Shinichiro Sawa

10.6k total citations · 1 hit paper
133 papers, 6.9k citations indexed

About

Shinichiro Sawa is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Shinichiro Sawa has authored 133 papers receiving a total of 6.9k indexed citations (citations by other indexed papers that have themselves been cited), including 120 papers in Plant Science, 85 papers in Molecular Biology and 14 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Shinichiro Sawa's work include Plant Molecular Biology Research (76 papers), Plant Reproductive Biology (64 papers) and Legume Nitrogen Fixing Symbiosis (26 papers). Shinichiro Sawa is often cited by papers focused on Plant Molecular Biology Research (76 papers), Plant Reproductive Biology (64 papers) and Legume Nitrogen Fixing Symbiosis (26 papers). Shinichiro Sawa collaborates with scholars based in Japan, United States and China. Shinichiro Sawa's co-authors include Hiroo Fukuda, Atsuko Kinoshita, Takashi Ishida, Shigeyuki Betsuyaku, Shigeo Yoshida, Hideki Goda, Yukihisa Shimada, Yuki Hirakawa, Tomokazu Koshiba and Kuninori Iwamoto and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Genes & Development.

In The Last Decade

Shinichiro Sawa

126 papers receiving 6.8k citations

Hit Papers

Dodeca-CLE Peptides as Suppressors of Plant Stem Cell Dif... 2006 2026 2012 2019 2006 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
Shinichiro Sawa Japan 41 6.3k 4.7k 298 172 136 133 6.9k
Keiko U. Torii United States 53 8.7k 1.4× 6.7k 1.4× 325 1.1× 78 0.5× 219 1.6× 117 9.7k
Steven E. Clark United States 35 8.0k 1.3× 6.8k 1.5× 386 1.3× 144 0.8× 129 0.9× 58 8.5k
Taku Demura Japan 47 7.8k 1.2× 6.9k 1.5× 362 1.2× 225 1.3× 273 2.0× 188 9.3k
Naomi Ori Israel 41 5.6k 0.9× 4.3k 0.9× 297 1.0× 75 0.4× 152 1.1× 63 6.1k
Bert De Rybel Belgium 41 5.9k 0.9× 4.5k 1.0× 207 0.7× 111 0.6× 171 1.3× 82 6.7k
Wei‐Cai Yang China 42 4.5k 0.7× 3.7k 0.8× 575 1.9× 271 1.6× 146 1.1× 97 5.4k
Yoshikatsu Matsubayashi Japan 47 7.5k 1.2× 5.9k 1.3× 368 1.2× 253 1.5× 101 0.7× 93 8.4k
Tatsuo Kakimoto Japan 38 8.5k 1.3× 7.3k 1.5× 360 1.2× 130 0.8× 558 4.1× 60 10.1k
Dorothee Staiger Germany 43 4.2k 0.7× 4.1k 0.9× 199 0.7× 77 0.4× 69 0.5× 121 6.1k
Peter V. Bozhkov Sweden 35 3.4k 0.5× 3.4k 0.7× 247 0.8× 107 0.6× 332 2.4× 83 4.8k

Countries citing papers authored by Shinichiro Sawa

Since Specialization
Citations

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

Fields of papers citing papers by Shinichiro Sawa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinichiro Sawa

This figure shows the co-authorship network connecting the top 25 collaborators of Shinichiro Sawa. A scholar is included among the top collaborators of Shinichiro Sawa 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 Shinichiro Sawa. Shinichiro Sawa 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.
Islam, Md. Saidul, et al.. (2024). Mitigation of salt effect using graphene oxide as additives in plantation. Environmental Science Nano. 11(12). 4692–4697.
2.
Nakagami, Satoru, Michitaka Notaguchi, Tatsuhiko Kondo, et al.. (2023). Root-knot nematode modulates plant CLE3-CLV1 signaling as a long-distance signal for successful infection. Science Advances. 9(22). eadf4803–eadf4803. 11 indexed citations
3.
Furumizu, Chihiro & Shinichiro Sawa. (2023). A rapid method for detection of the root-knot nematode resistance gene, <i>Mi-1.2</i>, in tomato cultivars. Plant Biotechnology. 40(1). 105–108. 3 indexed citations
4.
Zhang, Yi, Shuya Tan, Yuhan Gao, et al.. (2022). CLE42 delays leaf senescence by antagonizing ethylene pathway in Arabidopsis. New Phytologist. 235(2). 550–562. 39 indexed citations
5.
Islam, Md. Saidul, et al.. (2022). High water adsorption features of graphene oxide: potential of graphene oxide-based desert plantation. Materials Advances. 3(8). 3418–3422. 12 indexed citations
6.
Kanno, Yuri, Patricia Abril‐Urías, Mitsunori Seo, et al.. (2022). Local auxin synthesis mediated by YUCCA4 induced during root-knot nematode infection positively regulates gall growth and nematode development. Frontiers in Plant Science. 13. 1019427–1019427. 9 indexed citations
7.
Asaoka, Mariko, Pascale Milani, Gorou Horiguchi, et al.. (2021). Stem integrity in Arabidopsis thaliana requires a load-bearing epidermis. Development. 148(4). 16 indexed citations
8.
Furumizu, Chihiro, Anders K. Krabberød, Marta Hammerstad, et al.. (2021). The sequenced genomes of nonflowering land plants reveal the innovative evolutionary history of peptide signaling. The Plant Cell. 33(9). 2915–2934. 43 indexed citations
9.
Cabrera, Javier, Virginia Ruíz‐Ferrer, Marta Barcala, et al.. (2020). Root‐knot nematodes induce gall formation by recruiting developmental pathways of post‐embryonic organogenesis and regeneration to promote transient pluripotency. New Phytologist. 227(1). 200–215. 42 indexed citations
10.
Yamaguchi, Yasuka L., Javier Cabrera, Satoru Nakagami, et al.. (2017). Root-Knot and Cyst Nematodes Activate Procambium-Associated Genes in Arabidopsis Roots. Frontiers in Plant Science. 8. 1195–1195. 48 indexed citations
11.
Higaki, Takumi, et al.. (2017). A New Form of Gastrodia pubilabiata (Orchidaceae). 68(1). 45–52.
12.
Tabata, Ryo & Shinichiro Sawa. (2014). Maturation processes and structures of small secreted peptides in plants. Frontiers in Plant Science. 5. 311–311. 35 indexed citations
13.
Tabata, Ryo, Takehiro Kamiya, Shuji Shigenobu, et al.. (2013). Identification of an EMS-induced causal mutation in a gene required for boron-mediated root development by low-coverage genome re-sequencing inArabidopsis. Plant Signaling & Behavior. 8(1). e22534–e22534. 33 indexed citations
14.
HARA, Toshiaki, Hirokazu Tanaka, Tatsuhiko Kondo, et al.. (2013). Differential Effects of the Peptides Stomagen, EPF1 and EPF2 on Activation of MAP Kinase MPK6 and the SPCH Protein Level. Plant and Cell Physiology. 54(8). 1253–1262. 58 indexed citations
15.
Yamada, Masashi & Shinichiro Sawa. (2012). The roles of peptide hormones during plant root development. Current Opinion in Plant Biology. 16(1). 56–61. 38 indexed citations
16.
Hirakawa, Yuki, Hidefumi Shinohara, Yuki Kondo, et al.. (2008). Non-cell-autonomous control of vascular stem cell fate by a CLE peptide/receptor system. Proceedings of the National Academy of Sciences. 105(39). 15208–15213. 425 indexed citations
17.
Ito, Yasuko, Hiroyasu Motose, Kuninori Iwamoto, et al.. (2006). Dodeca-CLE Peptides as Suppressors of Plant Stem Cell Differentiation. Science. 313(5788). 842–845. 518 indexed citations breakdown →
18.
Kondo, Tatsuhiko, Shinichiro Sawa, Atsuko Kinoshita, et al.. (2006). A Plant Peptide Encoded by CLV3 Identified by in Situ MALDI-TOF MS Analysis. Science. 313(5788). 845–848. 381 indexed citations
19.
Nakamura, Ayako, Hideki Goda, M Fujiwara, et al.. (2003). Brassinolide Induces IAA5, IAA19 , and DR5, a Synthetic Auxin Response Element in Arabidopsis, Implying a Cross Talk Point of Brassinosteroid and Auxin Signaling. PLANT PHYSIOLOGY. 133(4). 1843–1853. 183 indexed citations
20.
Sawa, Shinichiro. (2002). Overexpression of the AtmybL2 Gene Represses Trichome Development in Arabidopsis. DNA Research. 9(2). 31–34. 32 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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