Dinesh A. Nagegowda

4.5k total citations · 1 hit paper
52 papers, 3.3k citations indexed

About

Dinesh A. Nagegowda is a scholar working on Molecular Biology, Plant Science and Biotechnology. According to data from OpenAlex, Dinesh A. Nagegowda has authored 52 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 13 papers in Plant Science and 11 papers in Biotechnology. Recurrent topics in Dinesh A. Nagegowda's work include Plant biochemistry and biosynthesis (39 papers), Phytochemicals and Medicinal Plants (10 papers) and Microbial Natural Products and Biosynthesis (8 papers). Dinesh A. Nagegowda is often cited by papers focused on Plant biochemistry and biosynthesis (39 papers), Phytochemicals and Medicinal Plants (10 papers) and Microbial Natural Products and Biosynthesis (8 papers). Dinesh A. Nagegowda collaborates with scholars based in India, United States and France. Dinesh A. Nagegowda's co-authors include Natalia Dudareva, Irina Orlova, Florence Negre, Priyanka Gupta, Ajit Kumar Shasany, Michael Gutensohn, Mee‐Len Chye, Avanish Rai, Anup K. Singh and Thomas J. Bach and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Plant Cell and PLANT PHYSIOLOGY.

In The Last Decade

Dinesh A. Nagegowda

51 papers receiving 3.2k citations

Hit Papers

Plant Volatiles: Recent Advances and Future Perspectives 2006 2026 2012 2019 2006 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dinesh A. Nagegowda India 27 2.3k 1.3k 527 478 472 52 3.3k
Alain Tissier Germany 34 3.1k 1.4× 2.3k 1.8× 425 0.8× 255 0.5× 409 0.9× 82 4.5k
John C. D’Auria Germany 23 2.4k 1.0× 1.6k 1.2× 379 0.7× 232 0.5× 334 0.7× 51 3.3k
Einat Bar Israel 36 2.4k 1.1× 1.7k 1.3× 400 0.8× 779 1.6× 211 0.4× 74 4.0k
Irina Orlova United States 16 2.4k 1.0× 1.3k 1.0× 634 1.2× 443 0.9× 448 0.9× 20 3.4k
Efraim Lewinsohn Israel 34 3.1k 1.4× 2.0k 1.5× 693 1.3× 1.2k 2.4× 494 1.0× 66 5.1k
David V. Huhman United States 33 2.9k 1.3× 2.2k 1.6× 255 0.5× 260 0.5× 225 0.5× 50 4.3k
Christine M. Kish United States 16 2.2k 1.0× 1.1k 0.8× 682 1.3× 385 0.8× 257 0.5× 18 2.9k
Qian Shen China 35 2.8k 1.2× 1.3k 1.0× 158 0.3× 424 0.9× 274 0.6× 117 3.8k
Christian Paetz Germany 30 1.2k 0.5× 1.1k 0.8× 307 0.6× 201 0.4× 576 1.2× 106 2.6k
Joëlle K. Mühlemann United States 14 1.6k 0.7× 1.4k 1.1× 733 1.4× 390 0.8× 336 0.7× 16 2.7k

Countries citing papers authored by Dinesh A. Nagegowda

Since Specialization
Citations

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

Fields of papers citing papers by Dinesh A. Nagegowda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dinesh A. Nagegowda

This figure shows the co-authorship network connecting the top 25 collaborators of Dinesh A. Nagegowda. A scholar is included among the top collaborators of Dinesh A. Nagegowda 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 Dinesh A. Nagegowda. Dinesh A. Nagegowda 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.
Nagegowda, Dinesh A., et al.. (2025). Three Rho of Plant (ROP)-GTPase regulatory proteins control ROP-mediated alkaloid biosynthesis in Catharanthus roseus. PLANT PHYSIOLOGY. 197(4). 1 indexed citations
2.
Nagegowda, Dinesh A., et al.. (2025). Characterization of two glycosyltransferases that modulate withanolide biosynthesis and defense in Withania somnifera. Molecular Biology Reports. 52(1). 675–675. 1 indexed citations
3.
Nagegowda, Dinesh A., et al.. (2024). Biosynthesis of the triterpenoid withanolides in Withania somnifera. Current Opinion in Plant Biology. 81. 102576–102576. 5 indexed citations
4.
Nagegowda, Dinesh A., et al.. (2024). Phylogenetically distant enzymes localized in cytosol and plastids drive citral biosynthesis in lemongrass. The Plant Journal. 120(5). 1901–1919. 3 indexed citations
5.
6.
Carqueijeiro, Inês, et al.. (2024). ROP GTPases with a geranylgeranylation motif modulate alkaloid biosynthesis in Catharanthus roseus. PLANT PHYSIOLOGY. 195(3). 2213–2233. 2 indexed citations
7.
Gupta, Priyanka, et al.. (2024). Analysis of root volatiles and functional characterization of a root-specific germacrene A synthase in Artemisia pallens. Planta. 259(3). 58–58. 2 indexed citations
8.
Gupta, Priyanka, Anuj Sharma, & Dinesh A. Nagegowda. (2023). Multi-omics: Powerful accelerator for uncovering plant specialized metabolic pathways: The case of leonurine. Molecular Plant. 17(1). 13–15. 3 indexed citations
9.
Nagegowda, Dinesh A., et al.. (2022). Agrobacterium-Mediated in Planta Transformation in Periwinkle. Methods in molecular biology. 2505. 301–315. 4 indexed citations
10.
Carqueijeiro, Inês, Κωνσταντίνος Κουδούνας, Emily Amor Stander, et al.. (2022). Identification of a second 16-hydroxytabersonine-O-methyltransferase suggests an evolutionary relationship between alkaloid and flavonoid metabolisms in Catharanthus roseus. PROTOPLASMA. 260(2). 607–624. 3 indexed citations
11.
Kumar, Sarma Rajeev, et al.. (2020). Virus-Induced Gene Silencing for Functional Genomics in Withania somnifera, an Important Indian Medicinal Plant. Methods in molecular biology. 2172. 139–154. 5 indexed citations
12.
Singh, Anup K., Varun Dwivedi, Avanish Rai, et al.. (2015). Virus‐induced gene silencing of Withania somnifera squalene synthase negatively regulates sterol and defence‐related genes resulting in reduced withanolides and biotic stress tolerance. Plant Biotechnology Journal. 13(9). 1287–1299. 72 indexed citations
14.
Liao, Pan, Hui Wang, Andréa Hemmerlin, et al.. (2014). Past achievements, current status and future perspectives of studies on 3-hydroxy-3-methylglutaryl-CoA synthase (HMGS) in the mevalonate (MVA) pathway. Plant Cell Reports. 33(7). 1005–1022. 58 indexed citations
15.
Klempien, Antje, Yasuhisa Kaminaga, Anthony Qualley, et al.. (2012). Contribution of CoA Ligases to Benzenoid Biosynthesis in Petunia Flowers. The Plant Cell. 24(5). 2015–2030. 137 indexed citations
16.
Wang, Hui, Dinesh A. Nagegowda, Reetika Rawat, et al.. (2011). Overexpression of Brassica juncea wild‐type and mutant HMG‐CoA synthase 1 in Arabidopsis up‐regulates genes in sterol biosynthesis and enhances sterol production and stress tolerance. Plant Biotechnology Journal. 10(1). 31–42. 105 indexed citations
17.
Nagegowda, Dinesh A.. (2010). The small subunit of geranyl diphosphate synthase: a tool to improve aroma and flavour by metabolic engineering. Journal of Biosciences. 35(2). 167–169. 2 indexed citations
18.
Nagegowda, Dinesh A., David Rhodes, & Natalia Dudareva. (2010). The Role of the Methyl-Erythritol-Phosphate Pathway in Rhythmic Emission of Volatiles. 2 indexed citations
19.
Dudareva, Natalia, Florence Negre, Dinesh A. Nagegowda, & Irina Orlova. (2006). Plant Volatiles: Recent Advances and Future Perspectives. Critical Reviews in Plant Sciences. 25(5). 417–440. 955 indexed citations breakdown →
20.
Nagegowda, Dinesh A., Sathishkumar Ramalingam, Andréa Hemmerlin, Thomas J. Bach, & Mee‐Len Chye. (2005). Brassica juncea HMG-CoA synthase: localization of mRNA and protein. Planta. 221(6). 844–856. 28 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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