Joaquı́n Arenas

12.3k total citations · 1 hit paper
307 papers, 8.9k citations indexed

About

Joaquı́n Arenas is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Joaquı́n Arenas has authored 307 papers receiving a total of 8.9k indexed citations (citations by other indexed papers that have themselves been cited), including 182 papers in Molecular Biology, 103 papers in Clinical Biochemistry and 94 papers in Rheumatology. Recurrent topics in Joaquı́n Arenas's work include Mitochondrial Function and Pathology (127 papers), Metabolism and Genetic Disorders (103 papers) and Glycogen Storage Diseases and Myoclonus (78 papers). Joaquı́n Arenas is often cited by papers focused on Mitochondrial Function and Pathology (127 papers), Metabolism and Genetic Disorders (103 papers) and Glycogen Storage Diseases and Myoclonus (78 papers). Joaquı́n Arenas collaborates with scholars based in Spain, United States and Italy. Joaquı́n Arenas's co-authors include Miguel A. Martı́n, Yolanda Campos, Carlos Rubio-Terrés, Pilar del Hoyo, Alejandro Lucía, Antoni L. Andreu, Cristina Ugalde, José Antonio Navarro, Gisela Nogales‐Gadea and Félix Javier Jiménez‐Jiménez and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The EMBO Journal and PLoS ONE.

In The Last Decade

Joaquı́n Arenas

305 papers receiving 8.7k citations

Hit Papers

Defective Hepatic Mitocho... 2003 2026 2010 2018 2003 100 200 300 400 500

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Joaquı́n Arenas 4.7k 1.9k 1.6k 1.5k 1.1k 307 8.9k
Rafael Artuch 3.7k 0.8× 2.5k 1.3× 1.2k 0.7× 1.1k 0.7× 853 0.8× 291 6.9k
Rita Horváth 7.1k 1.5× 3.2k 1.7× 473 0.3× 884 0.6× 823 0.7× 280 9.4k
Fernando Scaglia 4.8k 1.0× 3.0k 1.5× 495 0.3× 1.0k 0.7× 1.1k 1.0× 168 7.1k
Gerard T. Berry 3.1k 0.7× 3.3k 1.7× 716 0.4× 1.1k 0.8× 984 0.9× 213 7.1k
Leonardo Salviati 6.7k 1.4× 1.3k 0.7× 376 0.2× 2.1k 1.4× 545 0.5× 162 9.5k
S. DiMauro 12.7k 2.7× 8.0k 4.1× 1.9k 1.1× 1.5k 1.0× 1.2k 1.1× 237 15.9k
Nenad Blau 7.5k 1.6× 8.4k 4.4× 2.3k 1.4× 3.9k 2.6× 1.7k 1.6× 339 14.5k
Edwin C.M. Mariman 4.4k 0.9× 470 0.2× 1.4k 0.8× 2.0k 1.4× 2.1k 1.9× 242 10.1k
Richard J. Rodenburg 8.2k 1.8× 3.4k 1.8× 328 0.2× 959 0.6× 952 0.9× 250 10.9k
Anne Lombès 7.1k 1.5× 3.5k 1.8× 307 0.2× 982 0.7× 431 0.4× 145 9.5k

Countries citing papers authored by Joaquı́n Arenas

Since Specialization
Citations

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

Fields of papers citing papers by Joaquı́n Arenas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joaquı́n Arenas

This figure shows the co-authorship network connecting the top 25 collaborators of Joaquı́n Arenas. A scholar is included among the top collaborators of Joaquı́n Arenas 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 Joaquı́n Arenas. Joaquı́n Arenas 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.
Martı́n, Miguel A., et al.. (2024). Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene. International Journal of Molecular Sciences. 25(13). 7240–7240.
2.
Ceballos, Francisco C., Pablo Serrano‐Lorenzo, Laura Bermejo‐Guerrero, et al.. (2024). Clinical and Genetic Analysis of Patients With TK2 Deficiency. Neurology Genetics. 10(2). e200138–e200138. 4 indexed citations
3.
Delmiro, Aitor, María Morán, Cristina Domínguez‐González, et al.. (2022). High‐dose oral glutamine supplementation reduces elevated glutamate levels in cerebrospinal fluid in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke‐like episodes syndrome. European Journal of Neurology. 30(2). 538–547. 6 indexed citations
4.
Delmiro, Aitor, María Morán, Cristina Domínguez‐González, et al.. (2022). Elevated glutamate and decreased glutamine levels in the cerebrospinal fluid of patients with MELAS syndrome. Journal of Neurology. 269(6). 3238–3248. 6 indexed citations
5.
García‐Consuegra, Inés, Tomàs Pinós, Cristina Domínguez‐González, et al.. (2022). Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis. International Journal of Molecular Sciences. 23(9). 4650–4650. 1 indexed citations
6.
Domínguez‐González, Cristina, Laura Bermejo‐Guerrero, Germán Morís, et al.. (2022). Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational study. Neuromuscular Disorders. 32(9). 728–735. 5 indexed citations
7.
Laine-Menéndez, Sara, Carmen Fiuza‐Luces, Aitor Delmiro, et al.. (2022). Apoptosis-Inducing Factor Deficiency Induces Tissue-Specific Alterations in Autophagy: Insights from a Preclinical Model of Mitochondrial Disease and Exercise Training Effects. Antioxidants. 11(3). 510–510. 1 indexed citations
8.
García‐Consuegra, Inés, Rafael Garesse, Joaquı́n Arenas, et al.. (2022). Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. International Journal of Molecular Sciences. 23(22). 13964–13964. 8 indexed citations
9.
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
10.
Peñas, Ana, Sara Laine-Menéndez, David Lora, et al.. (2021). Plasma Gelsolin Reinforces the Diagnostic Value of FGF-21 and GDF-15 for Mitochondrial Disorders. International Journal of Molecular Sciences. 22(12). 6396–6396. 10 indexed citations
11.
Bermejo‐Guerrero, Laura, Pablo Serrano‐Lorenzo, Alberto Blázquez, et al.. (2021). Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to TWNK Mutations. Journal of Clinical Medicine. 11(1). 22–22. 6 indexed citations
12.
Peñas, Ana, Lorena Marín-Buera, Cristina Domínguez‐González, et al.. (2020). Altered Expression Ratio of Actin-Binding Gelsolin Isoforms Is a Novel Hallmark of Mitochondrial OXPHOS Dysfunction. Cells. 9(9). 1922–1922. 8 indexed citations
13.
Rodríguez‐Gómez, Irene, Alfredo Santalla, Diego Munguía‐Izquierdo, et al.. (2020). Sex Differences and the Influence of an Active Lifestyle on Adiposity in Patients with McArdle Disease. International Journal of Environmental Research and Public Health. 17(12). 4334–4334. 3 indexed citations
14.
Blázquez, Alberto, Pablo Serrano‐Lorenzo, Gerardo Gutiérrez‐Gutiérrez, et al.. (2020). Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia. Journal of Medical Genetics. 57(9). 643–646. 20 indexed citations
15.
Luna, Noemí de, Astrid Brull, Miguel A. Martı́n, et al.. (2019). Absence of p.R50X Pygm read-through in McArdle disease cellular models. Disease Models & Mechanisms. 13(1). 10 indexed citations
16.
Serrano‐Lorenzo, Pablo, et al.. (2019). A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish Population. Genes. 10(10). 785–785. 8 indexed citations
17.
García‐Consuegra, Inés, Rosario Francisco‐Velilla, Tomàs Pinós, et al.. (2018). Missense mutations have unexpected consequences: The McArdle disease paradigm. Human Mutation. 39(10). 1338–1343. 12 indexed citations
18.
Fiuza‐Luces, Carmen, Alejandro Santos‐Lozano, Francisco Llavero, et al.. (2018). Muscle molecular adaptations to endurance exercise training are conditioned by glycogen availability: a proteomics‐based analysis in the McArdle mouse model. The Journal of Physiology. 596(6). 1035–1061. 21 indexed citations
19.
Coenen, Daniëlle M., Ignacio Ara, Carlos Rodríguez-López, et al.. (2018). Manifesting heterozygotes in McArdle disease: a myth or a reality—role of statins. Journal of Inherited Metabolic Disease. 41(6). 1027–1035. 3 indexed citations
20.
Pérez-Carreras, M, Pilar del Hoyo, Miguel A. Martı́n, et al.. (2003). Defective Hepatic Mitochondrial Respiratory Chain in Patients With Nonalcoholic Steatohepatitis. Hepatology. 38(4). 999–1007. 570 indexed citations breakdown →

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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