Grigory Maksaev

1.5k total citations
24 papers, 1.1k citations indexed

About

Grigory Maksaev is a scholar working on Molecular Biology, Physiology and Plant Science. According to data from OpenAlex, Grigory Maksaev has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 11 papers in Physiology and 7 papers in Plant Science. Recurrent topics in Grigory Maksaev's work include Ion channel regulation and function (18 papers), Erythrocyte Function and Pathophysiology (11 papers) and Plant Stress Responses and Tolerance (5 papers). Grigory Maksaev is often cited by papers focused on Ion channel regulation and function (18 papers), Erythrocyte Function and Pathophysiology (11 papers) and Plant Stress Responses and Tolerance (5 papers). Grigory Maksaev collaborates with scholars based in United States, Austria and Russia. Grigory Maksaev's co-authors include Elizabeth S. Haswell, Peng Yuan, Zengqin Deng, Colin G. Nichols, Gregory S. Jensen, James A. J. Fitzpatrick, Andrew Katims, Eric S. Hamilton, Margaret E. Wilson and Michael Rau and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Grigory Maksaev

24 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Grigory Maksaev United States 14 735 383 217 187 102 24 1.1k
Xinliang Zhou United States 14 786 1.1× 394 1.0× 208 1.0× 375 2.0× 219 2.1× 21 1.2k
Yoshitaka Nakayama Australia 18 584 0.8× 256 0.7× 225 1.0× 50 0.3× 82 0.8× 36 885
Ann Batiza United States 9 547 0.7× 149 0.4× 207 1.0× 80 0.4× 77 0.8× 13 730
Veena Khanna India 14 928 1.3× 386 1.0× 75 0.3× 91 0.5× 233 2.3× 97 1.4k
Nathalie Pochon France 10 351 0.5× 247 0.6× 144 0.7× 80 0.4× 45 0.4× 10 766
Stephen H. Loukin United States 22 1.1k 1.5× 406 1.1× 333 1.5× 541 2.9× 321 3.1× 32 1.8k
Alan R. Penheiter United States 17 638 0.9× 169 0.4× 51 0.2× 149 0.8× 113 1.1× 36 1.1k
Raphaël Courjaret Qatar 19 527 0.7× 54 0.1× 132 0.6× 191 1.0× 281 2.8× 38 1.0k
Ruth A. Pumroy United States 14 540 0.7× 87 0.2× 46 0.2× 326 1.7× 93 0.9× 25 897
Anna Drews United Kingdom 15 229 0.3× 68 0.2× 206 0.9× 188 1.0× 148 1.5× 27 795

Countries citing papers authored by Grigory Maksaev

Since Specialization
Citations

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

Fields of papers citing papers by Grigory Maksaev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Grigory Maksaev

This figure shows the co-authorship network connecting the top 25 collaborators of Grigory Maksaev. A scholar is included among the top collaborators of Grigory Maksaev 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 Grigory Maksaev. Grigory Maksaev 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.
Maksaev, Grigory, Peng Yuan, & Colin G. Nichols. (2023). Blockade of TRPV channels by intracellular spermine. The Journal of General Physiology. 155(5). 3 indexed citations
2.
Dicks, Amanda, Grigory Maksaev, Alireza Savadipour, et al.. (2023). Skeletal dysplasia-causing TRPV4 mutations suppress the hypertrophic differentiation of human iPSC-derived chondrocytes. eLife. 12. 12 indexed citations
3.
Zhang, Jingying, Grigory Maksaev, & Peng Yuan. (2023). Open structure and gating of the Arabidopsis mechanosensitive ion channel MSL10. Nature Communications. 14(1). 6284–6284. 9 indexed citations
4.
Maksaev, Grigory, et al.. (2023). Subunit gating resulting from individual protonation events in Kir2 channels. Nature Communications. 14(1). 4538–4538. 7 indexed citations
5.
Kleist, Thomas J., et al.. (2022). OzTracs: Optical Osmolality Reporters Engineered from Mechanosensitive Ion Channels. Biomolecules. 12(6). 787–787. 1 indexed citations
6.
Maksaev, Grigory, et al.. (2022). Structural basis for mechanotransduction in a potassium-dependent mechanosensitive ion channel. Nature Communications. 13(1). 6904–6904. 12 indexed citations
7.
Deng, Zengqin, Zhihui He, Grigory Maksaev, et al.. (2020). Cryo-EM structures of the ATP release channel pannexin 1. Nature Structural & Molecular Biology. 27(4). 373–381. 91 indexed citations
8.
Deng, Zengqin, Grigory Maksaev, Michael Rau, et al.. (2020). Gating of human TRPV3 in a lipid bilayer. Nature Structural & Molecular Biology. 27(7). 635–644. 52 indexed citations
9.
Deng, Zengqin, Grigory Maksaev, Jingying Zhang, et al.. (2020). Structural mechanism for gating of a eukaryotic mechanosensitive channel of small conductance. Nature Communications. 11(1). 3690–3690. 37 indexed citations
10.
Zangerl‐Plessl, Eva‐Maria, Sun‐Joo Lee, Grigory Maksaev, et al.. (2019). Atomistic basis of opening and conduction in mammalian inward rectifier potassium (Kir2.2) channels. The Journal of General Physiology. 152(1). jgp.201912422–jgp.201912422. 24 indexed citations
11.
Wang, Shizhen, et al.. (2019). Potassium channel selectivity filter dynamics revealed by single-molecule FRET. Nature Chemical Biology. 15(4). 377–383. 27 indexed citations
12.
13.
Deng, Zengqin, Navid Paknejad, Grigory Maksaev, et al.. (2018). Cryo-EM and X-ray structures of TRPV4 reveal insight into ion permeation and gating mechanisms. Nature Structural & Molecular Biology. 25(3). 252–260. 167 indexed citations
14.
Herrera, Nadia, Grigory Maksaev, Elizabeth S. Haswell, & Douglas C. Rees. (2018). Elucidating a role for the cytoplasmic domain in the Mycobacterium tuberculosis mechanosensitive channel of large conductance. Scientific Reports. 8(1). 14566–14566. 7 indexed citations
15.
Hamilton, Eric S., et al.. (2015). Mechanosensitive channel MSL8 regulates osmotic forces during pollen hydration and germination. Science. 350(6259). 438–441. 153 indexed citations
16.
Maksaev, Grigory & Elizabeth S. Haswell. (2015). Expressing and Characterizing Mechanosensitive Channels in Xenopus Oocytes. Methods in molecular biology. 1309. 151–169. 11 indexed citations
17.
Wilson, Margaret E., Grigory Maksaev, & Elizabeth S. Haswell. (2013). MscS-like Mechanosensitive Channels in Plants and Microbes. Biochemistry. 52(34). 5708–5722. 54 indexed citations
18.
Maksaev, Grigory, Adina L. Milac, Andriy Anishkin, H. Robert Guy, & Sergei Sukharev. (2010). Analyses of gating thermodynamics and effects of deletions in the mechanosensitive channel TREK-1. Channels. 5(1). 34–42. 18 indexed citations
19.
Dubovskii, Peter V., М. Н. Жмак, Grigory Maksaev, & Alexander S. Arseniev. (2004). A New Water-Soluble Analogue of the Fusion Peptide of Influenza Virus Hemagglutinin: Synthesis and Properties. Russian Journal of Bioorganic Chemistry. 30(2). 196–198. 2 indexed citations
20.
Basáñez, Gorka, Jun Zhang, B. Nelson Chau, et al.. (2001). Pro-apoptotic Cleavage Products of Bcl-xL Form Cytochrome c-conducting Pores in Pure Lipid Membranes. Journal of Biological Chemistry. 276(33). 31083–31091. 124 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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