Kyoko Yamashiro

1.1k total citations
17 papers, 908 citations indexed

About

Kyoko Yamashiro is a scholar working on Immunology, Molecular Biology and Genetics. According to data from OpenAlex, Kyoko Yamashiro has authored 17 papers receiving a total of 908 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Immunology, 6 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Kyoko Yamashiro's work include Mast cells and histamine (4 papers), Asthma and respiratory diseases (4 papers) and Eosinophilic Disorders and Syndromes (3 papers). Kyoko Yamashiro is often cited by papers focused on Mast cells and histamine (4 papers), Asthma and respiratory diseases (4 papers) and Eosinophilic Disorders and Syndromes (3 papers). Kyoko Yamashiro collaborates with scholars based in Japan and United States. Kyoko Yamashiro's co-authors include Nobuo Tsuruoka, Yasuhiro Hayashi, Yoshiyuki Hizukuri, Hiroshi Nakazato, Nozomi Yamaguchi, Masao Murakawa, Masafumi Tsujimoto, Shiho Kodama, Takaharu Tanaka and Kazuhiro Yoneda and has published in prestigious journals such as Biochemical and Biophysical Research Communications, European Journal of Biochemistry and Biochemical Pharmacology.

In The Last Decade

Kyoko Yamashiro

17 papers receiving 879 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kyoko Yamashiro Japan 13 250 233 214 194 142 17 908
Geraldine Flynn United Kingdom 17 414 1.7× 254 1.1× 247 1.2× 89 0.5× 120 0.8× 29 1.1k
Maddalena Ruggieri Italy 21 501 2.0× 228 1.0× 132 0.6× 169 0.9× 196 1.4× 55 1.4k
E. Corsini Italy 19 587 2.3× 386 1.7× 570 2.7× 144 0.7× 117 0.8× 48 1.6k
Ruben Papoian United States 18 447 1.8× 538 2.3× 178 0.8× 65 0.3× 121 0.9× 35 1.4k
Ljiljana Križanac-Bengez United States 14 225 0.9× 88 0.4× 147 0.7× 63 0.3× 326 2.3× 22 891
A Zicca Italy 18 283 1.1× 506 2.2× 156 0.7× 144 0.7× 29 0.2× 39 1.2k
Sandrine Pouly Switzerland 16 344 1.4× 753 3.2× 201 0.9× 62 0.3× 212 1.5× 31 1.4k
Anser C. Azim United States 14 450 1.8× 218 0.9× 39 0.2× 332 1.7× 188 1.3× 22 1.2k
Mayi Arcellana‐Panlilio Canada 16 671 2.7× 265 1.1× 97 0.5× 168 0.9× 44 0.3× 23 1.3k
H.‐P. Hartung Germany 18 340 1.4× 352 1.5× 308 1.4× 31 0.2× 194 1.4× 62 1.6k

Countries citing papers authored by Kyoko Yamashiro

Since Specialization
Citations

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

Fields of papers citing papers by Kyoko Yamashiro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kyoko Yamashiro

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

All Works

17 of 17 papers shown
1.
Saito, Yoichi, Yukio Fujiwara, Yasuka L. Yamaguchi, et al.. (2025). Rodent monocyte‐derived macrophages do not express CD163: Comparative analysis using macrophages from living boreoeutherians. Developmental Dynamics. 1 indexed citations
2.
Miyazaki, Kazuo, Kouichi Uoto, Maki Terakawa, et al.. (2020). Design, synthesis, and optimization of a series of 2-azaspiro[3.3]heptane derivatives as orally bioavailable fetal hemoglobin inducers. Bioorganic & Medicinal Chemistry Letters. 30(19). 127425–127425. 4 indexed citations
3.
Makino, Tomohiro, et al.. (2019). Phenotypic-screening generates active novel fetal globin-inducers that downregulate Bcl11a in a monkey model. Biochemical Pharmacology. 171. 113717–113717. 6 indexed citations
4.
Fujiwara, Yukio, Yoshiyuki Hizukuri, Kyoko Yamashiro, et al.. (2016). Guanylate‐binding protein 5 is a marker of interferon‐γ‐induced classically activated macrophages. Clinical & Translational Immunology. 5(11). e111–e111. 63 indexed citations
5.
Hizukuri, Yoshiyuki, et al.. (2014). IL-10 enhances the phenotype of M2 macrophages induced by IL-4 and confers the ability to increase eosinophil migration. International Immunology. 27(3). 131–141. 168 indexed citations
6.
Saito, Kayo, Tsuyoshi Muto, Yoshiaki Tomimori, et al.. (2003). Mouse mast cell protease-1 cleaves angiotensin I to form angiotensin II. Biochemical and Biophysical Research Communications. 302(4). 773–777. 17 indexed citations
7.
Tomimori, Yoshiaki, Tsuyoshi Muto, Harukazu Fukami, et al.. (2002). Mast Cell Chymase Regulates Dermal Mast Cell Number in Mice. Biochemical and Biophysical Research Communications. 290(5). 1478–1482. 23 indexed citations
8.
Tomimori, Yoshiaki, Tsuyoshi Muto, Harukazu Fukami, et al.. (2002). Chymase Participates in Chronic Dermatitis by Inducing Eosinophil Infiltration. Laboratory Investigation. 82(6). 789–794. 47 indexed citations
9.
Tomimori, Yoshiaki, Nobuo Tsuruoka, Harukazu Fukami, et al.. (2002). Role of mast cell chymase in allergen-induced biphasic skin reaction. Biochemical Pharmacology. 64(7). 1187–1193. 22 indexed citations
10.
Matsumoto, Hideko, Tomohiro Rogi, Kyoko Yamashiro, et al.. (2000). Characterization of a recombinant soluble form of human placental leucine aminopeptidase/oxytocinase expressed in Chinese hamster ovary cells. European Journal of Biochemistry. 267(1). 46–52. 97 indexed citations
11.
Mitsui, Shinichi, Nobuo Tsuruoka, Kyoko Yamashiro, Hiroshi Nakazato, & Nozomi Yamaguchi. (1999). A novel form of human neuropsin, a brain‐related serine protease, is generated by alternative splicing and is expressed preferentially in human adult brain. European Journal of Biochemistry. 260(3). 627–634. 61 indexed citations
12.
Sobue, Kazuya, Naoki Yamamoto, Kazuhiro Yoneda, et al.. (1999). Induction of blood–brain barrier properties in immortalized bovine brain endothelial cells by astrocytic factors. Neuroscience Research. 35(2). 155–164. 169 indexed citations
13.
Yamashiro, Kyoko, Nobuo Tsuruoka, Shiho Kodama, et al.. (1997). Molecular cloning of a novel trypsin-like serine protease (neurosin) preferentially expressed in brain. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1350(1). 11–14. 155 indexed citations
14.
Yamashiro, Kyoko, et al.. (1997). Molecular Cloning of a Novel Brain-Specific Serine Protease with a Kringle-like Structure and Three Scavenger Receptor Cysteine-Rich Motifs1. Biochemical and Biophysical Research Communications. 239(2). 386–392. 40 indexed citations
15.
Enokihara, H, et al.. (1996). Eosinophils Negatively Regulate Eosinophilopoiesis by Decreasing IL-5 Levels. International Archives of Allergy and Immunology. 111(1). 2–4. 1 indexed citations
16.
Enokihara, H, Haruhiko Ninomiya, Kyoko Yamashiro, et al.. (1995). Serum concentrations of IL‐5, GM‐CSF, and IL‐3 and the production by lymphocytes in various eosinophilia. American Journal of Hematology. 50(2). 98–102. 14 indexed citations
17.
Enokihara, H, Kyoko Yamashiro, Nobuo Tsuruoka, et al.. (1994). IL‐5 mRNA expression in blood lymphocytes from patients with Kimura's disease and parasite infection. American Journal of Hematology. 47(2). 69–73. 20 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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