Eliécer Coto

26.6k total citations
304 papers, 8.1k citations indexed

About

Eliécer Coto is a scholar working on Molecular Biology, Immunology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Eliécer Coto has authored 304 papers receiving a total of 8.1k indexed citations (citations by other indexed papers that have themselves been cited), including 123 papers in Molecular Biology, 66 papers in Immunology and 60 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Eliécer Coto's work include Cardiomyopathy and Myosin Studies (31 papers), Psoriasis: Treatment and Pathogenesis (25 papers) and Ion channel regulation and function (21 papers). Eliécer Coto is often cited by papers focused on Cardiomyopathy and Myosin Studies (31 papers), Psoriasis: Treatment and Pathogenesis (25 papers) and Ion channel regulation and function (21 papers). Eliécer Coto collaborates with scholars based in Spain, United States and United Kingdom. Eliécer Coto's co-authors include Victoria Álvarez, Carlos López‐Larrea, Julián R. Reguero, Juan Gómez, Roser Torrá, David Ravine, Martijn H. Breuning, César Morı́s, Pablo Coto‐Segura and Pelayo González and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Eliécer Coto

300 papers receiving 7.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eliécer Coto Spain	45	3.3k	2.1k	1.6k	1.1k	797	304	8.1k
David Chitayat Canada	55	4.8k 1.5×	3.3k 1.6×	789 0.5×	686 0.6×	577 0.7×	403	11.6k
Michael A. Simpson United Kingdom	44	2.7k 0.8×	1.2k 0.6×	859 0.5×	486 0.4×	375 0.5×	161	6.3k
Victoria Álvarez Spain	42	1.8k 0.6×	660 0.3×	768 0.5×	886 0.8×	498 0.6×	199	5.4k
Robin J. Leach United States	47	4.8k 1.5×	2.2k 1.1×	490 0.3×	803 0.7×	601 0.8×	248	9.3k
Shigeo Kure Japan	44	4.1k 1.3×	1.1k 0.5×	781 0.5×	241 0.2×	1.4k 1.7×	322	8.0k
André Mégarbané Lebanon	43	4.1k 1.3×	2.1k 1.0×	806 0.5×	221 0.2×	367 0.5×	276	7.0k
Keiichi Ozono Japan	55	4.2k 1.3×	2.3k 1.1×	559 0.4×	297 0.3×	1.4k 1.8×	432	10.6k
Rodney E. Kellems United States	56	4.3k 1.3×	1.5k 0.7×	1.7k 1.1×	513 0.5×	240 0.3×	187	8.9k
Roger C. Wiggins United States	51	3.5k 1.1×	1.2k 0.6×	1.4k 0.9×	279 0.3×	361 0.5×	195	9.7k
Martin Farrall United Kingdom	47	3.1k 1.0×	3.2k 1.6×	1.5k 0.9×	1.8k 1.6×	366 0.5×	123	10.2k

Countries citing papers authored by Eliécer Coto

Since Specialization

Citations

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

Fields of papers citing papers by Eliécer Coto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eliécer Coto

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

All Works

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20 of 20 papers shown

Menéndez‐González, Manuel, et al.. (2024). Assessing the association between common functional Nuclear Factor Kappa-b gene polymorphisms (NFKB1, NFKBIZ, NFKBIA) and Alzheimer´s disease. Behavioural Brain Research. 476. 115264–115264. 1 indexed citations

Coto‐Segura, Pablo, et al.. (2023). The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs. Late-Onset Skin Disease and Increases the Risk of Arthritis in a Spanish Cohort of Psoriasis. International Journal of Molecular Sciences. 24(19). 14803–14803. 3 indexed citations

Gómez, Juan, Ceferino Martínez‐Faedo, Edelmiro Menéndez Torre, et al.. (2023). Clinical Evaluation of Patients with Genetically Confirmed Familial Hypercholesterolemia. Journal of Clinical Medicine. 12(3). 1030–1030. 2 indexed citations

Coto, Eliécer, Guillermo M. Albaiceta, Laura Amado‐Rodríguez, et al.. (2022). FURIN gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID‐19. Journal of Medical Virology. 94(8). 3589–3595. 13 indexed citations

Rodríguez, Ramón María Alvargonzález, María P. Hernández-Fuentes, María Laura Sáiz, et al.. (2021). Defining a Methylation Signature Associated With Operational Tolerance in Kidney Transplant Recipients. Frontiers in Immunology. 12. 709164–709164. 6 indexed citations

Lorca, Rebeca, Luca Pannone, Elías Cuesta‐Llavona, et al.. (2020). Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders. Clinical Genetics. 99(3). 457–461. 3 indexed citations

Lorca, Rebeca, Marı́a Martı́n, Isaac Pascual, et al.. (2020). Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome. Journal of Clinical Medicine. 9(12). 3846–3846. 1 indexed citations

Lorca, Rebeca, Marı́a Martı́n, Isaac Pascual, et al.. (2020). Characterization of Left Ventricular Non-Compaction Cardiomyopathy. Journal of Clinical Medicine. 9(8). 2524–2524. 15 indexed citations

Coto, Eliécer, Salvador Tranche, Julián R. Reguero, et al.. (2018). Genetic Variation in the H19 - IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function. DNA and Cell Biology. 37(7). 617–625. 6 indexed citations

10.

Calvo, David, Irene Valverde, José M. Rubín, et al.. (2016). Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope. International Journal of Cardiology. 218. 69–74. 8 indexed citations

11.

Vidal-Castiñeira, José Ramón, Antonio López‐Vázquez, Roberto Díaz‐Peña, et al.. (2016). A Single Nucleotide Polymorphism in the Il17ra Promoter Is Associated with Functional Severity of Ankylosing Spondylitis. PLoS ONE. 11(7). e0158905–e0158905. 17 indexed citations

12.

Gómez, Juan, Ikram Kammoun, Salem Kachboura, et al.. (2016). Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients. Genetic Testing and Molecular Biomarkers. 20(11). 674–679. 9 indexed citations

13.

Tavira, Beatriz, et al.. (2014). A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman’s syndrome patients. Journal of Human Genetics. 59(7). 376–380. 14 indexed citations

14.

González‐Lara, Leire, Noemí Eirís, Marta Díaz, et al.. (2013). SNP rs11652075 in the CARD14 Gene as a Risk Factor for Psoriasis (PSORS2) in a Spanish Cohort. DNA and Cell Biology. 32(10). 601–604. 25 indexed citations

15.

Coto‐Segura, Pablo, Jorge Santos‐Juanes, Juan Gómez, et al.. (2011). Common European Mitochondrial Haplogroups in the Risk for Psoriasis and Psoriatic Arthritis. Genetic Testing and Molecular Biomarkers. 16(6). 621–623. 9 indexed citations

16.

Sáiz, Pilar A., María Paz García‐Portilla, Celso Arango, et al.. (2008). Association study of the interleukin-1 gene complex and tumor necrosis factor alpha gene with suicide attempts. Psychiatric Genetics. 18(3). 147–150. 13 indexed citations

17.

Fernández-L, Africa, Francisco Sanz‐Rodríguez, Roberto Zarrabeitia, et al.. (2006). Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1. Human Mutation. 27(3). 295–295. 44 indexed citations

18.

Consugar, Mark, Sarah Anderson, Sandro Rossetti, et al.. (2005). Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease. American Journal of Kidney Diseases. 45(1). 77–87. 24 indexed citations

19.

Morales, Blanca, Pilar A. Sáiz, Clara V. Álvarez, et al.. (2000). Variación de los genes 5-HT2A y enzima conversiva de la angiotensina en pacientes esquizofrénicos. Psiquiatría Biológica. 7(1). 1–7. 2 indexed citations

20.

Álvarez, Rubén, Victoria Álvarez, Carlos Lahoz, et al.. (1999). Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's disease. Journal of Neurology Neurosurgery & Psychiatry. 67(6). 733–736. 83 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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