Taijun Myosho

1.3k total citations
20 papers, 874 citations indexed

About

Taijun Myosho is a scholar working on Genetics, Physiology and Reproductive Medicine. According to data from OpenAlex, Taijun Myosho has authored 20 papers receiving a total of 874 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 9 papers in Physiology and 6 papers in Reproductive Medicine. Recurrent topics in Taijun Myosho's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Reproductive biology and impacts on aquatic species (9 papers) and Sperm and Testicular Function (6 papers). Taijun Myosho is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers), Reproductive biology and impacts on aquatic species (9 papers) and Sperm and Testicular Function (6 papers). Taijun Myosho collaborates with scholars based in Japan, United Kingdom and Norway. Taijun Myosho's co-authors include Mitsuru Sakaizumi, Satoshi Hamaguchi, Masaru Matsuda, Yoko Kuroki, Kiyoshi Naruse, Asao Fujiyama, Hiroyuki Otake, Yusuke Takehana, Tadasu Shin‐I and Atsushi Toyoda and has published in prestigious journals such as Nature Communications, Environmental Science & Technology and The Science of The Total Environment.

In The Last Decade

Taijun Myosho

17 papers receiving 868 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Taijun Myosho Japan 10 794 456 185 165 118 20 874
Masatoshi Nakamoto Japan 16 1.0k 1.3× 723 1.6× 315 1.7× 311 1.9× 72 0.6× 19 1.2k
M. Oura Japan 5 526 0.7× 365 0.8× 104 0.6× 118 0.7× 45 0.4× 5 586
Masashi Fujita Japan 5 509 0.6× 232 0.5× 121 0.7× 69 0.4× 103 0.9× 5 575
Zhihong Shan United States 6 699 0.9× 313 0.7× 270 1.5× 174 1.1× 136 1.2× 8 785
Ayaka Yano France 13 997 1.3× 621 1.4× 204 1.1× 192 1.2× 136 1.2× 19 1.2k
Mateus Contar Adolfi Germany 13 387 0.5× 220 0.5× 120 0.6× 79 0.5× 70 0.6× 26 503
Sullip Kumar Majhi India 9 517 0.7× 411 0.9× 106 0.6× 157 1.0× 49 0.4× 29 681
Qingping Xie China 14 417 0.5× 243 0.5× 188 1.0× 118 0.7× 34 0.3× 29 639
Marina Govoroun France 17 1.1k 1.4× 863 1.9× 338 1.8× 347 2.1× 54 0.5× 24 1.4k
En‐Lieng Lau Taiwan 12 522 0.7× 439 1.0× 102 0.6× 161 1.0× 30 0.3× 12 619

Countries citing papers authored by Taijun Myosho

Since Specialization
Citations

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

Fields of papers citing papers by Taijun Myosho

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taijun Myosho

This figure shows the co-authorship network connecting the top 25 collaborators of Taijun Myosho. A scholar is included among the top collaborators of Taijun Myosho 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 Taijun Myosho. Taijun Myosho 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.
Myosho, Taijun, et al.. (2026). Effects of cyp19a1a and cyp19a1b Knockout on Germ Cell Kinetics During Gonadal Sex Differentiation in Medaka. Development Growth & Differentiation. 68(1). e70038–e70038.
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Hirasaka, Katsuya, et al.. (2024). Environmental DNA Reveals Geographic Distributions of Two eel Species, Anguilla japonica and A. marmorata, in Western Kyushu, Japan. ZOOLOGICAL SCIENCE. 41(4). 392–399. 1 indexed citations
4.
Fujimoto, Shingo, Taijun Myosho, Mitsuharu Yagi, et al.. (2024). Evolution of Size‐Fecundity Relationship in Medaka Fish From Different Latitudes. Molecular Ecology. 33(23). e17578–e17578. 4 indexed citations
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Kanamori, Akira, A. Oota, Taijun Myosho, et al.. (2023). Wnt4a Is Indispensable for Genital Duct Elongation but Not for Gonadal Sex Differentiation in the Medaka, Oryzias latipes. ZOOLOGICAL SCIENCE. 40(5). 348–359. 1 indexed citations
7.
Myosho, Taijun, et al.. (2023). Levonorgestrel causes feminization and dose-dependent masculinization in medaka fish (Oryzias latipes): Endocrine-disruption activity and its correlation with sex reversal. The Science of The Total Environment. 876. 162740–162740. 22 indexed citations
8.
Fujimoto, Shingo, et al.. (2022). Population admixtures in medaka inferred by multiple arbitrary amplicon sequencing. Scientific Reports. 12(1). 19989–19989. 2 indexed citations
9.
Myosho, Taijun, et al.. (2022). Preself-Feeding Medaka Fry Provides a Suitable Screening System for in Vivo Assessment of Thyroid Hormone-Disrupting Potential. Environmental Science & Technology. 56(10). 6479–6490. 12 indexed citations
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Myosho, Taijun, Tadashi Sato, Jun Yamamoto, et al.. (2019). Inter- and Intraspecific Variation in Sex Hormone-Induced Sex-Reversal in Medaka, Oryzias latipes and Oryzias sakaizumii. ZOOLOGICAL SCIENCE. 36(5). 425–425. 7 indexed citations
12.
Myosho, Taijun, Hideya Takahashi, Tadashi Sato, et al.. (2018). Hyperosmotic tolerance of adult fish and early embryos are determined by discrete, single loci in the genus Oryzias. Scientific Reports. 8(1). 6897–6897. 12 indexed citations
13.
Ogino, Yukiko, Anke Lange, Taijun Myosho, et al.. (2017). Establishment of estrogen receptor 1 (ESR1)‐knockout medaka: ESR1 is dispensable for sexual development and reproduction in medaka, Oryzias latipes. Development Growth & Differentiation. 59(6). 552–561. 29 indexed citations
14.
Kobayashi, Tohru, Ayaka Chiba, Tadashi Sato, et al.. (2017). Estrogen alters gonadal soma-derived factor (Gsdf)/Foxl2 expression levels in the testes associated with testis-ova differentiation in adult medaka, Oryzias latipes. Aquatic Toxicology. 191. 209–218. 27 indexed citations
15.
Horie, Yoshifumi, Taijun Myosho, Tadashi Sato, et al.. (2016). Androgen induces gonadal soma-derived factor, Gsdf, in XX gonads correlated to sex-reversal but not Dmrt1 directly, in the teleost fish, northern medaka (Oryzias sakaizumii). Molecular and Cellular Endocrinology. 436. 141–149. 41 indexed citations
16.
Myosho, Taijun, Yusuke Takehana, Satoshi Hamaguchi, & Mitsuru Sakaizumi. (2015). Turnover of Sex Chromosomes in Celebensis Group Medaka Fishes. G3 Genes Genomes Genetics. 5(12). 2685–2691. 71 indexed citations
17.
Takehana, Yusuke, Masaru Matsuda, Taijun Myosho, et al.. (2014). Co-option of Sox3 as the male-determining factor on the Y chromosome in the fish Oryzias dancena. Nature Communications. 5(1). 4157–4157. 245 indexed citations
18.
Myosho, Taijun, Hiroyuki Otake, Masaru Matsuda, et al.. (2012). Tracing the Emergence of a Novel Sex-Determining Gene in Medaka, Oryzias luzonensis. Genetics. 191(1). 163–170. 376 indexed citations
19.
Myosho, Taijun, Yusuke Takehana, Tadashi Sato, Satoshi Hamaguchi, & Mitsuru Sakaizumi. (2012). The origin of the large metacentric chromosome pair in Chinese medaka (Oryzias sinensis). Ichthyological Research. 59(4). 384–388. 5 indexed citations
20.
Otake, Hiroyuki, Ai Shinomiya, Taijun Myosho, et al.. (2009). Heritable artificial sex chromosomes in the medaka, Oryzias latipes. Heredity. 105(3). 247–256. 14 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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