Keiko Yoshioka

5.7k total citations
97 papers, 4.0k citations indexed

About

Keiko Yoshioka is a scholar working on Plant Science, Molecular Biology and Animal Science and Zoology. According to data from OpenAlex, Keiko Yoshioka has authored 97 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Plant Science, 36 papers in Molecular Biology and 9 papers in Animal Science and Zoology. Recurrent topics in Keiko Yoshioka's work include Plant-Microbe Interactions and Immunity (36 papers), Plant Stress Responses and Tolerance (27 papers) and Plant Molecular Biology Research (16 papers). Keiko Yoshioka is often cited by papers focused on Plant-Microbe Interactions and Immunity (36 papers), Plant Stress Responses and Tolerance (27 papers) and Plant Molecular Biology Research (16 papers). Keiko Yoshioka collaborates with scholars based in Canada, Japan and United States. Keiko Yoshioka's co-authors include Wolfgang Moeder, Daniel F. Klessig, Feng Cao, Darrell Desveaux, Pradeep Kachroo, Thomas A. DeFalco, Kimberley Chin, Hideo Nakashita, Isamu Yamaguchi and Jyoti Shah and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Angewandte Chemie International Edition and PLoS ONE.

In The Last Decade

Keiko Yoshioka

95 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Keiko Yoshioka Canada 37 3.2k 1.4k 302 165 156 97 4.0k
Anne Frary Türkiye 31 4.7k 1.5× 2.1k 1.5× 308 1.0× 260 1.6× 176 1.1× 98 5.7k
Christian Godon France 9 1.7k 0.5× 2.0k 1.4× 158 0.5× 199 1.2× 147 0.9× 11 2.9k
Ana María Rincón Spain 16 1.1k 0.3× 591 0.4× 441 1.5× 91 0.6× 78 0.5× 22 1.8k
Heinrich Kauss Germany 25 1.5k 0.5× 846 0.6× 173 0.6× 134 0.8× 79 0.5× 50 2.0k
María Coca Spain 28 1.9k 0.6× 1.4k 1.0× 198 0.7× 274 1.7× 179 1.1× 36 2.7k
Dandan Zhang China 30 1.7k 0.5× 1.2k 0.8× 340 1.1× 69 0.4× 359 2.3× 101 2.3k
N.C.A. de Ruijter Netherlands 21 1.4k 0.4× 1.1k 0.8× 277 0.9× 68 0.4× 55 0.4× 40 2.0k
Baofang Fan United States 33 5.3k 1.7× 3.7k 2.6× 323 1.1× 269 1.6× 293 1.9× 53 6.4k
Meena L. Narasimhan United States 29 2.6k 0.8× 2.0k 1.4× 245 0.8× 214 1.3× 335 2.1× 50 3.7k
Jung Ro Lee South Korea 27 1.2k 0.4× 2.0k 1.4× 236 0.8× 81 0.5× 227 1.5× 181 3.2k

Countries citing papers authored by Keiko Yoshioka

Since Specialization
Citations

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

Fields of papers citing papers by Keiko Yoshioka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Keiko Yoshioka

This figure shows the co-authorship network connecting the top 25 collaborators of Keiko Yoshioka. A scholar is included among the top collaborators of Keiko Yoshioka 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 Keiko Yoshioka. Keiko Yoshioka 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.
Laflamme, Bradley, Richard Trilles, Jennifer L. Roizen, et al.. (2025). A cationic amphiphilic drug synergizes with strobilurin fungicides to control fungal-borne plant diseases. Cell chemical biology. 32(6). 872–884.e7. 1 indexed citations
2.
Hussain, Saad Abdulrahman, et al.. (2024). Calcium signaling triggers early high humidity responses in Arabidopsis thaliana. Proceedings of the National Academy of Sciences. 121(51). e2416270121–e2416270121. 6 indexed citations
3.
Wang, Ren, Ellie Himschoot, Matteo Grenzi, et al.. (2022). Auxin analog-induced Ca2+ signaling is independent of inhibition of endosomal aggregation in Arabidopsis roots. Journal of Experimental Botany. 73(8). 2308–2319. 5 indexed citations
4.
Wang, Limin, Jian Sun, Katie A. Wilkins, et al.. (2022). Arabidopsis thaliana CYCLIC NUCLEOTIDE‐GATED CHANNEL2 mediates extracellular ATP signal transduction in root epidermis. New Phytologist. 234(2). 412–421. 22 indexed citations
5.
Toyota, Masatsugu, Wolfgang Moeder, Kimberley Chin, et al.. (2021). CYCLIC NUCLEOTIDE-GATED ION CHANNEL 2 modulates auxin homeostasis and signaling. PLANT PHYSIOLOGY. 187(3). 1690–1703. 29 indexed citations
6.
Ebine, Kazuo, et al.. (2017). Triphosphate Tunnel Metalloenzyme Function in Senescence Highlights a Biological Diversification of This Protein Superfamily. PLANT PHYSIOLOGY. 175(1). 473–485. 16 indexed citations
7.
DeFalco, Thomas A., Christopher B. Marshall, Kim Munro, et al.. (2016). Multiple Calmodulin-binding Sites Positively and Negatively Regulate Arabidopsis CYCLIC NUCLEOTIDE-GATED CHANNEL12. The Plant Cell. 28(7). tpc.00870.2015–tpc.00870.2015. 84 indexed citations
8.
Chin, Kimberley, Thomas A. DeFalco, Wolfgang Moeder, & Keiko Yoshioka. (2013). The Arabidopsis Cyclic Nucleotide-Gated Ion Channels AtCNGC2 and AtCNGC4 Work in the Same Signaling Pathway to Regulate Pathogen Defense and Floral Transition   . PLANT PHYSIOLOGY. 163(2). 611–624. 118 indexed citations
9.
Carviel, Jessie, et al.. (2009). Forward and reverse genetics to identify genes involved in the age‐related resistance response in Arabidopsis thaliana. Molecular Plant Pathology. 10(5). 621–634. 36 indexed citations
10.
Moeder, Wolfgang, W. E. S. Urquhart, Dea Shahinas, et al.. (2008). Identification of a functionally essential amino acid for Arabidopsis cyclic nucleotide gated ion channels using the chimeric AtCNGC11/12 gene. The Plant Journal. 56(3). 457–469. 33 indexed citations
11.
Yoshioka, Keiko & Eric Kellerman. (2006). Gestural introduction of Ground reference in L2 narrative discourse. IRAL - International Review of Applied Linguistics in Language Teaching. 44(2). 22 indexed citations
12.
Ikeuchi, Yoshihide, Keiko Yoshioka, & Atsushi Suzuki. (2006). Recent Advanced Topics on Application of High Pressure Technology to Meat Processing. The Review of High Pressure Science and Technology. 16(1). 17–25. 5 indexed citations
13.
14.
Yoshioka, Keiko, et al.. (1997). PROBENAZOLE, AN INDUCER OF BLAST FUNGUS RESISTANCE IN RICE PLANT, ACTIVATES SYSTEMIC ACQUIRED RESISTANCE IN TOBACCO AND ARABIDOPSIS. Plant and Cell Physiology. 38. 1 indexed citations
15.
Yoshioka, Keiko, et al.. (1993). Virus Resistance in Transgenic Melon Plants That Express the Cucumber Mosaic Virus Coat Protein Gene and in Their Progeny.. Ikushugaku zasshi. 43(4). 629–634. 17 indexed citations
16.
17.
Ishii, Masamitsu, et al.. (1990). A Case of Sweet's Syndrome Associated with Myelodysplastic Syndrome. Skin research. 32(4). 491–497.
18.
Kitamikado, Manabu, Chong‐Sheng Yuan, Keiko Yoshioka, & Ryuji Ueno. (1988). A routine method and test paper method for the differentiation between frozen-thawed and unfrozen fish.. NIPPON SUISAN GAKKAISHI. 54(12). 2149–2151. 1 indexed citations
19.
Yoshioka, Keiko & Manabu Kitamikado. (1988). Differentiation of freeze-thawed fish fillet from fresh fish fillet by the examination of erythrocyte.. NIPPON SUISAN GAKKAISHI. 54(7). 1221–1225. 3 indexed citations
20.
Yoshioka, Keiko & Manabu Kitamikado. (1983). Differentiation of Freeze-Thawed Fish from Fresh Fish by the Examination of Medulla of Crystalline Lens. NIPPON SUISAN GAKKAISHI. 49(1). 151–151. 9 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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