Takeshi Kawamoto

9.7k total citations · 2 hit papers
157 papers, 8.0k citations indexed

About

Takeshi Kawamoto is a scholar working on Molecular Biology, Endocrine and Autonomic Systems and Oncology. According to data from OpenAlex, Takeshi Kawamoto has authored 157 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 26 papers in Endocrine and Autonomic Systems and 25 papers in Oncology. Recurrent topics in Takeshi Kawamoto's work include Circadian rhythm and melatonin (26 papers), Osteoarthritis Treatment and Mechanisms (13 papers) and Light effects on plants (11 papers). Takeshi Kawamoto is often cited by papers focused on Circadian rhythm and melatonin (26 papers), Osteoarthritis Treatment and Mechanisms (13 papers) and Light effects on plants (11 papers). Takeshi Kawamoto collaborates with scholars based in Japan, United States and China. Takeshi Kawamoto's co-authors include Yukio Kato, Mitsuhide Noshiro, Masahiko Negishi, Katsumi Fujimoto, Igor N. Zelko, Tatsuya Sueyoshi, Sato Honma, Rick Moore, Ken‐ichi Honma and Fuyuki Sato and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Takeshi Kawamoto

147 papers receiving 7.9k citations

Hit Papers

The Repressed Nuclear Receptor CAR Responds to Phenobarbi... 1999 2026 2008 2017 1999 2002 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
Takeshi Kawamoto Japan 51 3.3k 1.4k 1.4k 1.3k 1.3k 157 8.0k
O. Wesley McBride United States 57 7.3k 2.2× 1.6k 1.1× 945 0.7× 733 0.6× 177 0.1× 131 12.2k
Atsushi Ichikawa Japan 61 6.2k 1.9× 2.4k 1.7× 422 0.3× 393 0.3× 331 0.3× 324 14.6k
Stephen R. Farmer United States 59 7.6k 2.3× 862 0.6× 226 0.2× 697 0.5× 453 0.4× 116 13.9k
Shmuel Muallem United States 80 12.1k 3.7× 796 0.6× 313 0.2× 383 0.3× 615 0.5× 276 20.1k
James M. Trzăskos United States 34 4.7k 1.4× 2.1k 1.4× 284 0.2× 309 0.2× 164 0.1× 71 11.4k
Kenneth Paigen United States 47 6.2k 1.9× 2.5k 1.7× 418 0.3× 945 0.7× 105 0.1× 139 10.9k
Leonard D. Kohn United States 63 6.2k 1.9× 2.0k 1.4× 184 0.1× 5.5k 4.2× 357 0.3× 324 13.9k
Jochen Buck United States 55 6.5k 1.9× 1.0k 0.7× 174 0.1× 428 0.3× 279 0.2× 149 11.3k
Hisashi Hidaka Japan 56 7.4k 2.2× 636 0.4× 190 0.1× 602 0.5× 193 0.2× 272 12.8k
Karen Reue United States 76 8.4k 2.5× 1.6k 1.1× 161 0.1× 1.4k 1.1× 339 0.3× 202 16.0k

Countries citing papers authored by Takeshi Kawamoto

Since Specialization
Citations

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

Fields of papers citing papers by Takeshi Kawamoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takeshi Kawamoto

This figure shows the co-authorship network connecting the top 25 collaborators of Takeshi Kawamoto. A scholar is included among the top collaborators of Takeshi Kawamoto 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 Kawamoto. Takeshi Kawamoto 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.
Myoken, Yoshinari, et al.. (2024). Orolabial angioedema as a rare complication of dental resin cement. International Journal of Dermatology. 63(7). 964–965.
2.
Myoken, Yoshiko, et al.. (2022). Evaluation of dental hygiene learning outcomes through smartphone‐based educational slides targeting dental hygienists: A pilot study. International Journal of Dental Hygiene. 21(3). 541–548. 1 indexed citations
3.
Nugraha, Alexander Patera, Chiquitа Prаhаsаnti, Diah Savitri Ernawati, et al.. (2022). Study of Alveolar Bone Remodeling Using Deciduous Tooth Stem Cells and Hydroxyapatite by Vascular Endothelial Growth Factor Enhancement and Inhibition of Matrix Metalloproteinase-8 Expression in vivo. Universitas Airlangga Repository (Universitas Airlangga). 9 indexed citations
4.
Noshiro, Mitsuhide, Takeshi Kawamoto, Ayumu Nakashima, et al.. (2020). DEC1 regulates the rhythmic expression of PPARγ target genes involved in lipid metabolism in white adipose tissue. Genes to Cells. 25(4). 232–241. 20 indexed citations
5.
Nishimura, Masahiro, et al.. (2010). Impact of Zinc Fingers and Homeoboxes 3 on the Regulation of Mesenchymal Stem Cell Osteogenic Differentiation. Stem Cells and Development. 20(9). 1539–1547. 16 indexed citations
6.
Liu, Yang, Fuyuki Sato, Takeshi Kawamoto, et al.. (2010). Anti‐apoptotic effect of the basic helix‐loop‐helix (bHLH) transcription factor DEC2 in human breast cancer cells. Genes to Cells. 15(4). 315–325. 61 indexed citations
7.
Kato, Yukio, Mitsuhide Noshiro, Katsumi Fujimoto, & Takeshi Kawamoto. (2010). Roles of Dec1 and Dec2 in the core loop of the circadian clock, and clock outputs to metabolism. [Emerging Frontiers in Brain Research: Crossroads of metabolic regulaltion, stress response and disease. The 11th Meeting of Hirosaki International Forum of Medical Science. Communication Center of Hirosaki University School of Medicine. March 27-28,2009. Hirosaki, Japan.]. 61. 1 indexed citations
8.
Kon, Naohiro, Tsuyoshi Hirota, Takeshi Kawamoto, et al.. (2008). Activation of TGF-β/activin signalling resets the circadian clock through rapid induction of Dec1 transcripts. Nature Cell Biology. 10(12). 1463–1469. 110 indexed citations
9.
Nakashima, Ayumu, Takeshi Kawamoto, K. Honda, et al.. (2008). DEC1 Modulates the Circadian Phase of Clock Gene Expression. Molecular and Cellular Biology. 28(12). 4080–4092. 128 indexed citations
10.
Fujimoto, Katsumi, Tadahiro Nakamura, Takeshi Kawamoto, et al.. (2007). Transcriptional repression by the basic helix-loop-helix protein Dec2: Multiple mechanisms through E-box elements. International Journal of Molecular Medicine. 19(6). 925–32. 50 indexed citations
11.
Ohtake, Hiroshi, et al.. (2007). Collocational Analysis of Life Science English (4) : Lists of common collocates of affinity, aim, difference, growth, importance, knowledge, observation, understanding. 41(41). 67–107.
12.
Kondo, Jun, Fuyuki Sato, Katsumi Fujimoto, et al.. (2006). 57Arg in the bHLH transcription factor DEC2 is essential for the suppression of CLOCK/BMAL2-mediated transactivation. International Journal of Molecular Medicine. 17(6). 1053–6. 12 indexed citations
13.
Kawamoto, Takeshi, et al.. (2005). Collocational Analysis of Life Science English (2) : Lists of common collocates of carry, confer, contribute, detect, elucidate, give, know, obtain, raise, understand. 39(39). 55–88. 1 indexed citations
14.
Butler, Matthew P., Sato Honma, Tatsuya Fukumoto, et al.. (2004). Dec1 and Dec2 Expression is Disrupted in the Suprachiasmatic Nuclei of Clock Mutant Mice. Journal of Biological Rhythms. 19(2). 126–134. 24 indexed citations
15.
Fujimoto, Katsumi, Takeshi Kawamoto, Mitsuhide Noshiro, et al.. (2004). Expression of the gene for Dec2, a basic helix–loop–helix transcription factor, is regulated by a molecular clock system. Biochemical Journal. 382(1). 43–50. 78 indexed citations
16.
Miyazaki, Kazuko, Takeshi Kawamoto, Keiji Tanimoto, et al.. (2002). Identification of Functional Hypoxia Response Elements in the Promoter Region of the DEC1 and DEC2 Genes. Journal of Biological Chemistry. 277(49). 47014–47021. 195 indexed citations
17.
Kawamoto, Takeshi. (2000). Estrogen Activation of the Nuclear Orphan Receptor CAR (Constitutive Active Receptor) in Induction of the Mouse Cyp2b10 Gene. Molecular Endocrinology. 14(11). 1897–1905. 36 indexed citations
18.
Shen, Ming, Takeshi Kawamoto, Weiqun Yan, et al.. (1997). Molecular Characterization of the Novel Basic Helix–Loop–Helix Protein DEC1 Expressed in Differentiated Human Embryo Chondrocytes. Biochemical and Biophysical Research Communications. 236(2). 294–298. 131 indexed citations
19.
Yoshida, Yuzo, M. Noshiro, Yumi Aoyama, et al.. (1997). Structural and Evolutionary Studies on Sterol 14-Demethylase P450 (CYP51), the Most Conserved P450 Monooxygenase: II. Evolutionary Analysis of Protein and Gene Structures. The Journal of Biochemistry. 122(6). 1122–1128. 59 indexed citations
20.
Fujioka, S, et al.. (1987). 新規アルファ-グルコシダーゼ阻害剤、AO-128が肥満被験者の炭水化物代謝に与える影響. International Journal of Obesity. 11. 98. 1 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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