Santosh Misra

2.8k total citations
64 papers, 2.1k citations indexed

About

Santosh Misra is a scholar working on Plant Science, Molecular Biology and Biotechnology. According to data from OpenAlex, Santosh Misra has authored 64 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Plant Science, 41 papers in Molecular Biology and 19 papers in Biotechnology. Recurrent topics in Santosh Misra's work include Transgenic Plants and Applications (18 papers), Plant tissue culture and regeneration (16 papers) and Seed Germination and Physiology (14 papers). Santosh Misra is often cited by papers focused on Transgenic Plants and Applications (18 papers), Plant tissue culture and regeneration (16 papers) and Seed Germination and Physiology (14 papers). Santosh Misra collaborates with scholars based in Canada, United States and Sri Lanka. Santosh Misra's co-authors include Lashitew Gedamu, William W. Kay, Dmytro P. Yevtushenko, Milan Osusky, Robert E. W. Hancock, Ann Oaks, Timothy J. Tranbarger, Karen L. Jones, Isabel Leal and J. Derek Bewley and has published in prestigious journals such as Nature Biotechnology, PLoS ONE and PLANT PHYSIOLOGY.

In The Last Decade

Santosh Misra

62 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Santosh Misra Canada 26 1.3k 1.2k 444 440 137 64 2.1k
Yube Yamaguchi Japan 29 1.6k 1.3× 2.7k 2.2× 178 0.4× 127 0.3× 53 0.4× 47 3.3k
Olaf B. Styrvold Norway 18 822 0.6× 219 0.2× 342 0.8× 431 1.0× 181 1.3× 20 1.8k
Barbara De Coninck Belgium 31 1.4k 1.1× 2.4k 2.0× 307 0.7× 384 0.9× 65 0.5× 58 3.3k
Ryozo Imai Japan 37 2.4k 1.9× 2.4k 2.0× 217 0.5× 82 0.2× 172 1.3× 90 3.8k
Anthony J. Conner New Zealand 30 2.2k 1.7× 2.5k 2.0× 653 1.5× 80 0.2× 77 0.6× 127 3.2k
Alex Richman Canada 11 859 0.7× 538 0.4× 272 0.6× 39 0.1× 129 0.9× 11 1.5k
Jeong Dong Bahk South Korea 30 1.9k 1.5× 2.3k 1.9× 157 0.4× 43 0.1× 98 0.7× 72 3.2k
Charles M. Kenerley United States 34 1.8k 1.4× 3.9k 3.2× 307 0.7× 63 0.1× 130 0.9× 89 4.8k
Henrik U. Stotz United Kingdom 23 1.2k 0.9× 2.0k 1.7× 127 0.3× 151 0.3× 45 0.3× 52 2.6k
Miguel A. Matilla Spain 33 1.6k 1.3× 1.3k 1.0× 80 0.2× 117 0.3× 412 3.0× 95 2.9k

Countries citing papers authored by Santosh Misra

Since Specialization
Citations

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

Fields of papers citing papers by Santosh Misra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Santosh Misra

This figure shows the co-authorship network connecting the top 25 collaborators of Santosh Misra. A scholar is included among the top collaborators of Santosh Misra 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 Santosh Misra. Santosh Misra 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
2.
Yevtushenko, Dmytro P., et al.. (2021). Douglas‐fir LEAFY COTYLEDON1 (PmLEC1) is an active transcription factor during zygotic and somatic embryogenesis. Plant Direct. 5(7). e00333–e00333. 9 indexed citations
3.
Yevtushenko, Dmytro P. & Santosh Misra. (2019). Enhancing disease resistance in poplar through modification of its natural defense pathway. Plant Molecular Biology. 100(4-5). 481–494. 12 indexed citations
4.
Yevtushenko, Dmytro P. & Santosh Misra. (2018). Spatiotemporal activities of Douglas-fir BiP Pro1 promoter in transgenic potato. Planta. 248(6). 1569–1579. 3 indexed citations
5.
Rustagi, Anjana, Deepak Kumar, Shashi Shekhar, et al.. (2014). Transgenic Brassica juncea Plants Expressing MsrA1, a Synthetic Cationic Antimicrobial Peptide, Exhibit Resistance to Fungal Phytopathogens. Molecular Biotechnology. 56(6). 535–545. 16 indexed citations
6.
Yevtushenko, Dmytro P., et al.. (2005). Pathogen-induced expression of a cecropin A-melittin antimicrobial peptide gene confers antifungal resistance in transgenic tobacco. Journal of Experimental Botany. 56(416). 1685–1695. 72 indexed citations
7.
Osusky, Milan, et al.. (2004). Transgenic Potatoes Expressing a Novel Cationic Peptide are Resistant to Late Blight and Pink Rot. Transgenic Research. 13(2). 181–190. 78 indexed citations
8.
Yevtushenko, Dmytro P., et al.. (2004). 2S storage protein gene of Douglas-fir: characterization and activity of promoter in transgenic tobacco seeds. Plant Physiology and Biochemistry. 42(5). 417–423. 6 indexed citations
10.
Sivaprasad, V., et al.. (2003). Screening of Silkworm Breeds for Tolerance to Bombyx mori Nuclear Polyhedro Virus (BmNPV). International Journal of Industrial Entomology. 7(1). 87–91. 3 indexed citations
11.
Misra, Santosh, et al.. (2000). Characterization and expression of the Douglas-fir luminal binding protein (PmBiP). Planta. 212(1). 41–51. 13 indexed citations
12.
Osusky, Milan, et al.. (2000). Transgenic plants expressing cationic peptide chimeras exhibit broad-spectrum resistance to phytopathogens. Nature Biotechnology. 18(11). 1162–1166. 191 indexed citations
13.
Kaukinen, Karia H., Timothy J. Tranbarger, & Santosh Misra. (1996). Post-germination-induced and hormonally dependent expression of low-molecular-weight heat shock protein genes in Douglas fir. Plant Molecular Biology. 30(6). 1115–1128. 29 indexed citations
14.
Brick, David J., Michael J. Brumlik, J. Thomas Buckley, et al.. (1995). A new family of lipolytic plant enzymes with members in rice, arabidopsis and maize. FEBS Letters. 377(3). 475–480. 96 indexed citations
15.
Leal, Isabel & Santosh Misra. (1994). Molecular cloning and characterization of a legumin-like storage protein cDNA of Douglas fir seeds. Plant Molecular Biology. 26(3). 1019–1019. 1 indexed citations
16.
Misra, Santosh, et al.. (1989). Analysis of stress-induced gene expression in fish cell lines exposed to heavy metals and heat shock. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1007(3). 325–333. 92 indexed citations
17.
Kermode, Allison R., et al.. (1986). The Transition from Seed Development to Germination: A Key Role for Desiccation?. HortScience. 21(5). 1113–1118. 65 indexed citations
18.
Misra, Santosh & J. Derek Bewley. (1985). Reprogramming of Protein Synthesis from a Developmental to a Germinative Mode Induced by Desiccation of the Axes of Phaseolus vulgaris. PLANT PHYSIOLOGY. 78(4). 876–882. 23 indexed citations
19.
Oaks, Ann, et al.. (1980). Enzymes of nitrogen assimilation in maize roots. Planta. 148(5). 477–484. 101 indexed citations
20.
Oaks, Ann, Karen L. Jones, & Santosh Misra. (1979). A Comparison of Glutamate Synthase Obtained from Maize Endosperms and Roots. PLANT PHYSIOLOGY. 63(5). 793–795. 23 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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