Б. Б. Кузнецов

2.6k total citations
85 papers, 2.0k citations indexed

About

Б. Б. Кузнецов is a scholar working on Molecular Biology, Ecology and Environmental Chemistry. According to data from OpenAlex, Б. Б. Кузнецов has authored 85 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 55 papers in Ecology and 19 papers in Environmental Chemistry. Recurrent topics in Б. Б. Кузнецов's work include Microbial Community Ecology and Physiology (55 papers), Genomics and Phylogenetic Studies (37 papers) and Methane Hydrates and Related Phenomena (19 papers). Б. Б. Кузнецов is often cited by papers focused on Microbial Community Ecology and Physiology (55 papers), Genomics and Phylogenetic Studies (37 papers) and Methane Hydrates and Related Phenomena (19 papers). Б. Б. Кузнецов collaborates with scholars based in Russia, Netherlands and Tajikistan. Б. Б. Кузнецов's co-authors include T. P. Tourova, В. М. Горленко, Т. В. Колганова, E. A. Bonch-Osmolovskaya, N. A. Kostrikina, Н. В. Доронина, Eugenia Boulygina, Tatjana P. Tourova, N. A. Chernyh and R. N. Ivanovsky and has published in prestigious journals such as PLoS ONE, Journal of Bacteriology and Environmental Microbiology.

In The Last Decade

Б. Б. Кузнецов

84 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Б. Б. Кузнецов Russia 26 1.1k 948 408 380 229 85 2.0k
Kae Kyoung Kwon South Korea 27 1.3k 1.2× 1.1k 1.2× 236 0.6× 341 0.9× 153 0.7× 100 2.2k
Т. В. Колганова Russia 27 1.1k 1.0× 1.0k 1.1× 550 1.3× 243 0.6× 404 1.8× 87 2.1k
Tatjana P. Tourova Russia 26 594 0.6× 719 0.8× 419 1.0× 275 0.7× 215 0.9× 36 1.4k
Alexander Y. Merkel Russia 27 886 0.8× 1.2k 1.3× 825 2.0× 273 0.7× 201 0.9× 121 2.1k
Irina S. Kulichevskaya Russia 29 1.0k 1.0× 1.4k 1.5× 371 0.9× 287 0.8× 113 0.5× 57 2.2k
Kjeld Ingvorsen Denmark 30 901 0.8× 1.1k 1.1× 968 2.4× 419 1.1× 381 1.7× 48 2.6k
Yuri A. Trotsenko Russia 32 2.2k 2.0× 1.1k 1.2× 1.0k 2.5× 570 1.5× 367 1.6× 74 3.2k
Vitaly V. Kadnikov Russia 24 692 0.6× 874 0.9× 663 1.6× 289 0.8× 217 0.9× 99 1.7k
Ilya V. Kublanov Russia 29 1.4k 1.3× 1.2k 1.3× 624 1.5× 243 0.6× 495 2.2× 117 2.4k
So‐Jeong Kim South Korea 22 544 0.5× 839 0.9× 376 0.9× 545 1.4× 103 0.4× 73 1.5k

Countries citing papers authored by Б. Б. Кузнецов

Since Specialization
Citations

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

Fields of papers citing papers by Б. Б. Кузнецов

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Б. Б. Кузнецов

This figure shows the co-authorship network connecting the top 25 collaborators of Б. Б. Кузнецов. A scholar is included among the top collaborators of Б. Б. Кузнецов 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 Б. Б. Кузнецов. Б. Б. Кузнецов 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.
Bryantseva, I. A., Vasil A. Gaisin, Denis S. Grouzdev, et al.. (2017). Benthic phototrophic community from Kiran soda lake, south-eastern Siberia. Extremophiles. 22(2). 211–220. 10 indexed citations
2.
Кузнецов, Б. Б., et al.. (2016). Isolation and sequence analysis of pCS36-4CPA, a small plasmid from Citrobacter sp. 36-4CPA. Saudi Journal of Biological Sciences. 25(4). 660–671. 11 indexed citations
3.
Gaisin, Vasil A., et al.. (2015). Filamentous anoxygenic phototrophic bacteria from cyanobacterial mats of Alla hot springs (Barguzin Valley, Russia). Extremophiles. 19(6). 1067–1076. 16 indexed citations
4.
5.
Пименов, Н. В., E. E. Zakharova, Б. Б. Кузнецов, et al.. (2014). Activity and structure of the sulfate-reducing bacterial community in the sediments of the southern part of Lake Baikal. Microbiology. 83(1-2). 47–55. 23 indexed citations
7.
Баслеров, Р. В., et al.. (2013). Haloferax chudinovii sp. nov., a halophilic archaeon from Permian potassium salt deposits. Extremophiles. 17(3). 499–504. 19 indexed citations
8.
Ушакова, Н. А., Vyacheslav M. Abramov, В. С. Хлебников, et al.. (2012). Generation of uncultivable forms of Lactobacillus plantarum 8R-A3 under solid-state cultivation on wheat bran. Biology Bulletin. 39(6). 525–533. 1 indexed citations
9.
Mardanov, Andrey V., А. В. Белецкий, Т. В. Колганова, et al.. (2012). Reconstruction of iron metabolism pathways of bacteria Magnetospirillum aberrantis SpK spp. based on sequenced genome analysis. Doklady Biological Sciences. 444(1). 202–205. 4 indexed citations
10.
Ушакова, Н. А., Vyacheslav M. Abramov, В. С. Хлебников, et al.. (2012). Properties of the Probiotic Strain Lactobacillus plantarum 8-RA-3 Grown in a Biofilm by Solid Substrate Cultivation Method. Probiotics and Antimicrobial Proteins. 4(3). 180–186. 12 indexed citations
12.
Boulygina, Eugenia, А. Н. Игнатов, Svetlana Tsygankova, Eugene Korotkov, & Б. Б. Кузнецов. (2009). Interspecies relations between Bacillus thuringiensis strains studied by AP-PCR and sequence analysis of ribosomal operon regions. Microbiology. 78(6). 703–710.
13.
Mardanov, Andrey V., Nikolai V. Ravin, Б. Б. Кузнецов, et al.. (2008). Complete Sequence of the Duckweed (Lemna minor) Chloroplast Genome: Structural Organization and Phylogenetic Relationships to Other Angiosperms. Journal of Molecular Evolution. 66(6). 555–564. 98 indexed citations
14.
Tsygankova, Svetlana, Eugenia Boulygina, А. Н. Игнатов, Б. Б. Кузнецов, & Eugene Korotkov. (2008). Use of DIR-PCR for elaboration of molecular markers of intraspecies bacterial groups as exemplified by Bacillus thuringiensis. Microbiology. 77(1). 33–38. 2 indexed citations
15.
Tsygankova, Svetlana, et al.. (2004). Obtaining of Intrapopulational Dissociants of Some Bacilli and the Use of DIR-PCR for Their Identification. Microbiology. 73(3). 334–341. 6 indexed citations
16.
Spiridonova, E. M., Ivan A. Berg, Т. В. Колганова, et al.. (2004). An Oligonucleotide Primer System for Amplification of the Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Genes of Bacteria of Various Taxonomic Groups. Microbiology. 73(3). 316–325. 63 indexed citations
17.
Boulygina, Eugenia, Б. Б. Кузнецов, Alina I. Marusina, et al.. (2002). A Study of Nucleotide Sequences of nifH Genes of Some Methanotrophic Bacteria. Microbiology. 71(4). 425–432. 79 indexed citations
18.
Доронина, Н. В., Yuri A. Trotsenko, Tatjana P. Tourova, Б. Б. Кузнецов, & Thomas Leisinger. (2000). Methylopila helvetica sp. nov. and Methylobacterium dichloromethanicum sp. nov. — Novel Aerobic Facultatively Methylotrophic Bacteria Utilizing Dichloromethane. Systematic and Applied Microbiology. 23(2). 210–218. 81 indexed citations
19.
Tourova, T. P., et al.. (2000). Phylogenetic position of desulfurococcus amylolyticus. Microbiology. 69(3). 369–370. 5 indexed citations
20.
Slobodkin, A. I., T. P. Tourova, Б. Б. Кузнецов, et al.. (1999). Thermoanaerobacter siderophilus sp. nov., a novel dissimilatory Fe(III)-reducing, anaerobic, thermophilic bacterium. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY. 49(4). 1471–1478. 96 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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