Takeshi Todo

10.0k total citations · 1 hit paper
114 papers, 6.6k citations indexed

About

Takeshi Todo is a scholar working on Molecular Biology, Plant Science and Cellular and Molecular Neuroscience. According to data from OpenAlex, Takeshi Todo has authored 114 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 58 papers in Plant Science and 43 papers in Cellular and Molecular Neuroscience. Recurrent topics in Takeshi Todo's work include Light effects on plants (53 papers), Photoreceptor and optogenetics research (38 papers) and Circadian rhythm and melatonin (31 papers). Takeshi Todo is often cited by papers focused on Light effects on plants (53 papers), Photoreceptor and optogenetics research (38 papers) and Circadian rhythm and melatonin (31 papers). Takeshi Todo collaborates with scholars based in Japan, United States and Germany. Takeshi Todo's co-authors include Kenichi Hitomi, Chentao Lin, Tomoko Ishikawa, Haruko Ryo, Hiroyuki Toh, Shigenori Iwai, Yasuhiro Kamei, Aziz Sancar, Mituo Ikenaga and Taisei Nomura and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Takeshi Todo

114 papers receiving 6.5k citations

Hit Papers

Differential regulation of mammalian Period genes and cir... 1999 2026 2008 2017 1999 100 200 300 400 500

Peers

Takeshi Todo
André P. M. Eker Netherlands
Takeshi Todo
Citations per year, relative to Takeshi Todo Takeshi Todo (= 1×) peers André P. M. Eker

Countries citing papers authored by Takeshi Todo

Since Specialization
Citations

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

Fields of papers citing papers by Takeshi Todo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takeshi Todo

This figure shows the co-authorship network connecting the top 25 collaborators of Takeshi Todo. A scholar is included among the top collaborators of Takeshi Todo 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 Takeshi Todo. Takeshi Todo 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.
Sato, Ryuma, Ryuhei Harada, Kohei Shimizu, et al.. (2018). Coulomb and CH–π interactions in (6–4) photolyase–DNA complex dominate DNA binding and repair abilities. Nucleic Acids Research. 46(13). 6761–6772. 10 indexed citations
2.
Takasu, Nana N., Takahiro J. Nakamura, Isao T. Tokuda, et al.. (2015). Recovery from Age-Related Infertility under Environmental Light-Dark Cycles Adjusted to the Intrinsic Circadian Period. Cell Reports. 12(9). 1407–1413. 47 indexed citations
3.
Oliveri, Paola, Antonio Emidio Fortunato, Tomoko Ishikawa‐Fujiwara, et al.. (2014). The Cryptochrome/Photolyase Family in aquatic organisms. Marine Genomics. 14. 23–37. 66 indexed citations
4.
Ishikawa, Tokiro, Tetsuya Okada, Tomoko Ishikawa‐Fujiwara, et al.. (2013). ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish. Molecular Biology of the Cell. 24(9). 1387–1395. 50 indexed citations
5.
Yasuda, Takako, Shoji Oda, Yoshitaka Kimori, et al.. (2012). Gamma-ray irradiation promotes premature meiosis of spontaneously differentiating testis–ova in the testis of p53-deficient medaka (Oryzias latipes). Cell Death and Disease. 3(10). e395–e395. 26 indexed citations
6.
Negoro, Hiromitsu, Akihiro Kanematsu, Masao Doi, et al.. (2012). Involvement of urinary bladder Connexin43 and the circadian clock in coordination of diurnal micturition rhythm. Nature Communications. 3(1). 809–809. 110 indexed citations
7.
Nakajima, Hiroo, Kiyokazu Ozaki, Tadashi Hongyo, Isao Narama, & Takeshi Todo. (2011). A rapid and easy method for the qualitative detection of intracellular deposition of inhaled nanoparticles. Nanomedicine Nanotechnology Biology and Medicine. 7(6). 881–888. 6 indexed citations
8.
Ishikawa, Tomoko, Yasuhiro Kamei, Ayuko Sato, et al.. (2010). High-resolution melting curve analysis for rapid detection of mutations in a Medaka TILLING library. BMC Molecular Biology. 11(1). 70–70. 49 indexed citations
9.
Oda, Shoji, Yusuke Urushihara, Yasuhiro Kamei, et al.. (2010). Identification of a Functional Medaka Heat Shock Promoter and Characterization of Its Ability to Induce Exogenous Gene Expression in Medaka in Vitro and In Vivo. ZOOLOGICAL SCIENCE. 27(5). 410–415. 15 indexed citations
10.
Kamei, Yasuhiro, Motoshi Suzuki, Kenjiro Watanabe, et al.. (2008). Infrared laser–mediated gene induction in targeted single cells in vivo. Nature Methods. 6(1). 79–81. 153 indexed citations
11.
Ikeda, Hiroki, Yong Qing, Takeshi Kurose, et al.. (2007). Clock gene defect disrupts light-dependency of autonomic nerve activity. Biochemical and Biophysical Research Communications. 364(3). 457–463. 37 indexed citations
12.
Ishikawa, Tomoko, Tomohiro Masuda, Kanta Mizusawa, et al.. (2006). Molecular analysis of Dec1 and Dec2 in the peripheral circadian clock of zebrafish photosensitive cells. Biochemical and Biophysical Research Communications. 351(4). 1072–1077. 13 indexed citations
13.
Nozaki, D., Tatsuya Iwata, Tomoko Ishikawa, et al.. (2004). Role of Gln1029 in the Photoactivation Processes of the LOV2 Domain in Adiantum Phytochrome3. Biochemistry. 43(26). 8373–8379. 93 indexed citations
14.
Daiyasu, Hiromi, Tomoko Ishikawa, Kei‐ichi Kuma, et al.. (2004). Identification of cryptochrome DASH from vertebrates. Genes to Cells. 9(5). 479–495. 96 indexed citations
15.
Kotani, Eiji, Toshiharu Furusawa, Shunji Nagaoka, et al.. (2002). Somatic Mutation in Larvae of the Silkworm, Bombyx mori, Induced by Heavy Ion Irradiation to Diapause Eggs. Journal of Radiation Research. 43(S). S193–S198. 12 indexed citations
16.
Ishikawa, Tomoko, Akira Matsumoto, Tomohisa Kato, et al.. (1999). DCRY is a Drosophila photoreceptor protein implicated in light entrainment of circadian rhythm. Genes to Cells. 4(1). 57–65. 68 indexed citations
17.
Todo, Takeshi, Hideo Tsuji, Eriko Otoshi, et al.. (1997). Characterization of a human homolog of (6-4)photolyase. Mutation Research/DNA Repair. 384(3). 195–204. 35 indexed citations
18.
Hitomi, Kenichi, Sang‐Tae Kim, Shigenori Iwai, et al.. (1997). Binding and Catalytic Properties of Xenopus (6-4) Photolyase. Journal of Biological Chemistry. 272(51). 32591–32598. 98 indexed citations
19.
Kai, Mihoko, Toshiaki Takahashi, Takeshi Todo, & Kengo Sakaguchi. (1995). Novel DNA binding protiens highly specific to UV-damaged DNA sequences from embryos ofDrosophila melanogaster. Nucleic Acids Research. 23(14). 2600–2607. 9 indexed citations
20.
Todo, Takeshi & Haruko Ryo. (1992). Identification of cellular factors that recognize UV-damaged DNA in Drosophila melanogaster. Mutation Research/DNA Repair. 273(1). 85–93. 25 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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