Takashi Kiuchi

2.5k total citations · 1 hit paper
62 papers, 1.6k citations indexed

About

Takashi Kiuchi is a scholar working on Insect Science, Molecular Biology and Genetics. According to data from OpenAlex, Takashi Kiuchi has authored 62 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Insect Science, 30 papers in Molecular Biology and 16 papers in Genetics. Recurrent topics in Takashi Kiuchi's work include Silkworms and Sericulture Research (19 papers), Silk-based biomaterials and applications (15 papers) and Invertebrate Immune Response Mechanisms (14 papers). Takashi Kiuchi is often cited by papers focused on Silkworms and Sericulture Research (19 papers), Silk-based biomaterials and applications (15 papers) and Invertebrate Immune Response Mechanisms (14 papers). Takashi Kiuchi collaborates with scholars based in Japan, United States and China. Takashi Kiuchi's co-authors include Susumu Katsuma, Toru Shimada, Munetaka Kawamoto, Keisuke Shoji, Yutaka Suzuki, Sumio Sugano, Takaaki Daimon, Shinpei Kawaoka, Masataka G. Suzuki and Hiroki Sakai and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Takashi Kiuchi

60 papers receiving 1.6k citations

Hit Papers

A single female-specific piRNA is the primary determiner ... 2014 2026 2018 2022 2014 100 200 300

Peers

Takashi Kiuchi
Mi Young Noh South Korea
Takashi Kiuchi
Citations per year, relative to Takashi Kiuchi Takashi Kiuchi (= 1×) peers Mi Young Noh

Countries citing papers authored by Takashi Kiuchi

Since Specialization
Citations

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

Fields of papers citing papers by Takashi Kiuchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Takashi Kiuchi

This figure shows the co-authorship network connecting the top 25 collaborators of Takashi Kiuchi. A scholar is included among the top collaborators of Takashi Kiuchi 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 Takashi Kiuchi. Takashi Kiuchi 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, Jung, Takashi Kiuchi, Katsushi Yamaguchi, et al.. (2025). A chromosome-level genome assembly of wild silkmoth, Bombyx mandarina. Scientific Data. 12(1). 27–27. 2 indexed citations
2.
Kiuchi, Takashi, Keisuke Shoji, Natsuko Izumi, Yukihide Tomari, & Susumu Katsuma. (2023). Non-gonadal somatic piRNA pathways ensure sexual differentiation, larval growth, and wing development in silkworms. PLoS Genetics. 19(9). e1010912–e1010912. 5 indexed citations
3.
Shoji, Keisuke, et al.. (2023). Masculinizer is not post-transcriptionally regulated by female-specific piRNAs during sex determination in the Asian corn borer, Ostrinia furnacalis. Insect Biochemistry and Molecular Biology. 156. 103946–103946. 5 indexed citations
4.
Kawamoto, Munetaka, et al.. (2022). Masculinizer-induced dosage compensation is achieved by transcriptional downregulation of both copies of Z-linked genes in the silkworm, Bombyx mori. Biology Letters. 18(9). 20220116–20220116. 12 indexed citations
5.
Katsuma, Susumu, Kohei Nishino, Hidetaka Kosako, et al.. (2022). A Wolbachia factor for male killing in lepidopteran insects. Nature Communications. 13(1). 6764–6764. 43 indexed citations
6.
Izumi, Natsuko, Keisuke Shoji, Takashi Kiuchi, Susumu Katsuma, & Yukihide Tomari. (2022). The two Gtsf paralogs in silkworms orthogonally activate their partner PIWI proteins for target cleavage. RNA. 29(1). 18–29. 8 indexed citations
7.
Katsuma, Susumu, et al.. (2022). Transcriptome analysis in the silkworm Bombyx mori overexpressing piRNA-resistant Masculinizer gene. Biochemical and Biophysical Research Communications. 616. 104–109.
8.
Matsuzaki, Shohei, Kazutoshi Yoshitake, Kimiko Yamamoto, et al.. (2021). Mutations in a β-group of solute carrier gene are responsible for egg and eye coloration of the brown egg 4 (b-4) mutant in the silkworm, Bombyx mori. Insect Biochemistry and Molecular Biology. 137. 103624–103624. 2 indexed citations
9.
Ulmer, Jonathan, Takashi Kiuchi, Florent Dingli, et al.. (2020). CenH3-Independent Kinetochore Assembly in Lepidoptera Requires CCAN, Including CENP-T. Current Biology. 30(4). 561–572.e10. 45 indexed citations
10.
Shimada, Toru, et al.. (2019). CRISPR/Cas9-mediated somatic mutation of the sex-linked translucent (os) gene in the silkworm, Bombyx mori. Journal of insect biotechnology and sericology. 88(2). 4 indexed citations
11.
Kiuchi, Takashi, et al.. (2018). In vivo masculinizing function of the Ostrinia furnacalis Masculinizer gene. Biochemical and Biophysical Research Communications. 503(3). 1768–1772. 20 indexed citations
12.
Takai, Hiroki, Rika Ozawa, Junji Takabayashi, et al.. (2018). Silkworms suppress the release of green leaf volatiles by mulberry leaves with an enzyme from their spinnerets. Scientific Reports. 8(1). 11942–11942. 29 indexed citations
13.
Zhang, Haokun, Takashi Kiuchi, Chikara Hirayama, et al.. (2018). A reexamination on the deficiency of riboflavin accumulation in Malpighian tubules in larval translucent mutants of the silkworm, Bombyx mori. Genetica. 146(4-5). 425–431. 4 indexed citations
14.
15.
Sakai, Hiroki, Megumi Sumitani, Keiro Uchino, et al.. (2016). Transgenic Expression of the piRNA-Resistant Masculinizer Gene Induces Female-Specific Lethality and Partial Female-to-Male Sex Reversal in the Silkworm, Bombyx mori. PLoS Genetics. 12(8). e1006203–e1006203. 33 indexed citations
16.
Katsuma, Susumu, et al.. (2015). Two Conserved Cysteine Residues Are Required for the Masculinizing Activity of the Silkworm Masc Protein. Journal of Biological Chemistry. 290(43). 26114–26124. 29 indexed citations
17.
Katsuma, Susumu, Munetaka Kawamoto, & Takashi Kiuchi. (2014). Guardian small RNAs and sex determination. RNA Biology. 11(10). 1238–1242. 13 indexed citations
18.
Shoji, Keisuke, Munetaka Kawamoto, Takashi Kiuchi, et al.. (2014). Silkworm HP1a transcriptionally enhances highly expressed euchromatic genes via association with their transcription start sites. Nucleic Acids Research. 42(18). 11462–11471. 11 indexed citations
19.
Yagi, Naomi, et al.. (1999). Bioavailability and Diuretic Effect after Administration of Retarded Capsules of Bumetanide in Human Subjects.. Biological and Pharmaceutical Bulletin. 22(3). 275–280. 3 indexed citations
20.
Yagi, Naomi, et al.. (1996). Bioavailability and Diuretic Effect of Furosemide Following Administration of Tablets and Retarded Capsules to Human Subjects.. Biological and Pharmaceutical Bulletin. 19(4). 616–622. 6 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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