Eduardo Rı́os

10.4k total citations · 2 hit papers
141 papers, 8.8k citations indexed

About

Eduardo Rı́os is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Eduardo Rı́os has authored 141 papers receiving a total of 8.8k indexed citations (citations by other indexed papers that have themselves been cited), including 120 papers in Molecular Biology, 92 papers in Cellular and Molecular Neuroscience and 73 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Eduardo Rı́os's work include Ion channel regulation and function (110 papers), Cardiac electrophysiology and arrhythmias (63 papers) and Neuroscience and Neural Engineering (61 papers). Eduardo Rı́os is often cited by papers focused on Ion channel regulation and function (110 papers), Cardiac electrophysiology and arrhythmias (63 papers) and Neuroscience and Neural Engineering (61 papers). Eduardo Rı́os collaborates with scholars based in United States, Uruguay and Canada. Eduardo Rı́os's co-authors include Gustavo Brum, Gonzalo Pizarro, Michael D. Stern, Natalia Shirokova, Martin F. Schneider, Adom González, Roman Shirokov, W. Melzer, Lothar A. Blatter and Heping Cheng and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Eduardo Rı́os

140 papers receiving 8.7k citations

Hit Papers

Involvement of dihydropyridine receptors in excitation–co... 1987 2026 2000 2013 1987 1991 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eduardo Rı́os United States 54 7.7k 5.0k 4.2k 914 649 141 8.8k
Kurt G. Beam United States 51 7.3k 0.9× 4.5k 0.9× 3.1k 0.7× 438 0.5× 570 0.9× 126 8.1k
W. Gil Wier United States 52 6.7k 0.9× 4.0k 0.8× 5.1k 1.2× 343 0.4× 965 1.5× 101 8.7k
Angela F. Dulhunty Australia 46 5.6k 0.7× 2.0k 0.4× 2.5k 0.6× 790 0.9× 679 1.0× 193 6.9k
Yoshihisa Kurachi Japan 58 9.2k 1.2× 4.6k 0.9× 3.6k 0.9× 356 0.4× 887 1.4× 210 12.3k
Martin Morad United States 56 7.2k 0.9× 4.8k 1.0× 5.8k 1.4× 359 0.4× 470 0.7× 200 9.6k
Makoto Endo Japan 38 4.6k 0.6× 1.9k 0.4× 2.5k 0.6× 1.1k 1.2× 675 1.0× 113 6.6k
Karl L. Magleby United States 48 6.9k 0.9× 5.6k 1.1× 2.6k 0.6× 519 0.6× 405 0.6× 101 8.4k
Enrico Stefani United States 69 10.7k 1.4× 6.7k 1.3× 4.7k 1.1× 631 0.7× 1.2k 1.9× 226 14.2k
W. Jonathan Lederer United States 44 8.2k 1.1× 3.7k 0.7× 6.6k 1.6× 219 0.2× 714 1.1× 74 10.3k
Akinori Noma Japan 55 8.7k 1.1× 5.3k 1.1× 7.3k 1.7× 467 0.5× 483 0.7× 191 11.7k

Countries citing papers authored by Eduardo Rı́os

Since Specialization
Citations

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

Fields of papers citing papers by Eduardo Rı́os

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eduardo Rı́os

This figure shows the co-authorship network connecting the top 25 collaborators of Eduardo Rı́os. A scholar is included among the top collaborators of Eduardo Rı́os 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 Eduardo Rı́os. Eduardo Rı́os 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.
Rı́os, Eduardo, et al.. (2024). Artificial intelligence approaches to the volumetric quantification of glycogen granules in EM images of human tissue. The Journal of General Physiology. 156(9). 2 indexed citations
2.
Rı́os, Eduardo. (2024). Using neural networks for image analysis in general physiology. The Journal of General Physiology. 156(10). 1 indexed citations
3.
Figueroa, Lourdes, et al.. (2023). Distinct pathophysiological characteristics in developing muscle from patients susceptible to malignant hyperthermia. British Journal of Anaesthesia. 131(1). 47–55. 2 indexed citations
4.
Ferreira, Juan J., et al.. (2020). A chloride channel blocker prevents the suppression by inorganic phosphate of the cytosolic calcium signals that control muscle contraction. The Journal of Physiology. 599(1). 157–170. 3 indexed citations
5.
Moreno, Carlos A., Natalia Kraeva, Elena Zvaritch, et al.. (2020). A multi-dimensional analysis of genotype–phenotype discordance in malignant hyperthermia susceptibility. British Journal of Anaesthesia. 125(6). 995–1001. 5 indexed citations
6.
Rı́os, Eduardo, et al.. (2019). Growth and morphometric relationships of the bean clam Donax punctatostriatus Hanley, 1843 in a sandy beach of southern Sinaloa, Mexico. Latin American Journal of Aquatic Research. 47(5). 764–773. 1 indexed citations
7.
Manno, Carlo, Lourdes Figueroa, Dirk Gillespie, et al.. (2017). Calsequestrin depolymerizes when calcium is depleted in the sarcoplasmic reticulum of working muscle. Proceedings of the National Academy of Sciences. 114(4). E638–E647. 49 indexed citations
8.
Manno, Carlo, Lourdes Figueroa, Dirk Gillespie, et al.. (2017). Anisotropic Diffusion of Proteins in the Sarcoplasmic Reticulum of Skeletal Muscle. Biophysical Journal. 112(3). 233a–233a. 1 indexed citations
9.
Rı́os, Eduardo. (2014). El “cuplón”; unidad funcional del acoplamiento contráctil.. SHILAP Revista de lepidopterología. 1 indexed citations
10.
Santiago, Demetrio J., Eduardo Rı́os, & Thomas R. Shannon. (2013). Isoproterenol Increases the Fraction of Spark-Dependent RyR-Mediated Leak in Ventricular Myocytes. Biophysical Journal. 104(5). 976–985. 17 indexed citations
11.
Stern, Michael D., Eduardo Rı́os, & Victor A. Maltsev. (2013). Life and death of a cardiac calcium spark. The Journal of General Physiology. 142(4). 477–477. 47 indexed citations
12.
Manno, Carlo, Lourdes Figueroa, Leandro Royer, et al.. (2013). Altered Ca2+ concentration, permeability and buffering in the myofibre Ca2+ store of a mouse model of malignant hyperthermia. The Journal of Physiology. 591(18). 4439–4457. 21 indexed citations
13.
Launikonis, Bradley S., et al.. (2007). An action potential (AP)-activated Ca2+ current in the tubular system of mammalian skeletal muscle.. Biophysical Journal. 1 indexed citations
14.
Launikonis, Bradley S., Jingsong Zhou, Leandro Royer, et al.. (2006). Depletion “skraps” and dynamic buffering inside the cellular calcium store. Proceedings of the National Academy of Sciences. 103(8). 2982–2987. 77 indexed citations
15.
Launikonis, Bradley S., Jingsong Zhou, Demetrio J. Santiago, Gustavo Brum, & Eduardo Rı́os. (2006). The Changes in Ca2+ Sparks Associated with Measured Modifications of Intra-store Ca2+ Concentration in Skeletal Muscle. The Journal of General Physiology. 128(1). 45–54. 14 indexed citations
16.
Brum, Gustavo, et al.. (2005). Concerted vs. Sequential. Two Activation Patterns of Vast Arrays of Intracellular Ca2+ Channels in Muscle. The Journal of General Physiology. 126(4). 301–309. 19 indexed citations
17.
Rı́os, Eduardo. (2005). The Ca2+ spark of mammalian muscle. Physiology or pathology?. The Journal of Physiology. 565(3). 705–705. 4 indexed citations
18.
Shirokova, Natalia, Roman Shirokov, Daniela Rossi, et al.. (1999). Spatially segregated control of Ca2+ release in developing skeletal muscle of mice. The Journal of Physiology. 521(2). 483–495. 57 indexed citations
19.
Mejía-Alvarez, Rafael, Claudia Kettlun, Eduardo Rı́os, Michael D. Stern, & Michael Fill. (1999). Unitary Ca2+ Current through Cardiac Ryanodine Receptor Channels under Quasi-Physiological Ionic Conditions. The Journal of General Physiology. 113(2). 177–186. 122 indexed citations
20.
Ma, Jianjie, Kristin A. Anderson, Roman Shirokov, et al.. (1993). Effects of perchlorate on the molecules of excitation-contraction coupling of skeletal and cardiac muscle.. The Journal of General Physiology. 102(3). 423–448. 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.

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