Oleksandr Maximyuk

586 total citations
30 papers, 444 citations indexed

About

Oleksandr Maximyuk is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience. According to data from OpenAlex, Oleksandr Maximyuk has authored 30 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 7 papers in Cognitive Neuroscience. Recurrent topics in Oleksandr Maximyuk's work include Neuroscience and Neuropharmacology Research (13 papers), Ion channel regulation and function (13 papers) and Ion Transport and Channel Regulation (9 papers). Oleksandr Maximyuk is often cited by papers focused on Neuroscience and Neuropharmacology Research (13 papers), Ion channel regulation and function (13 papers) and Ion Transport and Channel Regulation (9 papers). Oleksandr Maximyuk collaborates with scholars based in Ukraine, United States and Germany. Oleksandr Maximyuk's co-authors include Oleg Krishtal, Dmytro Isaev, Elena Isaeva, Polina V. Lishko, Michael Nöldner, S. S. Chatterjee, Maksim Storozhuk, V. I. Teslenko, Alexei Verkhratsky and Tian‐Le Xu and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and The Journal of Physiology.

In The Last Decade

Oleksandr Maximyuk

26 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oleksandr Maximyuk Ukraine 12 270 161 54 49 49 30 444
Gábor L. Petheö Hungary 14 399 1.5× 218 1.4× 55 1.0× 35 0.7× 7 0.1× 22 661
Jaume Lillo Spain 11 134 0.5× 154 1.0× 23 0.4× 30 0.6× 29 0.6× 40 351
Ruslan I. Stanika Austria 17 454 1.7× 427 2.7× 20 0.4× 36 0.7× 15 0.3× 22 738
Linda Console‐Bram United States 10 170 0.6× 247 1.5× 48 0.9× 65 1.3× 49 1.0× 13 563
Xiao-Dong Peng China 9 271 1.0× 206 1.3× 17 0.3× 16 0.3× 19 0.4× 18 542
Mircea Oprica Sweden 14 144 0.5× 142 0.9× 61 1.1× 24 0.5× 8 0.2× 20 549
Fusao Nakamura Japan 11 220 0.8× 172 1.1× 21 0.4× 38 0.8× 16 0.3× 23 498
Katsutoshi Ido Japan 11 177 0.7× 205 1.3× 55 1.0× 32 0.7× 9 0.2× 14 601
Carla Torri Italy 10 166 0.6× 211 1.3× 57 1.1× 65 1.3× 11 0.2× 15 437
Akito Nakao Japan 11 140 0.5× 112 0.7× 27 0.5× 29 0.6× 9 0.2× 26 406

Countries citing papers authored by Oleksandr Maximyuk

Since Specialization
Citations

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

Fields of papers citing papers by Oleksandr Maximyuk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oleksandr Maximyuk

This figure shows the co-authorship network connecting the top 25 collaborators of Oleksandr Maximyuk. A scholar is included among the top collaborators of Oleksandr Maximyuk 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 Oleksandr Maximyuk. Oleksandr Maximyuk 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.
Platonov, Maxim O., et al.. (2024). 4-(Azolyl)-Benzamidines as a Novel Chemotype for ASIC1a Inhibitors. International Journal of Molecular Sciences. 25(7). 3584–3584.
2.
Mamenko, Mykola, Tamara K. Nowling, Joshua H. Lipschutz, et al.. (2024). PAR1-mediated Non-periodical Synchronized Calcium Oscillations in Human Mesangial Cells. Function. 5(5). 2 indexed citations
3.
Isaev, Dmytro, et al.. (2023). Temperature increase significantly enhances nociceptive responses of C-fibers to ATP, high K+, and acidic pH in mice. Frontiers in Cellular Neuroscience. 17. 1131643–1131643. 1 indexed citations
4.
Platonov, Maxim O., Oleksandr Maximyuk, Yuliia Holota, et al.. (2023). Integrated workflow for the identification of new GABAAR positive allosteric modulators based on the in silico screening with further in vitro validation. Case study using Enamine's stock chemical space. Molecular Informatics. 43(2). e202300156–e202300156. 1 indexed citations
5.
Storozhuk, Maksim, et al.. (2022). Triggering of Major Brain Disorders by Protons and ATP: The Role of ASICs and P2X Receptors. Neuroscience Bulletin. 39(5). 845–862. 9 indexed citations
6.
Maximyuk, Oleksandr, et al.. (2021). Mecamylamine inhibits seizure-like activity in CA1-CA3 hippocampus through antagonism to nicotinic receptors. PLoS ONE. 16(3). e0240074–e0240074. 1 indexed citations
7.
Shi, Haosong, Xin Qi, Chunyan Li, et al.. (2020). Bilirubin enhances the activity of ASIC channels to exacerbate neurotoxicity in neonatal hyperbilirubinemia in mice. Science Translational Medicine. 12(530). 31 indexed citations
8.
9.
Qi, Xin, Ying Li, Oleksandr Maximyuk, et al.. (2019). Protein Kinase C Lambda Mediates Acid-Sensing Ion Channel 1a-Dependent Cortical Synaptic Plasticity and Pain Hypersensitivity. Journal of Neuroscience. 39(29). 5773–5793. 25 indexed citations
10.
Maximyuk, Oleksandr, et al.. (2019). INHIBITION OF BRAIN ASICS AFFECTS HIPPOCAMPAL THETA-RHYTHM AND OPENFIELD BEHAVIOR IN RATS. Fìzìologìčnij žurnal. 65(1). 15–19. 4 indexed citations
11.
Li, Wei‐Guang, Yan‐Jiao Wu, Chen Huang, et al.. (2016). Acid-sensing ion channel 1a contributes to hippocampal LTP inducibility through multiple mechanisms. Scientific Reports. 6(1). 23350–23350. 39 indexed citations
12.
Maximyuk, Oleksandr, et al.. (2016). VOLTAGE-GATED CALCIUM CHANNELS: CLASSIFICATION AND PHARMACOLOGICAL PROPERTIES (PART I). PubMed. 62(4). 84–94.
13.
Isaev, Dmytro, Iryna Lushnikova, Oleksandr Maximyuk, et al.. (2015). Contribution of protease-activated receptor 1 in status epilepticus-induced epileptogenesis. Neurobiology of Disease. 78. 68–76. 21 indexed citations
14.
Maximyuk, Oleksandr, Vladana Vukojević, Igor Bazov, et al.. (2015). Plasma membrane poration by opioid neuropeptides: a possible mechanism of pathological signal transduction. Cell Death and Disease. 6(3). e1683–e1683. 14 indexed citations
15.
Chizhmakov, I. V., et al.. (2015). ROLE PHOSPHOINOSITID SIGNALING PATHWAY IN OPIOIDS CONTROL OF Р2Х3 RECEPTORS IN THE PRIMARY SENSORY NEURONS. PubMed. 61(4). 22–29. 2 indexed citations
16.
Isaev, Dmytro, et al.. (2013). Persistent sodium current properties in hippocampal CA1 pyramidal neurons of young and adult rats. Neuroscience Letters. 559. 30–33. 11 indexed citations
17.
Isaev, Dmytro, et al.. (2011). Surface charge impact in low-magnesium model of seizure in rat hippocampus. Journal of Neurophysiology. 107(1). 417–423. 41 indexed citations
18.
Maximyuk, Oleksandr, et al.. (2007). P2X3 receptor gating near normal body temperature. Pflügers Archiv - European Journal of Physiology. 456(2). 339–347. 39 indexed citations
19.
Chatterjee, S. S., et al.. (1999). Hyperforin attenuates various ionic conductance mechanisms in the isolated hippocampal neurons of rat. Life Sciences. 65(22). 2395–2405. 49 indexed citations
20.
Lishko, Polina V., Oleksandr Maximyuk, S. S. Chatterjee, Michael Nöldner, & Oleg Krishtal. (1998). The putative cognitive enhancer KA-672. HCl is an uncompetitive voltage-dependent NMDA receptor antagonist. Neuroreport. 9(18). 4193–4197. 9 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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