Sergey Zozulya

4.5k total citations
58 papers, 2.9k citations indexed

About

Sergey Zozulya is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry. According to data from OpenAlex, Sergey Zozulya has authored 58 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 17 papers in Cellular and Molecular Neuroscience and 16 papers in Organic Chemistry. Recurrent topics in Sergey Zozulya's work include Fluorine in Organic Chemistry (9 papers), Receptor Mechanisms and Signaling (9 papers) and Chemical Synthesis and Analysis (7 papers). Sergey Zozulya is often cited by papers focused on Fluorine in Organic Chemistry (9 papers), Receptor Mechanisms and Signaling (9 papers) and Chemical Synthesis and Analysis (7 papers). Sergey Zozulya collaborates with scholars based in Ukraine, Russia and United States. Sergey Zozulya's co-authors include Lubert Stryer, Trieu Nguyen, Fernando Echeverri, Kevin Flaherty, Mikhail L. Gishizky, Pavel K. Mykhailiuk, David B. McKay, Bahija Jallal, Valery Krasnoperov and Parkash S. Gill and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Sergey Zozulya

56 papers receiving 2.9k citations

Peers

Sergey Zozulya
Thomas Vorherr Switzerland
Steven I. Dworetzky United States
B. V. L. POTTER United Kingdom
Kimberli J. Kamer United States
Suzie Chen United States
Michael J. Plevin United Kingdom
Thomas Vorherr Switzerland
Sergey Zozulya
Citations per year, relative to Sergey Zozulya Sergey Zozulya (= 1×) peers Thomas Vorherr

Countries citing papers authored by Sergey Zozulya

Since Specialization
Citations

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

Fields of papers citing papers by Sergey Zozulya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergey Zozulya

This figure shows the co-authorship network connecting the top 25 collaborators of Sergey Zozulya. A scholar is included among the top collaborators of Sergey Zozulya 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 Sergey Zozulya. Sergey Zozulya 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.
Vashchenko, Bohdan V., Olga Kuchuk, В. С. Броварец, et al.. (2025). Expanding chemical space of N-acyl sulfonamides for carbonic anhydrase inhibitor discovery. European Journal of Medicinal Chemistry. 302(Pt 1). 118296–118296.
2.
Zozulya, Sergey, O. Yu. Sokolov, & Н. В. Кост. (2024). Effect of Neurotropic and Immunotropic Drugs on Leukocyte Elastase Activity In Vitro. Bulletin of Experimental Biology and Medicine. 176(5). 585–590. 1 indexed citations
3.
Kuchuk, Olga, et al.. (2024). Synthetic Amine Linkers for Efficient Sortagging. Bioconjugate Chemistry. 35(8). 1172–1181.
4.
Zozulya, Sergey, et al.. (2020). Exploration of the nitrogen heterocyclic periphery around the core of the advanced FFA1 agonist fasiglifam (TAK‐875). Archiv der Pharmazie. 354(4). e2000275–e2000275. 3 indexed citations
5.
Adams, Volker, et al.. (2020). Small-Molecule Chemical Knockdown of MuRF1 in Melanoma Bearing Mice Attenuates Tumor Cachexia Associated Myopathy. Cells. 9(10). 2272–2272. 22 indexed citations
6.
Luzina, Olga A., Iryna Pishel, Sergey Zozulya, et al.. (2020). Exploring bulky natural and natural-like periphery in the design of p-(benzyloxy)phenylpropionic acid agonists of free fatty acid receptor 1 (GPR40). Bioorganic Chemistry. 99. 103830–103830. 17 indexed citations
7.
Krasavin, Mikhail, et al.. (2017). Continued SAR exploration of 1,2,4-thiadiazole-containing scaffolds in the design of free fatty acid receptor 1 (GPR40) agonists. European Journal of Medicinal Chemistry. 140. 229–238. 10 indexed citations
8.
Krasavin, Mikhail, et al.. (2016). Novel free fatty acid receptor 1 (GPR40) agonists based on 1,3,4-thiadiazole-2-carboxamide scaffold. Bioorganic & Medicinal Chemistry. 24(13). 2954–2963. 22 indexed citations
9.
Krasavin, Mikhail, Roman Stavniichuk, Sergey Zozulya, et al.. (2016). Discovery of Strecker-type α-aminonitriles as a new class of human carbonic anhydrase inhibitors using differential scanning fluorimetry. Journal of Enzyme Inhibition and Medicinal Chemistry. 31(6). 1707–1711. 4 indexed citations
10.
Petrenko, Alexander G., Sergey Zozulya, I. E. Deyev, & Dominique Eladari. (2012). Insulin receptor-related receptor as an extracellular pH sensor involved in the regulation of acid–base balance. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1834(10). 2170–2175. 33 indexed citations
11.
Liang, Sheng-Ben, Young Trieu, Zhihua Li, et al.. (2011). Molecular Target Characterization and Antimyeloma Activity of the Novel, Insulin-like Growth Factor 1 Receptor Inhibitor, GTx-134. Clinical Cancer Research. 17(14). 4693–4704. 8 indexed citations
12.
Deyev, I. E., Fabien Sohet, О. В. Серова, et al.. (2011). Insulin Receptor-Related Receptor as an Extracellular Alkali Sensor. Cell Metabolism. 13(6). 679–689. 78 indexed citations
13.
Krasnoperov, Valery, Sunil Kumar, Eric J. Ley, et al.. (2010). Novel EphB4 Monoclonal Antibodies Modulate Angiogenesis and Inhibit Tumor Growth. American Journal Of Pathology. 176(4). 2029–2038. 72 indexed citations
14.
Masood, Rizwan, Sunil Kumar, Uttam K. Sinha, et al.. (2006). EphB4 provides survival advantage to squamous cell carcinoma of the head and neck. International Journal of Cancer. 119(6). 1236–1248. 62 indexed citations
15.
Серова, О. В., et al.. (2006). Effect of changes in ambient pH on phosphorylation of cellular proteins. Doklady Biochemistry and Biophysics. 408(1). 184–187. 15 indexed citations
16.
Hill, Ronald J., et al.. (2002). The lymphoid protein tyrosine phosphatase Lyp interacts with the adaptor molecule Grb2 and functions as a negative regulator of T-cell activation. Experimental Hematology. 30(3). 237–244. 109 indexed citations
17.
Zozulya, Sergey, Fernando Echeverri, & Trieu Nguyen. (2001). The human olfactory receptor repertoire. Genome biology. 2(6). RESEARCH0018–RESEARCH0018. 270 indexed citations
18.
Flaherty, Kevin, Sergey Zozulya, Lubert Stryer, & David B. McKay. (1993). Three-dimensional structure of recoverin, a calcium sensor in vision. Cell. 75(4). 709–716. 223 indexed citations
19.
Gurevich, Vsevolod V., et al.. (1991). Preparative in vitro mRNA synthesis using SP6 and T7 RNA polymerases. Analytical Biochemistry. 195(2). 207–213. 133 indexed citations
20.
Zozulya, Sergey, Vsevolod V. Gurevich, Tatyana Zvyaga, et al.. (1990). Functional expression in vitro of bovine visual rhodopsin. Protein Engineering Design and Selection. 3(5). 453–458. 22 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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