Hayato Yokoi

1.2k total citations
43 papers, 812 citations indexed

About

Hayato Yokoi is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Hayato Yokoi has authored 43 papers receiving a total of 812 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 20 papers in Genetics and 8 papers in Physiology. Recurrent topics in Hayato Yokoi's work include Developmental Biology and Gene Regulation (11 papers), Animal Genetics and Reproduction (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Hayato Yokoi is often cited by papers focused on Developmental Biology and Gene Regulation (11 papers), Animal Genetics and Reproduction (10 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Hayato Yokoi collaborates with scholars based in Japan, United States and Germany. Hayato Yokoi's co-authors include John H. Postlethwait, Cristian Cañestro, Tohru Suzuki, Julian Catchen, Minoru Tanaka, Yuko Wakamatsu, Hiroyuki Takeda, Kenjiro Ozato, Susumu Uji and Daisuke Kobayashi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Nature Reviews Genetics.

In The Last Decade

Hayato Yokoi

41 papers receiving 803 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hayato Yokoi Japan 16 374 360 194 90 81 43 812
Sumanty Tohari Singapore 9 319 0.9× 553 1.5× 233 1.2× 58 0.6× 92 1.1× 18 915
Peter Batzel United States 13 406 1.1× 468 1.3× 213 1.1× 64 0.7× 80 1.0× 21 927
Evelyn Chiang Taiwan 7 202 0.5× 432 1.2× 262 1.4× 50 0.6× 40 0.5× 8 640
Frédéric Sohm France 14 551 1.5× 276 0.8× 102 0.5× 216 2.4× 92 1.1× 19 1.1k
Jérémy Pasquier France 13 316 0.8× 425 1.2× 210 1.1× 44 0.5× 109 1.3× 21 842
Thomas Desvignes United States 18 490 1.3× 232 0.6× 146 0.8× 55 0.6× 125 1.5× 50 976
Tomasz Furmanek Norway 22 651 1.7× 473 1.3× 217 1.1× 140 1.6× 238 2.9× 55 1.5k
Rajini Sreenivasan Australia 15 578 1.5× 810 2.3× 426 2.2× 62 0.7× 57 0.7× 24 1.2k
Oriane Marchand France 9 392 1.0× 223 0.6× 158 0.8× 145 1.6× 132 1.6× 12 845
Francesco Aniello Italy 22 759 2.0× 202 0.6× 56 0.3× 62 0.7× 46 0.6× 78 1.4k

Countries citing papers authored by Hayato Yokoi

Since Specialization
Citations

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

Fields of papers citing papers by Hayato Yokoi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hayato Yokoi

This figure shows the co-authorship network connecting the top 25 collaborators of Hayato Yokoi. A scholar is included among the top collaborators of Hayato Yokoi 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 Hayato Yokoi. Hayato Yokoi 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.
Tsuda, T., Umberto Rosani, Hayato Yokoi, et al.. (2025). Simple Transgene Overexpression using Scallop Hemocyte Culture Platform Enables Functional Genetic Research in Molluscs. Marine Biotechnology. 27(3). 94–94.
2.
Yokoi, Hayato, et al.. (2023). Vitellogenin uptake activity in the intestinal ducts of intraovarian embryos in a viviparous teleost Xenotoca eiseni. Biochemical and Biophysical Research Communications. 644. 79–84.
3.
Iida, Atsuo, et al.. (2022). Endocytosis-mediated vitellogenin absorption and lipid metabolism in the hindgut-derived placenta of the viviparous teleost Xenotoca eiseni. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1867(9). 159183–159183. 2 indexed citations
4.
Iida, Atsuo, Hiroyuki Arai, Mayu Inokuchi, et al.. (2019). Mother-to-embryo vitellogenin transport in a viviparous teleost Xenotoca eiseni. Proceedings of the National Academy of Sciences. 116(44). 22359–22365. 22 indexed citations
5.
Suzuki, Nobuo, et al.. (2018). Identification of Sox10‐positive cells at the dorsal fin base of juvenile flounder that are correlated with blind‐side skin ectopic pigmentation. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 330(8). 427–437. 3 indexed citations
6.
Chen, Qiran, Hayato Yokoi, & Tohru Suzuki. (2018). Expression profiles of RA synthases and catabolic enzymes in newly hatched and metamorphosing larvae of Japanese flounder, Paralichthys olivaceus. General and Comparative Endocrinology. 269. 60–67. 1 indexed citations
7.
Wu, Xiaoming, Qiran Chen, Youhei Washio, Hayato Yokoi, & Tohru Suzuki. (2016). Excess Retinoic Acid Induces Fusion of Centra by Degenerating Intervertebral Ligament Cells in Japanese flounder, Paralichthys olivaceus. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 326(8). 464–473. 7 indexed citations
8.
Shen, Jialing, et al.. (2016). Diethylnitrosamine-induced expression of germline-specific genes and pluripotency factors, including vasa and oct4, in medaka somatic cells. Biochemical and Biophysical Research Communications. 478(2). 858–863. 4 indexed citations
10.
Matsuda, Masaru, et al.. (2014). TALEN‐mediated mutagenesis in zebrafish reveals a role for r‐spondin 2 in fin ray and vertebral development. FEBS Letters. 588(24). 4543–4550. 21 indexed citations
11.
Washio, Youhei, et al.. (2013). Ocular‐Side Lateralization of Adult‐Type Chromatophore Precursors: Development of Pigment Asymmetry in Metamorphosing Flounder Larvae. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 320(3). 151–165. 8 indexed citations
12.
Kawanishi, Toru, Takuya Kaneko, Masato Kinoshita, et al.. (2013). Modular development of the teleost trunk along the dorsoventral axis and zic1/zic4 as selector genes in the dorsal module. Development. 140(7). 1486–1496. 15 indexed citations
13.
Shimizu, Daisuke, et al.. (2012). Circadian pacemaker in the suprachiasmatic nuclei of teleost fish revealed by rhythmic period2 expression. General and Comparative Endocrinology. 178(2). 400–407. 37 indexed citations
14.
Yokoi, Hayato, Yi‐Lin Yan, Michael R. Miller, et al.. (2009). Expression profiling of zebrafish sox9 mutants reveals that Sox9 is required for retinal differentiation. Developmental Biology. 329(1). 1–15. 46 indexed citations
15.
Yan, Yi‐Lin, Xinjun He, Julian Catchen, et al.. (2009). Evolution of developmental regulation in the vertebrate FgfD subfamily. Journal of Experimental Zoology Part B Molecular and Developmental Evolution. 314B(1). 33–56. 26 indexed citations
16.
Nakamura, Shuhei, Daisuke Kobayashi, Yumiko Aoki, et al.. (2006). Identification and lineage tracing of two populations of somatic gonadal precursors in medaka embryos. Developmental Biology. 295(2). 678–688. 75 indexed citations
17.
Ohtsuka, Masato, Hayato Yokoi, Masato Kinoshita, et al.. (2004). Possible roles of zic1 and zic4, identified within the medaka Double anal fin (Da) locus, in dorsoventral patterning of the trunk-tail region (related to phenotypes of the Da mutant). Mechanisms of Development. 121(7-8). 873–882. 20 indexed citations
18.
Kudo, Hisaaki, Keiji Inohaya, Hayato Yokoi, et al.. (2004). A mutation in the gene for δ-aminolevulinic acid dehydratase (ALAD) causes hypochromic anemia in the medaka, Oryzias latipes. Mechanisms of Development. 121(7-8). 747–752. 18 indexed citations
19.
Yokoi, Hayato, et al.. (2003). Cloning and embryonic expression of six wnt genes in the medaka (Oryzias latipes) with special reference to expression of wnt5a in the pectoral fin buds. Development Growth & Differentiation. 45(1). 51–61. 17 indexed citations
20.
Yokoi, Hayato, Tohru Kobayashi, Minoru Tanaka, et al.. (2002). sox9 in a teleost fish, medaka (Oryzias latipes): Evidence for diversified function of Sox9 in gonad differentiation. Molecular Reproduction and Development. 63(1). 5–16. 90 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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