Naoya Ueda

956 total citations
22 papers, 664 citations indexed

About

Naoya Ueda is a scholar working on Infectious Diseases, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Naoya Ueda has authored 22 papers receiving a total of 664 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Infectious Diseases, 6 papers in Molecular Biology and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Naoya Ueda's work include Viral Infections and Vectors (7 papers), SARS-CoV-2 and COVID-19 Research (3 papers) and Viral Infections and Outbreaks Research (3 papers). Naoya Ueda is often cited by papers focused on Viral Infections and Vectors (7 papers), SARS-CoV-2 and COVID-19 Research (3 papers) and Viral Infections and Outbreaks Research (3 papers). Naoya Ueda collaborates with scholars based in Japan, Philippines and Australia. Naoya Ueda's co-authors include Yutaka Seino, Mitsuo Fukushima, Toshihiro Miura, Shumpei Watanabe, Yasuhiro Yoshikawa, Hiroomi Akashi, Tetsuo Kaneko, Koichiro Iha, Satoshi Taniguchi and Shigeru Kyuwa and has published in prestigious journals such as Journal of Neurochemistry, American Journal Of Pathology and Emerging infectious diseases.

In The Last Decade

Naoya Ueda

21 papers receiving 633 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naoya Ueda Japan 15 256 215 168 95 74 22 664
Santanu Raychaudhuri United States 16 157 0.6× 506 2.4× 24 0.1× 134 1.4× 75 1.0× 19 977
I Béládi Hungary 13 90 0.4× 187 0.9× 35 0.2× 85 0.9× 59 0.8× 66 571
P. Selvaraj India 14 25 0.1× 179 0.8× 49 0.3× 78 0.8× 95 1.3× 67 700
Geeta Devi Leishangthem India 13 53 0.2× 168 0.8× 15 0.1× 91 1.0× 44 0.6× 45 670
T. L. Chow United States 12 65 0.3× 131 0.6× 50 0.3× 58 0.6× 38 0.5× 30 617
Ursula Wegner Germany 13 83 0.3× 141 0.7× 22 0.1× 136 1.4× 13 0.2× 21 542
Hitoshi Horie Japan 16 243 0.9× 175 0.8× 119 0.7× 54 0.6× 72 1.0× 34 619
Manisha Saini India 13 140 0.5× 117 0.5× 18 0.1× 70 0.7× 24 0.3× 31 445
Chunyan Zhong China 10 74 0.3× 126 0.6× 46 0.3× 69 0.7× 53 0.7× 22 341
Vladimir Perović Serbia 15 127 0.5× 294 1.4× 11 0.1× 180 1.9× 10 0.1× 46 627

Countries citing papers authored by Naoya Ueda

Since Specialization
Citations

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

Fields of papers citing papers by Naoya Ueda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naoya Ueda

This figure shows the co-authorship network connecting the top 25 collaborators of Naoya Ueda. A scholar is included among the top collaborators of Naoya Ueda 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 Naoya Ueda. Naoya Ueda 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.
Ueda, Naoya, et al.. (2018). Elevated Membrane Cholesterol Disrupts Lysosomal Degradation to Induce β-Amyloid Accumulation. American Journal Of Pathology. 189(2). 391–404. 7 indexed citations
2.
Ueda, Naoya, Taisuke Tomita, Katsuhiko Yanagisawa, & Nobuyuki Kimura. (2016). Retromer and Rab2‐dependent trafficking mediate PS1 degradation by proteasomes in endocytic disturbance. Journal of Neurochemistry. 137(4). 647–658. 12 indexed citations
3.
Izumi‐Nakaseko, Hiroko, Yuji Nakamura, Xin Cao, et al.. (2014). Effects of selective IKr channel blockade by E-4031 on ventricular electro-mechanical relationship in the halothane-anesthetized dogs. European Journal of Pharmacology. 740. 263–270. 15 indexed citations
4.
Watanabe, Shumpei, Joseph S. Masangkay, Tetsuya Mizutani, et al.. (2012). Genomic and serological detection of bat coronavirus from bats in the Philippines. Archives of Virology. 157(12). 2349–2355. 20 indexed citations
5.
Shirato, Kazuya, Ken Maeda, Kazuo Suzuki, et al.. (2011). Detection of bat coronaviruses from Miniopterus fuliginosus in Japan. Virus Genes. 44(1). 40–44. 18 indexed citations
6.
Watanabe, Shumpei, Joseph S. Masangkay, Noriyo Nagata, et al.. (2010). Bat Coronaviruses and Experimental Infection of Bats, the Philippines. Emerging infectious diseases. 16(8). 1217–1223. 142 indexed citations
7.
Fujii, H, Shumpei Watanabe, Daisuke Yamane, et al.. (2010). Functional analysis of Rousettus aegyptiacus “signal transducer and activator of transcription 1” (STAT1). Developmental & Comparative Immunology. 34(5). 598–602. 12 indexed citations
8.
Watanabe, Shumpei, Ken Maeda, Kazuo Suzuki, et al.. (2010). Novel Betaherpesvirus in Bats. Emerging infectious diseases. 16(6). 986–988. 30 indexed citations
9.
Watanabe, Shumpei, Naoya Ueda, Koichiro Iha, et al.. (2009). Detection of a new bat gammaherpesvirus in the Philippines. Virus Genes. 39(1). 90–93. 24 indexed citations
10.
Iha, Koichiro, Tsutomu Omatsu, Shumpei Watanabe, et al.. (2009). Molecular Cloning and Sequencing of the cDNAs Encoding the Bat Interleukin (IL)-2, IL-4, IL-6, IL-10, IL-12p40, and Tumor Necrosis Factor-Alpha. Journal of Veterinary Medical Science. 71(12). 1691–1695. 9 indexed citations
11.
Yamada, Kotaro, Masaya Hosokawa, Shimpei Fujimoto, et al.. (2008). Effect of corosolic acid on gluconeogenesis in rat liver. Diabetes Research and Clinical Practice. 80(1). 48–55. 36 indexed citations
12.
Watanabe, Shumpei, Tsutomu Omatsu, Mary Elizabeth Miranda, et al.. (2008). Epizootology and experimental infection of Yokose virus in bats. Comparative Immunology Microbiology and Infectious Diseases. 33(1). 25–36. 9 indexed citations
13.
Yamada, Kotaro, Masaya Hosokawa, Shimpei Fujimoto, et al.. (2006). The spontaneously diabetic Torii rat with gastroenteropathy. Diabetes Research and Clinical Practice. 75(2). 127–134. 16 indexed citations
14.
Fukushima, M, Naoya Ueda, Katsuya Egawa, et al.. (2006). Effect of corosolic acid on postchallenge plasma glucose levels. Diabetes Research and Clinical Practice. 73(2). 174–177. 96 indexed citations
15.
Fukushima, Mitsuo, Yuichi Nishi, Naoya Ueda, et al.. (2005). Factors responsible for deteriorating glucose tolerance in newly diagnosed type 2 diabetes in Japanese men. Metabolism. 55(1). 53–58. 31 indexed citations
16.
Nishi, Yuichi, Mitsuo Fukushima, Haruhiko Suzuki, et al.. (2005). Insulin secretion and insulin sensitivity in Japanese subjects with impaired fasting glucose and isolated fasting hyperglycemia. Diabetes Research and Clinical Practice. 70(1). 46–52. 23 indexed citations
17.
Miura, Toshihiro, Yasushi Itoh, Tetsuo Kaneko, et al.. (2004). Corosolic Acid Induces GLUT4 Translocation in Genetically Type 2 Diabetic Mice. Biological and Pharmaceutical Bulletin. 27(7). 1103–1105. 62 indexed citations
18.
Yamasaki, Yoshimitsu, et al.. (1991). Assessment of early stage autonomic nerve dysfunction in diabetic subjects--application of power spectral analysis of heart rate variability.. PubMed. 17(2). 73–80. 16 indexed citations
19.
Ueda, Naoya, et al.. (1984). [Macroamylasemia, report of two cases].. PubMed. 59(4). 496–500. 1 indexed citations
20.
Fujii, Satoru, Shiro Tanaka, Naoya Ueda, et al.. (1978). C-peptide response to arginine infusion in insulin requiring diabetics.. PubMed. 24(1). 25–32.

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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