Takeshi Chujo

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

About

Takeshi Chujo is a scholar working on Molecular Biology, Cancer Research and Virology. According to data from OpenAlex, Takeshi Chujo has authored 27 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 5 papers in Cancer Research and 1 paper in Virology. Recurrent topics in Takeshi Chujo's work include RNA modifications and cancer (23 papers), RNA Research and Splicing (14 papers) and RNA and protein synthesis mechanisms (11 papers). Takeshi Chujo is often cited by papers focused on RNA modifications and cancer (23 papers), RNA Research and Splicing (14 papers) and RNA and protein synthesis mechanisms (11 papers). Takeshi Chujo collaborates with scholars based in Japan, United States and Australia. Takeshi Chujo's co-authors include Tetsuro Hirose, Tsutomu Suzuki, Tomohiro Yamazaki, Shinichi Nakagawa, Charles S. Bond, Archa H. Fox, Kazuhito Tomizawa, Sylvie Souquère, Simon Kobelke and Gérard Pierron and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Takeshi Chujo

26 papers receiving 2.0k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Functional Domains of NEAT1 Architectural lncRNA Induce Paraspeckle Assembly through Phase Separation

2018 422 citations Tomohiro Yamazaki, Sylvie Souquère et al. Molecular Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Takeshi Chujo Japan	15	1.8k	658	183	111	60	27	2.0k
Claudia Strein Germany	7	1.9k 1.0×	396 0.6×	58 0.3×	74 0.7×	128 2.1×	7	2.1k
Adam Burkholder United States	23	1.8k 1.0×	346 0.5×	163 0.9×	215 1.9×	98 1.6×	53	2.1k
Tamayo Uechi Japan	18	1.2k 0.7×	206 0.3×	58 0.3×	131 1.2×	111 1.9×	22	1.4k
Henrik Spåhr Sweden	24	2.2k 1.2×	191 0.3×	186 1.0×	117 1.1×	58 1.0×	33	2.3k
Elvan Böke Spain	11	922 0.5×	161 0.2×	58 0.3×	50 0.5×	24 0.4×	16	1.1k
Galt P Barber United States	4	805 0.4×	230 0.3×	99 0.5×	228 2.1×	67 1.1×	4	1.1k
Raymond T. O’Keefe United Kingdom	19	1.4k 0.7×	149 0.2×	122 0.7×	128 1.2×	25 0.4×	48	1.5k
Isabel X. Wang United States	11	1.1k 0.6×	165 0.3×	70 0.4×	130 1.2×	58 1.0×	12	1.2k
Annalisa Izzo Germany	16	1.1k 0.6×	113 0.2×	146 0.8×	158 1.4×	75 1.3×	22	1.3k
Guo-Liang Chew United States	12	1.1k 0.6×	221 0.3×	48 0.3×	44 0.4×	88 1.5×	15	1.5k

Countries citing papers authored by Takeshi Chujo

Since Specialization

Citations

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

Fields of papers citing papers by Takeshi Chujo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takeshi Chujo

This figure shows the co-authorship network connecting the top 25 collaborators of Takeshi Chujo. A scholar is included among the top collaborators of Takeshi Chujo 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 Takeshi Chujo. Takeshi Chujo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Mito, Mari, Kazuhito Tomizawa, Takeshi Chujo, et al.. (2025). Monitoring the complexity and dynamics of mitochondrial translation. Molecular Cell. 85(22). 4279–4297.e8.

Chujo, Takeshi & Kazuhito Tomizawa. (2025). Neurological Diseases Caused by Loss of Transfer RNA Modifications: Commonalities in Their Molecular Pathogenesis. Journal of Molecular Biology. 437(16). 169047–169047. 1 indexed citations

Akichika, Shinichiro, Fan‐Yan Wei, Tsutomu Suzuki, et al.. (2024). Human DUS1L catalyzes dihydrouridine modification at tRNA positions 16/17, and DUS1L overexpression perturbs translation. Communications Biology. 7(1). 1238–1238. 3 indexed citations

Yabuki, Yasushi, Kimi Araki, Yukie Takahashi, et al.. (2024). TRMT10A dysfunction perturbs codon translation of initiator methionine and glutamine and impairs brain functions in mice. Nucleic Acids Research. 52(15). 9230–9246. 9 indexed citations

Murakami, Yoshitaka, Fan‐Yan Wei, Yoshimi Kawamura, et al.. (2023). NSUN3-mediated mitochondrial tRNA 5-formylcytidine modification is essential for embryonic development and respiratory complexes in mice. Communications Biology. 6(1). 307–307. 22 indexed citations

Zeng, Chao, Takeshi Chujo, Tetsuro Hirose, & Michiaki Hamada. (2023). Landscape of semi-extractable RNAs across five human cell lines. Nucleic Acids Research. 51(15). 7820–7831. 3 indexed citations

Wu, Yong, Takeshi Chujo, Akiko Ogawa, et al.. (2023). Pathological mutations promote proteolysis of mitochondrial tRNA-specific 2-thiouridylase 1 (MTU1) via mitochondrial caseinolytic peptidase (CLPP). Nucleic Acids Research. 52(3). 1341–1358. 5 indexed citations

Oka, Kaori, Yoshimi Kawamura, Yoshihiro Komohara, et al.. (2022). Resistance to chemical carcinogenesis induction via a dampened inflammatory response in naked mole-rats. Communications Biology. 5(1). 287–287. 21 indexed citations

Chujo, Takeshi, Fan‐Yan Wei, Nozomu Takahashi, et al.. (2022). Extracellular N⁶-isopentenyladenosine (i⁶A) addition induces cotranscriptional i⁶A incorporation into ribosomal RNAs. RNA. 28(7). 1013–1027. 8 indexed citations

10.

Iwakiri, Junichi, Kumiko Tanaka, Takeshi Chujo, et al.. (2022). Remarkable improvement in detection of readthrough downstream-of-gene transcripts by semi-extractable RNA-sequencing. RNA. 29(2). 170–177. 3 indexed citations

11.

Fukuda, Hiroyuki, Takeshi Chujo, Fan‐Yan Wei, et al.. (2021). Cooperative methylation of human tRNA3Lys at positions A58 and U54 drives the early and late steps of HIV-1 replication. Nucleic Acids Research. 49(20). 11855–11867. 22 indexed citations

12.

Chujo, Takeshi, S. Hirata, Hiroki Nakatsuka, et al.. (2021). Loss of Ftsj1 perturbs codon-specific translation efficiency in the brain and is associated with X-linked intellectual disability. Science Advances. 7(13). 45 indexed citations

13.

Fukuda, Hiroyuki, Takeshi Chujo, Takahisa Kouwaki, et al.. (2021). Export of RNA-derived modified nucleosides by equilibrative nucleoside transporters defines the magnitude of autophagy response and Zika virus replication. RNA Biology. 18(sup1). 478–495. 6 indexed citations

14.

Wei, Fan‐Yan, Takeshi Chujo, Shinya Oki, et al.. (2020). FTO Demethylates Cyclin D1 mRNA and Controls Cell-Cycle Progression. Cell Reports. 31(1). 107464–107464. 72 indexed citations

15.

Yamazaki, Tomohiro, Sylvie Souquère, Takeshi Chujo, et al.. (2018). Functional Domains of NEAT1 Architectural lncRNA Induce Paraspeckle Assembly through Phase Separation. Molecular Cell. 70(6). 1038–1053.e7. 422 indexed citations breakdown →

16.

Chujo, Takeshi, Tomohiro Yamazaki, Tetsuya Kawaguchi, et al.. (2017). Unusual semi‐extractability as a hallmark of nuclear body‐associated architectural noncoding RNA s. The EMBO Journal. 36(10). 1447–1462. 102 indexed citations

17.

Bar-Yaacov, Dan, Idan Frumkin, Yuka Yashiro, et al.. (2016). Mitochondrial 16S rRNA Is Methylated by tRNA Methyltransferase TRMT61B in All Vertebrates. PLoS Biology. 14(9). e1002557–e1002557. 101 indexed citations

18.

West, Jason A., Mari Mito, Satoshi Kurosaka, et al.. (2016). Structural, super-resolution microscopy analysis of paraspeckle nuclear body organization. The Journal of Cell Biology. 214(7). 817–830. 253 indexed citations

19.

Chujo, Takeshi, Tomohiro Yamazaki, & Tetsuro Hirose. (2015). Architectural RNAs (arcRNAs): A class of long noncoding RNAs that function as the scaffold of nuclear bodies. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1859(1). 139–146. 126 indexed citations

20.

Chujo, Takeshi, Takayuki Ohira, Yuriko Sakaguchi, et al.. (2012). LRPPRC/SLIRP suppresses PNPase-mediated mRNA decay and promotes polyadenylation in human mitochondria. Nucleic Acids Research. 40(16). 8033–8047. 148 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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