В. А. Гвоздев

5.3k total citations · 2 hit papers
146 papers, 4.2k citations indexed

About

В. А. Гвоздев is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, В. А. Гвоздев has authored 146 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 109 papers in Molecular Biology, 88 papers in Plant Science and 36 papers in Genetics. Recurrent topics in В. А. Гвоздев's work include Chromosomal and Genetic Variations (76 papers), CRISPR and Genetic Engineering (33 papers) and Genomics and Chromatin Dynamics (32 papers). В. А. Гвоздев is often cited by papers focused on Chromosomal and Genetic Variations (76 papers), CRISPR and Genetic Engineering (33 papers) and Genomics and Chromatin Dynamics (32 papers). В. А. Гвоздев collaborates with scholars based in Russia, United States and France. В. А. Гвоздев's co-authors include Vasily V. Vagin, Chengjian Li, Alla A. Sigova, Phillip D. Zamore, Hervé Seitz, Alexei A. Aravin, Mikhail S. Klenov, Alexei V. Tulin, Alla Kalmykova and Anastasia D. Stolyarenko and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

В. А. Гвоздев

139 papers receiving 4.2k citations

Hit Papers

A Distinct Small RNA Pathway Silences Selfish Genetic Ele... 2001 2026 2009 2017 2006 2001 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
В. А. Гвоздев Russia 29 3.6k 2.7k 678 540 161 146 4.2k
Colin D. Malone United States 20 3.4k 1.0× 2.0k 0.7× 415 0.6× 580 1.1× 190 1.2× 21 4.0k
Sergio Pimpinelli Italy 40 4.5k 1.3× 2.8k 1.1× 1.1k 1.6× 198 0.4× 112 0.7× 99 5.4k
Hugh W. Brock Canada 42 4.9k 1.4× 981 0.4× 764 1.1× 330 0.6× 335 2.1× 86 5.6k
Todd S. Macfarlan United States 31 4.0k 1.1× 1.6k 0.6× 686 1.0× 310 0.6× 311 1.9× 48 4.7k
Frédéric Pâques France 28 4.5k 1.3× 840 0.3× 976 1.4× 422 0.8× 86 0.5× 44 4.8k
Claudia Kutter Sweden 21 3.3k 0.9× 1.2k 0.5× 471 0.7× 959 1.8× 162 1.0× 44 4.2k
Pamela Geyer United States 38 3.7k 1.0× 1.5k 0.6× 810 1.2× 115 0.2× 179 1.1× 75 4.1k
Alain Pélisson France 28 2.5k 0.7× 2.3k 0.8× 490 0.7× 160 0.3× 122 0.8× 50 3.0k
Keita Miyoshi Japan 21 2.7k 0.8× 1.6k 0.6× 204 0.3× 644 1.2× 154 1.0× 35 3.2k
Songtao Jia United States 25 3.7k 1.0× 1.4k 0.5× 362 0.5× 246 0.5× 124 0.8× 48 4.1k

Countries citing papers authored by В. А. Гвоздев

Since Specialization
Citations

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

Fields of papers citing papers by В. А. Гвоздев

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by В. А. Гвоздев. 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 В. А. Гвоздев. The network helps show where В. А. Гвоздев may publish in the future.

Co-authorship network of co-authors of В. А. Гвоздев

This figure shows the co-authorship network connecting the top 25 collaborators of В. А. Гвоздев. A scholar is included among the top collaborators of В. А. Гвоздев 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 В. А. Гвоздев. В. А. Гвоздев 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.
Pokholkova, Galina V., А. К. Головнин, В. А. Гвоздев, et al.. (2025). Drosophila architectural proteins M1BP and Opbp cooperatively form the active promoter of a ribosomal protein gene. Epigenetics & Chromatin. 18(1). 20–20. 2 indexed citations
3.
Mikhaleva, Elena A., et al.. (2021). Impaired function of rDNA transcription initiation machinery leads to derepression of ribosomal genes with insertions of R2 retrotransposon. Nucleic Acids Research. 50(2). 867–884. 9 indexed citations
4.
Ryazansky, Sergei, Anastasia D. Stolyarenko, Mikhail S. Klenov, & В. А. Гвоздев. (2017). Induction of transposon silencing in the Drosophila germline. Biochemistry (Moscow). 82(5). 565–571. 3 indexed citations
5.
Ryazansky, Sergei, et al.. (2016). RNA helicase Spn-E is required to maintain Aub and AGO3 protein levels for piRNA silencing in the germline of Drosophila. European Journal of Cell Biology. 95(9). 311–322. 15 indexed citations
6.
Гвоздев, В. А., et al.. (2013). Multifunctionality of PIWI proteins in control of germline stem cell fate. Biochemistry (Moscow). 78(6). 585–591. 3 indexed citations
7.
Гвоздев, В. А.. (2013). Regulatory small RNAs. Biochemistry (Moscow). 78(6). 561–561. 3 indexed citations
8.
Kogan, Galina L., et al.. (2012). Expansion and Evolution of the X-Linked Testis Specific Multigene Families in the melanogaster Species Subgroup. PLoS ONE. 7(5). e37738–e37738. 11 indexed citations
9.
Klenov, Mikhail S., et al.. (2011). Separation of stem cell maintenance and transposon silencing functions of Piwi protein. Proceedings of the National Academy of Sciences. 108(46). 18760–18765. 138 indexed citations
11.
Ryazansky, Sergei & В. А. Гвоздев. (2008). Small RNAs and cancerogenesis. Biochemistry (Moscow). 73(5). 514–527. 12 indexed citations
12.
Vagin, Vasily V., Alla A. Sigova, Chengjian Li, et al.. (2006). A Distinct Small RNA Pathway Silences Selfish Genetic Elements in the Germline. Science. 313(5785). 320–324. 1034 indexed citations breakdown →
13.
Kalmykova, Alla, Yuri Y. Shevelyov, Oksana Polesskaya, et al.. (2002). CK2βtes gene encodes a testis‐specific isoform of the regulatory subunit of casein kinase 2 in Drosophila melanogaster. European Journal of Biochemistry. 269(5). 1418–1427. 12 indexed citations
14.
Aravin, Alexei A., N. M. Naumova, Alexei V. Tulin, Mikhail S. Klenov, & В. А. Гвоздев. (2000). Studies of the interactions between the Stellate and Suppressor of Stellate paralogous tandem repeats in the genome of Drosophila melanogaster.. 36(4). 581–584. 1 indexed citations
15.
Kogan, Galina L., et al.. (2000). Molecular Evolution of Two Paralogous Tandemly Repeated Heterochromatic Gene Clusters Linked to the X and Y Chromosomes of Drosophila melanogaster. Molecular Biology and Evolution. 17(5). 697–702. 18 indexed citations
16.
Mikhaleva, Elena A., et al.. (1997). Insect mucin-type glycoprotein: Immunodetection of the O-glycosylated epitope in Drosophila melanogaster cells and tissues. Insect Biochemistry and Molecular Biology. 27(6). 513–521. 16 indexed citations
17.
Benevolenskaya, Elizaveta V., Dmitry I. Nurminsky, & В. А. Гвоздев. (1995). Structure of the Drosophila melanogaster Annexin X Gene. DNA and Cell Biology. 14(4). 349–357. 6 indexed citations
18.
Гвоздев, В. А.. (1978). [Genome organization in eukaryotes].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 12(1). 5–35. 1 indexed citations
19.
Гвоздев, В. А., et al.. (1975). Influence of ecdysterone on the growth of cells and synthesis of macromolecules in established cell lines of Drosophila melanogaster.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 5(1). 29–36. 4 indexed citations
20.
Гвоздев, В. А., et al.. (1971). Activity of a sex-linked gene in Drosophila melanogaster embryonic cell sublines.. PubMed. 2(3). 243–8. 3 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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