М. В. Веселова

772 total citations
31 papers, 614 citations indexed

About

М. В. Веселова is a scholar working on Molecular Biology, Plant Science and Pathology and Forensic Medicine. According to data from OpenAlex, М. В. Веселова has authored 31 papers receiving a total of 614 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 9 papers in Plant Science and 6 papers in Pathology and Forensic Medicine. Recurrent topics in М. В. Веселова's work include Bioactive natural compounds (9 papers), Plant tissue culture and regeneration (9 papers) and Phytochemistry and Biological Activities (6 papers). М. В. Веселова is often cited by papers focused on Bioactive natural compounds (9 papers), Plant tissue culture and regeneration (9 papers) and Phytochemistry and Biological Activities (6 papers). М. В. Веселова collaborates with scholars based in Russia, Serbia and Germany. М. В. Веселова's co-authors include Sergey A. Fedoreyev, Victor P. Bulgakov, Konstantin V. Kiselev, Yuri N. Zhuravlev, Alexandra S. Dubrovina, G. K. Tchernoded, Н. И. Кулеш, В. А. Денисенко, Yu. N. Zhuravlev and А.В. Герасименко and has published in prestigious journals such as Journal of Agricultural and Food Chemistry, Applied Microbiology and Biotechnology and Planta.

In The Last Decade

М. В. Веселова

31 papers receiving 595 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
М. В. Веселова Russia 13 474 256 82 80 68 31 614
Sakae Yamanouchi Japan 14 492 1.0× 261 1.0× 109 1.3× 58 0.7× 31 0.5× 24 775
Asif Zaman India 15 358 0.8× 256 1.0× 34 0.4× 35 0.4× 39 0.6× 68 673
Yusuke Tsurumaru Japan 6 360 0.8× 157 0.6× 104 1.3× 31 0.4× 22 0.3× 6 518
Gilbert Deccaux Wabo Fotso Kapche Cameroon 13 238 0.5× 118 0.5× 55 0.7× 19 0.2× 54 0.8× 26 434
Z Ovesná Slovakia 6 427 0.9× 152 0.6× 105 1.3× 12 0.1× 88 1.3× 9 668
Paul‐Henri Ducrot France 12 178 0.4× 135 0.5× 122 1.5× 41 0.5× 16 0.2× 23 452
Moon Hee Jang South Korea 7 239 0.5× 166 0.6× 105 1.3× 13 0.2× 32 0.5× 10 509
Youn-Chul Kim South Korea 13 330 0.7× 174 0.7× 45 0.5× 34 0.4× 11 0.2× 17 539
Natalia P. Mischenko Russia 12 463 1.0× 241 0.9× 30 0.4× 199 2.5× 12 0.2× 20 669
Ren‐Bo An China 19 472 1.0× 178 0.7× 73 0.9× 27 0.3× 11 0.2× 43 777

Countries citing papers authored by М. В. Веселова

Since Specialization
Citations

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

Fields of papers citing papers by М. В. Веселова

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of М. В. Веселова

This figure shows the co-authorship network connecting the top 25 collaborators of М. В. Веселова. A scholar is included among the top collaborators of М. В. Веселова 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 М. В. Веселова. М. В. Веселова 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.
Похило, Н. Д., et al.. (2021). Flavonoid Glycosides from the Aerial Part of Lespedeza tomentosa. Chemistry of Natural Compounds. 57(6). 1023–1028. 3 indexed citations
2.
Dyshlovoy, Sergey A., Sergey A. Fedoreyev, М. В. Веселова, et al.. (2020). Polyphenolic Compounds from Lespedeza Bicolor Root Bark Inhibit Progression of Human Prostate Cancer Cells via Induction of Apoptosis and Cell Cycle Arrest. Biomolecules. 10(3). 451–451. 16 indexed citations
3.
Fedoreyev, Sergey A., et al.. (2019). Cytotoxic polyphenolic compounds from Lespedeza bicolor stem bark. Fitoterapia. 135. 64–72. 10 indexed citations
4.
Веселова, М. В., et al.. (2017). Cytotoxic Prenylated Polyphenolic Compounds from Maackia amurensis Root Bark. Natural Product Communications. 12(7). 3 indexed citations
5.
Kiselev, Konstantin V., G. K. Tchernoded, Sergey A. Fedoreyev, et al.. (2016). RolB gene-induced production of isoflavonoids in transformed Maackia amurensis cells. Applied Microbiology and Biotechnology. 100(17). 7479–7489. 11 indexed citations
6.
Веселова, М. В., et al.. (2015). Polyphenolic Metabolites from Iris pseudacorus Roots. Chemistry of Natural Compounds. 51(3). 451–455. 10 indexed citations
7.
Кулеш, Н. И., et al.. (2014). [Hepatoprotective properties of isoflavonoids from roots of Maackia amurensis on experimental carbon tetrachloride-induced hepatic damage].. PubMed. 77(2). 26–30. 5 indexed citations
8.
Веселова, М. В., et al.. (2014). Polyphenolic Metabolites from Iris pseudacorus. Chemistry of Natural Compounds. 50(2). 363–365. 7 indexed citations
9.
Fedoreyev, Sergey A., et al.. (2013). Polyphenolic Compounds from Callus Cultures of Iris Pseudacorus. Natural Product Communications. 8(10). 1419–20. 7 indexed citations
10.
Zakharenko, Alexander M., et al.. (2011). Deglycosylation of isoflavonoid glycosides from Maackia amurensis cell culture by β−D-glucosidase from Littorina sitkana hepatopancrease. Chemistry of Natural Compounds. 47(2). 197–200. 2 indexed citations
11.
Bulgakov, Victor P., et al.. (2011). Catechin production in cultured cells of Taxus cuspidata and Taxus baccata. Biotechnology Letters. 33(9). 1879–1883. 17 indexed citations
12.
Dubrovina, Alexandra S., et al.. (2009). Enhanced resveratrol accumulation in rolB transgenic cultures of Vitis amurensis correlates with unusual changes in CDPK gene expression. Journal of Plant Physiology. 166(11). 1194–1206. 41 indexed citations
13.
Bulgakov, Victor P., et al.. (2007). High Rabdosiin and Rosmarinic Acid Production inEritrichium sericeumCallus Cultures and the Effect of the Calli on Masugi-Nephritis in Rats. Bioscience Biotechnology and Biochemistry. 71(5). 1286–1293. 23 indexed citations
14.
Kiselev, Konstantin V., Alexandra S. Dubrovina, М. В. Веселова, et al.. (2006). The rolB gene-induced overproduction of resveratrol in Vitis amurensis transformed cells. Journal of Biotechnology. 128(3). 681–692. 143 indexed citations
15.
Bulgakov, Victor P., М. В. Веселова, G. K. Tchernoded, et al.. (2005). Inhibitory effect of the Agrobacterium rhizogenes rolC gene on rabdosiin and rosmarinic acid production in Eritrichium sericeum and Lithospermum erythrorhizon transformed cell cultures. Planta. 221(4). 471–478. 50 indexed citations
16.
Fedoreyev, Sergey A., М. В. Веселова, Natalia P. Mischenko, et al.. (2005). Caffeic Acid Metabolites fromEritrichium sericeumCell Cultures. Planta Medica. 71(5). 446–451. 24 indexed citations
17.
Веселова, М. В., et al.. (2004). Maksar: A preparation based on Amur maackia. Pharmaceutical Chemistry Journal. 38(11). 605–610. 22 indexed citations
18.
Fedoreyev, Sergey A., et al.. (2000). Isoflavonoid production by callus cultures of Maackia amurensis. Fitoterapia. 71(4). 365–372. 43 indexed citations
19.
Уткина, Н. К., et al.. (1993). Synthesis of polybrominated diphenyl ethers of marine origin. Chemistry of Natural Compounds. 29(3). 291–293. 5 indexed citations
20.
Уткина, Н. К. & М. В. Веселова. (1990). New sesquiterpene quinones from marine sponges of the order dictyoceratida. Chemistry of Natural Compounds. 26(1). 37–40. 6 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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