Oleg Krishtal

8.0k total citations
173 papers, 6.5k citations indexed

About

Oleg Krishtal is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Oleg Krishtal has authored 173 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 126 papers in Cellular and Molecular Neuroscience, 105 papers in Molecular Biology and 43 papers in Cognitive Neuroscience. Recurrent topics in Oleg Krishtal's work include Neuroscience and Neuropharmacology Research (92 papers), Ion channel regulation and function (68 papers) and Neuroscience and Neural Engineering (30 papers). Oleg Krishtal is often cited by papers focused on Neuroscience and Neuropharmacology Research (92 papers), Ion channel regulation and function (68 papers) and Neuroscience and Neural Engineering (30 papers). Oleg Krishtal collaborates with scholars based in Ukraine, United States and Germany. Oleg Krishtal's co-authors include V.I. Pidoplichko, P. G. Kostyuk, С. М. Марченко, A. Ya. Tsyndrenko, Nikolai I. Kiskin, Ulyana Lalo, Norio Akaike, Yuri Pankratov, Alexei Verkhratsky and N. A. Lozovaya and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Physical Review Letters.

In The Last Decade

Oleg Krishtal

165 papers receiving 6.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oleg Krishtal Ukraine 41 3.9k 3.9k 1.3k 845 794 173 6.5k
Forrest F. Weight United States 51 5.4k 1.4× 4.1k 1.1× 569 0.5× 734 0.9× 1.2k 1.6× 131 7.8k
Amy B. MacDermott United States 44 5.6k 1.4× 5.2k 1.3× 658 0.5× 586 0.7× 1.0k 1.3× 77 8.5k
H. L. Haas Germany 47 4.3k 1.1× 3.1k 0.8× 592 0.5× 978 1.2× 1.9k 2.4× 115 7.1k
Lucia G. Sivilotti United Kingdom 36 2.6k 0.7× 3.5k 0.9× 691 0.6× 533 0.6× 323 0.4× 71 5.5k
L.F. Agnati Italy 51 4.9k 1.3× 4.0k 1.0× 401 0.3× 1.1k 1.3× 901 1.1× 230 8.6k
V. A. Derkach United States 24 3.7k 0.9× 2.7k 0.7× 408 0.3× 506 0.6× 925 1.2× 36 5.2k
P. G. Kostyuk Ukraine 45 5.1k 1.3× 4.6k 1.2× 305 0.2× 309 0.4× 781 1.0× 223 7.2k
Bruno G. Frenguelli United Kingdom 34 3.1k 0.8× 3.2k 0.8× 1.1k 0.9× 525 0.6× 1.1k 1.4× 81 6.6k
Alasdair J. Gibb United Kingdom 35 2.4k 0.6× 2.5k 0.6× 803 0.6× 480 0.6× 462 0.6× 76 4.3k
Mark R. Brann United States 49 6.4k 1.6× 7.8k 2.0× 360 0.3× 449 0.5× 533 0.7× 112 10.3k

Countries citing papers authored by Oleg Krishtal

Since Specialization
Citations

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

Fields of papers citing papers by Oleg Krishtal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oleg Krishtal

This figure shows the co-authorship network connecting the top 25 collaborators of Oleg Krishtal. A scholar is included among the top collaborators of Oleg Krishtal 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 Oleg Krishtal. Oleg Krishtal 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.
Qi, Xin, Yijun Liu, Jian Xiong, et al.. (2022). Pharmacological Validation of ASIC1a as a Druggable Target for Neuroprotection in Cerebral Ischemia Using an Intravenously Available Small Molecule Inhibitor. Frontiers in Pharmacology. 13. 849498–849498. 5 indexed citations
3.
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
4.
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
5.
Maximyuk, Oleksandr, et al.. (2016). VOLTAGE-GATED CALCIUM CHANNELS: CLASSIFICATION AND PHARMACOLOGICAL PROPERTIES (PART I). PubMed. 62(4). 84–94.
6.
Sarkisyan, Daniil, Hiroyuki Watanabe, Olga Kononenko, et al.. (2015). Downregulation of the endogenous opioid peptides in the dorsal striatum of human alcoholics. Frontiers in Cellular Neuroscience. 9. 187–187. 17 indexed citations
7.
Chizhmakov, I. V., Iryna A. Khasabova, Sergey G. Khasabov, et al.. (2015). Molecular mechanism for opioid dichotomy: bidirectional effect of μ-opioid receptors on P2X3 receptor currents in rat sensory neurones. Purinergic Signalling. 11(2). 171–181. 6 indexed citations
8.
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
9.
Storozhuk, Maksim, et al.. (2012). Is rapid effect of thyroxine on GABAergic IPSCs purely postsynaptic?. Pharmacological Reports. 64(6). 1573–1577. 2 indexed citations
10.
Mamenko, Mykola, I. V. Chizhmakov, T. M. Volkova, Alexei Verkhratsky, & Oleg Krishtal. (2010). Extracellular cAMP inhibits P2X3 receptors in rat sensory neurones through G protein‐mediated mechanism. Acta Physiologica. 199(2). 199–204. 2 indexed citations
11.
Grishin, Eugene V., Alexander A. Vassilevski, Yuliya V. Korolkova, et al.. (2009). Novel peptide from spider venom inhibits P2X3 receptors and inflammatory pain. Annals of Neurology. 67(5). 680–683. 51 indexed citations
12.
Tsintsadze, Timur, et al.. (2005). Acid sensing ionic channels: Modulation by redox reagents. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1745(1). 1–6. 45 indexed citations
13.
Krishtal, Oleg. (2003). The ASICs: Signaling molecules? Modulators?. Trends in Neurosciences. 26(9). 477–483. 367 indexed citations
14.
Krishtal, Oleg, et al.. (2002). Modulation of GABAA receptor-mediated currents by benzophenone derivatives in isolated rat Purkinje neurones. Neuropharmacology. 43(4). 764–777. 3 indexed citations
15.
Krishtal, Oleg, et al.. (2001). Modulation of Ion Channels in Rat Neurons by the Constituents of Hypericum Perforatum. Pharmacopsychiatry. 34(Suppl1). 74–82. 27 indexed citations
16.
Lozovaya, Natalia, et al.. (2000). Hyperforin modulates gating of P-type Ca2+ current in cerebellar Purkinje neurons. Pflügers Archiv - European Journal of Physiology. 440(3). 427–434. 26 indexed citations
17.
Pintor, Jesús, et al.. (1996). Diadenosine polyphosphates selectively potentiate N-type Ca2+ channels in rat central neurons. Neuroscience. 70(2). 353–360. 24 indexed citations
18.
Tsintsadze, Timur, et al.. (1996). NMDA receptor-mediated synapses between CA1 neurones. Neuroreport. 7(15). 2679–2682. 10 indexed citations
19.
Kiskin, Nikolai I., et al.. (1990). Araneidae toxins as an antagonists of excitatory amino-acid responses in isolated hippocampal neurons. 10(2). 6 indexed citations
20.
Krishtal, Oleg, С. М. Марченко, & Alexander G. Obukhov. (1988). Cationic channels activated by extracellular atp in rat sensory neurons. Neuroscience. 27(3). 995–1000. 141 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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