Gitta Coaker

11.9k total citations · 3 hit papers
96 papers, 8.3k citations indexed

About

Gitta Coaker is a scholar working on Plant Science, Molecular Biology and Cell Biology. According to data from OpenAlex, Gitta Coaker has authored 96 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Plant Science, 20 papers in Molecular Biology and 8 papers in Cell Biology. Recurrent topics in Gitta Coaker's work include Plant-Microbe Interactions and Immunity (71 papers), Plant Pathogenic Bacteria Studies (55 papers) and Legume Nitrogen Fixing Symbiosis (25 papers). Gitta Coaker is often cited by papers focused on Plant-Microbe Interactions and Immunity (71 papers), Plant Pathogenic Bacteria Studies (55 papers) and Legume Nitrogen Fixing Symbiosis (25 papers). Gitta Coaker collaborates with scholars based in United States, China and Israel. Gitta Coaker's co-authors include Brian J. Staskawicz, Brad Day, Stephen T. Chisholm, James R. Elmore, Jun Liu, Tania Y. Toruño, Ioannis Stergiopoulos, Johan H. J. Leveau, Gurdeep Rastogi and Danielle M. Stevens and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Gitta Coaker

94 papers receiving 8.2k citations

Hit Papers

Host-Microbe Interactions: Shaping the Evolution of the P... 2006 2026 2012 2019 2006 2016 2021 500 1000 1.5k 2.0k

Peers

Gitta Coaker
Ping He United States
John P. Rathjen Australia
Libo Shan United States
Doil Choi South Korea
Hailing Jin United States
Fumiaki Katagiri United States
Kinya Nomura United States
Gitta Coaker
Citations per year, relative to Gitta Coaker Gitta Coaker (= 1×) peers Kenichi Tsuda

Countries citing papers authored by Gitta Coaker

Since Specialization
Citations

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

Fields of papers citing papers by Gitta Coaker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gitta Coaker

This figure shows the co-authorship network connecting the top 25 collaborators of Gitta Coaker. A scholar is included among the top collaborators of Gitta Coaker 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 Gitta Coaker. Gitta Coaker 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.
Bjornson, Marta, Dominique D. A. Pincot, Peter M. Henry, et al.. (2025). Unraveling the Fusarium oxysporum f. sp. fragariae –Strawberry Interaction: Evolution, Infection, and Genetic Resistance. Molecular Plant-Microbe Interactions. 38(6). 812–824.
2.
Figueroa, Melania, Gitta Coaker, & K. Kanyuka. (2024). Focus on the Effectors at the Interface of Plant–Microbe Interactions. Molecular Plant-Microbe Interactions. 37(3). 168–170. 1 indexed citations
3.
Stevens, Danielle M., Alexandra J. Weisberg, Judith Fliegmann, et al.. (2024). Natural variation of immune epitopes reveals intrabacterial antagonism. Proceedings of the National Academy of Sciences. 121(23). e2319499121–e2319499121. 14 indexed citations
4.
Zhu, Jie, et al.. (2023). Single-cell profiling of Arabidopsis leaves to Pseudomonas syringae infection. Cell Reports. 42(7). 112676–112676. 59 indexed citations
5.
Li, Tianrun, Jessica Franco, Tania Y. Toruño, et al.. (2023). Variation in microbial feature perception in the Rutaceae family with immune receptor conservation in citrus. PLANT PHYSIOLOGY. 193(1). 689–707. 10 indexed citations
6.
Stevens, Danielle M., et al.. (2023). Overlapping Local and Systemic Defense Induced by an Oomycete Fatty Acid MAMP and Brown Seaweed Extract in Tomato. Molecular Plant-Microbe Interactions. 36(6). 359–371. 4 indexed citations
7.
Zhu, Jie, Andrew Breakspear, Shree Prasad Thapa, et al.. (2022). Effectors from a Bacterial Vector-Borne Pathogen Exhibit Diverse Subcellular Localization, Expression Profiles, and Manipulation of Plant Defense. Molecular Plant-Microbe Interactions. 35(12). 1067–1080. 7 indexed citations
8.
Ramasamy, Manikandan, et al.. (2022). Evaluation of Candidatus Liberibacter Asiaticus Efflux Pump Inhibition by Antimicrobial Peptides. Molecules. 27(24). 8729–8729. 7 indexed citations
9.
Rufián, José S., James R. Elmore, Eduardo R. Bejarano, Carmen R. Beuzón, & Gitta Coaker. (2021). ER Bodies Are Induced by Pseudomonas syringae and Negatively Regulate Immunity. Molecular Plant-Microbe Interactions. 34(9). 1001–1009. 9 indexed citations
10.
Xu, Ning, Deepak D. Bhandari, Dmitry Lapin, et al.. (2021). Bacterial effector targeting of a plant iron sensor facilitates iron acquisition and pathogen colonization. The Plant Cell. 33(6). 2015–2031. 52 indexed citations
11.
Klymiuk, Valentyna, Andrii Fatiukha, Dina Raats, et al.. (2020). Three previously characterized resistances to yellow rust are encoded by a single locus Wtk1. Journal of Experimental Botany. 71(9). 2561–2572. 23 indexed citations
12.
Stevens, Danielle M., et al.. (2020). Phosphorylation of the Pseudomonas Effector AvrPtoB by Arabidopsis SnRK2.8 Is Required for Bacterial Virulence. Molecular Plant. 13(10). 1513–1522. 28 indexed citations
13.
Pang, Zhiqian, Li Zhang, Gitta Coaker, et al.. (2020). Citrus CsACD2 Is a Target of Candidatus Liberibacter Asiaticus in Huanglongbing Disease. PLANT PHYSIOLOGY. 184(2). 792–805. 65 indexed citations
14.
Lee, Donghyuk, Neeraj Lal, Shisong Ma, et al.. (2020). Regulation of reactive oxygen species during plant immunity through phosphorylation and ubiquitination of RBOHD. Nature Communications. 11(1). 1838–1838. 217 indexed citations
15.
Bolus, Stephen, Eduard Akhunov, Gitta Coaker, & Jorge Dubcovsky. (2019). Dissection of Cell Death Induction by Wheat Stem Rust Resistance Protein Sr35 and Its Matching Effector AvrSr35. Molecular Plant-Microbe Interactions. 33(2). 308–319. 28 indexed citations
16.
Clark, Kelley J., Jessica Franco, Simon Schwizer, et al.. (2018). An effector from the Huanglongbing-associated pathogen targets citrus proteases. Nature Communications. 9(1). 1718–1718. 143 indexed citations
17.
Kadota, Yasuhiro, Thomas W. H. Liebrand, Y Goto, et al.. (2018). Quantitative phosphoproteomic analysis reveals common regulatory mechanisms between effector‐ and PAMP‐triggered immunity in plants. New Phytologist. 221(4). 2160–2175. 98 indexed citations
18.
Luo, Xuming, Ning Xu, Junkai Huang, et al.. (2017). A Lectin Receptor-Like Kinase Mediates Pattern-Triggered Salicylic Acid Signaling. PLANT PHYSIOLOGY. 174(4). 2501–2514. 72 indexed citations
19.
Henry, Elizabeth, Tania Y. Toruño, Alain Jauneau, Laurent Deslandes, & Gitta Coaker. (2017). Direct and Indirect Visualization of Bacterial Effector Delivery into Diverse Plant Cell Types during Infection. The Plant Cell. 29(7). 1555–1570. 40 indexed citations
20.
Coaker, Gitta, Arnold M. Falick, & Brian J. Staskawicz. (2005). Activation of a Phytopathogenic Bacterial Effector Protein by a Eukaryotic Cyclophilin. Science. 308(5721). 548–550. 183 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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