Alberto Blázquez

1.6k total citations
50 papers, 1.1k citations indexed

About

Alberto Blázquez is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Alberto Blázquez has authored 50 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 24 papers in Clinical Biochemistry and 16 papers in Rheumatology. Recurrent topics in Alberto Blázquez's work include Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (24 papers) and ATP Synthase and ATPases Research (15 papers). Alberto Blázquez is often cited by papers focused on Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (24 papers) and ATP Synthase and ATPases Research (15 papers). Alberto Blázquez collaborates with scholars based in Spain, United States and Belgium. Alberto Blázquez's co-authors include Miguel A. Martı́n, Joaquı́n Arenas, Cristina Ugalde, María Morán, Antoni L. Andreu, María Dolores Ledesma, Carla Mazzeo, Rebeca Acín‐Pérez, Enrique Gabandé‐Rodríguez and Carolina Villarroya‐Beltri and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and Neurology.

In The Last Decade

Alberto Blázquez

49 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alberto Blázquez Spain 18 750 323 185 146 141 50 1.1k
Diana Ballhausen Switzerland 19 546 0.7× 356 1.1× 158 0.9× 141 1.0× 167 1.2× 46 1.1k
Caterina Garone Italy 21 1.3k 1.8× 641 2.0× 126 0.7× 44 0.3× 182 1.3× 45 1.7k
Denise Cassandrini Italy 23 735 1.0× 228 0.7× 315 1.7× 99 0.7× 176 1.2× 62 1.3k
Alessandra Maresca Italy 18 1.0k 1.4× 264 0.8× 43 0.2× 80 0.5× 91 0.6× 38 1.3k
Yolanda Cámara Spain 19 1.5k 2.0× 448 1.4× 84 0.5× 86 0.6× 137 1.0× 35 1.7k
Lynne A. Wolfe United States 15 742 1.0× 297 0.9× 50 0.3× 50 0.3× 264 1.9× 49 1.1k
Brendan C. Lanpher United States 17 581 0.8× 259 0.8× 175 0.9× 46 0.3× 465 3.3× 41 1.2k
Laura Gort Spain 24 629 0.8× 247 0.8× 226 1.2× 221 1.5× 104 0.7× 67 1.3k
Hendrik Rosewich Germany 18 567 0.8× 137 0.4× 41 0.2× 44 0.3× 120 0.9× 34 857
Shlomo Almashanu Israel 16 390 0.5× 271 0.8× 67 0.4× 62 0.4× 136 1.0× 45 838

Countries citing papers authored by Alberto Blázquez

Since Specialization
Citations

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

Fields of papers citing papers by Alberto Blázquez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alberto Blázquez

This figure shows the co-authorship network connecting the top 25 collaborators of Alberto Blázquez. A scholar is included among the top collaborators of Alberto Blázquez 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 Alberto Blázquez. Alberto Blázquez 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.
Bermejo‐Guerrero, Laura, et al.. (2024). Remarkable clinical improvement with oral nucleoside treatment in a patient with adult-onset TK2 deficiency: A case report. Mitochondrion. 76. 101879–101879. 5 indexed citations
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.
Ballesta‐Martínez, María Juliana, Pablo Serrano‐Lorenzo, Alberto Blázquez, et al.. (2023). A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene. International Journal of Molecular Sciences. 24(2). 1743–1743. 6 indexed citations
4.
Bermejo‐Guerrero, Laura, Alberto Blázquez, Pablo Serrano‐Lorenzo, et al.. (2023). Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome. Journal of Clinical Medicine. 12(6). 2435–2435. 7 indexed citations
5.
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
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.
Morén, Constanza, Francesc Josep García‐García, Alberto Blázquez, et al.. (2022). Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects. Antioxidants. 11(4). 741–741. 5 indexed citations
8.
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
9.
Arteche‐López, Ana, María José Gómez-Rodríguez, Alberto Blázquez, et al.. (2021). Biallelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2. European Journal of Human Genetics. 29(10). 1520–1526. 12 indexed citations
10.
Laine-Menéndez, Sara, Cristina Domínguez‐González, Alberto Blázquez, et al.. (2021). Preferent Diaphragmatic Involvement in TK2 Deficiency: An Autopsy Case Study. International Journal of Molecular Sciences. 22(11). 5598–5598. 5 indexed citations
11.
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
12.
García‐Consuegra, Inés, Amaya Bélanger-Quintana, Pablo Serrano‐Lorenzo, et al.. (2020). Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report. Genes. 11(8). 855–855. 11 indexed citations
13.
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
14.
Montoya, Julio, Sonia Emperador, Eduardo Ruiz‐Pesini, et al.. (2019). A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues. Mitochondrion. 50. 14–18. 7 indexed citations
15.
Blázquez, Alberto, et al.. (2017). Beyond cervical lipomas: myoclonus, gait disorder and multisystem involvement leading to mitochondrial disease. BMJ Case Reports. 2017. bcr–2016. 2 indexed citations
16.
García‐Consuegra, Inés, Alberto Blázquez, Carlos Rubio-Terrés, et al.. (2016). Taking advantage of an old concept, “illegitimate transcription”, for a proposed novel method of genetic diagnosis of McArdle disease. Genetics in Medicine. 18(11). 1128–1135. 8 indexed citations
17.
Cruz‐Bermúdez, Alberto, Ramiro J. Vicente-Blanco, Mayte Montero, et al.. (2016). Functional Characterization of Three Concomitant MtDNA LHON Mutations Shows No Synergistic Effect on Mitochondrial Activity. PLoS ONE. 11(1). e0146816–e0146816. 15 indexed citations
18.
Morán, María, Aitor Delmiro, Alberto Blázquez, et al.. (2014). Bulk autophagy, but not mitophagy, is increased in cellular model of mitochondrial disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(7). 1059–1070. 32 indexed citations
19.
Blázquez, Alberto, María Morán, Alfonso Verdú, et al.. (2009). Infantile mitochondrial encephalomyopathy with unusual phenotype caused by a novel BCS1L mutation in an isolated complex III-deficient patient. Neuromuscular Disorders. 19(2). 143–146. 33 indexed citations
20.
Rubio-Terrés, Carlos, Inés García‐Consuegra, Gisela Nogales‐Gadea, et al.. (2007). A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patients. Human Mutation. 28(2). 203–204. 42 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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