Miwa Aida

481 total citations
12 papers, 391 citations indexed

About

Miwa Aida is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Pharmacology. According to data from OpenAlex, Miwa Aida has authored 12 papers receiving a total of 391 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Pathology and Forensic Medicine and 3 papers in Pharmacology. Recurrent topics in Miwa Aida's work include Bioactive natural compounds (9 papers), Natural product bioactivities and synthesis (6 papers) and Phytoestrogen effects and research (4 papers). Miwa Aida is often cited by papers focused on Bioactive natural compounds (9 papers), Natural product bioactivities and synthesis (6 papers) and Phytoestrogen effects and research (4 papers). Miwa Aida collaborates with scholars based in Japan, United States and South Korea. Miwa Aida's co-authors include Taro Nomura, Yoshio Hano, Sachiko Okabe, K Park, Hirota Fujiki, Shinichi Ueda, Shozo Yamamoto, Natsuo Ueda, Takahiko Hada and Takatoshi Kawai and has published in prestigious journals such as Biochemical Pharmacology, Phytochemistry and Journal of Natural Products.

In The Last Decade

Miwa Aida

12 papers receiving 370 citations

Peers

Miwa Aida

MB

PFM

PHARM

BIOCH

PS

Keisuke Akagi Japan

Toshio Miyase Japan

Radhakrishnan Vinodhkumar India

Masao Hirose Japan

Guang‐Jian Du United States

Benjawan Wudtiwai Thailand

Harukuni Tokuda Japan

Kian Lam Lim Malaysia

Reiko Saijo Japan

A. Bu-Abbas United Kingdom

Keisuke Akagi Japan

Miwa Aida

207 ×0.8

MB

205 ×1.7

PFM

27 ×0.3

PHARM

176 ×2.8

BIOCH

65 ×1.4

PS

Citations per year, relative to Miwa Aida Miwa Aida (= 1×) peers Keisuke Akagi

Countries citing papers authored by Miwa Aida

Since Specialization

Citations

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

Fields of papers citing papers by Miwa Aida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miwa Aida

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

All Works

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12 of 12 papers shown

1.

Okabe, Sachiko, et al.. (1999). Mechanistic Aspects of Green Tea as a Cancer Preventive: Effect of Components on Human Stomach Cancer Cell Lines. Japanese Journal of Cancer Research. 90(7). 733–739. 119 indexed citations

2.

Nomura, Taro, Yoshio Hano, & Miwa Aida. (1998). Isoprenoid-substituted Flavonoids from Artocarpus Plants (Moraceae). Heterocycles. 47(2). 1179–1179. 75 indexed citations

3.

Aida, Miwa, et al.. (1997). Artonols A, B, C, D, and E, Five New Isoprenylated Phenols from the Bark of Artocarpus communis Forst.. Heterocycles. 45(1). 163–163. 13 indexed citations

4.

Nomura, Taro, et al.. (1996). Formation of Dihydrobenzoxanthone Skeleton from 3-Isoprenylated 2',4',5'-Trioxygenated Flavone. Heterocycles. 43(12). 2561–2561. 4 indexed citations

5.

Aida, Miwa, et al.. (1995). A diels-alder-type adduct from Artocarpus heterophyllus. Phytochemistry. 40(4). 1317–1319. 13 indexed citations

6.

Nomura, Taro, Miwa Aida, & Yoshio Hano. (1995). Ficusins A and B, Two New Cyclic-Monoterpene-substituted Isoflavones from Ficus septica Barm. F.. Heterocycles. 41(12). 2761–2761. 11 indexed citations

7.

Aida, Miwa, et al.. (1994). Artonins Q, R, S, T, and U, Five New Isoprenylated Phenoles from the Bark of Artocarpus heterophyllus Lamk. Heterocycles. 39(2). 847–847. 14 indexed citations

8.

Aida, Miwa, et al.. (1993). Artonins J, K, and L, Three New Isoprenylated Flavones from the Root Bark of Artocarpus heterophyllus Lamk.. Heterocycles. 36(3). 575–575. 17 indexed citations

9.

Hano, Yoshio, Miwa Aida, Taro Nomura, & Shinichi Ueda. (1992). A novel way of determining the structure of artonin I, an optically active Diels–Alder type adduct, with the aid of an enzyme system of Morus alba cell cultures. Journal of the Chemical Society Chemical Communications. 1177–1178. 23 indexed citations

10.

Ueda, Natsuo, Takahiko Hada, Shozo Yamamoto, et al.. (1991). A prenylflavone, artonin E, as arachidonate 5-lipoxygenase inhibitor. Biochemical Pharmacology. 41(1). 115–118. 48 indexed citations

11.

Hano, Yoshio, Miwa Aida, & Taro Nomura. (1990). Two New Natural Diels-Alder-Type Adducts from the Root Bark of Artocarpus heterophyllus. Journal of Natural Products. 53(2). 391–395. 23 indexed citations

12.

Nomura, Taro, et al.. (1989). Artonins A and B, Two New Prenylflavonoes from the Root Bark of Artocarpus heterophyllus Lamk. Heterocycles. 29(8). 1447–1447. 31 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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