Sergey Ivashuta

1.7k total citations
21 papers, 1.1k citations indexed

About

Sergey Ivashuta is a scholar working on Plant Science, Molecular Biology and Agronomy and Crop Science. According to data from OpenAlex, Sergey Ivashuta has authored 21 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Plant Science, 14 papers in Molecular Biology and 2 papers in Agronomy and Crop Science. Recurrent topics in Sergey Ivashuta's work include Plant Molecular Biology Research (9 papers), Chromosomal and Genetic Variations (7 papers) and Plant Virus Research Studies (4 papers). Sergey Ivashuta is often cited by papers focused on Plant Molecular Biology Research (9 papers), Chromosomal and Genetic Variations (7 papers) and Plant Virus Research Studies (4 papers). Sergey Ivashuta collaborates with scholars based in United States, Japan and Russia. Sergey Ivashuta's co-authors include Yuanji Zhang, B. Elizabeth Wiggins, J. Stephen Gantt, Kathryn A. VandenBosch, Jay S. Petrick, Bruna Bucciarelli, Carroll P. Vance, Deborah A. Samac, Gregory R. Heck and Mitsuru Gau and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Sergey Ivashuta

21 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergey Ivashuta United States 17 760 652 153 105 60 21 1.1k
B. Elizabeth Wiggins United States 10 471 0.6× 442 0.7× 174 1.1× 83 0.8× 18 0.3× 12 739
Burcu Alptekin United States 10 509 0.7× 303 0.5× 54 0.4× 66 0.6× 37 0.6× 17 637
Markus Wunderlich Germany 7 690 0.9× 652 1.0× 47 0.3× 33 0.3× 19 0.3× 10 908
Lijun Liu China 14 455 0.6× 367 0.6× 49 0.3× 28 0.3× 38 0.6× 28 629
Bala Anı Akpınar Türkiye 19 1.2k 1.5× 412 0.6× 35 0.2× 54 0.5× 109 1.8× 28 1.3k
Huixian Zhao China 21 864 1.1× 516 0.8× 89 0.6× 13 0.1× 56 0.9× 41 998
Céline Sorin France 14 1.3k 1.7× 771 1.2× 20 0.1× 37 0.4× 30 0.5× 18 1.4k
Suying Han China 18 776 1.0× 760 1.2× 19 0.1× 42 0.4× 20 0.3× 42 995
Éric Lasserre France 13 1.0k 1.4× 707 1.1× 28 0.2× 29 0.3× 23 0.4× 16 1.2k

Countries citing papers authored by Sergey Ivashuta

Since Specialization
Citations

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

Fields of papers citing papers by Sergey Ivashuta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergey Ivashuta

This figure shows the co-authorship network connecting the top 25 collaborators of Sergey Ivashuta. A scholar is included among the top collaborators of Sergey Ivashuta 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 Sergey Ivashuta. Sergey Ivashuta 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.
Kuwar, Suyog S., Ruchir Mishra, R. Banerjee, et al.. (2022). Engineering of Cry3Bb1 provides mechanistic insights toward countering western corn rootworm resistance. SHILAP Revista de lepidopterología. 2. 100033–100033. 2 indexed citations
2.
3.
Khajuria, Chitvan, Sergey Ivashuta, Lex Flagel, et al.. (2018). Development and characterization of the first dsRNA-resistant insect population from western corn rootworm, Diabrotica virgifera virgifera LeConte. PLoS ONE. 13(5). e0197059–e0197059. 157 indexed citations
4.
Ivashuta, Sergey, Yuanji Zhang, B. Elizabeth Wiggins, et al.. (2015). Environmental RNAi in herbivorous insects. RNA. 21(5). 840–850. 95 indexed citations
5.
Haag, Jeremy R., Brent D. Brower‐Toland, Lyudmila Sidorenko, et al.. (2014). Functional Diversification of Maize RNA Polymerase IV and V Subtypes via Alternative Catalytic Subunits. Cell Reports. 9(1). 378–390. 57 indexed citations
6.
Jensen, Peter D., Yuanji Zhang, B. Elizabeth Wiggins, et al.. (2013). Computational sequence analysis of predicted long dsRNA transcriptomes of major crops reveals sequence complementarity with human genes. GM crops & food. 4(2). 90–97. 19 indexed citations
7.
Zhang, Yuanji, et al.. (2012). RNA decoys. Plant Signaling & Behavior. 7(9). 1188–1193. 29 indexed citations
8.
Zhang, Yuanji, et al.. (2012). Analysis of plant-derived miRNAs in animal small RNA datasets. BMC Genomics. 13(1). 381–381. 108 indexed citations
9.
Ivashuta, Sergey, et al.. (2011). Regulation of Gene Expression in Plants through miRNA Inactivation. PLoS ONE. 6(6). e21330–e21330. 63 indexed citations
10.
Hoffer, Paul, Sergey Ivashuta, Olga Pontes, et al.. (2010). Posttranscriptional gene silencing in nuclei. Proceedings of the National Academy of Sciences. 108(1). 409–414. 68 indexed citations
11.
Yang, Heping, Jon J. Schmuke, James K. Roberts, et al.. (2009). A novel real‐time polymerase chain reaction method for high throughput quantification of small regulatory RNAs. Plant Biotechnology Journal. 7(7). 621–630. 24 indexed citations
12.
Ivashuta, Sergey, Jay S. Petrick, Yuanji Zhang, et al.. (2008). Endogenous small RNAs in grain: Semi-quantification and sequence homology to human and animal genes. Food and Chemical Toxicology. 47(2). 353–360. 39 indexed citations
13.
Chandran, Divya, N. Sharopova, Sergey Ivashuta, et al.. (2008). Transcriptome profiling identified novel genes associated with aluminum toxicity, resistance and tolerance in Medicago truncatula. Planta. 228(1). 151–166. 97 indexed citations
14.
Liu, Junqi, Susan S. Miller, Michelle A. Graham, et al.. (2006). Recruitment of Novel Calcium-Binding Proteins for Root Nodule Symbiosis in Medicago truncatula   . PLANT PHYSIOLOGY. 141(1). 167–177. 49 indexed citations
15.
Ivashuta, Sergey, Jinyuan Liu, Junqi Liu, et al.. (2005). RNA Interference Identifies a Calcium-Dependent Protein Kinase Involved inMedicago truncatulaRoot Development. The Plant Cell. 17(11). 2911–2921. 134 indexed citations
16.
Isobe, Sachiko, et al.. (2003). First RFLP linkage map of red clover (Trifolium pratense L.) based on cDNA probes and its transferability to other red clover germplasm. Theoretical and Applied Genetics. 108(1). 105–112. 38 indexed citations
17.
Ivashuta, Sergey, et al.. (2002). Genotype‐dependent transcriptional activation of novel repetitive elements during cold acclimation of alfalfa (Medicago sativa). The Plant Journal. 31(5). 615–627. 33 indexed citations
18.
Ivashuta, Sergey, et al.. (2002). Changes in chloroplast FtsH-like gene during cold acclimation in alfalfa (Medicago sativa). Journal of Plant Physiology. 159(1). 85–90. 17 indexed citations
20.
Ivashuta, Sergey, et al.. (1999). The Coupling of Differential Display and AFLP Approaches for Nonradioactive mRNA Fingerprinting. Molecular Biotechnology. 12(2). 137–142. 7 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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