Mark Kinkema

2.6k total citations · 2 hit papers
18 papers, 1.9k citations indexed

About

Mark Kinkema is a scholar working on Plant Science, Molecular Biology and Agronomy and Crop Science. According to data from OpenAlex, Mark Kinkema has authored 18 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Plant Science, 7 papers in Molecular Biology and 5 papers in Agronomy and Crop Science. Recurrent topics in Mark Kinkema's work include Legume Nitrogen Fixing Symbiosis (8 papers), Agronomic Practices and Intercropping Systems (5 papers) and Plant nutrient uptake and metabolism (4 papers). Mark Kinkema is often cited by papers focused on Legume Nitrogen Fixing Symbiosis (8 papers), Agronomic Practices and Intercropping Systems (5 papers) and Plant nutrient uptake and metabolism (4 papers). Mark Kinkema collaborates with scholars based in United States, Australia and Switzerland. Mark Kinkema's co-authors include Xinnian Dong, Weihua Fan, Peter M. Gresshoff, Xin Li, Yuelin Zhang, Dongxue Li, Sureeporn Nontachaiyapoom, Attila Kereszt, Arief Indrasumunar and Paul T. Scott and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Plant Cell and Journal of Molecular Biology.

In The Last Decade

Mark Kinkema

18 papers receiving 1.9k citations

Hit Papers

Interaction of NPR1 with basic leucine zipper protein tra... 1999 2026 2008 2017 1999 2000 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Kinkema United States 12 1.8k 683 188 112 67 18 1.9k
Laurence Godiard France 21 2.1k 1.2× 610 0.9× 171 0.9× 48 0.4× 213 3.2× 27 2.2k
Fasong Zhou China 22 2.2k 1.2× 659 1.0× 175 0.9× 44 0.4× 196 2.9× 35 2.5k
Zoltán Kevei United Kingdom 14 1.7k 1.0× 470 0.7× 387 2.1× 43 0.4× 84 1.3× 32 1.9k
Yang Yen United States 20 1.6k 0.9× 410 0.6× 71 0.4× 30 0.3× 240 3.6× 57 1.7k
Qinglu Zhang China 23 1.6k 0.9× 483 0.7× 38 0.2× 126 1.1× 65 1.0× 69 1.7k
Steffen Rietz Germany 15 1.7k 1.0× 712 1.0× 24 0.1× 95 0.8× 87 1.3× 27 1.9k
M. Bernard France 22 1.8k 1.0× 318 0.5× 213 1.1× 21 0.2× 48 0.7× 41 2.0k
Xinli Sun China 15 1.9k 1.1× 348 0.5× 54 0.3× 36 0.3× 103 1.5× 35 2.1k
Mercedes Díaz‐Mendoza Spain 20 1.1k 0.6× 872 1.3× 25 0.1× 143 1.3× 23 0.3× 27 1.4k
Jingjuan Yu China 26 1.5k 0.8× 1.0k 1.5× 78 0.4× 26 0.2× 35 0.5× 73 1.8k

Countries citing papers authored by Mark Kinkema

Since Specialization
Citations

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

Fields of papers citing papers by Mark Kinkema

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Kinkema

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Kinkema. A scholar is included among the top collaborators of Mark Kinkema 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 Mark Kinkema. Mark Kinkema is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Windus, Louisa, et al.. (2021). HearNPV susceptibility in Helicoverpa armigera and Helicoverpa punctigera strains resistant to Bt toxins Cry1Ac, Cry2Ab, and Vip3Aa. Journal of Invertebrate Pathology. 183. 107598–107598. 5 indexed citations
2.
Kinkema, Mark, R. J. Geijskes, Kylie Shand, et al.. (2013). An improved chemically inducible gene switch that functions in the monocotyledonous plant sugar cane. Plant Molecular Biology. 84(4-5). 443–454. 13 indexed citations
3.
Kinkema, Mark, Kylie Shand, Heather D. Coleman, et al.. (2013). Improved molecular tools for sugar cane biotechnology. Plant Molecular Biology. 84(4-5). 497–508. 9 indexed citations
4.
Harrison, Mark D., R. J. Geijskes, Heather D. Coleman, et al.. (2011). Accumulation of recombinant cellobiohydrolase and endoglucanase in the leaves of mature transgenic sugar cane. Plant Biotechnology Journal. 9(8). 884–896. 1 indexed citations
5.
Li, Dongxue, Mark Kinkema, & Peter M. Gresshoff. (2009). Autoregulation of nodulation (AON) in Pisum sativum (pea) involves signalling events associated with both nodule primordia development and nitrogen fixation. Journal of Plant Physiology. 166(9). 955–967. 40 indexed citations
6.
Hayashi, Satomi, Peter M. Gresshoff, & Mark Kinkema. (2008). Molecular Analysis of Lipoxygenases Associated with Nodule Development in Soybean. Molecular Plant-Microbe Interactions. 21(6). 843–853. 44 indexed citations
7.
Kinkema, Mark & Peter M. Gresshoff. (2008). Investigation of Downstream Signals of the Soybean Autoregulation of Nodulation Receptor Kinase GmNARK. Molecular Plant-Microbe Interactions. 21(10). 1337–1348. 70 indexed citations
8.
Dong, Xinnian, et al.. (2007). Regulation of Systemic Acquired Resistance by NPR1 and its Partners. Novartis Foundation symposium. 236. 165–175. 10 indexed citations
9.
Kereszt, Attila, Dongxue Li, Arief Indrasumunar, et al.. (2007). Agrobacterium rhizogenes-mediated transformation of soybean to study root biology. Nature Protocols. 2(4). 948–952. 418 indexed citations
10.
Nontachaiyapoom, Sureeporn, Paul T. Scott, A. Men, et al.. (2007). Promoters of OrthologousGlycine maxandLotus japonicusNodulation Autoregulation Genes Interchangeably Drive Phloem-Specific Expression in Transgenic Plants. Molecular Plant-Microbe Interactions. 20(7). 769–780. 70 indexed citations
11.
Hoffmann, Dana, Qunyi Jiang, A. Men, Mark Kinkema, & Peter M. Gresshoff. (2007). Nodulation deficiency caused by fast neutron mutagenesis of the model legume Lotus japonicus. Journal of Plant Physiology. 164(4). 460–469. 33 indexed citations
12.
Kinkema, Mark, Paul T. Scott, & Peter M. Gresshoff. (2006). Legume nodulation: successful symbiosis through short- and long-distance signalling. Functional Plant Biology. 33(8). 707–721. 70 indexed citations
13.
Kinkema, Mark, et al.. (2000). Nuclear Localization of NPR1 Is Required for Activation of PR Gene Expression. The Plant Cell. 12(12). 2339–2339. 27 indexed citations
14.
Kinkema, Mark, Weihua Fan, & Xinnian Dong. (2000). Nuclear Localization of NPR1 Is Required for Activation of PR Gene Expression. The Plant Cell. 12(12). 2339–2350. 536 indexed citations breakdown →
15.
Zhang, Yuelin, Weihua Fan, Mark Kinkema, Xin Li, & Xinnian Dong. (1999). Interaction of NPR1 with basic leucine zipper protein transcription factors that bind sequences required for salicylic acid induction of the PR-1 gene. Proceedings of the National Academy of Sciences. 96(11). 6523–6528. 538 indexed citations breakdown →
16.
Kinkema, Mark, Haiyang Wang, & John Schiefelbein. (1994). Molecular analysis of the myosin gene family in Arabidopsis thaliana. Plant Molecular Biology. 26(4). 1139–1153. 1 indexed citations
17.
Kinkema, Mark & John Schiefelbein. (1994). A Myosin from a Higher Plant has Structural Similarities to Class V Myosins. Journal of Molecular Biology. 239(4). 591–597. 2 indexed citations
18.
Bird, Kimon T., et al.. (1993). Agglutinins from marine macroalgae of the southeastern United States. Journal of Applied Phycology. 5(2). 213–218. 33 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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