Kazuyoshi Ikuta

10.4k total citations
394 papers, 7.9k citations indexed

About

Kazuyoshi Ikuta is a scholar working on Epidemiology, Infectious Diseases and Virology. According to data from OpenAlex, Kazuyoshi Ikuta has authored 394 papers receiving a total of 7.9k indexed citations (citations by other indexed papers that have themselves been cited), including 197 papers in Epidemiology, 142 papers in Infectious Diseases and 134 papers in Virology. Recurrent topics in Kazuyoshi Ikuta's work include HIV Research and Treatment (100 papers), Virology and Viral Diseases (71 papers) and Herpesvirus Infections and Treatments (56 papers). Kazuyoshi Ikuta is often cited by papers focused on HIV Research and Treatment (100 papers), Virology and Viral Diseases (71 papers) and Herpesvirus Infections and Treatments (56 papers). Kazuyoshi Ikuta collaborates with scholars based in Japan, Thailand and United States. Kazuyoshi Ikuta's co-authors include Shiro Kato, Keizō Tomonaga, Akikazu Sakudo, Takaaki Nakaya, Kanji Hirai, Y. Watanabe, Madiha S. Ibrahim, Masanori Kameoka, Takeshi Kobayashi and Shigeharu Ueda and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Kazuyoshi Ikuta

390 papers receiving 7.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kazuyoshi Ikuta Japan 44 3.7k 2.6k 1.9k 1.8k 1.2k 394 7.9k
Shigeru Morikawa Japan 53 2.3k 0.6× 4.7k 1.8× 1.6k 0.9× 1.9k 1.1× 1.8k 1.5× 361 9.8k
Tetsutaro Sata Japan 57 4.8k 1.3× 3.7k 1.4× 1.8k 0.9× 3.2k 1.7× 2.8k 2.2× 328 12.0k
Donald F. Smee United States 55 4.4k 1.2× 3.7k 1.4× 1.2k 0.6× 2.3k 1.3× 1.5k 1.2× 216 9.5k
Wolfgang Garten Germany 59 4.8k 1.3× 4.3k 1.7× 717 0.4× 2.9k 1.6× 1.7k 1.4× 131 10.3k
Zhen F. Fu China 47 1.9k 0.5× 2.9k 1.1× 2.7k 1.4× 1.8k 1.0× 966 0.8× 218 7.3k
Bernhard Dietzschold United States 61 4.0k 1.1× 2.9k 1.1× 5.7k 3.0× 2.2k 1.2× 1.4k 1.1× 169 9.5k
José F. Rodrígúez Spain 43 1.9k 0.5× 1.1k 0.4× 922 0.5× 1.2k 0.7× 478 0.4× 113 4.8k
Wayne A. Marasco United States 55 2.2k 0.6× 3.8k 1.5× 851 0.5× 4.2k 2.3× 2.7k 2.2× 165 11.3k
Keith G. Mansfield United States 46 2.2k 0.6× 2.2k 0.9× 2.5k 1.3× 1.9k 1.0× 2.2k 1.8× 161 7.6k
Benhur Lee United States 63 4.4k 1.2× 4.1k 1.6× 4.3k 2.3× 3.3k 1.8× 5.3k 4.3× 202 13.1k

Countries citing papers authored by Kazuyoshi Ikuta

Since Specialization
Citations

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

Fields of papers citing papers by Kazuyoshi Ikuta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kazuyoshi Ikuta

This figure shows the co-authorship network connecting the top 25 collaborators of Kazuyoshi Ikuta. A scholar is included among the top collaborators of Kazuyoshi Ikuta 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 Kazuyoshi Ikuta. Kazuyoshi Ikuta 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.
Matsumura, Takuhiro, Ryo Misaki, Masahiro Yutani, et al.. (2020). Fully Human Monoclonal Antibodies Effectively Neutralizing Botulinum Neurotoxin Serotype B. Toxins. 12(5). 302–302. 7 indexed citations
2.
Phanthanawiboon, Supranee, et al.. (2017). Construction of a high-yield dengue virus by replacing nonstructural proteins 3–4B without increasing virulence. Biochemical and Biophysical Research Communications. 495(1). 1221–1226. 3 indexed citations
3.
Sakai, Kaoru, Mikihiro Yunoki, Ritsuko Kubota‐Koketsu, et al.. (2013). Immunization of rabbits with synthetic peptides derived from a highly conserved β-sheet epitope region underneath the receptor binding site of influenza A virus. Biologics. 7. 233–233. 4 indexed citations
4.
Auwanit, Wattana, et al.. (2010). Appearance of Drug Resistance-Associated Mutations in Human Immunodeficiency Virus Type 1 CRF01_AE Integrase Derived from Drug-Naive Thai Patients. AIDS Research and Human Retroviruses. 26(12). 1341–1343. 6 indexed citations
5.
Yasunaga, Teruo, et al.. (2010). Genotypic Characterization of HIV Type 1 env gp160 Sequences from Three Regions in Thailand. AIDS Research and Human Retroviruses. 26(2). 223–227. 8 indexed citations
6.
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8.
Nakamura, Shota, Uamporn Siripanyaphinyo, Nuanjun Wichukchinda, et al.. (2008). Genotypic Characterization of CRF01_AE env Genes Derived from Human Immunodeficiency Virus Type 1-Infected Patients Residing in Central Thailand. AIDS Research and Human Retroviruses. 25(2). 229–236. 16 indexed citations
9.
Yanai, Hideyuki, Yohei Hayashi, Y. Watanabe, et al.. (2006). Development of a novel Borna disease virus reverse genetics system using RNA polymerase II promoter and SV40 nuclear import signal. Microbes and Infection. 8(6). 1522–1529. 34 indexed citations
10.
Yunoki, Mikihiro, et al.. (2003). Heat sensitivity of human parvovirus B19. Vox Sanguinis. 84(3). 164–169. 37 indexed citations
11.
Mukai, Tetsu, Satoshi Komoto, Takeshi Kurosu, et al.. (2002). Construction and Characterization of an Infectious Molecular Clone Derived from the CRF01_AE Primary Isolate of HIV Type 1. AIDS Research and Human Retroviruses. 18(8). 585–589. 10 indexed citations
12.
Komoto, Satoshi, Masanobu Kinomoto, Takeshi Kurosu, et al.. (2002). Ability to Induce p53 and Caspase-Mediated Apoptosis in Primary CD4 + T Cells Is Variable among Primary Isolates of Human Immunodeficiency Virus Type 1. AIDS Research and Human Retroviruses. 18(6). 435–446. 12 indexed citations
13.
Tobiume, Minoru, Koh Fujinaga, Satoko Suzuki, et al.. (2002). Extracellular Nef Protein Activates Signal Transduction Pathway from Ras to Mitogen-Activated Protein Kinase Cascades That Leads to Activation of Human Immunodeficiency Virus from Latency. AIDS Research and Human Retroviruses. 18(6). 461–467. 17 indexed citations
14.
Auwanit, Wattana, et al.. (2001). Full-Length Sequences of Two CRF01_AE (Subtype E) HIV Type 1 Isolates from 1995 Samples of Patients with Sexually Transmitted Diseases in Thailand. AIDS Research and Human Retroviruses. 17(9). 867–871. 8 indexed citations
15.
Kurosu, Takeshi, et al.. (2001). Variable Sequences in the Long Terminal Repeat and Its Downstream Region of Some of HIV Type 1 CRF01_AE Recently Distributing among Thai Carriers. AIDS Research and Human Retroviruses. 17(9). 863–866. 9 indexed citations
16.
Hagiwara, Katsuro, et al.. (2001). Seroprevalence of Borna disease virus in domestic animals in Xinjiang, China. Veterinary Microbiology. 80(4). 383–389. 24 indexed citations
17.
Nakaya, Takaaki, Mitsuhiro Tada, Hirokazu Takahashi, et al.. (1996). E Expression of Borna disease virus messages in clinical samples from patients with brain malignant tumors.. 19(7). 68–73. 1 indexed citations
18.
Nakaya, Takeo, et al.. (1996). E Varied prevalence of Borna disease virus infection in Arabic,thoroughbred and their cross-bred horses in Iran.. 19. 55–67. 1 indexed citations
19.
20.
Ikuta, Kazuyoshi, et al.. (1976). A lymphoblastoid cell line dually infected with Marek's disease virus and avian leukosis virus.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 19(1). 33–7. 4 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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