Makoto Yoshida

4.6k total citations
156 papers, 3.3k citations indexed

About

Makoto Yoshida is a scholar working on Molecular Biology, Plant Science and Biomedical Engineering. According to data from OpenAlex, Makoto Yoshida has authored 156 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 49 papers in Plant Science and 34 papers in Biomedical Engineering. Recurrent topics in Makoto Yoshida's work include Biofuel production and bioconversion (30 papers), Enzyme Production and Characterization (23 papers) and Enzyme-mediated dye degradation (18 papers). Makoto Yoshida is often cited by papers focused on Biofuel production and bioconversion (30 papers), Enzyme Production and Characterization (23 papers) and Enzyme-mediated dye degradation (18 papers). Makoto Yoshida collaborates with scholars based in Japan, United States and Slovakia. Makoto Yoshida's co-authors include Clea Fernandez, Kiyohiko Igarashi, Satoshi Kaneko, Masahiro Samejima, Hitomi Ichinose, Kiwamu Umezawa, Kiyoharu FUKUDA, Kensuke Kawarada, Yuan Liu and Satoshi Uchida and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Makoto Yoshida

152 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Makoto Yoshida Japan 32 1.1k 1.0k 729 537 461 156 3.3k
Henrik Hansson Sweden 24 1.1k 1.0× 1.2k 1.1× 397 0.5× 667 1.2× 235 0.5× 98 2.3k
Richard W. Pickersgill United Kingdom 36 2.2k 2.0× 766 0.7× 1.1k 1.4× 1.3k 2.3× 44 0.1× 121 3.8k
Charles Miller United States 32 862 0.8× 431 0.4× 373 0.5× 70 0.1× 371 0.8× 116 3.2k
Noam Adir Israel 37 2.8k 2.5× 246 0.2× 771 1.1× 163 0.3× 58 0.1× 111 4.5k
Peter L. Rogers Australia 42 3.1k 2.8× 2.4k 2.3× 368 0.5× 611 1.1× 37 0.1× 159 5.6k
John M. Wells United States 38 1.1k 1.0× 298 0.3× 1.5k 2.0× 360 0.7× 155 0.3× 175 4.6k
Marie Tichá Czechia 23 918 0.8× 210 0.2× 248 0.3× 127 0.2× 172 0.4× 125 1.9k
Michael Sauer Austria 41 4.6k 4.2× 2.2k 2.1× 443 0.6× 702 1.3× 17 0.0× 129 5.8k
Glenn R. Johnson United States 32 712 0.6× 503 0.5× 127 0.2× 56 0.1× 55 0.1× 87 3.0k
Sean R. Gallagher United States 26 1.7k 1.6× 207 0.2× 724 1.0× 199 0.4× 53 0.1× 119 2.9k

Countries citing papers authored by Makoto Yoshida

Since Specialization
Citations

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

Fields of papers citing papers by Makoto Yoshida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Makoto Yoshida

This figure shows the co-authorship network connecting the top 25 collaborators of Makoto Yoshida. A scholar is included among the top collaborators of Makoto 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 Makoto Yoshida. Makoto 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.
Yoshida, Makoto, et al.. (2024). Fungal invasion of cellulosic skeletal substrates with a hierarchical structure of wood. International Biodeterioration & Biodegradation. 192. 105826–105826.
2.
Kojima, Yuka, Naoki Sunagawa, Yoshiki Horikawa, et al.. (2024). A cellulose-binding domain specific for native crystalline cellulose in lytic polysaccharide monooxygenase from the brown-rot fungus Gloeophyllum trabeum. Carbohydrate Polymers. 347. 122651–122651. 2 indexed citations
3.
4.
Kojima, Yuka, Anikó Várnai, Vincent G. H. Eijsink, & Makoto Yoshida. (2020). The Role of Lytic Polysaccharide Monooxygenases in Wood Rotting Basidiomycetes. Trends in Glycoscience and Glycotechnology. 32(188). E135–E143. 3 indexed citations
5.
Yoshida, Makoto, et al.. (2019). Multiple iron reduction by methoxylated phenolic lignin structures and the generation of reactive oxygen species by lignocellulose surfaces. International Journal of Biological Macromolecules. 128. 340–346. 21 indexed citations
6.
Takeda, K., Kiwamu Umezawa, Anikó Várnai, et al.. (2018). Fungal PQQ-dependent dehydrogenases and their potential in biocatalysis. Current Opinion in Chemical Biology. 49. 113–121. 24 indexed citations
7.
Várnai, Anikó, Kiwamu Umezawa, Makoto Yoshida, & Vincent G. H. Eijsink. (2018). The Pyrroloquinoline-Quinone-Dependent Pyranose Dehydrogenase from Coprinopsis cinerea Drives Lytic Polysaccharide Monooxygenase Action. Applied and Environmental Microbiology. 84(11). 68 indexed citations
8.
Syukri, Daimon, Manasikan Thammawong, Hushna Ara Naznin, et al.. (2018). Identification of a freshness marker metabolite in stored soybean sprouts by comprehensive mass-spectrometric analysis of carbonyl compounds. Food Chemistry. 269. 588–594. 18 indexed citations
9.
Goodell, Barry, Yuan Zhu, Seong H. Kim, et al.. (2017). Modification of the nanostructure of lignocellulose cell walls via a non-enzymatic lignocellulose deconstruction system in brown rot wood-decay fungi. Biotechnology for Biofuels. 10(1). 179–179. 86 indexed citations
10.
Barajas-Solano, Andrés F., Makoto Yoshida, & Makiko Watanabe. (2016). Improvement of Biomass and Dha Production on a Semi-continuous Culture of Aurantiochytrium Sp Nyh-2. SHILAP Revista de lepidopterología. 49. 235–240. 1 indexed citations
11.
Yoshida, Makoto, et al.. (2013). Radioactive Caesium Contamination in Inago and Sustainability of Inago Cuisine in Fukushima. Food Hygiene and Safety Science (Shokuhin Eiseigaku Zasshi). 54(6). 410–414. 3 indexed citations
12.
Nakada, Yuji, et al.. (2013). Analysis of fugal community in stem of cherry tree (Somei-yoshino). MOKUZAI HOZON (Wood Protection). 39(3). 118–124. 1 indexed citations
13.
Yoshida, Makoto, et al.. (2013). Summary of visit to valuable water springs notes 1 to 100. Journal of Groundwater Hydrology. 55(2). 201–216. 2 indexed citations
14.
15.
Yoshida, Makoto, et al.. (2011). Detection of the genes encoding lignin and manganese peroxidases from white rot fungi. MOKUZAI HOZON (Wood Protection). 37(3). 111–121. 1 indexed citations
16.
Nakada, Yuji, Satoshi Nakaba, Yoko Katayama, et al.. (2010). Analysis of fungal community in decayed wood by PCR-based denaturing gradient gel electrophoresis. MOKUZAI HOZON (Wood Protection). 36(3). 100–110. 1 indexed citations
17.
Maehara, Tomoko, et al.. (2010). Development of a Gene Transfer System for the Mycelia ofFlammulina velutipesFv-1 Strain. Bioscience Biotechnology and Biochemistry. 74(5). 1126–1128. 10 indexed citations
18.
Yoshida, Makoto, et al.. (2010). Characterization of Glycoside Hydrolase Family 7 Cellobiohydrolases Produced by Flammulina velutipes in Cellulose-Degrading Culture. Mokuzai Gakkaishi. 56(6). 397–404. 1 indexed citations
19.
Yoshida, Makoto, Kan Sato, Satoshi Kaneko, & Kiyoharu FUKUDA. (2009). Cloning and Transcript Analysis of Multiple Genes Encoding the Glycoside Hydrolase Family 6 Enzyme fromCoprinopsis cinerea. Bioscience Biotechnology and Biochemistry. 73(1). 67–73. 17 indexed citations
20.
Satoh, Tazuko, et al.. (1995). Transfer of a new quinolone, fleroxacin, to the oral tissues of experimentally infected rabbits. 43(10). 903–906. 3 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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