Edward K. Gilding

2.8k total citations
48 papers, 1.6k citations indexed

About

Edward K. Gilding is a scholar working on Molecular Biology, Plant Science and Biotechnology. According to data from OpenAlex, Edward K. Gilding has authored 48 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 26 papers in Plant Science and 12 papers in Biotechnology. Recurrent topics in Edward K. Gilding's work include Biochemical and Structural Characterization (26 papers), Phytoplasmas and Hemiptera pathogens (16 papers) and Transgenic Plants and Applications (12 papers). Edward K. Gilding is often cited by papers focused on Biochemical and Structural Characterization (26 papers), Phytoplasmas and Hemiptera pathogens (16 papers) and Transgenic Plants and Applications (12 papers). Edward K. Gilding collaborates with scholars based in Australia, United States and United Kingdom. Edward K. Gilding's co-authors include David J. Craik, Mark A. Jackson, M. David Marks, Thomas Durek, Aaron G. Poth, Quentin Kaas, Jonathan P. Wenger, Marilyn A. Anderson, Karen S. Harris and Ian D. Godwin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Edward K. Gilding

48 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edward K. Gilding Australia 22 1.2k 734 257 160 129 48 1.6k
Aaron G. Poth Australia 21 1.3k 1.1× 534 0.7× 251 1.0× 319 2.0× 86 0.7× 31 1.4k
Mikhail A. Belozersky Russia 23 831 0.7× 647 0.9× 354 1.4× 70 0.4× 138 1.1× 64 1.4k
Yakov E. Dunaevsky Russia 20 623 0.5× 555 0.8× 231 0.9× 53 0.3× 104 0.8× 47 1.1k
Marina Vai Italy 29 1.8k 1.5× 776 1.1× 260 1.0× 102 0.6× 104 0.8× 72 2.6k
Ohkmae K. Park South Korea 32 2.0k 1.7× 2.9k 3.9× 103 0.4× 118 0.7× 178 1.4× 48 3.9k
Marina Franceschetti United Kingdom 27 1.4k 1.2× 1.9k 2.6× 197 0.8× 227 1.4× 130 1.0× 51 2.7k
Jan Sklenář United Kingdom 34 1.5k 1.3× 4.0k 5.4× 189 0.7× 140 0.9× 60 0.5× 63 4.6k
Jean‐Claude Kader France 29 2.1k 1.8× 1.7k 2.3× 235 0.9× 192 1.2× 36 0.3× 64 3.3k
Alexander Botzki Belgium 16 1.0k 0.9× 472 0.6× 40 0.2× 190 1.2× 74 0.6× 30 1.6k
Tsezi A. Egorov Russia 25 1.1k 0.9× 309 0.4× 288 1.1× 116 0.7× 32 0.2× 45 1.4k

Countries citing papers authored by Edward K. Gilding

Since Specialization
Citations

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

Fields of papers citing papers by Edward K. Gilding

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward K. Gilding. 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 Edward K. Gilding. The network helps show where Edward K. Gilding may publish in the future.

Co-authorship network of co-authors of Edward K. Gilding

This figure shows the co-authorship network connecting the top 25 collaborators of Edward K. Gilding. A scholar is included among the top collaborators of Edward K. Gilding 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 Edward K. Gilding. Edward K. Gilding 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.
Jackson, Mark A., Fabian B. H. Rehm, Deborah S. Barkauskas, et al.. (2024). Proximity Labelling Confirms the Involvement of Papain-Like Cysteine Proteases and Chaperones in Cyclotide Biosynthesis. Plant Molecular Biology Reporter. 42(3). 611–623. 2 indexed citations
2.
Huang, Yen‐Hua, et al.. (2024). Isolation and Characterization of Insecticidal Cyclotides from Viola communis. Journal of Natural Products. 88(1). 24–35. 1 indexed citations
3.
Jackson, Mark A., et al.. (2022). Rational domestication of a plant-based recombinant expression system expands its biosynthetic range. Journal of Experimental Botany. 73(18). 6103–6114. 9 indexed citations
4.
Campbell, Bradley C., Karen Massel, Anđelija Milić, et al.. (2022). Metabarcoding airborne pollen from subtropical and temperate eastern Australia over multiple years reveals pollen aerobiome diversity and complexity. The Science of The Total Environment. 862. 160585–160585. 9 indexed citations
5.
Xie, Jing, Samuel D. Robinson, Edward K. Gilding, et al.. (2022). Neurotoxic and cytotoxic peptides underlie the painful stings of the tree nettle Urtica ferox. Journal of Biological Chemistry. 298(8). 102218–102218. 5 indexed citations
6.
Huang, Yen‐Hua, et al.. (2021). Comparative analysis of cyclotide-producing plant cell suspensions presents opportunities for cyclotide plant molecular farming. Phytochemistry. 195. 113053–113053. 6 indexed citations
7.
Gilding, Edward K., Jennifer R. Deuis, Mathilde R. Israel, et al.. (2020). Neurotoxic peptides from the venom of the giant Australian stinging tree. Science Advances. 6(38). 19 indexed citations
8.
Jackson, Mark A., et al.. (2020). Make it or break it: Plant AEPs on stage in biotechnology. Biotechnology Advances. 45. 107651–107651. 19 indexed citations
9.
Jackson, Mark A., et al.. (2020). Production of a structurally validated cyclotide in rice suspension cells is enabled by a supporting biosynthetic enzyme. Planta. 252(6). 97–97. 11 indexed citations
10.
Pavasovic, Ana, Edward K. Gilding, Elise Pelzer, et al.. (2020). The Rapid Regenerative Response of a Model Sea Anemone Species Exaiptasia pallida Is Characterised by Tissue Plasticity and Highly Coordinated Cell Communication. Marine Biotechnology. 22(2). 285–307. 10 indexed citations
11.
Rehm, Fabian B. H., Mark A. Jackson, Kuok Yap, et al.. (2019). Papain-like cysteine proteases prepare plant cyclic peptide precursors for cyclization. Proceedings of the National Academy of Sciences. 116(16). 7831–7836. 50 indexed citations
12.
Jackson, Mark A., Kuok Yap, Aaron G. Poth, et al.. (2019). Rapid and Scalable Plant-Based Production of a Potent Plasmin Inhibitor Peptide. Frontiers in Plant Science. 10. 602–602. 24 indexed citations
13.
Li, Enpeng, Jovin Hasjim, Edward K. Gilding, et al.. (2019). The Role of Pullulanase in Starch Biosynthesis, Structure, and Thermal Properties by Studying Sorghum with Increased Pullulanase Activity. Starch - Stärke. 71(9-10). 14 indexed citations
14.
Jackson, Mark A., Edward K. Gilding, Thomas Shafee, et al.. (2018). Molecular basis for the production of cyclic peptides by plant asparaginyl endopeptidases. Nature Communications. 9(1). 2411–2411. 98 indexed citations
15.
Liu, Guoquan, Edward K. Gilding, Edward D. Kerr, et al.. (2018). Increasing protein content and digestibility in sorghum grain with a synthetic biology approach. Journal of Cereal Science. 85. 27–34. 20 indexed citations
16.
Poon, Simon, Karen S. Harris, Mark A. Jackson, et al.. (2017). Co-expression of a cyclizing asparaginyl endopeptidase enables efficient production of cyclic peptides in planta. Journal of Experimental Botany. 69(3). 633–641. 51 indexed citations
17.
Harris, Karen S., Thomas Durek, Quentin Kaas, et al.. (2015). Efficient backbone cyclization of linear peptides by a recombinant asparaginyl endopeptidase. Nature Communications. 6(1). 10199–10199. 207 indexed citations
18.
Mace, Emma, Shuaishuai Tai, David J. Innes, et al.. (2014). The plasticity of NBS resistance genes in sorghum is driven by multiple evolutionary processes. BMC Plant Biology. 14(1). 253–253. 1 indexed citations
19.
Gilding, Edward K. & M. David Marks. (2010). Analysis of purified glabra3-shapeshifter trichomes reveals a role for NOECK in regulating early trichome morphogenic events. The Plant Journal. 64(2). 304–317. 49 indexed citations
20.
Marks, M. David, Edward K. Gilding, & Jonathan P. Wenger. (2007). Genetic interaction between glabra3‐shapeshifter and siamese in Arabidopsis thaliana converts trichome precursors into cells with meristematic activity. The Plant Journal. 52(2). 352–361. 13 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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