Gerard J. Bishop

4.1k total citations
39 papers, 3.0k citations indexed

About

Gerard J. Bishop is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, Gerard J. Bishop has authored 39 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Plant Science, 30 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Gerard J. Bishop's work include Plant Molecular Biology Research (22 papers), Plant Reproductive Biology (15 papers) and Plant Stress Responses and Tolerance (14 papers). Gerard J. Bishop is often cited by papers focused on Plant Molecular Biology Research (22 papers), Plant Reproductive Biology (15 papers) and Plant Stress Responses and Tolerance (14 papers). Gerard J. Bishop collaborates with scholars based in United Kingdom, Japan and United States. Gerard J. Bishop's co-authors include T. Nomura, Kate Harrison, Takao Yokota, Jonathan D. G. Jones, Csaba Koncz, Yuji Kamiya, Suguru Takatsuto, Miklós Szekeres, Teresa Montoya and Steven R. Scofield and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Plant Cell.

In The Last Decade

Gerard J. Bishop

39 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gerard J. Bishop United Kingdom 25 2.5k 2.1k 89 86 82 39 3.0k
Bingkai Hou China 29 1.9k 0.7× 1.9k 0.9× 104 1.2× 143 1.7× 76 0.9× 49 2.7k
Susumu Hiraga Japan 24 1.8k 0.7× 812 0.4× 79 0.9× 126 1.5× 37 0.5× 44 2.2k
Hexin Tan China 21 970 0.4× 1.5k 0.7× 76 0.9× 132 1.5× 113 1.4× 38 1.7k
Ill–Sup Nou South Korea 30 2.2k 0.9× 1.8k 0.9× 196 2.2× 73 0.8× 69 0.8× 164 3.0k
Cathie Martin United Kingdom 4 3.2k 1.3× 3.5k 1.7× 105 1.2× 209 2.4× 74 0.9× 5 4.4k
Barunava Patra United States 23 1.5k 0.6× 1.9k 0.9× 37 0.4× 142 1.7× 140 1.7× 41 2.4k
Fengning Xiang China 29 2.6k 1.0× 2.0k 1.0× 84 0.9× 46 0.5× 42 0.5× 67 3.1k
Thomas D. McKnight United States 29 1.8k 0.7× 1.5k 0.7× 212 2.4× 190 2.2× 134 1.6× 46 2.5k
Wolfgang Dröge‐Laser Germany 32 4.6k 1.8× 3.4k 1.7× 91 1.0× 124 1.4× 38 0.5× 45 5.2k
Kyoung Hee Nam South Korea 27 4.1k 1.6× 3.0k 1.5× 82 0.9× 128 1.5× 56 0.7× 50 4.8k

Countries citing papers authored by Gerard J. Bishop

Since Specialization
Citations

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

Fields of papers citing papers by Gerard J. Bishop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerard J. Bishop. 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 Gerard J. Bishop. The network helps show where Gerard J. Bishop may publish in the future.

Co-authorship network of co-authors of Gerard J. Bishop

This figure shows the co-authorship network connecting the top 25 collaborators of Gerard J. Bishop. A scholar is included among the top collaborators of Gerard J. Bishop 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 Gerard J. Bishop. Gerard J. Bishop 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.
Bishop, Gerard J., et al.. (2021). Farmer preferred traits and genotype choices in Solanum aethiopicum L., Shum group. Journal of Ethnobiology and Ethnomedicine. 17(1). 27–27. 5 indexed citations
3.
Debnath, Samir C., D. B. McKenzie, Gerard J. Bishop, & David Percival. (2016). Strategic approaches to propagate berry crop nuclear stocks using a bioreactoraaSt. John’s Research and Development Centre Contribution No. 228.. Acta Horticulturae. 47–52. 2 indexed citations
4.
Haţegan, Lidia, et al.. (2014). Differential expression of the brassinosteroid receptor-encoding BRI1 gene in Arabidopsis. Planta. 239(5). 989–1001. 15 indexed citations
5.
Gregory, Peter, Gerard J. Bishop, Michelle T. Fountain, Richard J. Harrison, & Robert Saville. (2013). One hundred years of research at East Malling: science into practice for perennial fruit crops. Annals of Applied Biology. 163(1). 1–11. 7 indexed citations
6.
Schalkwyk, Antoinette van, Peter Wenzl, Sandra Smit, et al.. (2011). Bin mapping of tomato diversity array (DArT) markers to genomic regions of Solanum lycopersicum × Solanum pennellii introgression lines. Theoretical and Applied Genetics. 124(5). 947–956. 13 indexed citations
7.
Holton, Nicholas, Kate Harrison, Takao Yokota, & Gerard J. Bishop. (2008). Tomato BRI1 and systemin wound signalling. Plant Signaling & Behavior. 3(1). 54–55. 7 indexed citations
8.
Bishop, Gerard J.. (2007). Refining the plant steroid hormone biosynthesis pathway. Trends in Plant Science. 12(9). 377–380. 31 indexed citations
9.
Nomura, T., Tetsuo Kushiro, Takao Yokota, et al.. (2005). The Last Reaction Producing Brassinolide Is Catalyzed by Cytochrome P-450s, CYP85A3 in Tomato and CYP85A2 in Arabidopsis. Journal of Biological Chemistry. 280(18). 17873–17879. 176 indexed citations
10.
Szekeres, Miklós, et al.. (2005). Unique and overlapping expression patterns of Arabidopsis CYP85 genes involved in brassinosteroid C-6 oxidation. Plant Molecular Biology. 57(1). 129–140. 41 indexed citations
11.
Montoya, Teresa, T. Nomura, Takao Yokota, et al.. (2005). Patterns of Dwarf expression and brassinosteroid accumulation in tomato reveal the importance of brassinosteroid synthesis during fruit development. The Plant Journal. 42(2). 262–269. 110 indexed citations
12.
Nomura, T., Gerard J. Bishop, Tsuyoshi Kaneta, et al.. (2003). The LKA gene is a BRASSINOSTEROID INSENSITIVE 1 homolog of pea. The Plant Journal. 36(3). 291–300. 81 indexed citations
13.
Bishop, Gerard J.. (2003). Brassinosteroid Mutants of Crops. Journal of Plant Growth Regulation. 22(4). 325–335. 62 indexed citations
14.
Bishop, Gerard J. & Csaba Koncz. (2002). Brassinosteroids and Plant Steroid Hormone Signaling. The Plant Cell. 14(suppl 1). S97–S110. 199 indexed citations
15.
Bishop, Gerard J., et al.. (2001). Plants Steroid Hormones, Brassinosteroids: Current Highlights of Molecular Aspects on their Synthesis/Metabolism, Transport, Perception and Response. Plant and Cell Physiology. 42(2). 114–120. 204 indexed citations
16.
Nomura, T., Tatsuro Sato, Gerard J. Bishop, et al.. (2001). Accumulation of 6-deoxocathasterone and 6-deoxocastasterone in Arabidopsis, pea and tomato is suggestive of common rate-limiting steps in brassinosteroid biosynthesis. Phytochemistry. 57(2). 171–178. 75 indexed citations
17.
Czakó, Mihály, Rajendra Marathe, Cheng‐Bin Xiang, et al.. (1995). Variable expression of the herpes simplex virus thymidine kinase gene in Nicotiana tabacum affects negative selection. Theoretical and Applied Genetics. 91(8). 1242–1247. 4 indexed citations
18.
Carroll, Bernard J., Victor Klimyuk, C. M. Thomas, et al.. (1995). Germinal transpositions of the maize element Dissociation from T-DNA loci in tomato.. Genetics. 139(1). 407–420. 60 indexed citations
19.
Jones, David A., James J. English, Bernard J. Carroll, et al.. (1994). Analysis of the chromosomal distribution of transposon-carrying T-DNAs in tomato using the inverse polymerase chain reaction. Molecular and General Genetics MGG. 242(5). 573–585. 70 indexed citations
20.
Jones, Jonathan D. G., L. R. Shlumukov, Francine M. Carland, et al.. (1992). Effective vectors for transformation, expression of heterologous genes, and assaying transposon excision in transgenic plants. Transgenic Research. 1(6). 285–297. 272 indexed citations

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