Yutaka Banno

4.4k total citations
156 papers, 3.3k citations indexed

About

Yutaka Banno is a scholar working on Insect Science, Molecular Biology and Biomaterials. According to data from OpenAlex, Yutaka Banno has authored 156 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Insect Science, 72 papers in Molecular Biology and 66 papers in Biomaterials. Recurrent topics in Yutaka Banno's work include Silkworms and Sericulture Research (70 papers), Silk-based biomaterials and applications (66 papers) and Neurobiology and Insect Physiology Research (53 papers). Yutaka Banno is often cited by papers focused on Silkworms and Sericulture Research (70 papers), Silk-based biomaterials and applications (66 papers) and Neurobiology and Insect Physiology Research (53 papers). Yutaka Banno collaborates with scholars based in Japan, China and United States. Yutaka Banno's co-authors include Hiroshi Fujii, Kohji Yamamoto, Toru Shimada, Yoichi Aso, Susumu Katsuma, Kazuei Mita, Hideki Sezutsu, Tsuguru Fujii, Haruhiko Fujiwara and Kozo Tsuchida and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Yutaka Banno

150 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
Yutaka Banno Japan 35 1.7k 1.6k 1.1k 836 667 156 3.3k
Kostas Iatrou Greece 37 2.3k 1.4× 1.3k 0.8× 1.3k 1.2× 306 0.4× 1.0k 1.5× 103 3.7k
Keiko Kadono‐Okuda Japan 27 1.2k 0.7× 1.1k 0.7× 591 0.5× 386 0.5× 402 0.6× 63 2.2k
Qili Feng China 35 2.2k 1.3× 1.8k 1.1× 1.2k 1.0× 318 0.4× 781 1.2× 144 3.9k
Cheng Lu China 28 1.9k 1.1× 1.0k 0.6× 543 0.5× 457 0.5× 531 0.8× 194 2.9k
Luc Swevers Greece 38 2.0k 1.2× 1.6k 1.0× 959 0.9× 157 0.2× 598 0.9× 135 3.5k
Masafumi Iwami Japan 29 975 0.6× 679 0.4× 1.2k 1.1× 242 0.3× 631 0.9× 78 2.3k
Ping Zhao China 25 1.6k 1.0× 952 0.6× 715 0.6× 481 0.6× 555 0.8× 141 2.8k
Kozo Tsuchida Japan 20 729 0.4× 592 0.4× 659 0.6× 363 0.4× 284 0.4× 57 1.7k
Marek Jindra Czechia 31 1.5k 0.9× 1.6k 1.0× 2.6k 2.3× 172 0.2× 1.5k 2.2× 59 4.1k
Takaaki Daimon Japan 29 1.6k 0.9× 1.2k 0.8× 812 0.7× 296 0.4× 727 1.1× 71 2.7k

Countries citing papers authored by Yutaka Banno

Since Specialization
Citations

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

Fields of papers citing papers by Yutaka Banno

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yutaka Banno

This figure shows the co-authorship network connecting the top 25 collaborators of Yutaka Banno. A scholar is included among the top collaborators of Yutaka Banno 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 Yutaka Banno. Yutaka Banno 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.
Lee, Jae Man, Tsuguru Fujii, Hiroaki Mon, et al.. (2023). The biological role of core 1β1-3galactosyltransferase (T-synthase) in mucin-type O-glycosylation in Silkworm, Bombyx mori. Insect Biochemistry and Molecular Biology. 156. 103936–103936.
2.
Banno, Yutaka, et al.. (2018). Application of the v-cryoplate method for the cryopreservation of silkworm embryos. Journal of insect biotechnology and sericology. 87(3). 89–96. 2 indexed citations
3.
Kondo, Yusuke, T. Ando, Jun‐ichi Yamaguchi, et al.. (2017). Toll ligand Spätzle3 controls melanization in the stripe pattern formation in caterpillars. Proceedings of the National Academy of Sciences. 114(31). 8336–8341. 27 indexed citations
4.
Yamaguchi, Jun‐ichi, Kazuei Mita, Kimiko Yamamoto, et al.. (2014). The transcription factor Apontic-like controls diverse colouration pattern in caterpillars. Nature Communications. 5(1). 4936–4936. 35 indexed citations
5.
Yamamoto, Kazuo, et al.. (2011). Characterization of an omega‐class glutathione S‐transferase in the stress response of the silkmoth. Insect Molecular Biology. 20(3). 379–386. 36 indexed citations
6.
Banno, Yutaka, et al.. (2010). Integration of the twenty-fourth and twenty-seventh linkage groups of the silkwom, Bombyx mori. Journal of insect biotechnology and sericology. 79(2). 67–70. 2 indexed citations
7.
Futahashi, Ryo, Yan Meng, Takaaki Daimon, et al.. (2008). yellow and ebony Are the Responsible Genes for the Larval Color Mutants of the Silkworm Bombyx mori. Genetics. 180(4). 1995–2005. 112 indexed citations
8.
Lee, Jae Man, Hiroaki Mon, Masateru Takahashi, et al.. (2007). Screening of High-permissive Silkworm Strains for Efficient Recombinant Protein Production in Autographa californica Nuclear Polyhedrosis Virus (AcNPV). Journal of insect biotechnology and sericology. 76(2). 101–105. 10 indexed citations
9.
Kawanishi, Yuichi, et al.. (2007). Sequence Comparison of Mariner-like Elements among the Populations of Bombyx mandarina Inhabiting China, Korea and Japan. Journal of insect biotechnology and sericology. 76(2). 79–87. 4 indexed citations
10.
He, Ningjia, et al.. (2006). Genetic Analysis of Basic Chymotrypsin Inhibitors in the Hemolymph of the Silkworm, Bombyx mori. Journal of insect biotechnology and sericology. 75(2). 65–69. 2 indexed citations
11.
Takada, Naoko, Emiko Yamauchi, Hirofumi Fujimoto, et al.. (2006). A Novel Indicator for Radiation Sensitivity Using the Wing Size Reduction of Bombyx mori Pupae Caused by γ-ray Irradiation. Journal of insect biotechnology and sericology. 75(3). 161–165. 5 indexed citations
12.
Nakamura, Takashi, Yutaka Banno, & Hiroshi Fujii. (2001). Genetics of the "Wild Silkworm Translucent" Mutant (ows) Discovered in the Progenies after the Cross between the Domesticated Silkworm, Bombyx mori and the wild Mulberry Silkworm, Bombyx mandarina. 6. 7–10. 2 indexed citations
13.
Shirai, Koji, et al.. (2000). Purification of 35K protease from the digestive juice of Bombyx mori. Nihon sanshigaku zasshi. 69(1). 47–53. 4 indexed citations
14.
Miura, Yoshiko, et al.. (2000). Aseptic Rearing of the Mulberry Wild Silkworm, Bombyx mandarina. 5. 69–70.
15.
Kawaguchi, Yutaka, et al.. (1997). Genetic analysis of the “translucent-15” mutant in Bombyx mori. Nihon sanshigaku zasshi. 66(2). 113–115. 2 indexed citations
16.
Kawaguchi, Yutaka, et al.. (1996). Features and growth of the stemmata in the varnished eye mutant of Bombyx mori. Nihon sanshigaku zasshi. 65(6). 441–446. 1 indexed citations
17.
Kawaguchi, Yutaka, et al.. (1993). Inheritance of a new mutant, “shirotae-ran” in Bombyx mori. Nihon sanshigaku zasshi. 62(1). 88–90. 6 indexed citations
18.
Kawaguchi, Yutaka, Yutaka Banno, Katsumi Koga, & Hiroshi Fujii. (1992). Effect of 20-hydroxyecdysone application on the expression of the egg-shape determining genes in Bombyx mori. Nihon sanshigaku zasshi. 61(2). 145–149. 2 indexed citations
19.
Doira, Hiroshi, et al.. (1984). Genetical studies on the “non-molting dwarf” mutation in Bombyx mori. Nihon sanshigaku zasshi. 53(5). 427–431. 4 indexed citations
20.
Banno, Yutaka, Yutaka Kawaguchi, & Hiroshi Doira. (1984). Sexual dimorphism and developmental changes in hemolymph amylase of Bombyx mori. Nihon sanshigaku zasshi. 53(4). 335–340. 2 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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