Е. И. Кацы

545 total citations
49 papers, 365 citations indexed

About

Е. И. Кацы is a scholar working on Molecular Biology, Ecology and Biotechnology. According to data from OpenAlex, Е. И. Кацы has authored 49 papers receiving a total of 365 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 21 papers in Ecology and 13 papers in Biotechnology. Recurrent topics in Е. И. Кацы's work include Microbial Community Ecology and Physiology (15 papers), Enzyme Production and Characterization (13 papers) and Legume Nitrogen Fixing Symbiosis (10 papers). Е. И. Кацы is often cited by papers focused on Microbial Community Ecology and Physiology (15 papers), Enzyme Production and Characterization (13 papers) and Legume Nitrogen Fixing Symbiosis (10 papers). Е. И. Кацы collaborates with scholars based in Russia and United Kingdom. Е. И. Кацы's co-authors include Л. П. Петрова, А. В. Шелудько, L. Yu. Matora, Alexander Shirokov, Gennady L. Burygin, А. М. Буров, Anna V. Tugarova, L. P. Antonyuk, Boris N. Khlebtsov and Marina P. Chernyshova and has published in prestigious journals such as Canadian Journal of Microbiology, Microbiological Research and World Journal of Microbiology and Biotechnology.

In The Last Decade

Е. И. Кацы

40 papers receiving 354 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Е. И. Кацы Russia	12	198	157	150	56	47	49	365
А. В. Шелудько Russia	10	151 0.8×	106 0.7×	111 0.7×	31 0.6×	36 0.8×	43	261
Л. П. Петрова Russia	10	164 0.8×	105 0.7×	110 0.7×	34 0.6×	36 0.8×	50	276
N. Baida Lebanon	8	227 1.1×	190 1.2×	140 0.9×	28 0.5×	20 0.4×	9	416
Veerle Keijers Belgium	14	213 1.1×	338 2.2×	85 0.6×	54 1.0×	31 0.7×	19	533
Yuchao Ma China	15	281 1.4×	190 1.2×	118 0.8×	28 0.5×	10 0.2×	29	452
Yingbao Gai China	10	229 1.2×	54 0.3×	114 0.8×	93 1.7×	26 0.6×	16	351
Julian Quehenberger Austria	8	232 1.2×	136 0.9×	88 0.6×	46 0.8×	9 0.2×	19	422
Adrienne Zaprasis Germany	8	205 1.0×	60 0.4×	94 0.6×	24 0.4×	9 0.2×	8	372
Lummy Maria Oliveira Monteiro Brazil	11	203 1.0×	112 0.7×	68 0.5×	83 1.5×	7 0.1×	22	375
Jimena A. Ruiz Argentina	13	267 1.3×	138 0.9×	41 0.3×	25 0.4×	25 0.5×	19	520

Countries citing papers authored by Е. И. Кацы

Since Specialization

Citations

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

Fields of papers citing papers by Е. И. Кацы

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Е. И. Кацы. 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 Е. И. Кацы. The network helps show where Е. И. Кацы may publish in the future.

Co-authorship network of co-authors of Е. И. Кацы

This figure shows the co-authorship network connecting the top 25 collaborators of Е. И. Кацы. A scholar is included among the top collaborators of Е. И. Кацы 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 Е. И. Кацы. Е. И. Кацы 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

Петрова, Л. П., et al.. (2020). Plasmid gene for putative integral membrane protein affects formation of lipopolysaccharide and motility in Azospirillum brasilense Sp245. Folia Microbiologica. 65(6). 963–972. 1 indexed citations

Петрова, Л. П., et al.. (2020). Plasmid gene AZOBR_p60126 impacts biosynthesis of lipopolysaccharide II and swarming motility in Azospirillum brasilense Sp245. Journal of Basic Microbiology. 60(7). 613–623. 4 indexed citations

Шелудько, А. В., et al.. (2020). Анализ ультраструктуры клеток в составе биопленок бактерий Azospirillum brasilense . Микробиология. 89(1). 59–73.

Шелудько, А. В., et al.. (2019). Polar flagellum of the alphaproteobacterium Azospirillum brasilense Sp245 plays a role in biofilm biomass accumulation and in biofilm maintenance under stationary and dynamic conditions. World Journal of Microbiology and Biotechnology. 35(2). 19–19. 11 indexed citations

Шелудько, А. В., et al.. (2018). On the Contribution of Cell Aggregation and Extracellular DNA to Biofilm Formation and Stabilization in Azospirillum brasilense Bacteria. Izvestiya of Saratov University Chemistry Biology Ecology. 18(4). 399–406. 1 indexed citations

Кацы, Е. И., et al.. (2017). Analysis of Protease Effect on Biofilm Structure of Azospirillum Brasilense Strain Sp245 and Its Flagellation-Defective mmsB1 and fabG1 Mutants. Izvestiya of Saratov University Chemistry Biology Ecology. 17(4). 322–327. 1 indexed citations

Шелудько, А. В., et al.. (2017). Chromosomal flhB1 gene of the alphaproteobacterium Azospirillum brasilense Sp245 is essential for correct assembly of both constitutive polar flagellum and inducible lateral flagella. Folia Microbiologica. 63(2). 147–153. 7 indexed citations

Петрова, Л. П., et al.. (2017). Detection of putative polysaccharide biosynthesis genes in Azospirillum brasilense strains from serogroups I and II. Russian Journal of Genetics. 53(1). 39–48.

Шелудько, А. В., et al.. (2015). [Biofilm Formation by the Nonflagellated flhB1 Mutant of Azospirillum brasilense Sp245].. PubMed. 84(2). 175–83. 5 indexed citations

10.

Шелудько, А. В., et al.. (2013). Negative effect of alkylresorcinols on motility of rhizobacteria Azospirillum brasilense. Microbiology. 82(4). 434–438. 6 indexed citations

11.

Шелудько, А. В., et al.. (2011). Effect of genomic rearrangement on heavy metal tolerance in the plant-growth-promoting rhizobacterium Azospirillum brasilense Sp245. Folia Microbiologica. 57(1). 5–10. 9 indexed citations

12.

Петрова, Л. П., А. В. Шелудько, & Е. И. Кацы. (2010). Plasmid rearrangements and alterations in Azospirillum brasilense biofilm formation. Microbiology. 79(1). 121–124. 10 indexed citations

13.

Fedonenko, Yu. P., Е. И. Кацы, Л. П. Петрова, et al.. (2010). The structure of the O-specific polysaccharide from a mutant of nitrogen-fixing rhizobacterium Azospirillum brasilense Sp245 with an altered plasmid content. Russian Journal of Bioorganic Chemistry. 36(2). 219–223. 3 indexed citations

14.

Петрова, Л. П., А. В. Шелудько, & Е. И. Кацы. (2010). [Plasmid rearrangements and Azospirillum brasilense biofilm formation].. PubMed. 79(1). 129–32.

15.

Кацы, Е. И., et al.. (2009). Mobile elements of an Azospirillum brasilense Sp245 85-MDa plasmid involved in replicon fusions. Plasmid. 62(1). 22–29. 15 indexed citations

16.

Шелудько, А. В., et al.. (2009). Hemagglutinating activity and motility of the bacterium Azospirillum brasilense in the presence of various nitrogen sources. Microbiology. 78(6). 696–702. 11 indexed citations

17.

Tugarova, Anna V., et al.. (2007). Changes in motility of the rhizobacterium Azospirillum brasilense in the presence of plant lectins. Microbiological Research. 164(2). 149–156. 26 indexed citations

18.

Петрова, Л. П., et al.. (2007). Changes in Azospirillum brasilense motility and the effect of wheat seedling exudates. Microbiological Research. 164(5). 578–587. 10 indexed citations

19.

Шелудько, А. В., et al.. (2006). Effect of congo red on the motility of the bacterium Azospirillum brasilense. Microbiology. 75(1). 48–54. 8 indexed citations

20.

Кацы, Е. И., et al.. (2001). [Complementation analysis of mutants of the associative bacteria Azospirillum brasilense Sp245 and S27, defective in mobility and flagellation].. PubMed. 37(2). 190–6. 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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