Kei Okatsu

5.6k total citations · 3 hit papers
27 papers, 4.4k citations indexed

About

Kei Okatsu is a scholar working on Molecular Biology, Epidemiology and Neurology. According to data from OpenAlex, Kei Okatsu has authored 27 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Epidemiology and 11 papers in Neurology. Recurrent topics in Kei Okatsu's work include Autophagy in Disease and Therapy (16 papers), Ubiquitin and proteasome pathways (13 papers) and Mitochondrial Function and Pathology (11 papers). Kei Okatsu is often cited by papers focused on Autophagy in Disease and Therapy (16 papers), Ubiquitin and proteasome pathways (13 papers) and Mitochondrial Function and Pathology (11 papers). Kei Okatsu collaborates with scholars based in Japan, United States and Poland. Kei Okatsu's co-authors include Noriyuki Matsuda, Keiji Tanaka, Mayumi Kimura, Fumika Koyano, Masaaki Komatsu, Nobutaka Hattori, Shigeto Sato, Hidetaka Kosako, Yu‐shin Sou and Yasushi Saeki and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Kei Okatsu

21 papers receiving 4.4k citations

Hit Papers

PINK1 stabilized by mitochondrial depolarization recruits... 2010 2026 2015 2020 2010 2014 2012 500 1000 1.5k

Peers

Kei Okatsu
Wolfdieter Springer United States
Seok Min Jin United States
Fabienne C. Fiesel United States
Sven Geisler Germany
Ashish C. Massey United States
Joo‐Ho Shin South Korea
Wolfdieter Springer United States
Kei Okatsu
Citations per year, relative to Kei Okatsu Kei Okatsu (= 1×) peers Wolfdieter Springer

Countries citing papers authored by Kei Okatsu

Since Specialization
Citations

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

Fields of papers citing papers by Kei Okatsu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kei Okatsu

This figure shows the co-authorship network connecting the top 25 collaborators of Kei Okatsu. A scholar is included among the top collaborators of Kei Okatsu 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 Kei Okatsu. Kei Okatsu 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.
Okatsu, Kei, Reika Kikuchi, Noriyuki Matsuda, Shuya Fukai, & Koji Yamano. (2025). Functional and Structural Insights Into Complex Formation Between OPTN Leucine Zipper Domain and RAB8A. Genes to Cells. 30(5). e70043–e70043.
2.
Okatsu, Kei & Shuya Fukai. (2025). Ubiquitin signaling in PINK1/Parkin-dependent mitophagy. The Journal of Biochemistry. 179(3). 145–154.
3.
Yamaguchi, Takayuki, Kei Okatsu, Masato Kubota, et al.. (2025). Structural insights into heterohexameric assembly of epilepsy-related ligand–receptor complex LGI1–ADAM22. eLife. 14.
4.
Okatsu, Kei, et al.. (2024). Structural characterization of green fluorescent protein in the I-state. Scientific Reports. 14(1).
5.
Sato, Yusuke, et al.. (2024). Chemical Diversification of Enzymatically Assembled Polyubiquitin Chains to Decipher the Ubiquitin Codes Programmed on the Branch Structure. Journal of the American Chemical Society. 1 indexed citations
6.
Okatsu, Kei, Shuya Fukai, Hideo Ago, et al.. (2023). Structure of a putative immature form of a Rieske-type iron-sulfur protein in complex with zinc chloride. Communications Chemistry. 6(1). 190–190.
7.
Li, Yanjun, Kei Okatsu, Shuya Fukai, & Yusuke Sato. (2021). Structural basis for specific recognition of K6-linked polyubiquitin chains by the TAB2 NZF domain. Biophysical Journal. 120(16). 3355–3362. 5 indexed citations
8.
Yokoi, Norihiko, Yuko Fukata, Kei Okatsu, et al.. (2021). 14-3-3 proteins stabilize LGI1-ADAM22 levels to regulate seizure thresholds in mice. Cell Reports. 37(11). 110107–110107. 10 indexed citations
9.
Sato, Yusuke, Hikaru Tsuchiya, Atsushi Yamagata, et al.. (2019). Structural insights into ubiquitin recognition and Ufd1 interaction of Npl4. Nature Communications. 10(1). 5708–5708. 32 indexed citations
10.
Okatsu, Kei, Yusuke Sato, Koji Yamano, et al.. (2018). Structural insights into ubiquitin phosphorylation by PINK1. Scientific Reports. 8(1). 10382–10382. 32 indexed citations
11.
Sato, Yusuke, Kei Okatsu, Yasushi Saeki, et al.. (2017). Structural basis for specific cleavage of Lys6-linked polyubiquitin chains by USP30. Nature Structural & Molecular Biology. 24(11). 911–919. 61 indexed citations
12.
Akabane, Shiori, Shun‐ichi Yamashita, Kei Okatsu, et al.. (2016). Constitutive Activation of PINK1 Protein Leads to Proteasome-mediated and Non-apoptotic Cell Death Independently of Mitochondrial Autophagy. Journal of Biological Chemistry. 291(31). 16162–16174. 25 indexed citations
13.
Okatsu, Kei, Fumika Koyano, Mayumi Kimura, et al.. (2015). Phosphorylated ubiquitin chain is the genuine Parkin receptor. The Journal of Experimental Medicine. 212(4). 2124OIA14–2124OIA14. 1 indexed citations
14.
Iguchi, Masahiro, Kei Okatsu, Fumika Koyano, et al.. (2013). Parkin-catalyzed Ubiquitin-Ester Transfer Is Triggered by PINK1-dependent Phosphorylation. Journal of Biological Chemistry. 288(30). 22019–22032. 175 indexed citations
15.
Koyano, Fumika, Kei Okatsu, Shinsuke Ishigaki, et al.. (2013). The principal PINK1 and Parkin cellular events triggered in response to dissipation of mitochondrial membrane potential occur in primary neurons. Genes to Cells. 18(8). 672–681. 29 indexed citations
16.
Okatsu, Kei, Fumika Koyano, Mayumi Kimura, et al.. (2013). A Dimeric PINK1-containing Complex on Depolarized Mitochondria Stimulates Parkin Recruitment. Journal of Biological Chemistry. 288(51). 36372–36384. 185 indexed citations
17.
Okatsu, Kei, Toshihiko Oka, Masahiro Iguchi, et al.. (2012). PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria. Nature Communications. 3(1). 1016–1016. 415 indexed citations breakdown →
18.
Matsuda, Noriyuki, Shigeto Sato, Kahori Shiba, et al.. (2010). PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy. The Journal of Cell Biology. 189(2). 211–221. 1542 indexed citations breakdown →
19.
Okatsu, Kei, Kazuto Nakada, Hiroshi Shitara, et al.. (2010). p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria. Genes to Cells. 15(8). 887–900. 328 indexed citations
20.
Tanaka, Keiji, Noriyuki Matsuda, & Kei Okatsu. (2010). Mechanisms underling the cause of Parkinson's disease: The functions of Parkin/PINK1. Rinsho Shinkeigaku. 50(11). 867–867. 3 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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