Maiko Iida

504 total citations
23 papers, 401 citations indexed

About

Maiko Iida is a scholar working on Molecular Biology, Organic Chemistry and Microbiology. According to data from OpenAlex, Maiko Iida has authored 23 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Organic Chemistry and 7 papers in Microbiology. Recurrent topics in Maiko Iida's work include Antimicrobial Peptides and Activities (7 papers), Antimicrobial agents and applications (6 papers) and Antibiotic Resistance in Bacteria (4 papers). Maiko Iida is often cited by papers focused on Antimicrobial Peptides and Activities (7 papers), Antimicrobial agents and applications (6 papers) and Antibiotic Resistance in Bacteria (4 papers). Maiko Iida collaborates with scholars based in Japan, Brazil and United States. Maiko Iida's co-authors include Sho Takahata, Hideo Kitagawa, Tomohiro Ozawa, Jun Saito, Mototsugu Yamada, Masayuki Inoue, Naoki Shinohara, Shigeru Matsuoka, Hiromi Kumon and Hiroaki Itoh and has published in prestigious journals such as Angewandte Chemie International Edition, Gastroenterology and PLoS ONE.

In The Last Decade

Maiko Iida

22 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maiko Iida Japan 13 208 185 86 83 72 23 401
Walid A. M. Elgaher Germany 13 121 0.6× 207 1.1× 72 0.8× 34 0.4× 63 0.9× 30 428
Min Woo Ha South Korea 15 280 1.3× 205 1.1× 49 0.6× 70 0.8× 35 0.5× 49 606
Giannamaria Annunziato Italy 15 162 0.8× 352 1.9× 50 0.6× 93 1.1× 87 1.2× 27 643
Sean Trapp United States 5 207 1.0× 149 0.8× 65 0.8× 48 0.6× 38 0.5× 5 403
Mathieu F. Chellat Switzerland 7 193 0.9× 237 1.3× 76 0.9× 69 0.8× 102 1.4× 10 568
Varvara Pokrovskaya Israel 8 117 0.6× 259 1.4× 74 0.9× 57 0.7× 92 1.3× 8 388
Dhanaraju Mandalapu India 15 174 0.8× 272 1.5× 134 1.6× 72 0.9× 32 0.4× 30 551
Elena B. Isakova Russia 11 151 0.7× 172 0.9× 115 1.3× 42 0.5× 34 0.5× 30 367
Nishad Thamban Chandrika United States 12 280 1.3× 191 1.0× 80 0.9× 55 0.7× 54 0.8× 28 548
Aaron T. Garrison United States 14 240 1.2× 371 2.0× 57 0.7× 142 1.7× 115 1.6× 18 594

Countries citing papers authored by Maiko Iida

Since Specialization
Citations

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

Fields of papers citing papers by Maiko Iida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maiko Iida

This figure shows the co-authorship network connecting the top 25 collaborators of Maiko Iida. A scholar is included among the top collaborators of Maiko Iida 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 Maiko Iida. Maiko Iida 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
2.
Mawaribuchi, Shuuji, Maiko Iida, & Yoshikazu Haramoto. (2024). Fusion of breast cancer MCF-7 cells with mesenchymal stem cells rearranges interallelic gene expression and enhances cancer malignancy. Biochemical and Biophysical Research Communications. 736. 150887–150887. 2 indexed citations
3.
4.
Iida, Maiko, et al.. (2023). Liquid chromatography-mass spectrometry analyses of polyprenyl phosphates in Escherichia coli cells in which genes for isoprenoid synthesis are amplified. Journal of Bioscience and Bioengineering. 135(5). 382–388. 1 indexed citations
5.
Inaoka, D.K., Maiko Iida, Satoshi Hashimoto, et al.. (2017). Design and synthesis of potent substrate-based inhibitors of the Trypanosoma cruzi dihydroorotate dehydrogenase. Bioorganic & Medicinal Chemistry. 25(4). 1465–1470. 13 indexed citations
6.
Nishiyama, Mitsue, Masahiro Yamamoto, Seiichi Iizuka, et al.. (2017). Japanese Traditional Medicine Bofutsushosan Increased Akkermaisia Muciniphila in Gut Microbiota and Improved Non-Alcoholic Fatty Liver Disease in Obese Mice. Gastroenterology. 152(5). S1116–S1116. 1 indexed citations
7.
Inaoka, D.K., Maiko Iida, Teruki Honma, et al.. (2016). The Open Form Inducer Approach for Structure-Based Drug Design. PLoS ONE. 11(11). e0167078–e0167078. 9 indexed citations
8.
Satoh, Kazuko, et al.. (2016). Combinability of Animal Data in Relative Potency Estimations. 37(1). 45–65. 2 indexed citations
9.
Araki, Jun & Maiko Iida. (2016). Surface carboxylation of cellulose nanowhiskers using mPEG-TEMPO: its recovery and recycling. Polymer Journal. 48(10). 1029–1033. 14 indexed citations
10.
Matsuoka, Shigeru, et al.. (2011). Functional Analysis of Synthetic Substructures of Polytheonamide B: A Transmembrane Channel‐Forming Peptide. Angewandte Chemie International Edition. 50(21). 4879–4883. 17 indexed citations
11.
Matsuoka, Shigeru, et al.. (2011). Functional Analysis of Synthetic Substructures of Polytheonamide B: A Transmembrane Channel‐Forming Peptide. Angewandte Chemie. 123(21). 4981–4985. 5 indexed citations
12.
Inoue, Masayuki, et al.. (2010). Total synthesis of the large non-ribosomal peptide polytheonamide B. Nature Chemistry. 2(4). 280–285. 76 indexed citations
13.
Saito, Jun, Mototsugu Yamada, Takashi Watanabe, et al.. (2008). Crystal structure of enoyl–acyl carrier protein reductase (FabK) from Streptococcus pneumoniae reveals the binding mode of an inhibitor. Protein Science. 17(4). 691–699. 46 indexed citations
14.
Ozawa, Tomohiro, Hideo Kitagawa, Yasuo Yamamoto, et al.. (2007). Phenylimidazole derivatives as specific inhibitors of bacterial enoyl-acyl carrier protein reductase FabK. Bioorganic & Medicinal Chemistry. 15(23). 7325–7336. 12 indexed citations
16.
Kitagawa, Hideo, Tomohiro Ozawa, Sho Takahata, & Maiko Iida. (2007). Phenylimidazole derivatives as new inhibitors of bacterial enoyl-ACP reductase FabK. Bioorganic & Medicinal Chemistry Letters. 17(17). 4982–4986. 16 indexed citations
17.
Kitagawa, Hideo, Tomohiro Ozawa, Sho Takahata, et al.. (2007). Phenylimidazole Derivatives of 4-Pyridone as Dual Inhibitors of Bacterial Enoyl-Acyl Carrier Protein Reductases FabI and FabK. Journal of Medicinal Chemistry. 50(19). 4710–4720. 56 indexed citations
18.
Takahata, Sho, Maiko Iida, Yumi Osaki, et al.. (2006). AG205, a Novel Agent Directed against FabK of Streptococcus pneumoniae. Antimicrobial Agents and Chemotherapy. 50(8). 2869–2871. 21 indexed citations
19.
Kitagawa, Hideo, et al.. (2006). 4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI. Bioorganic & Medicinal Chemistry. 15(2). 1106–1116. 31 indexed citations
20.
Monden, Koichi, et al.. (2002). Role of fosfomycin in a synergistic combination with ofloxacin against Pseudomonas aeruginosa growing in a biofilm. Journal of Infection and Chemotherapy. 8(3). 218–226. 30 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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