С. Н. Щелкунов

4.5k total citations
165 papers, 3.5k citations indexed

About

С. Н. Щелкунов is a scholar working on Virology, Epidemiology and Molecular Biology. According to data from OpenAlex, С. Н. Щелкунов has authored 165 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Virology, 74 papers in Epidemiology and 68 papers in Molecular Biology. Recurrent topics in С. Н. Щелкунов's work include Poxvirus research and outbreaks (117 papers), Herpesvirus Infections and Treatments (69 papers) and Virus-based gene therapy research (40 papers). С. Н. Щелкунов is often cited by papers focused on Poxvirus research and outbreaks (117 papers), Herpesvirus Infections and Treatments (69 papers) and Virus-based gene therapy research (40 papers). С. Н. Щелкунов collaborates with scholars based in Russia, United States and Egypt. С. Н. Щелкунов's co-authors include А. В. Тотменин, L. S. Sandakhchiev, Igor V. Babkin, В. В. Гуторов, Vladimir M. Blinov, Pavel F. Safronov, E. V. Gavrilova, Olga I. Ryazankina, Rinat А. Maksyutov and Joseph J. Esposito and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Analytical Biochemistry.

In The Last Decade

С. Н. Щелкунов

160 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
С. Н. Щелкунов Russia	32	2.6k	2.0k	1.8k	590	586	165	3.5k
Joseph J. Esposito United States	28	3.4k 1.3×	2.6k 1.3×	2.1k 1.2×	636 1.1×	734 1.3×	57	4.1k
Victoria A. Olson United States	32	4.1k 1.6×	2.9k 1.5×	3.2k 1.8×	507 0.9×	421 0.7×	77	4.7k
Marion E. Perkus United States	21	1.6k 0.6×	1.6k 0.8×	657 0.4×	260 0.4×	966 1.6×	31	2.6k
Barbara E.H. Coupar Australia	35	1.2k 0.5×	1.4k 0.7×	840 0.5×	238 0.4×	970 1.7×	75	3.6k
David B. Boyle Australia	30	1.3k 0.5×	1.4k 0.7×	446 0.2×	337 0.6×	679 1.2×	67	2.9k
Flávio Guimarães da Fonseca Brazil	27	1.1k 0.4×	958 0.5×	564 0.3×	252 0.4×	341 0.6×	130	2.1k
Scott J. Goebel United States	25	1.0k 0.4×	1.0k 0.5×	666 0.4×	322 0.5×	547 0.9×	30	2.4k
Trudy G. Morrison United States	41	570 0.2×	3.2k 1.6×	1.1k 0.6×	314 0.5×	1.1k 1.9×	105	4.4k
Janice C. Knight United States	16	1.5k 0.6×	1.2k 0.6×	833 0.5×	303 0.5×	404 0.7×	18	1.8k

Countries citing papers authored by С. Н. Щелкунов

Since Specialization

Citations

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

Fields of papers citing papers by С. Н. Щелкунов

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by С. Н. Щелкунов. 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 С. Н. Щелкунов. The network helps show where С. Н. Щелкунов may publish in the future.

Co-authorship network of co-authors of С. Н. Щелкунов

This figure shows the co-authorship network connecting the top 25 collaborators of С. Н. Щелкунов. A scholar is included among the top collaborators of С. Н. Щелкунов 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 С. Н. Щелкунов. С. Н. Щелкунов is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Щелкунов, С. Н., et al.. (2025). The humoral and cellular immune response to the administration of OrthopoxVac vaccine to volunteers. PubMed. 17(3). 104–118.

Щелкунов, С. Н., et al.. (2024). Choice of Vaccination Regimen against Orthopoxvirus Infections in a Mouse Model. Molecular Genetics Microbiology and Virology. 39(2). 142–147. 1 indexed citations

Сергеев, А. А., et al.. (2023). Effect of the <i>ati</i> Gene Deletion on the Pathogenicity and Immunogenicity of the Vaccinia Virus. PubMed. 15(3). 82–90. 1 indexed citations

Щелкунов, С. Н., et al.. (2023). Preclinical Studies of the Specific Activity of the Live Culture Vaccine VACD6 against Smallpox and other Orthopoxvirus Infections. SHILAP Revista de lepidopterología. 21(6). 34–47. 3 indexed citations

Щелкунов, С. Н., et al.. (2023). Smallpox vaccination in a mouse model. Vavilov Journal of Genetics and Breeding. 27(6). 712–718. 1 indexed citations

Щелкунов, С. Н., et al.. (2022). Smallpox, Monkeypox and Other Human Orthopoxvirus Infections. Viruses. 15(1). 103–103. 45 indexed citations

Maksyutov, Rinat А., et al.. (2022). Genome stability of the vaccine strain VAC∆6. Vavilov Journal of Genetics and Breeding. 26(4). 394–401. 3 indexed citations

Щелкунов, С. Н., et al.. (2018). Virotherapy of the Malignant U87 Human Glioblastoma in the Orthotopic Xenotransplantation Mouse SCID Model. Doklady Biochemistry and Biophysics. 478(1). 30–33. 4 indexed citations

Щелкунов, С. Н., et al.. (2016). Highly immunogenic variant of attenuated vaccinia virus. Doklady Biochemistry and Biophysics. 466(1). 35–38. 17 indexed citations

10.

Шеховцов, С. В., et al.. (2015). TNF-Binding domain of the variola virus CrmB protein synthesized in Escherichia coli cells effectively interacts with human TNF. Doklady Biochemistry and Biophysics. 462(1). 176–180. 3 indexed citations

11.

Gavrilova, E. V., Rinat А. Maksyutov, & С. Н. Щелкунов. (2013). Orthopoxvirus Infections: Epidemiology, Clinical Picture, and Diagnostics (Scientific Review). SHILAP Revista de lepidopterología. 82–88. 1 indexed citations

12.

Gavrilova, E. V., et al.. (2010). [Identification of human pathogenic variola and monkeypox viruses by real-time polymerase chain reaction].. PubMed. 54(6). 28–33. 1 indexed citations

13.

Тотменин, А. В., et al.. (2005). [Expression of genes for orthopoxviral TNF-binding proteins and study resulted recombinant proteins].. PubMed. 39(2). 245–54. 6 indexed citations

14.

Babkin, Igor V., et al.. (2005). [Construction of DNA-fragments' libraries with complete genomes of different variola strains].. PubMed. 50(2). 18–23. 1 indexed citations

15.

Laassri, Majid, Vladimir Chizhikov, Maxim Mikheev, С. Н. Щелкунов, & Konstantin Chumakov. (2003). Detection and discrimination of orthopoxviruses using microarrays of immobilized oligonucleotides. Journal of Virological Methods. 112(1-2). 67–78. 63 indexed citations

16.

Щелкунов, С. Н., et al.. (2003). Development of a Candidate Polyvalent Live Vaccine against Human Immunodeficiency, Hepatitis B, and Orthopox Viruses. Doklady Biochemistry and Biophysics. 390(1-6). 180–183. 6 indexed citations

17.

Massung, Robert F., Vladimir N. Loparev, Janice C. Knight, et al.. (1996). Terminal Region Sequence Variations in Variola Virus DNA. Virology. 221(2). 291–300. 33 indexed citations

18.

Щелкунов, С. Н. & А. В. Тотменин. (1995). Two types of deletions in orthopoxvirus genomes. Virus Genes. 9(3). 231–245. 25 indexed citations

19.

Щелкунов, С. Н., Sergei Resenchuk, А. В. Тотменин, et al.. (1993). Comparison of the genetic maps of variola and vaccinia viruses. FEBS Letters. 327(3). 321–324. 50 indexed citations

20.

Ryazankina, Olga I., et al.. (1990). The molecular biological study of vaccinia virus genome. III. Identification of late gene 36K protein product from HindIII-P fragment of vaccinia virus strain L-IVP genome. 24(4). 977–983. 1 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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