Yoshihito Okamura

727 total citations
19 papers, 640 citations indexed

About

Yoshihito Okamura is a scholar working on Reproductive Medicine, Social Psychology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Yoshihito Okamura has authored 19 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Reproductive Medicine, 7 papers in Social Psychology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Yoshihito Okamura's work include Hypothalamic control of reproductive hormones (8 papers), Neuroendocrine regulation and behavior (7 papers) and Stress Responses and Cortisol (4 papers). Yoshihito Okamura is often cited by papers focused on Hypothalamic control of reproductive hormones (8 papers), Neuroendocrine regulation and behavior (7 papers) and Stress Responses and Cortisol (4 papers). Yoshihito Okamura collaborates with scholars based in Japan. Yoshihito Okamura's co-authors include Shigeo Daikoku, Hitoshi Kawano, Yoshihiro Tsuruo, Noboru Yanaihara, Setsuji Hisano, Masahiko Maegawa, Tamotsu Shibasaki, Ichiro Shimizu, Guangming Lu and Hirohito Honda and has published in prestigious journals such as Brain Research, Biochemical and Biophysical Research Communications and Developmental Biology.

In The Last Decade

Yoshihito Okamura

19 papers receiving 624 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshihito Okamura Japan 14 181 160 156 135 131 19 640
M. Priam France 14 206 1.1× 277 1.7× 384 2.5× 113 0.8× 125 1.0× 20 746
L. Désy Canada 12 130 0.7× 204 1.3× 277 1.8× 139 1.0× 65 0.5× 13 596
Valerie S. Densmore United States 7 131 0.7× 229 1.4× 197 1.3× 71 0.5× 53 0.4× 7 581
Csaba Vastagh Hungary 14 162 0.9× 163 1.0× 138 0.9× 102 0.8× 59 0.5× 26 545
Liesl De Sevilla United States 10 55 0.3× 161 1.0× 110 0.7× 75 0.6× 27 0.2× 12 578
Melissa Moholt-Siebert United States 7 137 0.8× 177 1.1× 141 0.9× 65 0.5× 42 0.3× 8 479
M Motta Italy 9 130 0.7× 108 0.7× 84 0.5× 79 0.6× 53 0.4× 21 456
Miklós Sárvári Hungary 15 100 0.6× 202 1.3× 83 0.5× 79 0.6× 48 0.4× 27 658
Sandrine De Seranno France 10 153 0.8× 241 1.5× 160 1.0× 139 1.0× 89 0.7× 10 686
G. B. Thomas Australia 15 85 0.5× 151 0.9× 71 0.5× 288 2.1× 35 0.3× 20 763

Countries citing papers authored by Yoshihito Okamura

Since Specialization
Citations

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

Fields of papers citing papers by Yoshihito Okamura

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoshihito Okamura

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshihito Okamura. A scholar is included among the top collaborators of Yoshihito Okamura 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 Yoshihito Okamura. Yoshihito Okamura is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Wang, Y., et al.. (2020). Metastable decomposition at the peptide C‐terminus: Possible use in protein identification. Rapid Communications in Mass Spectrometry. 34(9). e8734–e8734. 3 indexed citations
2.
Inoue, Hiroshi, Ichiro Shimizu, Guangming Lu, et al.. (2003). Idoxifene and Estradiol Enhance Antiapoptotic Activity Through Estrogen Receptor-β in Cultured Rat Hepatocytes. Digestive Diseases and Sciences. 48(3). 570–580. 39 indexed citations
3.
Ikemoto‐Uezumi, Madoka, Yoshihito Okamura, Katsuya Hirasaka, et al.. (2002). A Relative High Dose of Vitamin E Does Not Attenuate Unweighting-Induced Oxidative Stress and Ubiquitination in Rat Skeletal Muscle.. Journal of PHYSIOLOGICAL ANTHROPOLOGY and Applied Human Science. 21(5). 257–263. 30 indexed citations
4.
Shimizu, Ichiro, Yajun Zhou, Yoshihito Okamura, et al.. (2001). Effects of idoxifene and estradiol on NF‐κB activation in cultured rat hepatocytes undergoing oxidative stress. Liver International. 21(3). 183–191. 53 indexed citations
5.
Zhou, Yajun, Ichiro Shimizu, Guangming Lu, et al.. (2001). Hepatic Stellate Cells Contain the Functional Estrogen Receptor β but Not the Estrogen Receptor α in Male and Female Rats. Biochemical and Biophysical Research Communications. 286(5). 1059–1065. 62 indexed citations
7.
Okamura, Yoshihito, Hitoshi Kawano, & Shigeo Daikoku. (1991). Spatial-temporal appearance of developing immunoreactive TRH neurons in the neuroepithelial wall of the diencephalon. Developmental Brain Research. 63(1-2). 21–31. 15 indexed citations
8.
Okamura, Yoshihito, et al.. (1990). Development of the hypothalamic luteinizing hormone-releasing hormone-containing neuron system in the rat: In vivo and in transplantation studies. Developmental Biology. 140(2). 374–387. 91 indexed citations
9.
Daikoku, Shigeo, et al.. (1989). Hypothalamic neurons from a developmental aspect.. Archives of Histology and Cytology. 52(Suppl). 217–223. 3 indexed citations
10.
Daikoku, Shigeo, et al.. (1988). Development of hypothalamic neurons in intraventricular grafts: Expression of specific transmitter phenotypes. Developmental Biology. 126(2). 382–393. 16 indexed citations
11.
Daikoku, Shigeo, et al.. (1986). Ontogenesis of immunoreactive tyrosine hydroxylase-containing neurons in rat hypothalamus. Developmental Brain Research. 28(1). 85–98. 67 indexed citations
13.
Daikoku, Shigeo, Yoshihito Okamura, Hitoshi Kawano, et al.. (1985). CRF-containing neurons of the rat hypothalamus. Cell and Tissue Research. 240(3). 575–584. 46 indexed citations
14.
Daikoku, Shigeo, et al.. (1984). Development of immunoreactive lhrh neurons in the fetal rat hypothalamus. International Journal of Developmental Neuroscience. 2(2). 113–120. 13 indexed citations
15.
Hisano, Setsuji, Yoshihito Okamura, & Shigeo Daikoku. (1984). Synaptic regulation of hypothalamic neurons containing ACTH by substance P. Brain Research. 308(1). 162–165. 15 indexed citations
16.
Tsuruo, Yoshihiro, Setsuji Hisano, Yoshihito Okamura, Nobuhiro Tsukamoto, & Shigeo Daikoku. (1984). Hypothalamic substance P-containing neurons. Sex-dependent topographical differences and ultrastructural transformations associated with stages of the estrous cycle. Brain Research. 305(2). 331–341. 36 indexed citations
17.
Daikoku, Shigeo, Yoshihito Okamura, Hitoshi Kawano, et al.. (1984). Immunohistochemical study on the development of CRF-containing neurons in the hypothalamus of the rat. Cell and Tissue Research. 238(3). 539–44. 59 indexed citations
18.
Daikoku, Shigeo, et al.. (1983). Ontogenesis of hypothalamic immunoreactive ACTH cells in vivo and in vitro: Role of Rathke's pouch. Developmental Biology. 97(1). 81–88. 39 indexed citations
19.
Daikoku, Shigeo, Setsuji Hisano, Hitoshi Kawano, Yoshihito Okamura, & Yoshihiro Tsuruo. (1983). Ontogenetic studies on the topographical heterogeneity of somatostatin-containing neurons in rat hypothalamus. Cell and Tissue Research. 233(2). 347–54. 34 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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