Yoichiro Isohama

2.5k total citations
107 papers, 2.1k citations indexed

About

Yoichiro Isohama is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Physiology. According to data from OpenAlex, Yoichiro Isohama has authored 107 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 31 papers in Pulmonary and Respiratory Medicine and 24 papers in Physiology. Recurrent topics in Yoichiro Isohama's work include Neonatal Respiratory Health Research (17 papers), Asthma and respiratory diseases (14 papers) and Glycosylation and Glycoproteins Research (13 papers). Yoichiro Isohama is often cited by papers focused on Neonatal Respiratory Health Research (17 papers), Asthma and respiratory diseases (14 papers) and Glycosylation and Glycoproteins Research (13 papers). Yoichiro Isohama collaborates with scholars based in Japan, United States and Greece. Yoichiro Isohama's co-authors include Akinori Hisatsune, Takeshi Miyata, Hiroshi Katsuki, Hirofumi Kai, Yuki Kurauchi, Erik P. Lillehoj, Satoshi Mishima, Yoko Araki, Masanori Hijioka and Hideaki Matsushita and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Journal of Agricultural and Food Chemistry.

In The Last Decade

Yoichiro Isohama

106 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoichiro Isohama Japan 25 819 420 305 274 267 107 2.1k
Jacek Kurzepa Poland 21 557 0.7× 84 0.2× 139 0.5× 378 1.4× 110 0.4× 90 1.9k
Juan B. Salom Spain 28 822 1.0× 134 0.3× 548 1.8× 140 0.5× 59 0.2× 98 2.0k
Eun Jin Yang South Korea 21 499 0.6× 80 0.2× 215 0.7× 169 0.6× 116 0.4× 47 1.4k
Michael P. Neeper United States 20 922 1.1× 248 0.6× 426 1.4× 31 0.1× 518 1.9× 26 3.3k
Sofia Mariotto Italy 30 973 1.2× 100 0.2× 417 1.4× 48 0.2× 445 1.7× 55 2.8k
Akinori Hisatsune Japan 24 819 1.0× 190 0.5× 186 0.6× 29 0.1× 250 0.9× 73 1.7k
Marjan Gharagozloo Iran 28 816 1.0× 426 1.0× 241 0.8× 27 0.1× 682 2.6× 72 2.7k
Ik‐Hyun Cho South Korea 35 1.6k 1.9× 95 0.2× 777 2.5× 95 0.3× 559 2.1× 110 3.7k
Alexander G. Obukhov United States 32 2.2k 2.7× 217 0.5× 513 1.7× 35 0.1× 258 1.0× 88 4.6k

Countries citing papers authored by Yoichiro Isohama

Since Specialization
Citations

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

Fields of papers citing papers by Yoichiro Isohama

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yoichiro Isohama

This figure shows the co-authorship network connecting the top 25 collaborators of Yoichiro Isohama. A scholar is included among the top collaborators of Yoichiro Isohama 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 Yoichiro Isohama. Yoichiro Isohama 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.
Muramatsu, Shin‐ichi, et al.. (2025). A review of frequently used Kampo prescriptions; Part 6—Goreisan. Traditional & Kampo Medicine. 12(2). 121–134. 2 indexed citations
2.
Matsumoto, Chinami, et al.. (2023). Goreisan alleviates cerebral edema: Possibility of its involvement in inhibiting aquaporin‐4 function. Traditional & Kampo Medicine. 10(2). 168–176. 7 indexed citations
3.
Horie, Ichiro, et al.. (2021). Goreisan regulates AQP3 expression and improves diarrhea. Traditional & Kampo Medicine. 8(1). 91–99. 11 indexed citations
4.
Isohama, Yoichiro. (2014). Increase in aquaporin 3 expression in keratinocytes by Schizonepeta tenuifolia. Folia Pharmacologica Japonica. 143(3). 115–119. 2 indexed citations
5.
Maeda, Noriko, et al.. (2010). Interaction of ethyl pyruvate in vitro with NF-κB subunits, RelA and p50. European Journal of Pharmacology. 650(1). 151–156. 7 indexed citations
6.
Hisatsune, Akinori, et al.. (2009). Hypoxia enhances MUC1 expression in a lung adenocarcinoma cell line. Biochemical and Biophysical Research Communications. 379(4). 1060–1065. 30 indexed citations
7.
Michinaga, Shotaro, Akinori Hisatsune, Yoichiro Isohama, & Hiroshi Katsuki. (2009). Inhibition of neural activity depletes orexin from rat hypothalamic slice culture. Journal of Neuroscience Research. 88(1). 214–221. 7 indexed citations
8.
Kurauchi, Yuki, Akinori Hisatsune, Yoichiro Isohama, & Hiroshi Katsuki. (2008). Nitric oxide–cyclic GMP signaling pathway limits inflammatory degeneration of midbrain dopaminergic neurons: Cell type-specific regulation of heme oxygenase-1 expression. Neuroscience. 158(2). 856–866. 23 indexed citations
9.
Nomura, Johji, Akinori Hisatsune, Takeshi Miyata, & Yoichiro Isohama. (2007). The role of CpG methylation in cell type-specific expression of the aquaporin-5 gene. Biochemical and Biophysical Research Communications. 353(4). 1017–1022. 20 indexed citations
10.
Narita, Yukio, Johji Nomura, Shozo Ohta, et al.. (2006). Royal Jelly Stimulates Bone Formation: Physiologic and Nutrigenomic Studies with Mice and Cell Lines. Bioscience Biotechnology and Biochemistry. 70(10). 2508–2514. 52 indexed citations
11.
Mishima, Satoshi, et al.. (2005). Estrogenic effects of royal jelly. 22(1). 171–175. 7 indexed citations
12.
Lillehoj, Erik P., Akinori Hisatsune, Wenju Lu, et al.. (2005). Neutrophil elastase stimulatesMUC1gene expression through increased Sp1 binding to theMUC1promoter. American Journal of Physiology-Lung Cellular and Molecular Physiology. 289(2). L355–L362. 43 indexed citations
13.
Nomura, Johji, et al.. (2004). Lipopolysaccharide changes the subcellular distribution of aquaporin 5 and increases plasma membrane water permeability in mouse lung epithelial cells. Biochemical and Biophysical Research Communications. 326(3). 521–526. 19 indexed citations
14.
Fukushima, Hideo, et al.. (1998). Inhibition of glycine-induced current by morphine in nucleustractus solitarii neurones of guinea pigs. Methods and Findings in Experimental and Clinical Pharmacology. 20(2). 125–125. 2 indexed citations
15.
Miyata, Takeshi, Hirofumi Kai, Yoichiro Isohama, & K. Takahama. (1998). Current opinion of muco-active drug research: strategies and problems. European Respiratory Journal. 11(2). 480–491. 17 indexed citations
16.
Takahama, Kazuo, et al.. (1997). Inhibition of glycine currents by dextromethorphan in neurones dissociated from the guinea‐pig nucleus tractus solitarii. British Journal of Pharmacology. 120(4). 690–694. 15 indexed citations
17.
Isohama, Yoichiro, et al.. (1995). Changes in β1- and β2-adrenoceptor mRNA levels in alveolar type II cells during cultivation.. Folia Pharmacologica Japonica. 106(supplement). 112–116. 3 indexed citations
18.
Kai, Hirofumi, et al.. (1995). Activated Polymorphonuclear Leucocytes Stimulate the Loss of the Cell-associated High-molecular Weight Glycoconjugates from Hamster Tracheal Epithelial Cells in Culture. Pharmacy and Pharmacology Communications. 1(10). 475–478. 4 indexed citations
19.
20.
Kai, Hirofumi, et al.. (1992). The influence of neuraminidase treatment on tracheal smooth muscle contraction. European Journal of Pharmacology. 220(2-3). 181–185. 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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