Toru Sengoku

2.3k total citations
33 papers, 1.7k citations indexed

About

Toru Sengoku is a scholar working on Molecular Biology, Genetics and Pharmacology. According to data from OpenAlex, Toru Sengoku has authored 33 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pharmacology. Recurrent topics in Toru Sengoku's work include RNA modifications and cancer (13 papers), RNA and protein synthesis mechanisms (11 papers) and Epigenetics and DNA Methylation (7 papers). Toru Sengoku is often cited by papers focused on RNA modifications and cancer (13 papers), RNA and protein synthesis mechanisms (11 papers) and Epigenetics and DNA Methylation (7 papers). Toru Sengoku collaborates with scholars based in Japan, United States and Australia. Toru Sengoku's co-authors include Shigeyuki Yokoyama, Osamu Nureki, Akira Nakamura, Satoru Kobayashi, Karl B. Shpargel, Terry Magnuson, Kazuhiro Ogata, Hiroaki Suga, Takashi Umehara and Seketsu Fukuzawa and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Toru Sengoku

33 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toru Sengoku Japan 18 1.5k 267 92 73 72 33 1.7k
Kirk Clark United States 10 1.3k 0.9× 237 0.9× 119 1.3× 92 1.3× 93 1.3× 16 1.5k
Balraj Doray United States 19 1.1k 0.7× 180 0.7× 154 1.7× 127 1.7× 44 0.6× 36 1.6k
Jacob A. Galán United States 22 681 0.5× 377 1.4× 87 0.9× 81 1.1× 21 0.3× 49 1.1k
Yonka Christova United Kingdom 12 834 0.6× 196 0.7× 191 2.1× 95 1.3× 81 1.1× 18 1.2k
Christian Mielke Germany 22 1.7k 1.2× 326 1.2× 315 3.4× 80 1.1× 72 1.0× 38 1.9k
Sandrine Curtet France 12 1.5k 1.0× 163 0.6× 268 2.9× 47 0.6× 58 0.8× 14 1.6k
Hiroshi Onogi Japan 14 886 0.6× 96 0.4× 122 1.3× 71 1.0× 76 1.1× 16 1.2k
H. Christian Eberl Germany 17 1.5k 1.0× 118 0.4× 130 1.4× 218 3.0× 103 1.4× 27 1.7k

Countries citing papers authored by Toru Sengoku

Since Specialization
Citations

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

Fields of papers citing papers by Toru Sengoku

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Toru Sengoku

This figure shows the co-authorship network connecting the top 25 collaborators of Toru Sengoku. A scholar is included among the top collaborators of Toru Sengoku 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 Toru Sengoku. Toru Sengoku 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.
Carcavilla, Atilano, Arrate Pereda, Mami Miyado, et al.. (2025). Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypes. European Journal of Endocrinology. 192(4). 364–372. 1 indexed citations
2.
Sumida, Tomomi, Satoshi Hiraoka, Keiko Usui, et al.. (2024). Genetic and functional diversity of β-N-acetylgalactosamine-targeting glycosidases expanded by deep-sea metagenome analysis. Nature Communications. 15(1). 3543–3543. 3 indexed citations
3.
Nguyen, Dinh Thanh, Keisuke Hamada, Chikako Okada, et al.. (2024). De Novo Discovery of Pseudo‐Natural Prenylated Macrocyclic Peptide Ligands. Angewandte Chemie. 136(36). 1 indexed citations
4.
Nguyen, Dinh Thanh, Keisuke Hamada, Chikako Okada, et al.. (2024). De Novo Discovery of Pseudo‐Natural Prenylated Macrocyclic Peptide Ligands. Angewandte Chemie International Edition. 63(36). e202409973–e202409973. 5 indexed citations
5.
Hamada, Keisuke, Dinh Thanh Nguyen, Masayuki Satake, et al.. (2022). LimF is a versatile prenyltransferase for histidine-C-geranylation on diverse non-natural substrates. Nature Catalysis. 5(8). 682–693. 31 indexed citations
6.
Saida, Ken, Masayuki Sasaki, Eriko Koshimizu, et al.. (2021). Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Clinical Genetics. 100(6). 722–730. 18 indexed citations
7.
Sato, Ko, Keisuke Hamada, Chikako Okada, et al.. (2021). Structural basis of the regulation of the normal and oncogenic methylation of nucleosomal histone H3 Lys36 by NSD2. Nature Communications. 12(1). 6605–6605. 26 indexed citations
8.
Saida, Ken, Tokiko Fukuda, Daryl A. Scott, et al.. (2021). OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation. Frontiers in Cell and Developmental Biology. 9. 631428–631428. 6 indexed citations
9.
Mitsuhashi, Satomi, et al.. (2020). A novel PAK1 variant causative of neurodevelopmental disorder with postnatal macrocephaly. Journal of Human Genetics. 65(5). 481–485. 11 indexed citations
10.
Katoh, Takayuki, Toru Sengoku, Kunio Hirata, Kazuhiro Ogata, & Hiroaki Suga. (2020). Ribosomal synthesis and de novo discovery of bioactive foldamer peptides containing cyclic β-amino acids. Nature Chemistry. 12(11). 1081–1088. 92 indexed citations
11.
Niwa, Hideaki, Shin Sato, N. Handa, et al.. (2020). Development and Structural Evaluation of N‐Alkylated trans‐2‐Phenylcyclopropylamine‐Based LSD1 Inhibitors. ChemMedChem. 15(9). 787–793. 21 indexed citations
12.
13.
Sengoku, Toru, Takehiro Suzuki, Naoshi Dohmae, et al.. (2018). Structural basis of protein arginine rhamnosylation by glycosyltransferase EarP. Nature Chemical Biology. 14(4). 368–374. 18 indexed citations
14.
Tang, Zhanyun, Wei‐Yi Chen, Miho Shimada, et al.. (2013). SET1 and p300 Act Synergistically, through Coupled Histone Modifications, in Transcriptional Activation by p53. Cell. 154(2). 297–310. 135 indexed citations
15.
Kitamura, Aya, Madoka Nishimoto, Toru Sengoku, et al.. (2012). Characterization and Structure of the Aquifex aeolicus Protein DUF752. Journal of Biological Chemistry. 287(52). 43950–43960. 17 indexed citations
16.
Shpargel, Karl B., Toru Sengoku, Shigeyuki Yokoyama, & Terry Magnuson. (2012). UTX and UTY Demonstrate Histone Demethylase-Independent Function in Mouse Embryonic Development. PLoS Genetics. 8(9). e1002964–e1002964. 239 indexed citations
17.
Mimasu, Shinya, Toru Sengoku, Seketsu Fukuzawa, Takashi Umehara, & Shigeyuki Yokoyama. (2007). Crystal structure of histone demethylase LSD1 and tranylcypromine at 2.25 Å. Biochemical and Biophysical Research Communications. 366(1). 15–22. 108 indexed citations
18.
Kuratani, M., Ryohei Ishii, Yoshitaka Bessho, et al.. (2005). Crystal Structure of tRNA Adenosine Deaminase (TadA) from Aquifex aeolicus. Journal of Biological Chemistry. 280(16). 16002–16008. 48 indexed citations
19.
Kise, Yoshiaki, Sang‐Won Lee, Sang Gyu Park, et al.. (2004). A short peptide insertion crucial for angiostatic activity of human tryptophanyl-tRNA synthetase. Nature Structural & Molecular Biology. 11(2). 149–156. 63 indexed citations
20.
Sengoku, Toru, Osamu Nureki, Naoshi Dohmae, Akira Nakamura, & Shigeyuki Yokoyama. (2004). Crystallization and preliminary X-ray analysis of the helicase domains of Vasa complexed with RNA and an ATP analogue. Acta Crystallographica Section D Biological Crystallography. 60(2). 320–322. 5 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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