Kazuo Shin‐ya

16.6k total citations · 1 hit paper
391 papers, 13.0k citations indexed

About

Kazuo Shin‐ya is a scholar working on Molecular Biology, Pharmacology and Organic Chemistry. According to data from OpenAlex, Kazuo Shin‐ya has authored 391 papers receiving a total of 13.0k indexed citations (citations by other indexed papers that have themselves been cited), including 260 papers in Molecular Biology, 191 papers in Pharmacology and 92 papers in Organic Chemistry. Recurrent topics in Kazuo Shin‐ya's work include Microbial Natural Products and Biosynthesis (185 papers), Marine Sponges and Natural Products (64 papers) and DNA and Nucleic Acid Chemistry (43 papers). Kazuo Shin‐ya is often cited by papers focused on Microbial Natural Products and Biosynthesis (185 papers), Marine Sponges and Natural Products (64 papers) and DNA and Nucleic Acid Chemistry (43 papers). Kazuo Shin‐ya collaborates with scholars based in Japan, United States and South Korea. Kazuo Shin‐ya's co-authors include Motoki Takagi, Yoichi Hayakawa, Haruo Seto, Kazuo Furihata, Miho Izumikawa, Haruo Ikeda, Konstanty Wierzba, Robert M. Brosh, Satoshi Ōmura and Junko Hashimoto and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nucleic Acids Research.

In The Last Decade

Kazuo Shin‐ya

386 papers receiving 12.8k citations

Hit Papers

Terpene synthases are widely distributed in bacteria 2014 2026 2018 2022 2014 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kazuo Shin‐ya Japan 55 9.3k 4.4k 2.7k 2.0k 808 391 13.0k
Craig A. Townsend United States 55 6.9k 0.7× 4.7k 1.1× 2.4k 0.9× 997 0.5× 1.5k 1.8× 270 11.4k
Masami Ishibashi Japan 51 5.3k 0.6× 2.7k 0.6× 3.9k 1.5× 2.6k 1.3× 1.2k 1.4× 512 12.0k
Hideaki Kakeya Japan 39 3.4k 0.4× 1.7k 0.4× 2.3k 0.9× 738 0.4× 548 0.7× 229 6.7k
Dong‐Chan Oh South Korea 38 3.7k 0.4× 3.2k 0.7× 1.6k 0.6× 1.9k 0.9× 566 0.7× 234 7.7k
Jee H. Jung South Korea 44 2.9k 0.3× 1.8k 0.4× 1.3k 0.5× 1.6k 0.8× 825 1.0× 228 6.5k
Teruhiko Beppu Japan 54 7.3k 0.8× 2.4k 0.6× 938 0.4× 1.6k 0.8× 1.4k 1.7× 394 10.4k
John A. Porco United States 62 4.9k 0.5× 1.6k 0.4× 8.4k 3.2× 937 0.5× 781 1.0× 248 13.3k
MASA HAMADA Japan 45 4.5k 0.5× 2.2k 0.5× 2.4k 0.9× 975 0.5× 519 0.6× 229 7.5k
Hendrik Luesch United States 55 3.9k 0.4× 3.2k 0.7× 2.1k 0.8× 3.1k 1.6× 195 0.2× 190 8.1k
Joseph P. Noel United States 80 16.8k 1.8× 3.8k 0.9× 1.2k 0.5× 1.6k 0.8× 5.9k 7.3× 181 21.4k

Countries citing papers authored by Kazuo Shin‐ya

Since Specialization
Citations

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

Fields of papers citing papers by Kazuo Shin‐ya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kazuo Shin‐ya. 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 Kazuo Shin‐ya. The network helps show where Kazuo Shin‐ya may publish in the future.

Co-authorship network of co-authors of Kazuo Shin‐ya

This figure shows the co-authorship network connecting the top 25 collaborators of Kazuo Shin‐ya. A scholar is included among the top collaborators of Kazuo Shin‐ya 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 Kazuo Shin‐ya. Kazuo Shin‐ya 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.
Akiyama, Satoko, et al.. (2023). Carrier Protein Mediated Formation of the Dihydropyridazinone Ring in Actinopyridazinone Biosynthesis. Angewandte Chemie International Edition. 62(29). e202305155–e202305155. 5 indexed citations
2.
Sasaki, Kazuki, Tilman Schneider‐Poetsch, Akihiro Ito, et al.. (2022). Visualization of the dynamic interaction between nucleosomal histone H3K9 tri-methylation and HP1α chromodomain in living cells. Cell chemical biology. 29(7). 1153–1161.e5. 4 indexed citations
3.
Kagaya, Noritaka, Hikaru Suenaga, Manabu Fujie, et al.. (2022). New azodyrecins identified by a genome mining-directed reactivity-based screening. Beilstein Journal of Organic Chemistry. 18. 1017–1025. 4 indexed citations
4.
Katsuyama, Yohei, Naruhiko Adachi, Toshio Moriya, et al.. (2021). Structural and Functional Analyses of the Tridomain‐Nonribosomal Peptide Synthetase FmoA3 for 4‐Methyloxazoline Ring Formation. Angewandte Chemie International Edition. 60(26). 14554–14562. 21 indexed citations
5.
Yamamoto, Kyosuke, Yasuhiro Tanaka, Xian‐Ying Meng, et al.. (2021). Novel Plant-Associated Acidobacteria Promotes Growth of Common Floating Aquatic Plants, Duckweeds. Microorganisms. 9(6). 1133–1133. 32 indexed citations
6.
Hayakawa, Yoichi, et al.. (2020). Neocurromycin A, a new GRP78 downregulator from Streptomyces sp. RAI364. The Journal of Antibiotics. 73(11). 790–793. 4 indexed citations
7.
Romer, Eric J., et al.. (2020). Replication stress at microsatellites causes DNA double-strand breaks and break-induced replication. Journal of Biological Chemistry. 295(45). 15378–15397. 23 indexed citations
8.
Hashimoto, Takuya, Junko Hashimoto, Ikuko Kozone, et al.. (2020). In vitro Cas9-assisted editing of modular polyketide synthase genes to produce desired natural product derivatives. Nature Communications. 11(1). 4022–4022. 33 indexed citations
9.
Hashimoto, Takuya, Ikuko Kozone, Junko Hashimoto, et al.. (2020). Identification, cloning and heterologous expression of biosynthetic gene cluster for desertomycin. The Journal of Antibiotics. 73(9). 650–654. 10 indexed citations
10.
Ueoka, Reiko, Naoya Shinzato, Noritaka Kagaya, Hikaru Suenaga, & Kazuo Shin‐ya. (2020). Pseudoalteropeptide A, a novel lipopeptide from the marine bacterium Pseudoalteromonas piscicida SWA4_PA4 isolated from marine seaweed. The Journal of Antibiotics. 74(2). 105–110. 4 indexed citations
11.
Hashimoto, Takuya, Ikuko Kozone, Junko Hashimoto, et al.. (2019). Novel macrolactam compound produced by the heterologous expression of a large cryptic biosynthetic gene cluster of Streptomyces rochei IFO12908. The Journal of Antibiotics. 73(3). 171–174. 14 indexed citations
12.
Awakawa, Takayoshi, Lihan Zhang, Shotaro Hoshino, et al.. (2018). Reprogramming of the antimycin NRPS-PKS assembly lines inspired by gene evolution. Nature Communications. 9(1). 3534–3534. 47 indexed citations
13.
Zhang, Lihan, Takuya Hashimoto, Bin Qin, et al.. (2017). Characterization of Giant Modular PKSs Provides Insight into Genetic Mechanism for Structural Diversification of Aminopolyol Polyketides. Angewandte Chemie. 129(7). 1766–1771. 4 indexed citations
14.
Katsuyama, Yohei, et al.. (2017). Reconstitution of a Type II Polyketide Synthase that Catalyzes Polyene Formation. Angewandte Chemie. 130(7). 1972–1975. 7 indexed citations
15.
Nishizawa, Masato, Takahiro Hosoya, Takatsugu Hirokawa, Kazuo Shin‐ya, & Shigenori Kumazawa. (2014). NMR Spectroscopic Characterization of Inclusion Complexes of Theaflavin Digallate and Cyclodextrins. Food Science and Technology Research. 20(3). 663–670. 5 indexed citations
16.
Miyazaki, Takeshi, Kaushal Joshi, Bin Hu, et al.. (2012). Telomestatin Impairs Glioma Stem Cell Survival and Growth through the Disruption of Telomeric G-Quadruplex and Inhibition of the Proto-oncogene, c-Myb. Clinical Cancer Research. 18(5). 1268–1280. 97 indexed citations
17.
Shalaby, Tarek, André O. von Bueren, Giulio Fiaschetti, et al.. (2010). Disabling c-Myc in Childhood Medulloblastoma and Atypical Teratoid/Rhabdoid Tumor Cells by the Potent G-Quadruplex Interactive Agent S2T1-6OTD. Molecular Cancer Therapeutics. 9(1). 167–179. 39 indexed citations
18.
Kunoh, Tatsuki, Koichi Koseki, Motoki Takagi, et al.. (2010). A Novel Human Dynactin-Associated Protein, dynAP, Promotes Activation of Akt, and Ergosterol-Related Compounds Induce dynAP-Dependent Apoptosis of Human Cancer Cells. Molecular Cancer Therapeutics. 9(11). 2934–2942. 10 indexed citations
19.
Saito, Sakae, Junko Sakurai, Asami Sakamoto, et al.. (2009). Chemical Genomics Identifies the Unfolded Protein Response as a Target for Selective Cancer Cell Killing during Glucose Deprivation. Cancer Research. 69(10). 4225–4234. 137 indexed citations
20.
Yamashita, N., Takashi Harada, Kazuo Shin‐ya, & Haruo Seto. (1998). 6-HydroxytetranguloL a Ncw CPP32 Protease Inducer Produced by Streptomyca sp.. The Journal of Antibiotics. 51(1). 79–81. 16 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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