Masayuki Yamamoto

159.8k total citations · 44 hit papers
1.4k papers, 119.9k citations indexed

About

Masayuki Yamamoto is a scholar working on Molecular Biology, Physiology and Immunology. According to data from OpenAlex, Masayuki Yamamoto has authored 1.4k papers receiving a total of 119.9k indexed citations (citations by other indexed papers that have themselves been cited), including 917 papers in Molecular Biology, 131 papers in Physiology and 119 papers in Immunology. Recurrent topics in Masayuki Yamamoto's work include Genomics, phytochemicals, and oxidative stress (418 papers), Glutathione Transferases and Polymorphisms (175 papers) and Epigenetics and DNA Methylation (114 papers). Masayuki Yamamoto is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (418 papers), Glutathione Transferases and Polymorphisms (175 papers) and Epigenetics and DNA Methylation (114 papers). Masayuki Yamamoto collaborates with scholars based in Japan, United States and United Kingdom. Masayuki Yamamoto's co-authors include Ken Itoh, Hozumi Motohashi, Thomas W. Kensler, Takafumi Suzuki, James Douglas Engel, Nobunao Wakabayashi, Akira Kobayashi, Keiko Taguchi, Norio Suzuki and Yasutake Katoh and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Masayuki Yamamoto

1.3k papers receiving 118.5k citations

Hit Papers

Keap1 represses nuclear activation of antioxidant respons... 1990 2026 2002 2014 1999 2017 2010 2004 2002 1000 2.0k 3.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masayuki Yamamoto Japan 169 85.7k 11.1k 10.4k 9.2k 9.1k 1.4k 119.9k
Steven P. Gygi United States 166 88.4k 1.0× 7.9k 0.7× 15.6k 1.5× 14.5k 1.6× 18.1k 2.0× 695 121.5k
Bharat B. Aggarwal United States 166 48.7k 0.6× 16.0k 1.4× 7.7k 0.7× 5.8k 0.6× 3.1k 0.3× 574 104.9k
John C. Reed United States 161 73.3k 0.9× 20.4k 1.8× 4.6k 0.4× 10.6k 1.2× 10.1k 1.1× 799 107.5k
Ronald M. Evans United States 187 96.0k 1.1× 15.1k 1.4× 20.1k 1.9× 11.6k 1.3× 6.0k 0.7× 629 148.1k
Christopher K. Glass United States 149 61.4k 0.7× 19.3k 1.7× 10.0k 1.0× 8.8k 1.0× 3.4k 0.4× 375 96.6k
Roger J. Davis United States 146 62.3k 0.7× 13.6k 1.2× 8.3k 0.8× 7.5k 0.8× 11.7k 1.3× 572 92.6k
Douglas R. Green United States 178 80.9k 0.9× 35.3k 3.2× 6.9k 0.7× 18.8k 2.0× 9.0k 1.0× 613 125.1k
Lewis C. Cantley United States 183 104.9k 1.2× 16.8k 1.5× 11.7k 1.1× 8.7k 0.9× 19.6k 2.1× 710 150.4k
Harvey F. Lodish United States 150 49.1k 0.6× 8.7k 0.8× 15.7k 1.5× 11.1k 1.2× 12.2k 1.3× 646 82.0k
Frank J. Gonzalez United States 171 56.6k 0.7× 5.1k 0.5× 16.8k 1.6× 19.1k 2.1× 3.6k 0.4× 1.3k 119.2k

Countries citing papers authored by Masayuki Yamamoto

Since Specialization
Citations

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

Fields of papers citing papers by Masayuki Yamamoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masayuki Yamamoto

This figure shows the co-authorship network connecting the top 25 collaborators of Masayuki Yamamoto. A scholar is included among the top collaborators of Masayuki Yamamoto 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 Masayuki Yamamoto. Masayuki Yamamoto 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.
Wang, Ke, Liam Baird, & Masayuki Yamamoto. (2025). The clinical-grade CBP/ p300 inhibitor CCS1477 represses the global NRF2-dependent cytoprotective transcription program and re-sensitizes cancer cells to chemotherapeutic drugs. Free Radical Biology and Medicine. 233. 102–117. 2 indexed citations
2.
Okada, Hikaru, Masakazu Hachisu, Miki Ando, et al.. (2023). A rose flavor compound activating the NRF2 pathway in dendritic cells ameliorates contact hypersensitivity in mice. Frontiers in Nutrition. 10. 1081263–1081263. 3 indexed citations
3.
Sies, Helmut, Vsevolod V. Belousov, Navdeep S. Chandel, et al.. (2022). Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology. Nature Reviews Molecular Cell Biology. 23(7). 499–515. 1095 indexed citations breakdown →
4.
Touat‐Todeschini, Leila, Yuichi Shichino, Nicolas Thierry‐Mieg, et al.. (2017). Selective termination of lnc RNA transcription promotes heterochromatin silencing and cell differentiation. The EMBO Journal. 36(17). 2626–2641. 42 indexed citations
5.
Koshiba, S., Ikuko N. Motoike, Daisuke Saigusa, et al.. (2017). Japanese Multi Omics Reference Panel 2017 (jMorp2017). 1 indexed citations
6.
Hamanaka, Teruhiko, Nobuo Ishida, Jun Yasuda, et al.. (2017). A Histologic Categorization of Aqueous Outflow Routes in Familial Open-Angle Glaucoma and Associations With Mutations in the MYOC Gene in Japanese Patients. Investigative Ophthalmology & Visual Science. 58(5). 2818–2818. 11 indexed citations
7.
Hamada, Shin, Tooru Shimosegawa, Keiko Taguchi, et al.. (2017). Simultaneous K-ras activation and Keap1 deletion cause atrophy of pancreatic parenchyma. American Journal of Physiology-Gastrointestinal and Liver Physiology. 314(1). G65–G74. 19 indexed citations
8.
Zheng, Hongzhi, Jingqi Fu, Peng Xue, et al.. (2015). CNC-bZIP Protein Nrf1-Dependent Regulation of Glucose-Stimulated Insulin Secretion. Antioxidants and Redox Signaling. 22(10). 819–831. 56 indexed citations
9.
Canet, Mark J., Matthew D. Merrell, Bryan Harder, et al.. (2014). Identification of a Functional Antioxidant Response Element within the Eighth Intron of the Human ABCC3 Gene. Drug Metabolism and Disposition. 43(1). 93–99. 19 indexed citations
10.
Ida, Tomoaki, Tomohiro Sawa, Hideshi Ihara, et al.. (2014). Reactive cysteine persulfides and S-polythiolation regulate oxidative stress and redox signaling. Proceedings of the National Academy of Sciences. 111(21). 7606–7611. 768 indexed citations breakdown →
11.
Satoh, Hironori, Takashi Moriguchi, Jun Takai, Masahito Ebina, & Masayuki Yamamoto. (2013). Nrf2 Prevents Initiation but Accelerates Progression through the Kras Signaling Pathway during Lung Carcinogenesis. Cancer Research. 73(13). 4158–4168. 203 indexed citations
12.
Ohkoshi, Akira, Takafumi Suzuki, Masao Ono, Toshimitsu Kobayashi, & Masayuki Yamamoto. (2012). Roles of Keap1–Nrf2 System in Upper Aerodigestive Tract Carcinogenesis. Cancer Prevention Research. 6(2). 149–159. 60 indexed citations
13.
Narita, Masato, et al.. (2009). Tumescent local anesthesia in inguinal herniorrhaphy with a PROLENE Hernia System: original technique and results. The American Journal of Surgery. 198(2). e27–e31. 13 indexed citations
14.
Kurokawa, H., et al.. (2009). Structural Basis of Alternative DNA Recognition by Maf Transcription Factors. Molecular and Cellular Biology. 29(23). 6232–6244. 64 indexed citations
15.
Li, Jinqing, Tomonaga Ichikawa, Luis Villacorta, et al.. (2009). Nrf2 Protects Against Maladaptive Cardiac Responses to Hemodynamic Stress. Arteriosclerosis Thrombosis and Vascular Biology. 29(11). 1843–1850. 221 indexed citations
16.
Shibuya, Masato, et al.. (2007). Effectiveness of Odd Order Aspherical Surface. 36(11). 646–660. 4 indexed citations
17.
Satoh, Kimio, Yutaka Kagaya, Makoto Nakano, et al.. (2006). Important Role of Endogenous Erythropoietin System in Recruitment of Endothelial Progenitor Cells in Hypoxia-Induced Pulmonary Hypertension in Mice. Circulation. 113(11). 1442–1450. 151 indexed citations
18.
Yoshida, Shosei, Ayumi Takakura, Kazuyuki Ohbo, et al.. (2004). Neurogenin3 delineates the earliest stages of spermatogenesis in the mouse testis. Developmental Biology. 269(2). 447–458. 210 indexed citations
19.
Kobayashi, Makoto, Keizo Nishikawa, Takafumi Suzuki, & Masayuki Yamamoto. (2001). The Homeobox Protein Six3 Interacts with the Groucho Corepressor and Acts as a Transcriptional Repressor in Eye and Forebrain Formation. Developmental Biology. 232(2). 315–326. 152 indexed citations
20.
Chiba, Tomoki, Yasunobu Nagata, Kazuhiro Sakamaki, et al.. (1993). Induction of erythroid-specific gene expression in lymphoid cells.. Proceedings of the National Academy of Sciences. 90(24). 11593–11597. 68 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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