Koichi Suzuki

710 total citations
31 papers, 508 citations indexed

About

Koichi Suzuki is a scholar working on Cellular and Molecular Neuroscience, Insect Science and Ecology. According to data from OpenAlex, Koichi Suzuki has authored 31 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Cellular and Molecular Neuroscience, 15 papers in Insect Science and 9 papers in Ecology. Recurrent topics in Koichi Suzuki's work include Neurobiology and Insect Physiology Research (20 papers), Physiological and biochemical adaptations (9 papers) and Insect Utilization and Effects (7 papers). Koichi Suzuki is often cited by papers focused on Neurobiology and Insect Physiology Research (20 papers), Physiological and biochemical adaptations (9 papers) and Insect Utilization and Effects (7 papers). Koichi Suzuki collaborates with scholars based in Japan, Brazil and United States. Koichi Suzuki's co-authors include Eiichi Kuwano, Hiromasa Tanaka, Masato Sakai, Mitsuhiro Fujii, Gang Yu, Robert I. Glazer, Takashi Tsuruo, Shakeel Ahmad, Kenneth H. Cowan and Shigeo Ohno and has published in prestigious journals such as Peptides, Insect Biochemistry and Molecular Biology and Journal of Insect Physiology.

In The Last Decade

Koichi Suzuki

30 papers receiving 481 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Koichi Suzuki Japan 12 208 181 175 152 109 31 508
J.M. Van Doorn Netherlands 14 376 1.8× 226 1.2× 193 1.1× 116 0.8× 11 0.1× 25 653
Enen Guo China 8 273 1.3× 287 1.6× 243 1.4× 40 0.3× 37 0.3× 9 597
Anne‐Marie Courgeon France 13 265 1.3× 414 2.3× 175 1.0× 69 0.5× 11 0.1× 19 674
J K Kawooya United States 11 361 1.7× 246 1.4× 198 1.1× 91 0.6× 6 0.1× 13 761
Kun Qian China 15 84 0.4× 380 2.1× 309 1.8× 34 0.2× 24 0.2× 58 616
Damien Garrido France 10 111 0.5× 168 0.9× 75 0.4× 29 0.2× 18 0.2× 15 376
Julie C. Silver Canada 18 42 0.2× 528 2.9× 240 1.4× 123 0.8× 20 0.2× 39 835
Shiv Hiremath United States 14 96 0.5× 280 1.5× 185 1.1× 47 0.3× 10 0.1× 34 619
J. H. Sang United Kingdom 14 102 0.5× 294 1.6× 99 0.6× 30 0.2× 16 0.1× 31 497
Marina S. Defferrari Canada 13 114 0.5× 208 1.1× 160 0.9× 28 0.2× 19 0.2× 17 369

Countries citing papers authored by Koichi Suzuki

Since Specialization
Citations

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

Fields of papers citing papers by Koichi Suzuki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Koichi Suzuki

This figure shows the co-authorship network connecting the top 25 collaborators of Koichi Suzuki. A scholar is included among the top collaborators of Koichi Suzuki 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 Koichi Suzuki. Koichi Suzuki 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.
Kofujita, Hisayoshi, et al.. (2011). Morus alba leaf extract increases lifespan in Caenorhabditis elegans. Journal of insect biotechnology and sericology. 80(3). 89–92. 3 indexed citations
2.
GORYO, Masanobu, et al.. (2010). Hot-water extract of Paecilomyces tenuipes from the silkworm pupae improves d-galactose-induced brain aging in mice. Journal of insect biotechnology and sericology. 79(2). 45–51. 3 indexed citations
3.
Yang, Ping, Ying An, Kikukatsu Ito, et al.. (2010). A palmitoyl conjugate of insect pentapeptide Yamamarin arrests cell proliferation and respiration. Peptides. 31(5). 827–833. 7 indexed citations
4.
Kamiya, Masakatsu, Yoshinori Sato, Takuya Yokoyama, et al.. (2010). Structure–activity relationship of a novel pentapeptide with cancer cell growth‐inhibitory activity. Journal of Peptide Science. 16(5). 242–248. 3 indexed citations
5.
Yang, Ping, Hiromasa Tanaka, Eiichi Kuwano, & Koichi Suzuki. (2008). A novel cytochrome P450 gene (CYP4G25) of the silkmoth Antheraea yamamai: Cloning and expression pattern in pharate first instar larvae in relation to diapause. Journal of Insect Physiology. 54(3). 636–643. 28 indexed citations
6.
Yang, Ping, et al.. (2008). A Quinone Isolated from the Nest of Vespa simillima and Its Growth-Inhibitory Effect on Rat Liver Cancer Cells. Biological and Pharmaceutical Bulletin. 31(4). 722–725. 11 indexed citations
7.
Yang, Ping, et al.. (2007). A Palmitonyl Conjugate of an Insect Pentapeptide Causes Growth Arrest in Mammalian Cells and Mimics the Action of Diapause Hormone. Journal of insect biotechnology and sericology. 76(2). 6 indexed citations
8.
Fujita, Kosuke, et al.. (2005). Continuous rearing of an entomoresource, the leaf beetle, Gastrophysa atrocyanea Motschulsky (Coleoptera: Chrysomelidae) on artificial diets. Applied Entomology and Zoology. 40(1). 119–124. 7 indexed citations
9.
Yang, Ping, et al.. (2004). Growth Suppression of Rat Hepatoma Cells by a Pentapeptide from Antheraea yamamai. Journal of insect biotechnology and sericology. 73(1). 7–13. 20 indexed citations
10.
Tan, Anjiang, et al.. (2003). Identification of Novel Tissue-specific Proteins in the Suboesophageal Body of the Silkworm, Bombyx mori.. Journal of insect biotechnology and sericology. 72(1). 41–50. 13 indexed citations
11.
Tanaka, Hiromasa, Kenji Sato, Yoshimi Saito, et al.. (2003). Insect diapause-specific peptide from the leaf beetle has consensus with a putative iridovirus peptide. Peptides. 24(9). 1327–1333. 31 indexed citations
12.
Shimizu, Takayuki, et al.. (2002). Identification of an Imidazole Compound-Binding Protein from Diapausing Pharate First Instar Larvae of the Wild Silkmoth Antheraea yamamai. Journal of insect biotechnology and sericology. 71(1). 35–42. 6 indexed citations
13.
Song, Hongsheng, Ying An, Tetsuro Yamashita, & Koichi Suzuki. (2001). Antheraea yamamai paralytic peptide induces egg diapause as well as larval paralysis in Bombyx mori: The primary sequence-activity correlations. Journal of insect biotechnology and sericology. 70(1). 33–38. 2 indexed citations
14.
Sakai, Masato, Chengcang Wu, & Koichi Suzuki. (2001). Nucleotide and Deduced Amino Acid Sequences of a cDNA Encoding a Lipocalin Protein in the Central Nervous System of Bombyx mori. Journal of insect biotechnology and sericology. 70(2). 105–111. 10 indexed citations
15.
Sato, Yumiko, et al.. (1998). Identification of a novel member of the paralytic peptide family in the silkmoth Antheraea yamamai. Nihon sanshigaku zasshi. 67(6). 473–478. 6 indexed citations
16.
Goto, Michiyo, Mitsuhiro Fujii, Koichi Suzuki, & Masato Sakai. (1997). Factors affecting carbohydrate and free amino acid content in overwintering larvae of Enosima leucotaeniella. Journal of Insect Physiology. 44(1). 87–94. 51 indexed citations
18.
Suzuki, Koichi, et al.. (1986). Effect of anti-JH (KK-42) treatment on the breaking of the diapause of the eggs of the silkmoth, Antheraea yamamai. Nihon sanshigaku zasshi. 55(4). 305–308. 3 indexed citations
19.
Suzuki, Koichi, et al.. (1977). Studies on the Carbohydrate Metabolism of Diapause Eggs of Bombyx mori, with Special Reference to the Detection of Phosphofructokinase Activity. Nihon sanshigaku zasshi. 46(3). 213–219. 1 indexed citations
20.
Suzuki, Koichi, et al.. (1975). Studies on the Carbohydrate Metabolism in Diapause Eggs of the Silkworm, Bombyx mori, with Special Reference to Phosphofructokinase Activity. Nihon sanshigaku zasshi. 44(2). 88–97. 5 indexed citations

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