Yohei Katoh

3.2k total citations
64 papers, 2.4k citations indexed

About

Yohei Katoh is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Yohei Katoh has authored 64 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 42 papers in Genetics and 23 papers in Cell Biology. Recurrent topics in Yohei Katoh's work include Genetic and Kidney Cyst Diseases (40 papers), Protist diversity and phylogeny (22 papers) and Hedgehog Signaling Pathway Studies (15 papers). Yohei Katoh is often cited by papers focused on Genetic and Kidney Cyst Diseases (40 papers), Protist diversity and phylogeny (22 papers) and Hedgehog Signaling Pathway Studies (15 papers). Yohei Katoh collaborates with scholars based in Japan, China and United Kingdom. Yohei Katoh's co-authors include Kazuhisa Nakayama, Shohei Nozaki, Hiroyuki Takatsu, Hye‐Won Shin, Yoko Shiba, Senye Takahashi, Ryota Takei, Keiji Kubo, Satoshi Waguri and Atsuko Yabashi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Cell Biology.

In The Last Decade

Yohei Katoh

59 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yohei Katoh Japan 30 1.9k 1.3k 921 151 151 64 2.4k
Seng Hui Low United States 18 1.7k 0.9× 894 0.7× 1.2k 1.3× 61 0.4× 350 2.3× 28 2.4k
Ian R. Adams United Kingdom 29 3.2k 1.7× 809 0.6× 535 0.6× 151 1.0× 89 0.6× 55 3.7k
Kei‐ichiro Ishiguro Japan 22 2.8k 1.5× 412 0.3× 1.1k 1.1× 120 0.8× 112 0.7× 62 3.2k
Mikhail Bashkurov Canada 19 2.0k 1.0× 820 0.6× 821 0.9× 63 0.4× 69 0.5× 27 2.4k
Haruhiko Miyata Japan 24 1.1k 0.6× 613 0.5× 234 0.3× 44 0.3× 64 0.4× 69 2.0k
Tetsuo Kobayashi Japan 20 1.5k 0.8× 678 0.5× 580 0.6× 31 0.2× 61 0.4× 28 1.8k
Juliati Rahajeng United States 14 983 0.5× 261 0.2× 879 1.0× 20 0.1× 161 1.1× 15 1.4k
Kei Miyamoto Japan 31 1.8k 0.9× 320 0.2× 323 0.4× 43 0.3× 106 0.7× 86 2.6k
Catherine M. Abbott United Kingdom 27 1.8k 0.9× 577 0.4× 208 0.2× 30 0.2× 85 0.6× 96 2.4k
Alexander K. Haas Germany 15 1.1k 0.6× 282 0.2× 965 1.0× 15 0.1× 148 1.0× 23 1.7k

Countries citing papers authored by Yohei Katoh

Since Specialization
Citations

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

Fields of papers citing papers by Yohei Katoh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yohei Katoh

This figure shows the co-authorship network connecting the top 25 collaborators of Yohei Katoh. A scholar is included among the top collaborators of Yohei Katoh 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 Yohei Katoh. Yohei Katoh 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.
Yoshida, Saishu, Katsuhiko Aoki, Pattama Wiriyasermkul, et al.. (2024). Positive regulation of Hedgehog signaling via phosphorylation of GLI2/GLI3 by DYRK2 kinase. Proceedings of the National Academy of Sciences. 121(28). e2320070121–e2320070121. 5 indexed citations
3.
Stevenson, Nicola L., Kate J. Heesom, Shuhei Chiba, et al.. (2023). Multiple interactions of the dynein-2 complex with the IFT-B complex are required for effective intraflagellar transport. Journal of Cell Science. 136(5). 13 indexed citations
4.
Uddin, Borhan, Yohei Katoh, Tom Brown, et al.. (2022). Disease-associated mutations in WDR34 lead to diverse impacts on the assembly and function of dynein-2. Journal of Cell Science. 136(5). 5 indexed citations
5.
6.
Nakamura, Kentaro, et al.. (2021). CCRK/CDK20 regulates ciliary retrograde protein trafficking via interacting with BROMI/TBC1D32. PLoS ONE. 16(10). e0258497–e0258497. 7 indexed citations
7.
Nakamura, Kentaro, Mariko Takahara, Yoshihiro Omori, et al.. (2020). Anterograde trafficking of ciliary MAP kinase–like ICK/CILK1 by the intraflagellar transport machinery is required for intraciliary retrograde protein trafficking. Journal of Biological Chemistry. 295(38). 13363–13376. 30 indexed citations
8.
Katoh, Yohei, Shuhei Chiba, & Kazuhisa Nakayama. (2020). Practical method for superresolution imaging of primary cilia and centrioles by expansion microscopy using an amplibody for fluorescence signal amplification. Molecular Biology of the Cell. 31(20). 2195–2206. 22 indexed citations
9.
Katoh, Yohei, et al.. (2019). Interactions of the dynein-2 intermediate chain WDR34 with the light chains are required for ciliary retrograde protein trafficking. Molecular Biology of the Cell. 30(5). 658–670. 34 indexed citations
10.
Nozaki, Shohei, et al.. (2018). Interaction of WDR60 intermediate chain with TCTEX1D2 light chain of the dynein-2 complex is crucial for ciliary protein trafficking. Molecular Biology of the Cell. 29(13). 1628–1639. 48 indexed citations
11.
Takahara, Mariko, et al.. (2017). Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis. Human Molecular Genetics. 27(3). 516–528. 48 indexed citations
12.
Katoh, Yohei, et al.. (2017). Practical method for targeted disruption of cilia-related genes by using CRISPR/Cas9-mediated, homology-independent knock-in system. Molecular Biology of the Cell. 28(7). 898–906. 71 indexed citations
13.
Katoh, Yohei, et al.. (2015). Architectures of multisubunit complexes revealed by a visible immunoprecipitation assay using fluorescent fusion proteins. Journal of Cell Science. 128(12). 2351–2362. 134 indexed citations
14.
Makyio, Hisayoshi, Senye Takahashi, Hiroyuki Takatsu, et al.. (2012). Structural basis for Arf6–MKLP1 complex formation on the Flemming body responsible for cytokinesis. The EMBO Journal. 31(11). 2590–2603. 48 indexed citations
15.
Koga, Hiroshi, et al.. (2010). Functional Cross-Talk between Rab14 and Rab4 through a Dual Effector, RUFY1/Rabip4. Molecular Biology of the Cell. 21(15). 2746–2755. 54 indexed citations
16.
Akutsu, Masato, Masato Kawasaki, Yohei Katoh, et al.. (2005). Structural basis for recognition of ubiquitinated cargo by Tom1‐GAT domain. FEBS Letters. 579(24). 5385–5391. 30 indexed citations
17.
Katoh, Yohei, et al.. (2004). Tollip and Tom1 Form a Complex and Recruit Ubiquitin-conjugated Proteins onto Early Endosomes. Journal of Biological Chemistry. 279(23). 24435–24443. 131 indexed citations
18.
19.
Iioka, H, et al.. (1987). [The study on human placental DHA-S transport mechanism (using placental microvillous membrane vesicles)].. PubMed. 39(10). 1756–60. 2 indexed citations
20.
Kitajima, Takashi, et al.. (1986). Micromere differentiation and specific protein synthesis. Development Growth & Differentiation. 28(4). 377. 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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