Masaki Tomishima

860 total citations
18 papers, 633 citations indexed

About

Masaki Tomishima is a scholar working on Infectious Diseases, Pharmacology and Molecular Biology. According to data from OpenAlex, Masaki Tomishima has authored 18 papers receiving a total of 633 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Infectious Diseases, 6 papers in Pharmacology and 5 papers in Molecular Biology. Recurrent topics in Masaki Tomishima's work include Antifungal resistance and susceptibility (6 papers), Fungal Infections and Studies (5 papers) and Analytical Chemistry and Chromatography (3 papers). Masaki Tomishima is often cited by papers focused on Antifungal resistance and susceptibility (6 papers), Fungal Infections and Studies (5 papers) and Analytical Chemistry and Chromatography (3 papers). Masaki Tomishima collaborates with scholars based in Japan and United States. Masaki Tomishima's co-authors include Katsuyuki Maki, Hidenori Ohki, Akira Yamada, Fumiaki Ikeda, Tetsuji Kawamoto, Fumio Yoneda, Shuichi Tawara, Toshio Goto, Shōgo Kuwahara and Kazuo Sakane and has published in prestigious journals such as Journal of the American Chemical Society, Antimicrobial Agents and Chemotherapy and The Journal of Organic Chemistry.

In The Last Decade

Masaki Tomishima

18 papers receiving 617 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Masaki Tomishima Japan 13 291 243 182 163 148 18 633
Kazuo Sakane Japan 16 257 0.9× 485 2.0× 171 0.9× 193 1.2× 318 2.1× 66 975
Hidenori Ohki Japan 16 296 1.0× 356 1.5× 215 1.2× 182 1.1× 167 1.1× 24 817
F. Aileen Bouffard United States 12 314 1.1× 506 2.1× 239 1.3× 216 1.3× 166 1.1× 13 928
Raulo Parmegiani United States 14 286 1.0× 190 0.8× 210 1.2× 97 0.6× 102 0.7× 33 617
David N. Whittern United Kingdom 17 101 0.3× 469 1.9× 75 0.4× 289 1.8× 364 2.5× 29 915
Tingjunhong Ni China 14 213 0.7× 325 1.3× 118 0.6× 51 0.3× 116 0.8× 35 539
KOZO TOMATSU Japan 12 94 0.3× 246 1.0× 86 0.5× 203 1.2× 241 1.6× 17 564
Aparna S. Chothe India 7 161 0.6× 371 1.5× 99 0.5× 95 0.6× 179 1.2× 8 663
Robert A. Zambias United States 11 129 0.4× 175 0.7× 67 0.4× 110 0.7× 136 0.9× 15 434
L. J. J. Backx Belgium 5 129 0.4× 228 0.9× 130 0.7× 41 0.3× 75 0.5× 7 443

Countries citing papers authored by Masaki Tomishima

Since Specialization
Citations

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

Fields of papers citing papers by Masaki Tomishima

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masaki Tomishima

This figure shows the co-authorship network connecting the top 25 collaborators of Masaki Tomishima. A scholar is included among the top collaborators of Masaki Tomishima 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 Masaki Tomishima. Masaki Tomishima is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Morita, Masataka, Y. Amano, Hiroyuki Moriguchi, et al.. (2019). Synthesis, SAR study, and biological evaluation of novel 2,3-dihydro-1H-imidazo[1,2-a]benzimidazole derivatives as phosphodiesterase 10A inhibitors. Bioorganic & Medicinal Chemistry. 27(16). 3692–3706. 6 indexed citations
2.
Amano, Y., Ichiji Namatame, Kazuya Honbou, et al.. (2018). Fragment-Based Discovery of Pyrimido[1,2-<i>b</i>]indazole PDE10A Inhibitors. Chemical and Pharmaceutical Bulletin. 66(3). 286–294. 20 indexed citations
3.
Morikawa, Hiroshi, Masaki Tomishima, Takanobu Araki, et al.. (2014). Synthesis and antifungal activity of ASP9726, a novel echinocandin with potent Aspergillus hyphal growth inhibition. Bioorganic & Medicinal Chemistry Letters. 24(4). 1172–1175. 22 indexed citations
4.
Masuda, Naoyuki, Y. Amano, Kazuya Honbou, et al.. (2014). Novel benzimidazole derivatives as phosphodiesterase 10A (PDE10A) inhibitors with improved metabolic stability. Bioorganic & Medicinal Chemistry. 22(13). 3515–3526. 25 indexed citations
5.
Tomishima, Masaki, et al.. (2009). FR290581, a novel sordarin derivative: Synthesis and antifungal activity. Bioorganic & Medicinal Chemistry Letters. 19(5). 1465–1468. 30 indexed citations
6.
Garfunkle, Joie, F. Scott Kimball, John D. Trzupek, et al.. (2009). Total Synthesis of Chloropeptin II (Complestatin) and Chloropeptin I. Journal of the American Chemical Society. 131(44). 16036–16038. 98 indexed citations
7.
Tomishima, Masaki, Hidenori Ohki, Akira Yamada, Katsuyuki Maki, & Fumiaki Ikeda. (2008). Novel echinocandin antifungals. Part 2: Optimization of the side chain of the natural product FR901379. Discovery of micafungin. Bioorganic & Medicinal Chemistry Letters. 18(9). 2886–2890. 30 indexed citations
8.
Tomishima, Masaki, Hidenori Ohki, Akira Yamada, Katsuyuki Maki, & Fumiaki Ikeda. (2008). Novel echinocandin antifungals. Part 1: Novel side-chain analogs of the natural product FR901379. Bioorganic & Medicinal Chemistry Letters. 18(4). 1474–1477. 18 indexed citations
9.
Maki, Katsuyuki, Satoru Matsumoto, Masaki Tomishima, et al.. (2008). Use of a serum‐based antifungal susceptibility assay to predict the in vivo efficacy of novel echinocandin compounds. Microbiology and Immunology. 52(8). 383–391. 17 indexed citations
10.
Maki, Katsuyuki, Masaki Tomishima, Hidenori Ohki, et al.. (2006). Determination of Antifungal Activities in Serum Samples from Mice Treated with Different Antifungal Drugs Allows Detection of an Active Metabolite of Itraconazole. Microbiology and Immunology. 50(4). 281–292. 3 indexed citations
11.
Tawara, Shuichi, Fumiaki Ikeda, Katsuyuki Maki, et al.. (2000). In Vitro Activities of a New Lipopeptide Antifungal Agent, FK463, against a Variety of Clinically Important Fungi. Antimicrobial Agents and Chemotherapy. 44(1). 57–62. 260 indexed citations
12.
Ohno, Atsuyoshi, Jun Kunitomo, Yasushi Kawai, et al.. (1996). Atropisomeric Flavoenzyme Models with a Modified Pyrimidine Ring:  Syntheses, Physical Properties, and Stereochemistry in the Reactions with NAD(P)H Analogs. The Journal of Organic Chemistry. 61(26). 9344–9355. 29 indexed citations
13.
Kawamoto, Tetsuji, Yoshihiro Ikeuchi, Kazue Shimizu, et al.. (1995). Evaluation of differential hypoxic cytotoxicity and electrochemical studies of nitro 5-deazaflavins. Bioorganic & Medicinal Chemistry Letters. 5(18). 2115–2118. 8 indexed citations
14.
Kawamoto, Tetsuji, Yoshihiro Ikeuchi, Kazue Shimizu, et al.. (1995). Synthesis and evaluation of nitro 5-deazaflavins as novel bioreductive antitumor agents. Bioorganic & Medicinal Chemistry Letters. 5(18). 2109–2114. 16 indexed citations
15.
Ohno, Atsuyoshi, Jun Kunitomo, Tetsuji Kawamoto, et al.. (1994). Variation of reaction channel in a flavoenzyme model with a modified pyrimidine ring. Tetrahedron Letters. 35(52). 9729–9732. 3 indexed citations
16.
Kawamoto, Tetsuji, Masaki Tomishima, Fumio Yoneda, & Jun-ichi Hayami. (1992). Diastereoface differentiating “(net) hydride transfer” in novel 5-deazaflavins modified at pyrimidine ring. Tetrahedron Letters. 33(22). 3173–3176. 15 indexed citations
17.
Kawamoto, Tetsuji, Masaki Tomishima, Fumio Yoneda, & Jun-ichi Hayami. (1992). Synthesis and reaction of novel 5-deazaflavins with axial chirality at pyrimidine ring moiety. Tetrahedron Letters. 33(22). 3169–3172. 24 indexed citations
18.
Kawamoto, Tetsuji, Masaki Tomishima, Jun Kunitomo, Fumio Yoneda, & Jun-ichi Hayami. (1992). First example of “diastereotopic face activation” and chiral recognition without metal assistance. A novel 5-deazaflavin enzyme model.. Tetrahedron Letters. 33(47). 7173–7176. 9 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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