Steven J. Sollott

18.3k total citations · 6 hit papers
80 papers, 14.7k citations indexed

About

Steven J. Sollott is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Pathology and Forensic Medicine. According to data from OpenAlex, Steven J. Sollott has authored 80 papers receiving a total of 14.7k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 31 papers in Cardiology and Cardiovascular Medicine and 18 papers in Pathology and Forensic Medicine. Recurrent topics in Steven J. Sollott's work include Mitochondrial Function and Pathology (30 papers), Cardiac electrophysiology and arrhythmias (19 papers) and Cardiac Ischemia and Reperfusion (18 papers). Steven J. Sollott is often cited by papers focused on Mitochondrial Function and Pathology (30 papers), Cardiac electrophysiology and arrhythmias (19 papers) and Cardiac Ischemia and Reperfusion (18 papers). Steven J. Sollott collaborates with scholars based in United States, Russia and Australia. Steven J. Sollott's co-authors include Dmitry B. Zorov, Magdalena Juhaszova, Edward G. Lakatta, Jay L. Zweíer, Lars‐Oliver Klotz, Charles R. Filburn, Toren Finkel, Pascal J. Goldschmidt‐Clermont, Channing J. Der and Yong Xia and has published in prestigious journals such as Science, Journal of Biological Chemistry and Circulation.

In The Last Decade

Steven J. Sollott

79 papers receiving 14.5k citations

Hit Papers

Mitochondrial Reactive Oxygen Speci... 1997 2026 2006 2016 2014 2017 1997 2000 2006 1000 2.0k 3.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven J. Sollott United States 39 8.1k 2.4k 2.3k 2.2k 1.2k 80 14.7k
Takashi Matsui Japan 57 6.9k 0.8× 1.6k 0.7× 2.9k 1.2× 1.1k 0.5× 870 0.7× 271 13.0k
Dmitry B. Zorov Russia 48 8.9k 1.1× 2.0k 0.8× 997 0.4× 2.2k 1.0× 1.5k 1.3× 221 15.2k
Raymond C. Harris United States 82 8.6k 1.1× 2.5k 1.1× 3.0k 1.3× 1.7k 0.7× 1.2k 1.0× 334 22.5k
Magdalena Juhaszova United States 32 5.7k 0.7× 1.5k 0.6× 1.3k 0.6× 1.4k 0.6× 887 0.8× 56 11.1k
Wolfgang Dillmann United States 71 9.9k 1.2× 2.4k 1.0× 5.2k 2.2× 1.3k 0.6× 961 0.8× 212 16.2k
Edwin K. Jackson United States 71 5.8k 0.7× 2.4k 1.0× 3.0k 1.3× 1.2k 0.5× 1.4k 1.2× 502 19.4k
Giovanni E. Mann United Kingdom 62 5.6k 0.7× 3.3k 1.4× 1.2k 0.5× 1.2k 0.5× 731 0.6× 224 13.7k
Fabio Di Lisa Italy 59 7.7k 0.9× 2.0k 0.8× 1.9k 0.8× 2.9k 1.3× 906 0.8× 135 12.3k
Michael S. Goligorsky United States 72 5.0k 0.6× 3.5k 1.5× 2.0k 0.9× 1.1k 0.5× 777 0.7× 221 13.2k
Paul S. Brookes United States 60 8.2k 1.0× 4.0k 1.6× 992 0.4× 2.4k 1.1× 1.1k 1.0× 163 13.7k

Countries citing papers authored by Steven J. Sollott

Since Specialization
Citations

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

Fields of papers citing papers by Steven J. Sollott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven J. Sollott. 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 Steven J. Sollott. The network helps show where Steven J. Sollott may publish in the future.

Co-authorship network of co-authors of Steven J. Sollott

This figure shows the co-authorship network connecting the top 25 collaborators of Steven J. Sollott. A scholar is included among the top collaborators of Steven J. Sollott 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 Steven J. Sollott. Steven J. Sollott 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.
Morrell, Christopher H., Jack M. Moen, Melissa Krawczyk, et al.. (2023). A small erythropoietin derived non-hematopoietic peptide reduces cardiac inflammation, attenuates age associated declines in heart function and prolongs healthspan. Frontiers in Cardiovascular Medicine. 9. 1096887–1096887. 1 indexed citations
2.
Mancardi, Daniele, Pasquale Pagliaro, Lisa A. Ridnour, et al.. (2022). HNO Protects the Myocardium against Reperfusion Injury, Inhibiting the mPTP Opening via PKCε Activation. Antioxidants. 11(2). 382–382. 18 indexed citations
3.
Juhaszova, Magdalena, Evgeny Kobrinsky, Dmitry B. Zorov, et al.. (2022). ATP Synthase K+- and H+-fluxes Drive ATP Synthesis and Enable Mitochondrial K+-“Uniporter” Function: II. Ion and ATP Synthase Flux Regulation. Function. 3(2). zqac001–zqac001. 22 indexed citations
4.
Aon, Miguel A., Sonia Cortassa, Magdalena Juhaszova, et al.. (2021). Mitochondrial health is enhanced in rats with higher vs. lower intrinsic exercise capacity and extended lifespan. SHILAP Revista de lepidopterología. 7(1). 1–1. 17 indexed citations
5.
Juhaszova, Magdalena, Evgeny Kobrinsky, Dmitry B. Zorov, et al.. (2021). ATP Synthase K+- and H+-Fluxes Drive ATP Synthesis and Enable Mitochondrial K+-“Uniporter” Function: I. Characterization of Ion Fluxes. Function. 3(2). zqab065–zqab065. 32 indexed citations
6.
Cortassa, Sonia, Miguel A. Aon, Magdalena Juhaszova, et al.. (2021). Computational modeling of mitochondrial K+- and H+-driven ATP synthesis. Journal of Molecular and Cellular Cardiology. 165. 9–18. 5 indexed citations
7.
Cortassa, Sonia, Magdalena Juhaszova, Miguel A. Aon, Dmitry B. Zorov, & Steven J. Sollott. (2020). Mitochondrial Ca2+, redox environment and ROS emission in heart failure: Two sides of the same coin?. Journal of Molecular and Cellular Cardiology. 151. 113–125. 27 indexed citations
8.
Cortassa, Sonia, Viviane Caceres, Carlo G. Tocchetti, et al.. (2018). Metabolic remodelling of glucose, fatty acid and redox pathways in the heart of type 2 diabetic mice. The Journal of Physiology. 598(7). 1393–1415. 30 indexed citations
9.
Cortassa, Sonia, Steven J. Sollott, & Miguel A. Aon. (2018). Computational Modeling of Mitochondrial Function from a Systems Biology Perspective. Methods in molecular biology. 1782. 249–265. 9 indexed citations
10.
Zorova, Ljubava D., Vasily A. Popkov, Egor Y. Plotnikov, et al.. (2017). Mitochondrial membrane potential. Analytical Biochemistry. 552. 50–59. 1472 indexed citations breakdown →
11.
Maltsev, Victor A., Magdalena Juhaszova, Syevda Sirenko, et al.. (2016). Cardiac Pacemaker Cell Function at a Super-Resolution Scale of SIM: Distribution of RyRs, Calcium Dynamics, and Numerical Modeling. Biophysical Journal. 110(3). 267a–267a. 1 indexed citations
12.
Lukyanenko, Yevgeniya, Antoine Younès, Alexey E. Lyashkov, et al.. (2016). Ca2+/calmodulin-activated phosphodiesterase 1A is highly expressed in rabbit cardiac sinoatrial nodal cells and regulates pacemaker function. Journal of Molecular and Cellular Cardiology. 98. 73–82. 31 indexed citations
13.
Sirenko, Syevda, Magdalena Juhaszova, Jie Liu, et al.. (2014). Coupled-Clock Pacemaker System becomes Dysfunctional with Aging. Biophysical Journal. 106(2). 111a–112a. 1 indexed citations
14.
Yaniv, Yael, Magdalena Juhaszova, & Steven J. Sollott. (2013). Age-related changes of myocardial ATP supply and demand mechanisms. Trends in Endocrinology and Metabolism. 24(10). 495–505. 44 indexed citations
15.
Krishna, Manchugondanahalli S., et al.. (2008). Paracrine effects of hypoxic fibroblast-derived factors on the MPT-ROS threshold and viability of adult rat cardiac myocytes. American Journal of Physiology-Heart and Circulatory Physiology. 294(6). H2653–H2658. 24 indexed citations
16.
Chiara, Federica, Oriano Marin, Valeria Petronilli, et al.. (2008). Hexokinase II Detachment from Mitochondria Triggers Apoptosis through the Permeability Transition Pore Independent of Voltage-Dependent Anion Channels. PLoS ONE. 3(3). e1852–e1852. 241 indexed citations
17.
Juhaszova, Magdalena, Dmitry B. Zorov, Salvatore Pepe, et al.. (2004). Glycogen synthase kinase-3β mediates convergence of protection signaling to inhibit the mitochondrial permeability transition pore. Journal of Clinical Investigation. 113(11). 1535–1549. 832 indexed citations breakdown →
18.
Long, X, Michael T. Crow, Steven J. Sollott, et al.. (1998). Enhanced expression of p53 and apoptosis induced by blockade of the vacuolar proton ATPase in cardiomyocytes.. Journal of Clinical Investigation. 101(6). 1453–1461. 61 indexed citations
19.
Sollott, Steven J., et al.. (1996). Reactive oxygen species act as mediators in endothelial cell signalling pathways. Journal of the American College of Cardiology. 27(2). 385–385. 1 indexed citations
20.
Sollott, Steven J., L.M. Cheng, Rebecca Pauly, et al.. (1995). Taxol inhibits neointimal smooth muscle cell accumulation after angioplasty in the rat.. Journal of Clinical Investigation. 95(4). 1869–1876. 201 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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