Shinsuke Kutsuna

1.5k total citations · 1 hit paper
15 papers, 1.1k citations indexed

About

Shinsuke Kutsuna is a scholar working on Molecular Biology, Plant Science and Endocrine and Autonomic Systems. According to data from OpenAlex, Shinsuke Kutsuna has authored 15 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Plant Science and 6 papers in Endocrine and Autonomic Systems. Recurrent topics in Shinsuke Kutsuna's work include Photosynthetic Processes and Mechanisms (10 papers), Light effects on plants (10 papers) and Circadian rhythm and melatonin (6 papers). Shinsuke Kutsuna is often cited by papers focused on Photosynthetic Processes and Mechanisms (10 papers), Light effects on plants (10 papers) and Circadian rhythm and melatonin (6 papers). Shinsuke Kutsuna collaborates with scholars based in Japan, United States and Germany. Shinsuke Kutsuna's co-authors include Takao Kondo, Masahiro Ishiura, Susan S. Golden, Carl Hirschie Johnson, Setsuyuki Aoki, Hideo Iwasaki, Akio Tanabe, Carol R. Andersson, Nicholas F. Tsinoremas and Mitsunori Katayama and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Shinsuke Kutsuna

14 papers receiving 1.1k citations

Hit Papers

Expression of a Gene Cluster kaiABC as a Circadian Feedba... 1998 2026 2007 2016 1998 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
Shinsuke Kutsuna Japan 9 718 588 576 302 196 15 1.1k
Setsuyuki Aoki Japan 17 904 1.3× 734 1.2× 452 0.8× 255 0.8× 235 1.2× 33 1.3k
Yoriko Murayama Japan 7 775 1.1× 568 1.0× 696 1.2× 438 1.5× 145 0.7× 7 1.3k
Carol R. Andersson United States 11 1.1k 1.5× 1.1k 1.9× 713 1.2× 344 1.1× 240 1.2× 13 2.0k
Yohko Kitayama Japan 10 881 1.2× 587 1.0× 679 1.2× 472 1.6× 176 0.9× 13 1.2k
Florence Corellou France 20 924 1.3× 842 1.4× 418 0.7× 220 0.7× 318 1.6× 30 1.6k
Carl A. Strayer United States 10 1.4k 2.0× 1.8k 3.0× 685 1.2× 220 0.7× 133 0.7× 12 2.4k
Guogang Dong United States 9 444 0.6× 239 0.4× 250 0.4× 166 0.5× 148 0.8× 12 645
Jun Tomita Japan 14 382 0.5× 307 0.5× 562 1.0× 586 1.9× 87 0.4× 29 1.1k
Leland N. Edmunds United States 22 666 0.9× 465 0.8× 327 0.6× 449 1.5× 342 1.7× 56 1.3k
N. F. Tsinoremas United States 7 422 0.6× 273 0.5× 189 0.3× 91 0.3× 190 1.0× 9 581

Countries citing papers authored by Shinsuke Kutsuna

Since Specialization
Citations

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

Fields of papers citing papers by Shinsuke Kutsuna

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinsuke Kutsuna

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

All Works

15 of 15 papers shown
1.
Uesaka, Kazuma, Robert A. Kanaly, Shinsuke Kutsuna, et al.. (2023). The GGDEF protein Dgc2 suppresses both motility and biofilm formation in the filamentous cyanobacterium Leptolyngbya boryana. Microbiology Spectrum. 11(5). e0483722–e0483722. 7 indexed citations
2.
Kanaly, Robert A., et al.. (2022). Quantification of cyanobacterial cyclic di-guanosine monophosphate (c-di-GMP) by liquid chromatography electrospray ionization tandem mass spectrometry. Journal of Microbiological Methods. 196. 106468–106468. 3 indexed citations
3.
Kobayashi, Shoko, Aya Miura, Kiyoshi Onai, et al.. (2021). Circadian Clock inArabidopsis thalianaDetermines Flower Opening Time Early in the Morning and Dominantly Closes Early in the Afternoon. Plant and Cell Physiology. 62(5). 883–893. 10 indexed citations
4.
Kobayashi, Takayuki, Yohko Kitayama, Kyohei Arita, et al.. (2015). Analysis of the Fine-Tuning of Cyanobacterial Circadian Phase by Monochromatic Light and Long-Day Conditions. Plant and Cell Physiology. 57(1). 105–114.
5.
Kondou, Youichi, Shinsuke Kutsuna, Mika Kawashima, et al.. (2013). Overexpression of DWARF AND LESION FORMATION 1 (DLE1) causes altered activation of plant defense system in Arabidopsis thaliana. Plant Biotechnology. 30(4). 385–392. 7 indexed citations
6.
Tanaka, Hiromitsu, Yoko Nakano, Mitsunori Katayama, et al.. (2012). CmpR is Important for Circadian Phasing and Cell Growth. Plant and Cell Physiology. 53(9). 1561–1569. 6 indexed citations
7.
Kutsuna, Shinsuke, et al.. (2007). The Circadian Clock-Related Gene pex Regulates a Negative cis Element in the kaiA Promoter Region. Journal of Bacteriology. 189(21). 7690–7696. 24 indexed citations
8.
Arita, Kyohei, et al.. (2006). Structural and Biochemical Characterization of a Cyanobacterium Circadian Clock-modifier Protein. Journal of Biological Chemistry. 282(2). 1128–1135. 23 indexed citations
9.
Takai, Naoki, et al.. (2006). Expression of the Circadian Clock-Related Gene pex in Cyanobacteria Increases in Darkness and Is Required to Delay the Clock. Journal of Biological Rhythms. 21(4). 235–244. 20 indexed citations
10.
Kutsuna, Shinsuke, Yoichi Nakahira, Mitsunori Katayama, Masahiro Ishiura, & Takao Kondo. (2005). Transcriptional regulation of the circadian clock operon kaiBC by upstream regions in cyanobacteria. Molecular Microbiology. 57(5). 1474–1484. 24 indexed citations
11.
Nakahira, Yoichi, Mitsunori Katayama, Hiroshi Miyashita, et al.. (2004). Global gene repression by KaiC as a master process of prokaryotic circadian system. Proceedings of the National Academy of Sciences. 101(3). 881–885. 99 indexed citations
12.
Kondou, Youichi, Shinsuke Kutsuna, Miki Nakazawa, et al.. (2002). Bipolar Localization of Putative Photoreceptor Protein for Phototaxis in Thermophilic Cyanobacterium Synechococcus elongatus. Plant and Cell Physiology. 43(12). 1585–1588. 8 indexed citations
13.
Kutsuna, Shinsuke, Takao Kondo, Setsuyuki Aoki, & Masahiro Ishiura. (1998). A Period-Extender Gene, pex , That Extends the Period of the Circadian Clock in the Cyanobacterium Synechococcus sp. Strain PCC 7942. Journal of Bacteriology. 180(8). 2167–2174. 67 indexed citations
14.
Ishiura, Masahiro, Shinsuke Kutsuna, Setsuyuki Aoki, et al.. (1998). Expression of a Gene Cluster kaiABC as a Circadian Feedback Process in Cyanobacteria. Science. 281(5382). 1519–1523. 571 indexed citations breakdown →
15.
Kondo, Takao, Nicholas F. Tsinoremas, Susan S. Golden, et al.. (1994). Circadian Clock Mutants of Cyanobacteria. Science. 266(5188). 1233–1236. 238 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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