Shizuo Akira

334.6k total citations · 91 hit papers
1.2k papers, 261.0k citations indexed

About

Shizuo Akira is a scholar working on Immunology, Molecular Biology and Cancer Research. According to data from OpenAlex, Shizuo Akira has authored 1.2k papers receiving a total of 261.0k indexed citations (citations by other indexed papers that have themselves been cited), including 863 papers in Immunology, 299 papers in Molecular Biology and 206 papers in Cancer Research. Recurrent topics in Shizuo Akira's work include Immune Response and Inflammation (604 papers), interferon and immune responses (222 papers) and Immune Cell Function and Interaction (206 papers). Shizuo Akira is often cited by papers focused on Immune Response and Inflammation (604 papers), interferon and immune responses (222 papers) and Immune Cell Function and Interaction (206 papers). Shizuo Akira collaborates with scholars based in Japan, United States and Germany. Shizuo Akira's co-authors include Taro Kawai, Kiyoshi Takeda, Osamu Takeuchi, Satoshi Uematsu, Tsuneyasu Kaisho, Shintaro Sato, Katsuaki Hoshino, Hiroaki Hemmi, Masahiro Yamamoto and Ken J. Ishii and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Shizuo Akira

1.2k papers receiving 256.9k citations

Hit Papers

Pathogen Recognition and ... 1990 2026 2002 2014 2006 2010 2010 2004 2003 2.5k 5.0k 7.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shizuo Akira Japan 239 164.0k 79.6k 48.5k 29.0k 27.9k 1.2k 261.0k
Richard A. Flavell United States 219 86.8k 0.5× 75.7k 1.0× 19.7k 0.4× 13.8k 0.5× 23.1k 0.8× 1.2k 179.2k
Guido Kroemer France 228 51.4k 0.3× 128.2k 1.6× 47.5k 1.0× 28.9k 1.0× 45.9k 1.6× 1.4k 235.5k
Alberto Mantovani Italy 173 91.5k 0.6× 42.5k 0.5× 13.7k 0.3× 16.5k 0.6× 45.1k 1.6× 1.1k 157.6k
Michael Karin United States 229 60.2k 0.4× 113.1k 1.4× 23.0k 0.5× 56.6k 2.0× 45.8k 1.6× 652 212.6k
Kiyoshi Takeda Japan 118 57.1k 0.3× 27.9k 0.4× 14.7k 0.3× 10.5k 0.4× 9.7k 0.3× 463 92.8k
Kenneth J. Livak United States 42 26.2k 0.2× 95.0k 1.2× 12.1k 0.2× 23.5k 0.8× 11.6k 0.4× 95 199.5k
Ruslan Medzhitov United States 114 61.3k 0.4× 27.9k 0.4× 13.4k 0.3× 8.9k 0.3× 7.3k 0.3× 227 97.2k
Charles A. Dinarello United States 174 47.0k 0.3× 36.8k 0.5× 15.9k 0.3× 5.5k 0.2× 11.9k 0.4× 873 108.0k
Ulrich K. Laemmli Switzerland 62 24.1k 0.1× 154.2k 1.9× 12.7k 0.3× 10.0k 0.3× 15.2k 0.5× 84 261.7k
David Baltimore United States 190 46.6k 0.3× 76.2k 1.0× 11.4k 0.2× 32.4k 1.1× 18.2k 0.6× 804 141.8k

Countries citing papers authored by Shizuo Akira

Since Specialization
Citations

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

Fields of papers citing papers by Shizuo Akira

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shizuo Akira

This figure shows the co-authorship network connecting the top 25 collaborators of Shizuo Akira. A scholar is included among the top collaborators of Shizuo Akira 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 Shizuo Akira. Shizuo Akira 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.
Niitsu, Takayuki, Kiyoharu Fukushima, Daisuke Motooka, et al.. (2025). Spatial transcriptomics identifies SPARC as a prognostic marker in interstitial lung diseases. The Journal of Pathology. 267(1). 79–91.
2.
Nayer, Bhavana, Jean L. Tan, Yen‐Zhen Lu, et al.. (2024). Local administration of regulatory T cells promotes tissue healing. Nature Communications. 15(1). 7863–7863. 28 indexed citations
3.
Lu, Yen‐Zhen, Bhavana Nayer, Shailendra Kumar Singh, et al.. (2024). CGRP sensory neurons promote tissue healing via neutrophils and macrophages. Nature. 628(8008). 604–611. 145 indexed citations breakdown →
4.
Saltykova, Irina V., Sergio Li Calzi, Takashi Satoh, et al.. (2021). Tribbles Homolog 3 Mediates the Development and Progression of Diabetic Retinopathy. Diabetes. 70(8). 1738–1753. 18 indexed citations
5.
Julier, Ziad, Bhavana Nayer, Yen‐Zhen Lu, et al.. (2020). Enhancing the regenerative effectiveness of growth factors by local inhibition of interleukin-1 receptor signaling. Science Advances. 6(24). eaba7602–eaba7602. 28 indexed citations
6.
Omiya, Shigemiki, Yosuke Omori, Manabu Taneike, et al.. (2020). Cytokine mRNA Degradation in Cardiomyocytes Restrains Sterile Inflammation in Pressure-Overloaded Hearts. Circulation. 141(8). 667–677. 22 indexed citations
7.
Tanaka, Hiroki, Yasunobu Arima, Daisuke Kamimura, et al.. (2019). Phosphorylation-dependent Regnase-1 release from endoplasmic reticulum is critical in IL-17 response. The Journal of Experimental Medicine. 216(6). 1431–1449. 50 indexed citations
8.
Komine, Okiru, Hirofumi Yamashita, Noriko Fujimori-Tonou, et al.. (2018). Innate immune adaptor TRIF deficiency accelerates disease progression of ALS mice with accumulation of aberrantly activated astrocytes. Cell Death and Differentiation. 25(12). 2130–2146. 48 indexed citations
9.
Kawasaki, Takumi, Kosuke Ito, Haruhiko Miyata, Shizuo Akira, & Taro Kawai. (2017). Deletion of PIK fyve alters alveolar macrophage populations and exacerbates allergic inflammation in mice. The EMBO Journal. 36(12). 1707–1718. 23 indexed citations
10.
Iwasaki, Hidenori, Osamu Takeuchi, Shunsuke Teraguchi, et al.. (2011). The IκB kinase complex regulates the stability of cytokine-encoding mRNA induced by TLR–IL-1R by controlling degradation of regnase-1. Nature Immunology. 12(12). 1167–1175. 228 indexed citations
11.
Jung, In Duk, Soo Kyung Jeong, Chang-Min Lee, et al.. (2011). Enhanced Efficacy of Therapeutic Cancer Vaccines Produced by Co-Treatment with Mycobacterium tuberculosis Heparin-Binding Hemagglutinin, a Novel TLR4 Agonist. Cancer Research. 71(8). 2858–2870. 77 indexed citations
12.
Kawai, Taro & Shizuo Akira. (2010). The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors. Nature Immunology. 11(5). 373–384. 7035 indexed citations breakdown →
13.
Matsumoto, Koichiro, Keiko Kan‐o, Satoru Fukuyama, et al.. (2010). Essential Role of B7-H1 in Double-Stranded RNA–Induced Augmentation of an Asthma Phenotype in Mice. American Journal of Respiratory Cell and Molecular Biology. 45(1). 31–39. 11 indexed citations
14.
Pichlmair, Andreas, Oliver Schulz, Jan Rehwinkel, et al.. (2009). Activation of MDA5 Requires Higher-Order RNA Structures Generated during Virus Infection. Journal of Virology. 83(20). 10761–10769. 369 indexed citations
15.
Swann, Jeremy B., Matthew D. Vesely, Anabel Silva, et al.. (2008). Demonstration of inflammation-induced cancer and cancer immunoediting during primary tumorigenesis. Proceedings of the National Academy of Sciences. 105(2). 652–656. 244 indexed citations
16.
Jounai, Nao, Fumihiko Takeshita, Kouji Kobiyama, et al.. (2007). The Atg5–Atg12 conjugate associates with innate antiviral immune responses. Proceedings of the National Academy of Sciences. 104(35). 14050–14055. 486 indexed citations
17.
Roberts, Zachary, Nadège Goutagny, Pin‐Yu Perera, et al.. (2007). The chemotherapeutic agent DMXAA potently and specifically activates the TBK1–IRF-3 signaling axis. The Journal of Experimental Medicine. 204(7). 1559–1569. 127 indexed citations
18.
Loo, Yueh–Ming, Jamie L. Fornek, Gagan Bajwa, et al.. (2007). Distinct RIG-I and MDA5 Signaling by RNA Viruses in Innate Immunity. Journal of Virology. 82(1). 335–345. 843 indexed citations breakdown →
19.
Yamamoto, Masahiro, Shintaro Sato, Hiroaki Hemmi, et al.. (2003). Role of Adaptor TRIF in the MyD88-Independent Toll-Like Receptor Signaling Pathway. Science. 301(5633). 640–643. 2604 indexed citations breakdown →
20.
Sano, Shigetoshi, Satoshi Itami, Kentaro Takeda, et al.. (1999). Functional involvement of Stat3 in skin remodeling including hair cycle and wound healing. Journal of Investigative Dermatology. 112(4). 529. 2 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026