Rie Terada

3.9k total citations · 1 hit paper
38 papers, 2.7k citations indexed

About

Rie Terada is a scholar working on Molecular Biology, Plant Science and Biotechnology. According to data from OpenAlex, Rie Terada has authored 38 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 30 papers in Plant Science and 9 papers in Biotechnology. Recurrent topics in Rie Terada's work include Plant tissue culture and regeneration (23 papers), CRISPR and Genetic Engineering (14 papers) and Chromosomal and Genetic Variations (12 papers). Rie Terada is often cited by papers focused on Plant tissue culture and regeneration (23 papers), CRISPR and Genetic Engineering (14 papers) and Chromosomal and Genetic Variations (12 papers). Rie Terada collaborates with scholars based in Japan, United Kingdom and China. Rie Terada's co-authors include Ko Shimamoto, Shigeru Iida, Takeshi Izawa, Hideya Fujimoto, Zenpei Shimatani, Yoshishige Inagaki, Kazuo Tsugane, Yasuyo Johzuka‐Hisatomi, Soryu Nishibayashi and Hiroko Urawa and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Rie Terada

38 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Targeted base editing in rice and tomato using a CRISPR-Cas9 cytidine deaminase fusion

2017 544 citations Zenpei Shimatani, Sachiko Kashojiya et al. Nature Biotechnology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rie Terada Japan	27	2.3k	2.2k	517	274	120	38	2.7k
Bronwyn Frame United States	20	1.7k 0.7×	1.5k 0.7×	659 1.3×	152 0.6×	60 0.5×	24	2.0k
David M. Tricoli United States	17	1.2k 0.5×	1.3k 0.6×	315 0.6×	103 0.4×	100 0.8×	24	1.6k
Jeffrey Townsend United States	9	1.4k 0.6×	1.3k 0.6×	489 0.9×	180 0.7×	61 0.5×	9	1.8k
Zhanyuan J. Zhang United States	22	1.3k 0.6×	1.4k 0.7×	310 0.6×	102 0.4×	70 0.6×	33	1.8k
Qiwei Shan China	6	1.8k 0.8×	1.9k 0.9×	206 0.4×	251 0.9×	259 2.2×	10	2.3k
Huirong Gao United States	12	1.3k 0.6×	1.2k 0.6×	157 0.3×	217 0.8×	150 1.3×	16	1.7k
Jean‐Luc Gallois France	26	1.7k 0.8×	2.1k 1.0×	152 0.3×	113 0.4×	264 2.2×	48	2.4k
Kaijun Zhao China	23	1.2k 0.5×	1.6k 0.7×	139 0.3×	269 1.0×	148 1.2×	55	2.0k
Ivan Ingelbrecht Nigeria	18	786 0.3×	1.1k 0.5×	244 0.5×	182 0.7×	50 0.4×	54	1.4k
Yingxiao Zhang United States	17	1.7k 0.8×	1.1k 0.5×	140 0.3×	161 0.6×	328 2.7×	27	1.9k

Countries citing papers authored by Rie Terada

Since Specialization

Citations

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

Fields of papers citing papers by Rie Terada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rie Terada

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

All Works

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20 of 20 papers shown

Taoka, Ken‐ichiro, Shoko Shinya, Kenichi Harada, et al.. (2022). Multifunctional chemical inhibitors of the florigen activation complex discovered by structure‐based high‐throughput screening. The Plant Journal. 112(6). 1337–1349. 6 indexed citations

Higo, Asuka, Fumihito Miura, Shojiro Tamaki, et al.. (2020). DNA methylation is reconfigured at the onset of reproduction in rice shoot apical meristem. Nature Communications. 11(1). 4079–4079. 45 indexed citations

Shimatani, Zenpei, Ushio Fujikura, Hisaki Ishii, et al.. (2018). Inheritance of co-edited genes by CRISPR-based targeted nucleotide substitutions in rice. Plant Physiology and Biochemistry. 131. 78–83. 31 indexed citations

Shimatani, Zenpei, Sachiko Kashojiya, M. Takayama, et al.. (2017). Targeted base editing in rice and tomato using a CRISPR-Cas9 cytidine deaminase fusion. Nature Biotechnology. 35(5). 441–443. 544 indexed citations breakdown →

Shimatani, Zenpei, Ayako Nishizawa‐Yokoi, M. Endo, Seiichi Toki, & Rie Terada. (2015). Positiveâ€“negative-selection-mediated gene targeting in rice. Frontiers in Plant Science. 5. 748–748. 35 indexed citations

Yamauchi, Takaki, Yasuyo Johzuka‐Hisatomi, Rie Terada, Ikuo Nakamura, & Shigeru Iida. (2014). The MET1b gene encoding a maintenance DNA methyltransferase is indispensable for normal development in rice. Plant Molecular Biology. 85(3). 219–232. 57 indexed citations

Dang, Thu Thi, Zenpei Shimatani, Yoji Kawano, Rie Terada, & Ko Shimamoto. (2013). Gene Editing a Constitutively Active OsRac1 by Homologous Recombination-Based Gene Targeting Induces Immune Responses in Rice. Plant and Cell Physiology. 54(12). 2058–2070. 21 indexed citations

Moritoh, Satoru, Chang‐Ho Eun, A. Ono, et al.. (2012). Targeted disruption of an orthologue of DOMAINS REARRANGED METHYLASE 2, OsDRM2 , impairs the growth of rice plants by abnormal DNA methylation. The Plant Journal. 71(1). 85–98. 100 indexed citations

Shimatani, Zenpei, Kyoko Takagi, Masahiko Maekawa, et al.. (2009). Characterization of autonomous Dart1 transposons belonging to the hAT superfamily in rice. Molecular Genetics and Genomics. 281(3). 329–344. 15 indexed citations

10.

Yamauchi, Takaki, Yasuyo Johzuka‐Hisatomi, Sachiko Fukada‐Tanaka, et al.. (2009). Homologous recombination‐mediated knock‐in targeting of the MET1a gene for a maintenance DNA methyltransferase reproducibly reveals dosage‐dependent spatiotemporal gene expression in rice. The Plant Journal. 60(2). 386–396. 42 indexed citations

11.

Iida, Shigeru & Rie Terada. (2005). Modification of Endogenous Natural Genes by Gene Targeting in Rice and Other Higher Plants. Plant Molecular Biology. 59(1). 205–219. 45 indexed citations

12.

Terada, Rie, et al.. (2004). A large-scale Agrobacterium -mediated transformation procedure with a strong positive-negative selection for gene targeting in rice ( Oryza sativa L.). Plant Cell Reports. 22(9). 653–659. 47 indexed citations

13.

Iida, Shigeru & Rie Terada. (2004). A tale of two integrations, transgene and T-DNA: gene targeting by homologous recombination in rice. Current Opinion in Biotechnology. 15(2). 132–138. 33 indexed citations

14.

Terada, Rie, Hiroko Urawa, Yoshishige Inagaki, Kazuo Tsugane, & Shigeru Iida. (2002). Efficient gene targeting by homologous recombination in rice. Nature Biotechnology. 20(10). 1030–1034. 229 indexed citations

15.

Ignacimuthu, S., et al.. (2000). Genetic transformation of rice: current status and future prospects.. Current Science. 79(2). 186–195. 17 indexed citations

16.

Terada, Rie, Midori Nakajima, Masayuki Isshiki, et al.. (2000). Antisense Waxy Genes with Highly Active Promoters Effectively Suppress Waxy Gene Expression in Transgenic Rice. Plant and Cell Physiology. 41(7). 881–888. 48 indexed citations

17.

Terada, Rie, Takuya Nakayama, Masaki Iwabuchi, & Ko Shimamoto. (1995). A type I element composed of the hexamer (ACGTCA) and octamer (CGCGGATC) motifs plays a role(s) in meristematic expression of a wheat histone H3 gene in transgenic rice plants. Plant Molecular Biology. 27(1). 17–26. 26 indexed citations

18.

Ohtsubo, Norihiro, Takuya Nakayama, Rie Terada, Ko Shimamoto, & Masaki Iwabuchi. (1993). Proximal promoter region of the wheat histone H3 gene confers S phase-specific gene expression in transformed rice cells. Plant Molecular Biology. 23(3). 553–565. 24 indexed citations

19.

Shimamoto, Ko, Chikara Miyazaki, Hisako Hashimoto, et al.. (1993). Trans-activation and stable integration of the maize transposable element Ds cotransfected with the Ac transposase gene in transgenic rice plants. Molecular and General Genetics MGG. 239(3). 354–360. 45 indexed citations

20.

Terada, Rie, Yoko Yamashita, Soryu Nishibayashi, & Ko Shimamoto. (1987). Somatic hybrids between Brassica oleracea and B. campestris: selection by the use of iodoacetamide inactivation and regeneration ability. Theoretical and Applied Genetics. 73(3). 379–384. 66 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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