
3.
Blesa, Rafael, et al.. (2007). Molecular Genetics of a Patient with Mohr–Tranebjaerg Syndrome due to a New Mutation in the DDP1 Gene. NeuroMolecular Medicine. 9(4). 285–291. 19 indexed citations
4.
Carod-Artal, Francisco Javier, et al.. (2006). Deleciones en el ADN mitocondrial asociadas a oftalmoplejía crónica extrínseca progresiva con fibras rojas rasgadas en 2 pacientes brasileños. Medicina Clínica. 126(12). 457–460. 2 indexed citations
5.
Guallar, Jordi P, Maya R. Vilà, Ester López‐Gallardo, et al.. (2006). Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNALys point mutations in mitochondrial DNA. Molecular Genetics and Metabolism. 89(3). 283–285. 18 indexed citations
6.
García‐Arumí, Elena, David Lligé, Ramón Martí, et al.. (2005). Free radicals‐mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA. FEBS Letters. 579(30). 6909–6913. 29 indexed citations
7.
Pineda, Merçè, Aída Ormazábal, Ester López‐Gallardo, et al.. (2005). Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion. Annals of Neurology. 59(2). 394–398. 119 indexed citations
8.
Solano, Abelardo, Giovanna Russo, Maria Giovanna Parisi, et al.. (2004). De Toni-Debr�-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA. Pediatric Nephrology. 19(7). 790–793. 8 indexed citations
9.
Pineda, Mercédes, Abelardo Solano, Rafael Artuch, et al.. (2004). Peripheral Neuropathy with Ataxia in Childhood as a Result of the G8363A Mutation in Mitochondrial DNA. Pediatric Research. 56(1). 55–59. 8 indexed citations
10.
Solano, Abelardo, Manuel G. Roig, Cristòfol Vives-Bauzá, et al.. (2003). Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene. Annals of Neurology. 54(4). 527–530. 53 indexed citations
11.
Herráiz, Maite, Naiara Beraza, Abelardo Solano, et al.. (2003). Liver Failure Caused by Herpes Simplex Virus Thymidine Kinase Plus Ganciclovir Therapy Is Associated with Mitochondrial Dysfunction and Mitochondrial DNA Depletion. Human Gene Therapy. 14(5). 463–472. 32 indexed citations
12.
Vives-Bauzá, Cristòfol, Josep Gámez, Paz Briones, et al.. (2001). Exercise intolerance resulting: from a muscle-restricted mutation in the mitochondrial tRNALeu(CUN)gene. Annals of Medicine. 33(7). 493–496. 20 indexed citations
13.
Solano, Abelardo, et al.. (2001). Enfermedades genéticas del ADN mitocondrial humano. Salud Pública de México. 43(2). 151–161. 15 indexed citations
14.
Vilà, Maya R., Josep Gámez, Abelardo Solano, et al.. (2000). Uncoupling Protein-1 mRNA Expression in Lipomas from Patients Bearing Pathogenic Mitochondrial DNA Mutations. Biochemical and Biophysical Research Communications. 278(3). 800–802. 26 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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