Alexander Surin

1.5k total citations
49 papers, 1.2k citations indexed

About

Alexander Surin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Alexander Surin has authored 49 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 32 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Alexander Surin's work include Neuroscience and Neuropharmacology Research (27 papers), Mitochondrial Function and Pathology (17 papers) and Ion channel regulation and function (9 papers). Alexander Surin is often cited by papers focused on Neuroscience and Neuropharmacology Research (27 papers), Mitochondrial Function and Pathology (17 papers) and Ion channel regulation and function (9 papers). Alexander Surin collaborates with scholars based in Russia, United States and Finland. Alexander Surin's co-authors include Jarda T. Wroblewski, Michael R. Duchen, Jake Jacobson, Pinelis Vg, Barbara Wróblewska, Joseph H. Neale, Yingxian Xiao, Kenneth J. Kellar, Erin L. Meyer and B. I. Khodorov and has published in prestigious journals such as FEBS Letters, International Journal of Molecular Sciences and Biophysical Journal.

In The Last Decade

Alexander Surin

47 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
Alexander Surin Russia 16 811 496 156 80 65 49 1.2k
Nathaniel Calloway United States 9 582 0.7× 434 0.9× 177 1.1× 63 0.8× 54 0.8× 9 1.1k
С. М. Антонов Russia 22 714 0.9× 700 1.4× 162 1.0× 61 0.8× 23 0.4× 67 1.1k
Kathiresan Krishnan United States 23 1.1k 1.4× 709 1.4× 240 1.5× 83 1.0× 78 1.2× 56 1.8k
Amal Kanti Bera India 22 1.1k 1.3× 320 0.6× 147 0.9× 57 0.7× 57 0.9× 59 1.5k
Svetlana Leschiner Israel 20 541 0.7× 324 0.7× 91 0.6× 91 1.1× 68 1.0× 36 1.0k
María F. Cano‐Abad Spain 17 731 0.9× 337 0.7× 154 1.0× 57 0.7× 83 1.3× 40 1.2k
Takeo Oshima Japan 9 571 0.7× 780 1.6× 113 0.7× 221 2.8× 44 0.7× 15 1.2k
Mark L. Weber United States 20 560 0.7× 517 1.0× 240 1.5× 115 1.4× 96 1.5× 31 1.3k
Jeffrey M. Brown United States 20 800 1.0× 674 1.4× 81 0.5× 60 0.8× 75 1.2× 33 1.5k
Masami Nakai Japan 20 712 0.9× 374 0.8× 100 0.6× 141 1.8× 77 1.2× 37 1.5k

Countries citing papers authored by Alexander Surin

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Surin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Surin

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Surin. A scholar is included among the top collaborators of Alexander Surin 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 Alexander Surin. Alexander Surin 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.
Fatkhudinov, Timur, et al.. (2024). Neuroprotective and anti-inflammatory properties of proteins secreted by glial progenitor cells derived from human iPSCs. Frontiers in Cellular Neuroscience. 18. 1449063–1449063.
2.
Weidinger, Adelheid, Arthur Hosmann, J. Catharina Duvigneau, et al.. (2023). Oxoglutarate dehydrogenase complex controls glutamate-mediated neuronal death. Redox Biology. 62. 102669–102669. 21 indexed citations
3.
Surin, Alexander, et al.. (2023). Neurodegeneration and Neuroinflammation: The Role of Pannexin 1. Neurochemical Journal. 17(4). 727–739. 1 indexed citations
4.
Surin, Alexander, et al.. (2022). Boris Izrailevich Khodorov: Scientist and Teacher. Neurochemical Journal. 16(4). 389–395.
5.
Surin, Alexander, et al.. (2022). Perinatal stroke: modelling and the potential of neurovisualization. Russian Pediatric Journal. 25(2). 128–138. 1 indexed citations
6.
7.
Belosludtsev, Konstantin N., et al.. (2021). The effect of DS16570511, a new inhibitor of mitochondrial calcium uniporter, on calcium homeostasis, metabolism, and functional state of cultured cortical neurons and isolated brain mitochondria. Biochimica et Biophysica Acta (BBA) - General Subjects. 1865(5). 129847–129847. 12 indexed citations
8.
Surin, Alexander, et al.. (2020). Neuroprotective Potential of Peptides HFRWPGP (ACTH6–9PGP), KKRRPGP, and PyrRP in Cultured Cortical Neurons at Glutamate Excitotoxicity. Doklady Biochemistry and Biophysics. 491(1). 62–66. 13 indexed citations
9.
Efremov, Yuri M., Ekaterina A. Grebenik, Svetlana Kotova, et al.. (2020). Viscoelasticity and Volume of Cortical Neurons under Glutamate Excitotoxicity and Osmotic Challenges. Biophysical Journal. 119(9). 1712–1723. 15 indexed citations
10.
Grebenik, Ekaterina A., Alexander Surin, Kseniia N. Bardakova, et al.. (2019). Chitosan-g-oligo(L,L-lactide) copolymer hydrogel for nervous tissue regeneration in glutamate excitotoxicity: in vitro feasibility evaluation. Biomedical Materials. 15(1). 15011–15011. 21 indexed citations
11.
Помыткин, И. А., et al.. (2019). Excitotoxic glutamate causes neuronal insulin resistance by inhibiting insulin receptor/Akt/mTOR pathway. Molecular Brain. 12(1). 112–112. 26 indexed citations
12.
Surin, Alexander, Е. Г. Сорокина, Аndrey P. Fisenko, et al.. (2019). Insulin Protects Cortical Neurons Against Glutamate Excitotoxicity. Frontiers in Neuroscience. 13. 1027–1027. 27 indexed citations
13.
Горбачева, Л. Р., et al.. (2019). ASTROCYTES AND THEIR ROLE IN THE PATHOLOGY OF THE CENTRAL NERVOUS SYSTEM. Russian Pediatric Journal. 21(1). 46–53. 5 indexed citations
14.
Surin, Alexander, et al.. (2017). Disruption of functional activity of mitochondria during MTT assay of viability of cultured neurons. Biochemistry (Moscow). 82(6). 737–749. 43 indexed citations
15.
Avlonitis, Nicolaos, Rashid Giniatullin, Craig McDougall, et al.. (2009). Synthesis, photolysis studies and in vitro photorelease of caged TRPV1 agonists and antagonists. Organic & Biomolecular Chemistry. 7(22). 4695–4695. 9 indexed citations
16.
Afzalov, Ramil, et al.. (2007). Calcium-dependent trapping of mitochondria near plasma membrane in stimulated astrocytes. PubMed. 35(1). 75–86. 20 indexed citations
17.
Surin, Alexander, et al.. (2006). Arachidonic acid enhances intracellular [Ca2+]i increase and mitochondrial depolarization induced by glutamate in cerebellar granule cells. Biochemistry (Moscow). 71(8). 864–870. 6 indexed citations
18.
Shchepotin, I., В А Солдатенков, Jarda T. Wroblewski, et al.. (1997). Apoptosis induced by hyperthermia and verapamilin vitroin a human colon cancer cell line. International Journal of Hyperthermia. 13(5). 547–557. 12 indexed citations
19.
Tückmantel, Werner, et al.. (1996). Synthesis and biology of the regidified glutamate analogue, trans-2-carboxyazetidine-3-acetic acid (t-CAA). Bioorganic & Medicinal Chemistry. 2559–2564. 8 indexed citations
20.
Surin, Alexander, et al.. (1990). Cholera toxin and its B subunit do not change cytosolic free calcium concentration. Cell Calcium. 11(6). 419–423. 4 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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