Miyuki Kanda

2.5k total citations · 1 hit paper
29 papers, 1.4k citations indexed

About

Miyuki Kanda is a scholar working on Ecology, Molecular Biology and Global and Planetary Change. According to data from OpenAlex, Miyuki Kanda has authored 29 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Ecology, 9 papers in Molecular Biology and 9 papers in Global and Planetary Change. Recurrent topics in Miyuki Kanda's work include Coral and Marine Ecosystems Studies (7 papers), Marine Ecology and Invasive Species (6 papers) and Ichthyology and Marine Biology (4 papers). Miyuki Kanda is often cited by papers focused on Coral and Marine Ecosystems Studies (7 papers), Marine Ecology and Invasive Species (6 papers) and Ichthyology and Marine Biology (4 papers). Miyuki Kanda collaborates with scholars based in Japan, United States and Ireland. Miyuki Kanda's co-authors include Y. Otsuki, Kazuhiko Sugimoto, Hidehito Tsugawa, Hirohiko Hirochika, Noriyuki Satoh, Ryo Koyanagi, Manabu Fujie, Chuya Shinzato, Yi‐Jyun Luo and Takeshi Takeuchi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Development.

In The Last Decade

Miyuki Kanda

28 papers receiving 1.4k citations

Hit Papers

Retrotransposons of rice involved in mutations induced by... 1996 2026 2006 2016 1996 100 200 300 400 500
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Retrotransposons of rice involved in mutations induced by tissue culture.
    1996 596 citations Hirohiko Hirochika, Kazuhiko Sugimoto et al. Proceedings of the National Academy of Sciences profile →

Peers

Miyuki Kanda
Guifré Torruella France
Oliver Voigt Germany
Xavier Grau‐Bové Spain
Jaime E. Blair United States
Muriel Jager France
Béatrice Roure Canada
Galina V. Aglyamova United States
Walker Pett United States
Craig Michell Saudi Arabia
Nathan J. Kenny United Kingdom
Guifré Torruella France
Miyuki Kanda
Citations per year, relative to Miyuki Kanda Miyuki Kanda (= 1×) peers Guifré Torruella

Countries citing papers authored by Miyuki Kanda

Since Specialization
Citations

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

Fields of papers citing papers by Miyuki Kanda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miyuki Kanda

This figure shows the co-authorship network connecting the top 25 collaborators of Miyuki Kanda. A scholar is included among the top collaborators of Miyuki Kanda 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 Miyuki Kanda. Miyuki Kanda 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.
Mukhopadhyay, Asish K., Goutam Chowdhury, Fumito Maruyama, et al.. (2024). Genomic epidemiology and genetic characteristics of clinical Campylobacter species cocirculating in West Bengal, India, 2019, using whole genome analysis. Antimicrobial Agents and Chemotherapy. 69(1). e0110824–e0110824. 1 indexed citations
2.
Shikina, Shinya, Yuki Yoshioka, T. Uchida, et al.. (2024). Genome and tissue-specific transcriptomes of the large-polyp coral, Fimbriaphyllia (Euphyllia) ancora: a recipe for a coral polyp. Communications Biology. 7(1). 899–899. 1 indexed citations
3.
Higashiura, Akifumi, Yoko Mizoguchi, Takao Hashiguchi, et al.. (2023). Structural basis of spike RBM-specific human antibodies counteracting broad SARS-CoV-2 variants. Communications Biology. 6(1). 395–395. 5 indexed citations
4.
Tsutani, Yasuhiro, Miyuki Kanda, Yuki Yamamoto, et al.. (2020). Diagnostic performance of peripheral leukocyte telomere G‐tail length for detecting breast cancer. Cancer Science. 111(5). 1856–1861. 9 indexed citations
5.
Khalturin, Konstantin, Chuya Shinzato, Mayuko Hamada, et al.. (2019). Publisher Correction: Medusozoan genomes inform the evolution of the jellyfish body plan. Nature Ecology & Evolution. 3(6). 989–989. 1 indexed citations
6.
Khalturin, Konstantin, Chuya Shinzato, Mayuko Hamada, et al.. (2019). Medusozoan genomes inform the evolution of the jellyfish body plan. Nature Ecology & Evolution. 3(5). 811–822. 83 indexed citations
7.
Lu, Tsai-Ming, Miyuki Kanda, Hidetaka Furuya, & Noriyuki Satoh. (2019). Dicyemid Mesozoans: A Unique Parasitic Lifestyle and a Reduced Genome. Genome Biology and Evolution. 11(8). 2232–2243. 17 indexed citations
8.
Phuong, Nguyen Thanh, Eiichi Shoguchi, Kanako Hisata, et al.. (2018). A draft genome of the striped catfish, Pangasianodon hypophthalmus, for comparative analysis of genes relevant to development and a resource for aquaculture improvement. BMC Genomics. 19(1). 733–733. 35 indexed citations
9.
Lu, Tsai-Ming, Miyuki Kanda, Noriyuki Satoh, & Hidetaka Furuya. (2017). The phylogenetic position of dicyemid mesozoans offers insights into spiralian evolution. Zoological Letters. 3(1). 6–6. 32 indexed citations
10.
Luo, Yi‐Jyun, Miyuki Kanda, Ryo Koyanagi, et al.. (2017). Nemertean and phoronid genomes reveal lophotrochozoan evolution and the origin of bilaterian heads. Nature Ecology & Evolution. 2(1). 141–151. 90 indexed citations
11.
Nakano, Hiroaki, Akiteru Maeno, Toshihiko Shiroishi, et al.. (2017). A new species of Xenoturbella from the western Pacific Ocean and the evolution of Xenoturbella. BMC Evolutionary Biology. 17(1). 245–245. 11 indexed citations
12.
Campbell, Matthew A., Jørgen Nielsen, Tetsuya Sado, et al.. (2017). Evolutionary affinities of the unfathomable Parabrotulidae: Molecular data indicate placement of Parabrotula within the family Bythitidae, Ophidiiformes. Molecular Phylogenetics and Evolution. 109. 337–342. 8 indexed citations
13.
Takeuchi, Takeshi, Ryo Koyanagi, Fuki Gyoja, et al.. (2016). Bivalve-specific gene expansion in the pearl oyster genome: implications of adaptation to a sessile lifestyle. Zoological Letters. 2(1). 3–3. 125 indexed citations
14.
Luo, Yi‐Jyun, Takeshi Takeuchi, Ryo Koyanagi, et al.. (2015). The Lingula genome provides insights into brachiopod evolution and the origin of phosphate biomineralization. Nature Communications. 6(1). 8301–8301. 145 indexed citations
15.
Kanda, Miyuki, et al.. (2013). Retinoid X receptor-mediated transdifferentiation cascade in budding tunicates. Developmental Biology. 384(2). 343–355. 17 indexed citations
16.
Kanda, Miyuki, et al.. (2013). Identification of a retinoic acid‐responsive neural enhancer in the Ciona intestinalis Hox1 gene. Development Growth & Differentiation. 55(2). 260–269. 9 indexed citations
17.
Sasakura, Yasunori, Miyuki Kanda, Takeo Horie, et al.. (2012). Retinoic acid-driven Hox1 is required in the epidermis for forming the otic/atrial placodes during ascidian metamorphosis. Development. 139(12). 2156–2160. 43 indexed citations
18.
Kanda, Miyuki, Hiroshi Wada, & Shigeki Fujiwara. (2009). Epidermal expression of Hox1 is directly activated by retinoic acid in the Ciona intestinalis embryo. Developmental Biology. 335(2). 454–463. 26 indexed citations
19.
Hirochika, Hirohiko, Kazuhiko Sugimoto, Y. Otsuki, Hidehito Tsugawa, & Miyuki Kanda. (1996). Retrotransposons of rice involved in mutations induced by tissue culture.. Proceedings of the National Academy of Sciences. 93(15). 7783–7788. 596 indexed citations breakdown →
20.
Mitsunaga‐Nakatsubo, Keiko, Miyuki Kanda, Ken Yamazaki, et al.. (1992). Expression of Na+, K+‐ATPase α‐Subunit in Animalized and Vegetalized Embryos of the Sea Urchin, Hemicentrotus pulcherrimus.. Development Growth & Differentiation. 34(6). 677–684. 5 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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