Tetsuji Naka

17.1k total citations · 4 hit papers
202 papers, 13.4k citations indexed

About

Tetsuji Naka is a scholar working on Oncology, Immunology and Molecular Biology. According to data from OpenAlex, Tetsuji Naka has authored 202 papers receiving a total of 13.4k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Oncology, 62 papers in Immunology and 60 papers in Molecular Biology. Recurrent topics in Tetsuji Naka's work include Cytokine Signaling Pathways and Interactions (51 papers), Clusterin in disease pathology (18 papers) and Immune Cell Function and Interaction (15 papers). Tetsuji Naka is often cited by papers focused on Cytokine Signaling Pathways and Interactions (51 papers), Clusterin in disease pathology (18 papers) and Immune Cell Function and Interaction (15 papers). Tetsuji Naka collaborates with scholars based in Japan, United States and Australia. Tetsuji Naka's co-authors include Tadamitsu Kishimoto, Minoru Fujimoto, Akihiko Yoshimura, Masato Kubo, Satoshi Serada, Akihiro Kimura, Norihiro Nishimoto, Masashi Narazaki, Shizuo Akira and Tomoshige Matsumoto and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Journal of Experimental Medicine.

In The Last Decade

Tetsuji Naka

196 papers receiving 13.2k citations

Hit Papers

SOCS proteins, cytokine signalling and immune regul... 1994 2026 2004 2015 2007 1997 1994 2002 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tetsuji Naka Japan 54 6.4k 5.1k 3.7k 1.5k 1.4k 202 13.4k
Matthias Ernst Australia 68 5.6k 0.9× 5.7k 1.1× 5.6k 1.5× 2.0k 1.3× 1.2k 0.9× 220 15.2k
Fred Schaper Germany 40 4.3k 0.7× 5.0k 1.0× 3.3k 0.9× 1.2k 0.8× 1.0k 0.8× 96 9.9k
Valeria Poli Italy 66 5.0k 0.8× 5.1k 1.0× 6.1k 1.7× 2.1k 1.4× 2.4k 1.8× 148 16.0k
Christian Schindler United States 46 5.9k 0.9× 5.1k 1.0× 3.5k 0.9× 1.3k 0.9× 1.3k 1.0× 82 10.7k
Massimo Gadina United States 55 6.4k 1.0× 4.1k 0.8× 3.5k 1.0× 794 0.5× 1.1k 0.8× 126 13.2k
Lionel Feigenbaum United States 61 9.0k 1.4× 4.3k 0.8× 4.5k 1.2× 879 0.6× 1.2k 0.9× 123 15.1k
Iris Behrmann Germany 46 4.4k 0.7× 5.0k 1.0× 5.9k 1.6× 1.9k 1.3× 1000 0.7× 92 11.6k
Yuka Kanno United States 59 11.4k 1.8× 3.9k 0.8× 4.3k 1.2× 1.2k 0.8× 1.1k 0.8× 97 17.3k
Arian Laurence United States 50 10.1k 1.6× 3.9k 0.8× 2.7k 0.7× 811 0.5× 1.2k 0.9× 98 15.0k
Brendan J. Jenkins Australia 43 3.8k 0.6× 4.0k 0.8× 2.8k 0.8× 1.2k 0.8× 644 0.5× 113 8.6k

Countries citing papers authored by Tetsuji Naka

Since Specialization
Citations

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

Fields of papers citing papers by Tetsuji Naka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tetsuji Naka

This figure shows the co-authorship network connecting the top 25 collaborators of Tetsuji Naka. A scholar is included among the top collaborators of Tetsuji Naka 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 Tetsuji Naka. Tetsuji Naka 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.
Ikenaga, Naoki, Tsuyoshi Takahashi, Koji Tanaka, et al.. (2025). Overexpression of Transferrin Receptor in Esophageal Squamous Cell Cancer Suggests Poor Prognosis and Potential Therapy. Cancer Science. 117(2). 393–406.
2.
Takahashi, Tsuyoshi, Koji Tanaka, Kazuyoshi Yamamoto, et al.. (2024). Lipolysis-stimulated lipoprotein receptor promote lipid uptake and fatty acid oxidation in gastric cancer. Gastric Cancer. 27(6). 1258–1272. 5 indexed citations
3.
Serada, Satoshi, Minoru Fujimoto, Tomoharu Ohkawara, et al.. (2021). Gene therapy with SOCS1 induces potent preclinical antitumor activities in oral squamous cell carcinoma. Journal of Oral Pathology and Medicine. 51(2). 126–133. 6 indexed citations
4.
Nakajima, Hideki, Kimiko Nakajima, Mikiro Takaishi, et al.. (2021). The Skin–Liver Axis Modulates the Psoriasiform Phenotype and Involves Leucine-Rich α-2 Glycoprotein. The Journal of Immunology. 206(7). 1469–1477. 8 indexed citations
5.
Matsuzaki, Shinya, Satoshi Serada, Koji Matsuo, et al.. (2021). CD70 antibody‐drug conjugate: A potential novel therapeutic agent for ovarian cancer. Cancer Science. 112(9). 3655–3668. 13 indexed citations
6.
Serada, Satoshi, Tsuyoshi Takahashi, Takashi Matsunaga, et al.. (2021). Anti-Glypican-1 Antibody–drug Conjugate as Potential Therapy Against Tumor Cells and Tumor Vasculature for Glypican-1–Positive Cholangiocarcinoma. Molecular Cancer Therapeutics. 20(9). 1713–1722. 15 indexed citations
7.
Kato, Daiki, Tomonori Yaguchi, Takashi Iwata, et al.. (2020). GPC1 specific CAR-T cells eradicate established solid tumor without adverse effects and synergize with anti-PD-1 Ab. eLife. 9. 47 indexed citations
8.
Kitagawa, Koichi, Yuka Fukui, Hiroki Saito, et al.. (2019). Overexpression of SOCS3 mediated by adenovirus vector in mouse and human castration-resistant prostate cancer cells increases the sensitivity to NK cells in vitro and in vivo. Cancer Gene Therapy. 26(11-12). 388–399. 16 indexed citations
9.
Serada, Satoshi, et al.. (2019). Myosin heavy chain, a novel allergen for fish allergy in patients with atopic dermatitis. British Journal of Dermatology. 181(6). 1322–1324. 5 indexed citations
10.
Nakagawa, Satoshi, Satoshi Serada, Kosuke Hiramatsu, et al.. (2018). Intratumoral Delivery of an Adenoviral Vector Carrying the SOCS-1 Gene Enhances T-Cell–Mediated Antitumor Immunity By Suppressing PD-L1. Molecular Cancer Therapeutics. 17(9). 1941–1950. 8 indexed citations
11.
Sugase, Takahito, Tsuyoshi Takahashi, Satoshi Serada, et al.. (2017). SOCS1 Gene Therapy Improves Radiosensitivity and Enhances Irradiation-Induced DNA Damage in Esophageal Squamous Cell Carcinoma. Cancer Research. 77(24). 6975–6986. 37 indexed citations
12.
Hiramatsu, Kosuke, Satoshi Serada, Takayuki Enomoto, et al.. (2017). LSR Antibody Therapy Inhibits Ovarian Epithelial Tumor Growth by Inhibiting Lipid Uptake. Cancer Research. 78(2). 516–527. 33 indexed citations
13.
Shinzaki, Shinichiro, Hideki Iijima, Hironobu Fujii, et al.. (2017). A novel pathogenesis of inflammatory bowel disease from the perspective of glyco-immunology. The Journal of Biochemistry. 161(5). 409–415. 7 indexed citations
14.
Umegaki‐Arao, Noriko, Katsuto Tamai, Keisuke Nimura, et al.. (2013). Karyopherin Alpha2 Is Essential for rRNA Transcription and Protein Synthesis in Proliferative Keratinocytes. PLoS ONE. 8(10). e76416–e76416. 9 indexed citations
15.
Ishii, Hiroshi, Shihori Tanabe, Masaki Ueno, et al.. (2013). ifn-γ-dependent secretion of IL-10 from Th1 cells and microglia/macrophages contributes to functional recovery after spinal cord injury. Cell Death and Disease. 4(7). e710–e710. 55 indexed citations
16.
Shinzaki, Shinichiro, Hideki Iijima, Hironobu Fujii, et al.. (2012). Lectin-based Immunoassay for Aberrant IgG Glycosylation as the Biomarker for Crohnʼs Disease. Inflammatory Bowel Diseases. 19(2). 321–331. 36 indexed citations
17.
Ohguro, Nobuyuki, Kei Nakai, Fumitaka Terabe, et al.. (2010). Blockade of interleukin-6 signaling suppresses experimental autoimmune uveoretinitis by the inhibition of inflammatory Th17 responses. Experimental Eye Research. 91(2). 162–170. 82 indexed citations
18.
Terabe, Fumitaka, Minoru Fujimoto, Satoshi Serada, et al.. (2010). Comparative analysis of the effects of anti-IL-6 receptor mAb and anti-TNF mAb treatment on CD4+ T-cell responses in murine colitis. Inflammatory Bowel Diseases. 17(2). 491–502. 14 indexed citations
19.
Kimura, Akihiro, Tetsuji Naka, Keiko Nohara, Yoshiaki Fujii‐Kuriyama, & Tadamitsu Kishimoto. (2008). Aryl hydrocarbon receptor regulates Stat1 activation and participates in the development of Th17 cells. Proceedings of the National Academy of Sciences. 105(28). 9721–9726. 429 indexed citations
20.
Hirano, Tôru, Shinji Higa, Junsuke Arimitsu, et al.. (2005). Luteolin, a flavonoid, inhibits AP-1 activation by basophils. Biochemical and Biophysical Research Communications. 340(1). 1–7. 68 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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