Minoru Yoshida

61.7k total citations · 17 hit papers
1.2k papers, 49.6k citations indexed

About

Minoru Yoshida is a scholar working on Molecular Biology, Oncology and Animal Science and Zoology. According to data from OpenAlex, Minoru Yoshida has authored 1.2k papers receiving a total of 49.6k indexed citations (citations by other indexed papers that have themselves been cited), including 501 papers in Molecular Biology, 149 papers in Oncology and 109 papers in Animal Science and Zoology. Recurrent topics in Minoru Yoshida's work include Histone Deacetylase Inhibitors Research (111 papers), Animal Nutrition and Physiology (93 papers) and Ubiquitin and proteasome pathways (56 papers). Minoru Yoshida is often cited by papers focused on Histone Deacetylase Inhibitors Research (111 papers), Animal Nutrition and Physiology (93 papers) and Ubiquitin and proteasome pathways (56 papers). Minoru Yoshida collaborates with scholars based in Japan, United States and United Kingdom. Minoru Yoshida's co-authors include Sueharu Horinouchi, Ed Seto, Motoharu Seiki, Toru Beppu, Akihiro Ito, Teruhiko Beppu, Mutsuhito Ohno, Iain W. Mattaj, Maarten Fornerod and Motomu Akita and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Minoru Yoshida

1.1k papers receiving 48.2k citations

Hit Papers

HDAC6 is a microtubule-as... 1984 2026 1998 2012 2002 1997 1990 2014 1997 500 1000 1.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Minoru Yoshida 32.1k 7.2k 6.9k 3.9k 3.8k 1.2k 49.6k
Adi F. Gazdar 36.4k 1.1× 7.6k 1.1× 28.3k 4.1× 2.9k 0.7× 2.7k 0.7× 654 70.7k
John D. Minna 42.2k 1.3× 8.8k 1.2× 26.3k 3.8× 3.0k 0.8× 2.8k 0.7× 803 73.8k
Prescott L. Deininger 62.5k 1.9× 6.6k 0.9× 6.6k 1.0× 844 0.2× 2.4k 0.6× 197 98.6k
Yukio Ando 16.5k 0.5× 3.6k 0.5× 6.6k 0.9× 649 0.2× 995 0.3× 2.8k 56.0k
Alan Coulson 58.3k 1.8× 6.1k 0.8× 4.1k 0.6× 834 0.2× 1.8k 0.5× 56 85.2k
Richard J. Simpson 27.6k 0.9× 7.4k 1.0× 5.2k 0.8× 698 0.2× 982 0.3× 558 42.5k
Wolfgang Huber 67.0k 2.1× 12.8k 1.8× 7.0k 1.0× 1.5k 0.4× 2.6k 0.7× 249 109.8k
Christian von Mering 45.6k 1.4× 5.6k 0.8× 4.3k 0.6× 547 0.1× 1.1k 0.3× 134 69.7k
Simon Anders 51.5k 1.6× 10.7k 1.5× 5.6k 0.8× 1.4k 0.4× 2.3k 0.6× 59 87.9k
Frederick Sanger 61.4k 1.9× 6.2k 0.9× 4.5k 0.6× 841 0.2× 1.8k 0.5× 78 89.2k

Countries citing papers authored by Minoru Yoshida

Since Specialization
Citations

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

Fields of papers citing papers by Minoru Yoshida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Minoru Yoshida

This figure shows the co-authorship network connecting the top 25 collaborators of Minoru Yoshida. A scholar is included among the top collaborators of Minoru Yoshida 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 Minoru Yoshida. Minoru Yoshida 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.
Tsugawa, Hiroshi, Satoshi Kimura, Akihisa Matsuyama, et al.. (2025). Formation of giant ER sheets by pentadecanoic acid causes lipotoxicity in fission yeast. Proceedings of the National Academy of Sciences. 122(22). e2422126122–e2422126122.
2.
Wang, Ying, Danni Chen, Hiroyuki Osada, et al.. (2025). GENI as an AMPK Activator Binds α and γ Subunits and Improves the Memory Dysfunction of Alzheimer’s Disease Mouse Models via Autophagy and Neuroprotection. Antioxidants. 14(1). 57–57. 1 indexed citations
4.
Dileep, K.V., Naoki Sakai, Kentaro Ihara, et al.. (2024). Identification of benzimidazole-6-carboxamide based inhibitors of secretory glutaminyl cyclase for the treatment of Alzheimer's disease. International Journal of Biological Macromolecules. 293. 139320–139320.
5.
Oniki, Kentaro, Masatsune Ogura, Hiroshi Watanabe, et al.. (2024). Impaired Cholesterol Efflux Capacity rather than Low HDL-C Reflects Oxidative Stress under Acute Myocardial Infarction. Journal of Atherosclerosis and Thrombosis. 31(8). 1149–1161. 2 indexed citations
6.
Sohtome, Yoshihiro, Daisuke Hashizume, Mai Akakabe, et al.. (2024). Catalytic Aerobic Carbooxygenation for the Construction of Vicinal Tetrasubstituted Centers: Application to the Synthesis of Hexasubstituted γ‐Lactones. Angewandte Chemie International Edition. 63(36). e202405876–e202405876. 3 indexed citations
7.
Suzuki, Akihiro & Minoru Yoshida. (2023). Design of dispersion-flattened photonic crystal fiber with 800 nm wide low-dispersion band. Results in Optics. 12. 100474–100474.
8.
Chen, Bin, Qing Zhai, Chi Zhang, et al.. (2023). UBL3 Interacts with Alpha-Synuclein in Cells and the Interaction Is Downregulated by the EGFR Pathway Inhibitor Osimertinib. Biomedicines. 11(6). 1685–1685. 7 indexed citations
9.
Yan, Jing, Md. Shoriful Islam, Tomohito Sato, et al.. (2023). UBL3 Interaction with α-Synuclein Is Downregulated by Silencing MGST3. Biomedicines. 11(9). 2491–2491. 6 indexed citations
10.
Takayama, Ken‐ichi, Teruki Honma, Takashi Suzuki, et al.. (2021). Targeting Epigenetic and Posttranscriptional Gene Regulation by PSF Impairs Hormone Therapy–Refractory Cancer Growth. Cancer Research. 81(13). 3495–3508. 15 indexed citations
12.
Sekine, Daisuke, Akihiro Ito, Satoko Maeda, et al.. (2019). Synthesis of All Stereoisomers of Monomeric Spectomycin A1/A2 and Evaluation of Their Protein SUMOylation‐Inhibitory Activity. Chemistry - A European Journal. 25(35). 8387–8392. 6 indexed citations
13.
Nelson, Justin, Scott W. Simpkins, Sheena C. Li, et al.. (2017). MOSAIC: a chemical-genetic interaction data repository and web resource for exploring chemical modes of action. Bioinformatics. 34(7). 1251–1252. 9 indexed citations
14.
Li, Ge, Melissa N. Poulsen, Yoko Yashiroda, et al.. (2017). Characterization of cytopathic factors through genome-wide analysis of the Zika viral proteins in fission yeast. Proceedings of the National Academy of Sciences. 114(3). E376–E385. 51 indexed citations
15.
Deshpande, Raamesh, Michael K. Asiedu, Mitchell Klebig, et al.. (2013). A Comparative Genomic Approach for Identifying Synthetic Lethal Interactions in Human Cancer. Cancer Research. 73(20). 6128–6136. 47 indexed citations
16.
Williams, David E., Doralyn S. Dalisay, Brian O. Patrick, et al.. (2011). Padanamides A and B, Highly Modified Linear Tetrapeptides Produced in Culture by a Streptomyces sp. Isolated from a Marine Sediment. Organic Letters. 13(15). 3936–3939. 46 indexed citations
17.
Yoshida, Minoru, et al.. (1990). First discovery of fossil ice of 1000–1700 year B.P. in Japan. Journal of Glaciology. 36(123). 258–259. 13 indexed citations
18.
Yoshida, Minoru, et al.. (1987). Bottom Topography and Internal Layers in East Dronning Maud Land, East Antarctica, from 179 MHz Radio Echo-Sounding. Annals of Glaciology. 9. 221–224. 8 indexed citations
19.
Inoue, Katsuhiro, et al.. (1981). . The Quaternary Research (Daiyonki-Kenkyu). 20(2). 61–73. 4 indexed citations
20.
Yoshida, Minoru, et al.. (1966). Nutritive Value of Various Energy Sources for Poultry Feed. Japanese poultry science. 3(1). 29–34. 7 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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