Tatsuya Maeda

7.2k total citations · 3 hit papers
79 papers, 5.8k citations indexed

About

Tatsuya Maeda is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Tatsuya Maeda has authored 79 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 20 papers in Cell Biology and 14 papers in Plant Science. Recurrent topics in Tatsuya Maeda's work include Fungal and yeast genetics research (30 papers), PI3K/AKT/mTOR signaling in cancer (15 papers) and Cellular transport and secretion (10 papers). Tatsuya Maeda is often cited by papers focused on Fungal and yeast genetics research (30 papers), PI3K/AKT/mTOR signaling in cancer (15 papers) and Cellular transport and secretion (10 papers). Tatsuya Maeda collaborates with scholars based in Japan, United States and France. Tatsuya Maeda's co-authors include Haruo Saito, Terunao Takahara, Mutsuhiro Takekawa, Francesc Posas, Tran C. Thai, Hiroyuki Sorimachi, Masayuki Yamamoto, Tetsuo Meshi, Michio Hayashi and Elizabeth Witten and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Tatsuya Maeda

78 papers receiving 5.7k citations

Hit Papers

A two-component system that regulates an osmosensing MAP ... 1994 2026 2004 2015 1994 1996 1995 250 500 750

Peers

Tatsuya Maeda
Michael C. Gustin United States
Charles S. Hoffman United States
Stephen A. Osmani United States
Kyle W. Cunningham United States
Cora A. Styles United States
Douglas I. Johnson United States
Michael C. Gustin United States
Tatsuya Maeda
Citations per year, relative to Tatsuya Maeda Tatsuya Maeda (= 1×) peers Michael C. Gustin

Countries citing papers authored by Tatsuya Maeda

Since Specialization
Citations

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

Fields of papers citing papers by Tatsuya Maeda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tatsuya Maeda

This figure shows the co-authorship network connecting the top 25 collaborators of Tatsuya Maeda. A scholar is included among the top collaborators of Tatsuya Maeda 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 Tatsuya Maeda. Tatsuya Maeda 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.
Nakajima, Toshio, et al.. (2023). Overexpression of polyphosphate polymerases and deletion of polyphosphate phosphatases shorten the replicative lifespan in yeast. FEBS Letters. 597(18). 2316–2333. 1 indexed citations
2.
Sakamaki, Jun-Ichi, et al.. (2023). The pH-sensing Rim101 pathway regulates cell size in budding yeast. Journal of Biological Chemistry. 299(3). 102973–102973. 2 indexed citations
3.
Tahara, Yuhei O., et al.. (2022). Coordinated regulation of TORC2 signaling by MCC/eisosome‐associated proteins, Pil1 and tetraspan membrane proteins during the stress response. Molecular Microbiology. 117(5). 1227–1244. 12 indexed citations
4.
Ito, Kenji, Kohei Nagata, Sho Ohta, et al.. (2022). The oncogene-dependent resistance to reprogramming unveils cancer therapeutic targets. Cell Reports. 39(4). 110721–110721. 10 indexed citations
5.
Tani, Motohiro, et al.. (2021). Regulation of sphingolipid biosynthesis in the endoplasmic reticulum via signals from the plasma membrane in budding yeast. FEBS Journal. 289(2). 457–472. 10 indexed citations
6.
Yamamoto, Katsuyoshi, Satoru Nagatoishi, Koji Nagata, et al.. (2021). A glutamine sensor that directly activates TORC1. Communications Biology. 4(1). 1093–1093. 25 indexed citations
7.
Watanabe, Daisuke, Yan Zhou, Jiawen Chen, et al.. (2018). Nutrient Signaling via the TORC1-Greatwall-PP2A B55δ Pathway Is Responsible for the High Initial Rates of Alcoholic Fermentation in Sake Yeast Strains of Saccharomyces cerevisiae. Applied and Environmental Microbiology. 85(1). 16 indexed citations
8.
Kassai, Hidetoshi, Yuki Sugaya, Kazuki Nakao, et al.. (2014). Selective Activation of mTORC1 Signaling Recapitulates Microcephaly, Tuberous Sclerosis, and Neurodegenerative Diseases. Cell Reports. 7(5). 1626–1639. 76 indexed citations
9.
Goranov, Alexi I., Noah Dephoure, Terunao Takahara, et al.. (2013). Changes in Cell Morphology Are Coordinated with Cell Growth through the TORC1 Pathway. Current Biology. 23(14). 1269–1279. 31 indexed citations
10.
Takahara, Terunao & Tatsuya Maeda. (2013). Evolutionarily conserved regulation of TOR signalling. The Journal of Biochemistry. 154(1). 1–10. 47 indexed citations
11.
Oku, Masahide, et al.. (2013). Hyper-Activation of the Target of Rapamycin (Tor) Kinase 1 Decreases Intracellular Glutathione Content inSaccharomyces cerevisiaeas Revealed by LC-MS/MS Analysis. Bioscience Biotechnology and Biochemistry. 77(7). 1608–1611. 2 indexed citations
12.
Takahara, Terunao & Tatsuya Maeda. (2012). Transient Sequestration of TORC1 into Stress Granules during Heat Stress. Molecular Cell. 47(2). 242–252. 219 indexed citations
13.
Furukawa, Kentaro, et al.. (2005). Aspergillus nidulans HOG pathway is activated only by two‐component signalling pathway in response to osmotic stress. Molecular Microbiology. 56(5). 1246–1261. 153 indexed citations
14.
Hayashi, Michio, et al.. (2005). Constitutive Activation of the pH-Responsive Rim101 Pathway in Yeast Mutants Defective in Late Steps of the MVB/ESCRT Pathway. Molecular and Cellular Biology. 25(21). 9478–9490. 84 indexed citations
15.
Ozawa, Heita, Satoshi Ashizawa, Masanori Naito, et al.. (2004). Paired-like homeodomain protein ESXR1 possesses a cleavable C-terminal region that inhibits cyclin degradation. Oncogene. 23(39). 6590–6602. 15 indexed citations
16.
Futai, Eugene, et al.. (2001). Molecular cloning of PalBH, a mammalian homologue of the Aspergillus atypical calpain PalB. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1517(2). 316–319. 40 indexed citations
17.
Maeda, Tatsuya. (1999). [Osmotic response of the yeast Saccharomyces cerevisiae].. PubMed. 44(15 Suppl). 2206–13. 3 indexed citations
18.
Maeda, Tatsuya, et al.. (1998). A novel human RasGAP‐like gene that maps within the prostate cancer susceptibility locus at chromosome 1q25. FEBS Letters. 441(1). 127–131. 18 indexed citations
19.
Posas, Francesc, et al.. (1996). Yeast HOG1 MAP Kinase Cascade Is Regulated by a Multistep Phosphorelay Mechanism in the SLN1–YPD1–SSK1 “Two-Component” Osmosensor. Cell. 86(6). 865–875. 745 indexed citations breakdown →
20.
Maeda, Tatsuya, et al.. (1994). A two-component system that regulates an osmosensing MAP kinase cascade in yeast. Nature. 369(6477). 242–245. 931 indexed citations breakdown →

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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