Ayako Yoshida

1.1k total citations
18 papers, 912 citations indexed

About

Ayako Yoshida is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Ayako Yoshida has authored 18 papers receiving a total of 912 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Ophthalmology, 7 papers in Radiology, Nuclear Medicine and Imaging and 3 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Ayako Yoshida's work include Retinal Diseases and Treatments (12 papers), Retinal and Optic Conditions (4 papers) and Ocular Diseases and Behçet’s Syndrome (4 papers). Ayako Yoshida is often cited by papers focused on Retinal Diseases and Treatments (12 papers), Retinal and Optic Conditions (4 papers) and Ocular Diseases and Behçet’s Syndrome (4 papers). Ayako Yoshida collaborates with scholars based in Japan, United States and Poland. Ayako Yoshida's co-authors include Shigeo Yoshida, Tatsuro Ishibashi, Victor M. Elner, H Inomata, Ahmad Khalil, M Kuwano, Zong-Mei Bian, Steven L. Kunkel, Miho Miyazaki and Yutaka Kiyohara and has published in prestigious journals such as American Journal of Ophthalmology, Journal of Leukocyte Biology and Journal of Histochemistry & Cytochemistry.

In The Last Decade

Ayako Yoshida

18 papers receiving 891 citations

Peers

Ayako Yoshida

OPHTH

RNMI

IMMUN

NEURO

S. Kawahara Japan

Tine Van Bergen Belgium

Yohei Tomita Japan

Meihua Ju United States

Mrinali Patel United States

Y Moromizato United States

Shinsuke Miyahara Japan

Takao Tobe Japan

Stephan Hoffmann Germany

Murilo Wendeborn Rodrigues United States

S. Kawahara Japan

Ayako Yoshida

468 ×0.9

OPHTH

343 ×1.1

439 ×1.4

RNMI

65 ×0.4

IMMUN

39 ×0.3

NEURO

Citations per year, relative to Ayako Yoshida Ayako Yoshida (= 1×) peers S. Kawahara

Countries citing papers authored by Ayako Yoshida

Since Specialization

Citations

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

Fields of papers citing papers by Ayako Yoshida

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ayako Yoshida

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

All Works

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18 of 18 papers shown

Ishikawa, Keijiro, Shigeo Yoshida, Shintaro Nakao, et al.. (2011). Bone marrow-derived monocyte lineage cells recruited by MIP-1β promote physiological revascularization in mouse model of oxygen-induced retinopathy. Laboratory Investigation. 92(1). 91–101. 37 indexed citations

Yoshida, Shigeo, Keijiro Ishikawa, Ryo Asato, et al.. (2011). Increased Expression of Periostin in Vitreous and Fibrovascular Membranes Obtained from Patients with Proliferative Diabetic Retinopathy. Investigative Ophthalmology & Visual Science. 52(8). 5670–5670. 46 indexed citations

Yoshida, Shigeo, et al.. (2010). Reduced concentrations of angiogenesis-related factors in vitreous after vitrectomy in patients with proliferative diabetic retinopathy. Graefe s Archive for Clinical and Experimental Ophthalmology. 248(6). 799–804. 20 indexed citations

Yoshida, Ayako, Kouji Kato, Shigeo Yoshida, et al.. (2006). Apoptosis in perforated cornea of a patient with graft-versus-host disease. Canadian Journal of Ophthalmology. 41(4). 472–475. 18 indexed citations

Yoshida, Ayako, et al.. (2005). Serous retinal detachment in an elderly patient with Philadelphia-chromosome-positive acute lymphoblastic leukemia. American Journal of Ophthalmology. 139(2). 348–349. 12 indexed citations

Miyazaki, Miho, Yutaka Kiyohara, Ayako Yoshida, et al.. (2005). The 5-Year Incidence and Risk Factors for Age-Related Maculopathy in a General Japanese Population: The Hisayama Study. Investigative Ophthalmology & Visual Science. 46(6). 1907–1907. 80 indexed citations

Yoshida, Shigeo, Ayako Yoshida, & Tatsuro Ishibashi. (2004). Induction of IL-8, MCP-1, and bFGF by TNF-α in retinal glial cells: implications for retinal neovascularization during post-ischemic inflammation. Graefe s Archive for Clinical and Experimental Ophthalmology. 242(5). 409–413. 125 indexed citations

Elner, Victor M., Ayako Yoshida, Robert D. Dick, & George J. Brewer. (2004). Effects of Tetrathiomolybdate in a Mouse Model of Retinal Neovascularization. Investigative Ophthalmology & Visual Science. 46(1). 299–299. 12 indexed citations

Yoshida, Shigeo, et al.. (2003). Involvement of Macrophage Chemotactic Protein-1 and Interleukin-1β During Inflammatory but Not Basic Fibroblast Growth Factor–Dependent Neovascularization in the Mouse Cornea. Laboratory Investigation. 83(7). 927–938. 44 indexed citations

10.

Yoshida, Shigeo, Ayako Yoshida, Tatsuro Ishibashi, & Victor M. Elner. (2003). Role of MCP-1 and MIP-1α in retinal neovascularization during postischemic inflammation in a mouse model of retinal neovascularization. Journal of Leukocyte Biology. 73(1). 137–144. 145 indexed citations

11.

Yoshida, Ayako, et al.. (2003). Activated Monocytes Induce Human Retinal Pigment Epithelial Cell Apoptosis Through Caspase-3 Activation. Laboratory Investigation. 83(8). 1117–1129. 13 indexed citations

12.

Elner, Victor M., et al.. (2003). Human RPE cell apoptosis induced by activated monocytes is mediated by caspase-3 activation.. PubMed. 101. 77–89; discussion 89. 8 indexed citations

13.

Yoshida, Shigeo, et al.. (2002). Two brothers with gelatinous drop-like dystrophy at different stages of the disease: role of mutational analysis. American Journal of Ophthalmology. 133(6). 830–832. 17 indexed citations

14.

Bian, Zong-Mei, et al.. (2001). Activation of p38, ERK1/2 and NIK Pathways is Required for IL-1β and TNF-α-induced Chemokine Expression in Human Retinal Pigment Epithelial Cells. Experimental Eye Research. 73(1). 111–121. 75 indexed citations

15.

Yoshida, Ayako. (2000). Familial Cases with Age-Related Macular Degeneration. Japanese Journal of Ophthalmology. 44(3). 290–295. 11 indexed citations

16.

Yoshida, Ayako, Shigeo Yoshida, Tatsuro Ishibashi, M Kuwano, & H Inomata. (1999). Suppression of retinal neovascularization by the NF-kappaB inhibitor pyrrolidine dithiocarbamate in mice.. PubMed. 40(7). 1624–9. 114 indexed citations

17.

Yoshida, Ayako, et al.. (1998). Role of NF-kappaB-mediated interleukin-8 expression in intraocular neovascularization.. PubMed. 39(7). 1097–106. 104 indexed citations

18.

Yoshida, Ayako, Shigeo Yoshida, Yasuaki Hata, et al.. (1998). The Role of NF-κB in Retinal Neovascularization in the Rat: Possible Involvement of Cytokine-induced Neutrophil Chemoattractant (CINC), a Member of the Interleukin-8 Family. Journal of Histochemistry & Cytochemistry. 46(4). 429–436. 31 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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