M. A. Eldarov

733 total citations
44 papers, 612 citations indexed

About

M. A. Eldarov is a scholar working on Molecular Biology, Biotechnology and Genetics. According to data from OpenAlex, M. A. Eldarov has authored 44 papers receiving a total of 612 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 12 papers in Biotechnology and 8 papers in Genetics. Recurrent topics in M. A. Eldarov's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (8 papers), Fungal and yeast genetics research (8 papers) and Vitamin K Research Studies (6 papers). M. A. Eldarov is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (8 papers), Fungal and yeast genetics research (8 papers) and Vitamin K Research Studies (6 papers). M. A. Eldarov collaborates with scholars based in Russia, Ukraine and Netherlands. M. A. Eldarov's co-authors include Natalya Kouprina, Michael A. Resnick, V. Larionov, Alexander A. Zhgun, K. G. Skryabin, Victoria C.H.F. de Regt, O.I. Georgiev, Rudi J. Planta, A.A. Hadjiolov and Vladimir Larionov and has published in prestigious journals such as Nucleic Acids Research, Biochimica et Biophysica Acta (BBA) - General Subjects and Genomics.

In The Last Decade

M. A. Eldarov

43 papers receiving 590 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. A. Eldarov Russia	15	459	126	76	67	64	44	612
Pedro Castanheira Portugal	14	242 0.5×	105 0.8×	19 0.3×	50 0.7×	28 0.4×	23	436
Qinyu Zhang China	11	239 0.5×	62 0.5×	28 0.4×	20 0.3×	32 0.5×	27	431
Pilar Eraso Spain	18	871 1.9×	215 1.7×	38 0.5×	31 0.5×	28 0.4×	27	1.1k
C.D. Raghavendra Gowda India	9	161 0.4×	87 0.7×	33 0.4×	99 1.5×	119 1.9×	14	401
Makoto Tsuboi Japan	9	169 0.4×	70 0.6×	101 1.3×	19 0.3×	39 0.6×	25	370
Janice L. Bleibaum United States	7	596 1.3×	203 1.6×	32 0.4×	59 0.9×	46 0.7×	7	781
Ismael Navarro Spain	15	177 0.4×	73 0.6×	69 0.9×	87 1.3×	22 0.3×	29	554
Dong-Uk Kim South Korea	18	648 1.4×	90 0.7×	50 0.7×	12 0.2×	74 1.2×	39	892
Xiaowen Wang United States	12	845 1.8×	58 0.5×	11 0.1×	45 0.7×	29 0.5×	29	991
M. Ruszkowski Poland	16	465 1.0×	228 1.8×	13 0.2×	22 0.3×	14 0.2×	51	652

Countries citing papers authored by M. A. Eldarov

Since Specialization

Citations

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

Fields of papers citing papers by M. A. Eldarov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. A. Eldarov. 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 M. A. Eldarov. The network helps show where M. A. Eldarov may publish in the future.

Co-authorship network of co-authors of M. A. Eldarov

This figure shows the co-authorship network connecting the top 25 collaborators of M. A. Eldarov. A scholar is included among the top collaborators of M. A. Eldarov 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 M. A. Eldarov. M. A. Eldarov 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

Andreeva, N. A., et al.. (2020). Inorganic Polyphosphate and Physiological Properties of Saccharomyces cerevisiae Yeast Overexpressing Ppn2. Biochemistry (Moscow). 85(4). 516–522. 4 indexed citations

Serebryakova, Marina V., M. A. Eldarov, Alexandra A. Kulikova, et al.. (2020). S-glutathionylation of human glyceraldehyde-3-phosphate dehydrogenase and possible role of Cys152-Cys156 disulfide bridge in the active site of the protein. Biochimica et Biophysica Acta (BBA) - General Subjects. 1864(6). 129560–129560. 18 indexed citations

Eldarov, M. A., et al.. (2020). Natural Yeast Strains of Saccharomyces cerevisiae that are Promising for Sherry Production. Applied Biochemistry and Microbiology. 56(3). 329–335. 2 indexed citations

Kulakovskaya, T. V., et al.. (2019). The acid phosphatase Pho5 of Saccharomyces cerevisiae is not involved in polyphosphate breakdown. Folia Microbiologica. 64(6). 867–873. 6 indexed citations

Zhgun, Alexander A., et al.. (2018). Role of acetyl-CoA Synthetase and LovE Regulator Protein of Polyketide Biosynthesis in Lovastatin Production by Wild-Type and Overproducing Aspergillus terreus Strains. Applied Biochemistry and Microbiology. 54(2). 188–197. 15 indexed citations

Тишков, В. И., et al.. (2018). Rational Design of Practically Important Enzymes. Moscow University Chemistry Bulletin. 73(1). 1–6. 20 indexed citations

Eldarov, M. A., et al.. (2017). Isolation of recombinant human untagged glyceraldehyde-3-phosphate dehydrogenase from E. coli producer strain. Protein Expression and Purification. 137. 1–6. 13 indexed citations

Eldarov, M. A., et al.. (2016). Genomics and biochemistry of Saccharomyces cerevisiae wine yeast strains. Biochemistry (Moscow). 81(13). 1650–1668. 31 indexed citations

Trilisenko, L. V., et al.. (2015). Polyphosphates and polyphosphatase activity in the yeast Saccharomyces cerevisiae during overexpression of the DDP1 gene. Biochemistry (Moscow). 80(10). 1312–1317. 7 indexed citations

10.

Zhgun, Alexander A., et al.. (2014). Comparative gene expression profiling reveals key changes in expression levels of cephalosporin C biosynthesis and transport genes between low and high-producing strains of Acremonium chrysogenum. World Journal of Microbiology and Biotechnology. 30(11). 2933–2941. 19 indexed citations

11.

Trilisenko, L. V., et al.. (2014). Purification and properties of recombinant exopolyphosphatase PPN1 and effects of its overexpression on polyphosphate in Saccharomyces cerevisiae. Journal of Bioscience and Bioengineering. 119(1). 52–56. 6 indexed citations

12.

Lichko, L. P., et al.. (2014). PPX1 gene overexpression has no influence on polyphosphates in Saccharomyces cerevisiae. Biochemistry (Moscow). 79(11). 1211–1215. 14 indexed citations

13.

Eldarov, M. A., Maksim V. Baranov, N. A. Andreeva, et al.. (2013). Polyphosphates and exopolyphosphatase activities in the yeast Saccharomyces cerevisiae under overexpression of homologous and heterologous PPN1 genes. Biochemistry (Moscow). 78(8). 946–953. 22 indexed citations

14.

Zhgun, Alexander A., et al.. (2012). Chromosomal polymorphism of Acremonium chrysogenum strains producing cephalosporin C. Russian Journal of Genetics. 48(8). 778–784. 18 indexed citations

15.

Eldarov, M. A., et al.. (2011). Expression of modified oxidase of D-aminoacids of Trigonopsis variabilis in methylotrophic yeasts Pichia pastoris. Applied Biochemistry and Microbiology. 47(1). 32–37. 1 indexed citations

16.

Eldarov, M. A., et al.. (2010). Recombinant human sperm-specific glyceraldehyde-3-phosphate dehydrogenase: Structural basis for enhanced stability. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1804(12). 2207–2212. 29 indexed citations

17.

Trilisenko, L. V., V. M. Vagabov, I. S. Kulaev, et al.. (2010). The concentration dynamics of inorganic polyphosphates during the cephalosporin C synthesis by Acremonium chrysogenum. Applied Biochemistry and Microbiology. 46(2). 184–190. 6 indexed citations

18.

Skryabin, K. G., et al.. (2004). Differential Expression of the Isoforms of Human Vascular Endothelial Growth Factor and New Approaches to Therapeutic Angiogenesis. Doklady Biological Sciences. 397(1-6). 298–300. 2 indexed citations

19.

Larionov, V., Natalya Kouprina, M. A. Eldarov, et al.. (1994). Transformation‐associated recombination between diverged and homologous DNA repeats is induced by strand breaks. Yeast. 10(1). 93–104. 45 indexed citations

20.

Kouprina, Natalya, M. A. Eldarov, Robert K. Moyzis, Michael A. Resnick, & V. Larionov. (1994). A Model System to Assess the Integrity of Mammalian YACs during Transformation and Propagation in Yeast. Genomics. 21(1). 7–17. 42 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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