Ester López‐Gallardo

2.0k total citations
57 papers, 1.2k citations indexed

About

Ester López‐Gallardo is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, Ester López‐Gallardo has authored 57 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 26 papers in Clinical Biochemistry and 9 papers in Epidemiology. Recurrent topics in Ester López‐Gallardo's work include Mitochondrial Function and Pathology (44 papers), Metabolism and Genetic Disorders (26 papers) and ATP Synthase and ATPases Research (15 papers). Ester López‐Gallardo is often cited by papers focused on Mitochondrial Function and Pathology (44 papers), Metabolism and Genetic Disorders (26 papers) and ATP Synthase and ATPases Research (15 papers). Ester López‐Gallardo collaborates with scholars based in Spain, Brazil and Venezuela. Ester López‐Gallardo's co-authors include Julio Montoya, Eduardo Ruiz‐Pesini, Manuel J. López‐Pérez, David Pacheu‐Grau, Aurora Gómez-Durán, Carmen Díez‐Sánchez, Paz Briones, Rafael Artuch, Sonia Emperador and A. Nascimento and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Ester López‐Gallardo

57 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ester López‐Gallardo Spain 19 936 493 135 107 104 57 1.2k
Carl Fratter United Kingdom 26 945 1.0× 530 1.1× 184 1.4× 158 1.5× 72 0.7× 47 1.3k
Daniela Skladal Austria 16 705 0.8× 461 0.9× 82 0.6× 137 1.3× 71 0.7× 32 994
S. Lane Rutledge United States 19 844 0.9× 519 1.1× 252 1.9× 104 1.0× 85 0.8× 31 1.3k
Edith Müller Germany 17 688 0.7× 685 1.4× 148 1.1× 128 1.2× 119 1.1× 51 1.3k
H. Ogier de Baulny France 17 626 0.7× 808 1.6× 136 1.0× 274 2.6× 252 2.4× 33 1.2k
D. R. Johns United States 18 781 0.8× 382 0.8× 77 0.6× 89 0.8× 33 0.3× 20 1.0k
Parayil Sankaran Bindu India 19 386 0.4× 177 0.4× 80 0.6× 170 1.6× 108 1.0× 92 1.1k
Abraham B. Eastwood United States 13 654 0.7× 248 0.5× 76 0.6× 121 1.1× 129 1.2× 19 984
Ying Jin China 15 258 0.3× 136 0.3× 210 1.6× 56 0.5× 57 0.5× 52 865
Yolanda Campos Spain 31 1.9k 2.0× 1.1k 2.2× 274 2.0× 292 2.7× 275 2.6× 118 2.7k

Countries citing papers authored by Ester López‐Gallardo

Since Specialization
Citations

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

Fields of papers citing papers by Ester López‐Gallardo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ester López‐Gallardo. 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 Ester López‐Gallardo. The network helps show where Ester López‐Gallardo may publish in the future.

Co-authorship network of co-authors of Ester López‐Gallardo

This figure shows the co-authorship network connecting the top 25 collaborators of Ester López‐Gallardo. A scholar is included among the top collaborators of Ester López‐Gallardo 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 Ester López‐Gallardo. Ester López‐Gallardo 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.
López‐Gallardo, Ester, Sonia Emperador, David Pacheu‐Grau, et al.. (2022). Toxic and nutritional factors trigger Leber hereditary optic neuropathy due to a mitochondrial tRNA mutation. Clinical Genetics. 102(4). 339–344. 2 indexed citations
2.
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
3.
López‐Gallardo, Ester, Francisco Cammarata‐Scalisi, Sonia Emperador, et al.. (2020). Mitochondrial DNA pathogenic mutations in multiple symmetric lipomatosis. Clinical Genetics. 97(5). 731–735. 8 indexed citations
4.
Bayona‐Bafaluy, M. Pilar, Ester López‐Gallardo, Sonia Emperador, et al.. (2020). Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathy. Mutation Research/Reviews in Mutation Research. 786. 108334–108334. 6 indexed citations
5.
Emperador, Sonia, et al.. (2019). Ketogenic treatment reduces the percentage of a LHON heteroplasmic mutation and increases mtDNA amount of a LHON homoplasmic mutation. Orphanet Journal of Rare Diseases. 14(1). 150–150. 20 indexed citations
6.
López‐Gallardo, Ester, et al.. (2018). Food derived respiratory complex I inhibitors modify the effect of Leber hereditary optic neuropathy mutations. Food and Chemical Toxicology. 120. 89–97. 6 indexed citations
7.
Emperador, Sonia, M. Pilar Bayona‐Bafaluy, Ana Fernández‐Marmiesse, et al.. (2016). Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy. European Journal of Human Genetics. 25(1). 153–156. 16 indexed citations
8.
Montoya, Julio, et al.. (2015). Side Effects of Culture Media Antibiotics on Cell Differentiation. Tissue Engineering Part C Methods. 21(11). 1143–1147. 30 indexed citations
9.
Emperador, Sonia, Mercè Pineda, Ester López‐Gallardo, et al.. (2015). Mutation loads in different tissues from six pathogenic mtDNA point mutations. Mitochondrion. 22. 17–22. 11 indexed citations
10.
Lorente, Leonardo, María M. Martín, Ester López‐Gallardo, et al.. (2015). Decrease of oxidative phosphorylation system function in severe septic patients. Journal of Critical Care. 30(5). 935–939. 24 indexed citations
11.
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
12.
Montoya, Julio, Ester López‐Gallardo, Sonia Emperador, & Eduardo Ruiz‐Pesini. (2012). Enfermedades del ADN mitocondrial. 1 indexed citations
13.
Gómez-Durán, Aurora, David Pacheu‐Grau, Ester López‐Gallardo, et al.. (2012). Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(8). 1216–1222. 81 indexed citations
14.
Pacheu‐Grau, David, et al.. (2012). Mitochondrial antibiograms in personalized medicine. Human Molecular Genetics. 22(6). 1132–1139. 34 indexed citations
15.
Pacheu‐Grau, David, Aurora Gómez-Durán, Ester López‐Gallardo, et al.. (2011). ‘Progress’ renders detrimental an ancient mitochondrial DNA genetic variant. Human Molecular Genetics. 20(21). 4224–4231. 11 indexed citations
16.
López‐Gallardo, Ester, et al.. (2011). OXPHOS toxicogenomics and Parkinson's disease. Mutation Research/Reviews in Mutation Research. 728(3). 98–106. 15 indexed citations
17.
Bayona‐Bafaluy, M. Pilar, Ester López‐Gallardo, Julio Montoya, & Eduardo Ruiz‐Pesini. (2010). Maternally inherited susceptibility to cancer. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1807(6). 643–649. 11 indexed citations
18.
Ascaso, Francisco J., et al.. (2010). Macular lesion resembling adult‐onset vitelliform macular dystrophy in Kearns–Sayre syndrome with multiple mtDNA deletions. Clinical and Experimental Ophthalmology. 38(8). 812–816. 18 indexed citations
19.
López‐Gallardo, Ester, Antoni L. Andreu, Antonio Herrera, et al.. (2009). NARP syndrome in a patient harbouring an insertion in the MT-ATP6 gene that results in a truncated protein. Journal of Medical Genetics. 46(1). 64–67. 40 indexed citations
20.
Montoya, Julio, Ester López‐Gallardo, Carmen Díez‐Sánchez, Manuel J. López‐Pérez, & Eduardo Ruiz‐Pesini. (2008). 20 years of human mtDNA pathologic point mutations: Carefully reading the pathogenicity criteria. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1787(5). 476–483. 45 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Carl Fratter Breakdown of academic impact, for papers by Daniela Skladal Breakdown of academic impact, for papers by S. Lane Rutledge Breakdown of academic impact, for papers by Edith Müller Breakdown of academic impact, for papers by H. Ogier de Baulny Breakdown of academic impact, for papers by D. R. Johns Breakdown of academic impact, for papers by Parayil Sankaran Bindu Breakdown of academic impact, for papers by Abraham B. Eastwood Breakdown of academic impact, for papers by Ying Jin Breakdown of academic impact, for papers by Yolanda Campos
Rankless by CCL
2026