Futoshi Suizu

2.8k total citations · 1 hit paper
44 papers, 2.0k citations indexed

About

Futoshi Suizu is a scholar working on Molecular Biology, Epidemiology and Cell Biology. According to data from OpenAlex, Futoshi Suizu has authored 44 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 9 papers in Epidemiology and 9 papers in Cell Biology. Recurrent topics in Futoshi Suizu's work include Protist diversity and phylogeny (8 papers), Protein Kinase Regulation and GTPase Signaling (7 papers) and Ubiquitin and proteasome pathways (6 papers). Futoshi Suizu is often cited by papers focused on Protist diversity and phylogeny (8 papers), Protein Kinase Regulation and GTPase Signaling (7 papers) and Ubiquitin and proteasome pathways (6 papers). Futoshi Suizu collaborates with scholars based in Japan, United States and Egypt. Futoshi Suizu's co-authors include Kun Ping Lu, Gerburg M. Wulf, Masayuki Noguchi, Noriyuki Hirata, Akihide Ryo, Yasuhiro Yoshida, Shoji Yamaoka, Robert Rottapel, Yih‐Cherng Liou and Kilian Perrem and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and The EMBO Journal.

In The Last Decade

Futoshi Suizu

41 papers receiving 2.0k citations

Hit Papers

Regulation of NF-κB Signaling by Pin1-Dependent Prolyl Is... 2003 2026 2010 2018 2003 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
Futoshi Suizu Japan 20 1.4k 617 511 311 287 44 2.0k
Shu‐ichi Matsuzawa United States 29 1.9k 1.3× 664 1.1× 528 1.0× 404 1.3× 442 1.5× 65 2.6k
Melissa J. Parsons United States 11 1.8k 1.2× 418 0.7× 381 0.7× 233 0.7× 393 1.4× 18 2.3k
Yongge Zhao United States 21 1.6k 1.1× 751 1.2× 401 0.8× 322 1.0× 444 1.5× 35 2.4k
Arnaud Jacquel France 33 1.7k 1.2× 718 1.2× 514 1.0× 332 1.1× 455 1.6× 64 3.0k
Matthias Germer Germany 12 1.6k 1.1× 800 1.3× 376 0.7× 370 1.2× 283 1.0× 16 2.2k
Ralph K. Lindemann Germany 20 1.5k 1.0× 669 1.1× 421 0.8× 197 0.6× 240 0.8× 27 2.2k
Hwain Shin United States 10 2.0k 1.4× 521 0.8× 407 0.8× 326 1.0× 356 1.2× 12 2.4k
Victoria C. Pham United States 20 1.5k 1.1× 511 0.8× 388 0.8× 279 0.9× 338 1.2× 35 1.9k
Sandra S. Zinkel United States 20 2.2k 1.5× 424 0.7× 441 0.9× 272 0.9× 386 1.3× 34 2.8k
Hangjun Duan United States 15 2.0k 1.4× 598 1.0× 485 0.9× 286 0.9× 285 1.0× 16 2.4k

Countries citing papers authored by Futoshi Suizu

Since Specialization
Citations

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

Fields of papers citing papers by Futoshi Suizu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Futoshi Suizu

This figure shows the co-authorship network connecting the top 25 collaborators of Futoshi Suizu. A scholar is included among the top collaborators of Futoshi Suizu 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 Futoshi Suizu. Futoshi Suizu 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.
Saito, Ryota, Tomohiro Suzuki, Manfred Wanner, et al.. (2025). Salinity tolerance in resting cysts of colpodid ciliates: Comparative transcriptomics analysis and chemical analysis of cyst walls to investigate their tolerance capability. Current Research in Microbial Sciences. 8. 100371–100371.
2.
Suizu, Futoshi, Keiko Yamakawa, Hiroyuki Yoneyama, et al.. (2024). Intra-tumoral administration of CHST15 siRNA remodels tumor microenvironment and augments tumor-infiltrating T cells in pancreatic cancer. SHILAP Revista de lepidopterología. 32(2). 200812–200812. 2 indexed citations
3.
Sogame, Yoichiro, Makoto Ogata, Yuta Saito, et al.. (2024). α,β-trehalose, an intracellular substance in resting cyst of colpodid ciliates as a key to environmental tolerances. Biochemical and Biophysical Research Communications. 716. 149971–149971. 1 indexed citations
4.
Yamakawa, Keiko, et al.. (2024). Discrepancies Between Morphological and Immunohistochemical Classifications Are Associated With Prognoses and Subtypes of Lung Cancer. Anticancer Research. 44(2). 711–722. 1 indexed citations
5.
Miyai, Yumi, Hiroyuki Mima, Masaki Magari, et al.. (2023). Transcriptional, biochemical, and immunohistochemical analyses of CaMKKβ/2 splice variants that co-localize with CaMKIV in spermatids. Cell Calcium. 117. 102820–102820.
6.
Takeya, Kosuke, et al.. (2023). PHI-1, an Endogenous Inhibitor Protein for Protein Phosphatase-1 and a Pan-Cancer Marker, Regulates Raf-1 Proteostasis. Biomolecules. 13(12). 1741–1741. 1 indexed citations
7.
Saito, Ryota, et al.. (2023). ATP accumulation in early resting cyst formation towards cryptobiosis in Colpoda Cucullus. Acta Protozoologica. 62. 39–44. 4 indexed citations
8.
Suizu, Futoshi, Keiko Yamakawa, Motohiko Kato, et al.. (2023). Silencing of tumoral carbohydrate sulfotransferase 15 reactivates lymph node pancreatic cancer T cells in mice. European Journal of Immunology. 53(9). e2250160–e2250160. 2 indexed citations
9.
Noguchi, Masayuki, Noriyuki Hirata, Tsutomu Tanaka, et al.. (2020). Autophagy as a modulator of cell death machinery. Cell Death and Disease. 11(7). 517–517. 147 indexed citations
10.
Hirata, Noriyuki, Futoshi Suizu, Mami Matsuda‐Lennikov, et al.. (2018). Functional characterization of lysosomal interaction of Akt with VRK2. Oncogene. 37(40). 5367–5386. 21 indexed citations
11.
Suizu, Futoshi, Noriyuki Hirata, Tsutomu Tanaka, et al.. (2016). Phosphorylation‐dependent Akt–Inversin interaction at the basal body of primary cilia. The EMBO Journal. 35(12). 1346–1363. 43 indexed citations
12.
Sogame, Yoichiro, Katsuhiko Kojima, Toshikazu Takeshita, et al.. (2016). Morphogenetic and molecular analyses of cyst wall components in the ciliated protozoanColpoda cucullusNag-1. FEMS Microbiology Letters. 363(18). fnw203–fnw203. 9 indexed citations
13.
Noguchi, Masayuki, Noriyuki Hirata, & Futoshi Suizu. (2014). The links between AKT and two intracellular proteolytic cascades: Ubiquitination and autophagy. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1846(2). 342–352. 82 indexed citations
14.
Hashimoto, Manabu, Futoshi Suizu, Wataru Tokuyama, et al.. (2013). Protooncogene TCL1b functions as an Akt kinase co-activator that exhibits oncogenic potency in vivo. Oncogenesis. 2(9). e70–e70. 12 indexed citations
15.
Lee, Tae Ho, Chun-Hau Chen, Futoshi Suizu, et al.. (2011). Death-Associated Protein Kinase 1 Phosphorylates Pin1 and Inhibits Its Prolyl Isomerase Activity and Cellular Function. Molecular Cell. 42(2). 147–159. 144 indexed citations
16.
Matsuda, Mami, Futoshi Suizu, Noriyuki Hirata, et al.. (2010). Characterization of the interaction of influenza virus NS1 with Akt. Biochemical and Biophysical Research Communications. 395(3). 312–317. 22 indexed citations
17.
Hiromura, Makoto, et al.. (2006). Identification of Nerve Growth Factor-responsive Element of the TCL1 Promoter as a Novel Negative Regulatory Element. Journal of Biological Chemistry. 281(38). 27753–27764. 13 indexed citations
18.
Wulf, Gerburg M., Greg Finn, Futoshi Suizu, & Kun Ping Lu. (2005). Phosphorylation-specific prolyl isomerization: is there an underlying theme?. Nature Cell Biology. 7(5). 435–441. 194 indexed citations
19.
Suizu, Futoshi, Kozue Ueda, Takahiro Iwasaki, Maki Murata‐Hori, & Hiroshi Hosoya. (2000). Activation of Action-Activated MgATPase Activity of Myosin II by Phyosphorylation with MAPK-Activated Protein Kinase-1b (RSK-2). The Journal of Biochemistry. 128(3). 435–440. 24 indexed citations
20.
Suizu, Futoshi, et al.. (1996). Growth Characteristics of Tetrahymena paravorax. Journal of protozoology research. 6(4). 94–100. 2 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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