Shinya Sakaguchi

2.7k total citations
31 papers, 1.8k citations indexed

About

Shinya Sakaguchi is a scholar working on Immunology, Oncology and Molecular Biology. According to data from OpenAlex, Shinya Sakaguchi has authored 31 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Immunology, 10 papers in Oncology and 9 papers in Molecular Biology. Recurrent topics in Shinya Sakaguchi's work include Immune Cell Function and Interaction (14 papers), T-cell and B-cell Immunology (12 papers) and Immunotherapy and Immune Responses (7 papers). Shinya Sakaguchi is often cited by papers focused on Immune Cell Function and Interaction (14 papers), T-cell and B-cell Immunology (12 papers) and Immunotherapy and Immune Responses (7 papers). Shinya Sakaguchi collaborates with scholars based in Austria, Japan and United States. Shinya Sakaguchi's co-authors include Tadatsugu Taniguchi, Kenya Honda, Hideo Negishi, Hideyuki Yanai, Wilfried Ellmeier, Chigusa Nakajima, Akinori Takaoka, Hiroshi Takayanagi, Masahiro Shinohara and Xinshou Ouyang and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Shinya Sakaguchi

31 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shinya Sakaguchi Austria 17 1.2k 615 428 238 173 31 1.8k
David A. Savitsky United States 12 1.8k 1.5× 788 1.3× 588 1.4× 288 1.2× 267 1.5× 28 2.6k
Joan Ní Gabhann Ireland 19 1.0k 0.9× 583 0.9× 258 0.6× 145 0.6× 188 1.1× 35 1.6k
Sachiko Suematsu Japan 18 1.6k 1.3× 782 1.3× 430 1.0× 276 1.2× 183 1.1× 31 2.6k
Anna Yarilina United States 13 947 0.8× 576 0.9× 407 1.0× 167 0.7× 135 0.8× 15 1.7k
Kiri Honma Japan 16 1.6k 1.4× 629 1.0× 293 0.7× 182 0.8× 177 1.0× 22 2.2k
Tatsukata Kawagoe Japan 17 1.7k 1.5× 859 1.4× 272 0.6× 412 1.7× 257 1.5× 39 2.6k
Ji‐Yang Wang Japan 22 930 0.8× 663 1.1× 232 0.5× 162 0.7× 112 0.6× 60 1.7k
L. Otten Switzerland 15 1.8k 1.5× 565 0.9× 417 1.0× 141 0.6× 176 1.0× 23 2.3k
Victor C. de Vries United States 18 1.8k 1.5× 404 0.7× 525 1.2× 113 0.5× 206 1.2× 21 2.5k
Omar Duramad United States 14 2.3k 1.9× 605 1.0× 300 0.7× 163 0.7× 280 1.6× 19 3.2k

Countries citing papers authored by Shinya Sakaguchi

Since Specialization
Citations

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

Fields of papers citing papers by Shinya Sakaguchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shinya Sakaguchi

This figure shows the co-authorship network connecting the top 25 collaborators of Shinya Sakaguchi. A scholar is included among the top collaborators of Shinya Sakaguchi 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 Shinya Sakaguchi. Shinya Sakaguchi 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.
Kutschat, Ana P., Thomas Krausgruber, Christoph Bock, et al.. (2025). HDAC1 controls the generation and maintenance of effector-like CD8+ T cells during chronic viral infection. The Journal of Experimental Medicine. 222(8). 1 indexed citations
2.
Hladik, Anastasiya, Sandra Högler, Omar Sharif, et al.. (2021). The Tyrosine Kinase Tec Regulates Effector Th17 Differentiation, Pathogenicity, and Plasticity in T-Cell-Driven Intestinal Inflammation. Frontiers in Immunology. 12. 750466–750466. 11 indexed citations
3.
Takata, Fuyuko, Shinya Dohgu, Shinya Sakaguchi, et al.. (2019). Oncostatin-M-Reactive Pericytes Aggravate Blood–Brain Barrier Dysfunction by Activating JAK/STAT3 Signaling In Vitro. Neuroscience. 422. 12–20. 20 indexed citations
4.
Tizian, Caroline, Liisa Andersen, Tatjana Stojaković, et al.. (2019). The zinc-finger transcription factor MAZR regulates iNKT cell subset differentiation. Cellular and Molecular Life Sciences. 76(21). 4391–4404. 6 indexed citations
5.
Preglej, Teresa, Caroline Tizian, Sawako Muroi, et al.. (2019). Differential Requirement of Cd8 Enhancers E8I and E8VI in Cytotoxic Lineage T Cells and in Intestinal Intraepithelial Lymphocytes. Frontiers in Immunology. 10. 409–409. 5 indexed citations
6.
Müller, Lena, Teresa Preglej, Nicole Boucheron, et al.. (2017). The corepressor NCOR1 regulates the survival of single-positive thymocytes. Scientific Reports. 7(1). 15928–15928. 8 indexed citations
7.
Newman, Dane M., Shinya Sakaguchi, Aaron T. L. Lun, et al.. (2016). Acetylation of the Cd8 Locus by KAT6A Determines Memory T Cell Diversity. Cell Reports. 16(12). 3311–3321. 21 indexed citations
8.
Deniz, Emre, Tülin Erşahin, Rengül Çetin-Atalay, et al.. (2015). PATZ1 Is a DNA Damage-Responsive Transcription Factor That Inhibits p53 Function. Molecular and Cellular Biology. 35(10). 1741–1753. 28 indexed citations
9.
Sakaguchi, Shinya, Caroline Tizian, Hirokazu Tanaka, et al.. (2015). MAZR and Runx Factors Synergistically Repress ThPOK during CD8+ T Cell Lineage Development. The Journal of Immunology. 195(6). 2879–2887. 23 indexed citations
10.
Procházková, Jana, Shinya Sakaguchi, Abdelghani Mazouzi, et al.. (2015). DNA Repair Cofactors ATMIN and NBS1 Are Required to Suppress T Cell Activation. PLoS Genetics. 11(11). e1005645–e1005645. 12 indexed citations
11.
Boucheron, Nicole, Roland Tschismarov, Lisa Göschl, et al.. (2014). CD4+ T cell lineage integrity is controlled by the histone deacetylases HDAC1 and HDAC2. Nature Immunology. 15(5). 439–448. 63 indexed citations
12.
Sakaguchi, Shinya, Hirokazu Tanaka, Nighat Yasmin, et al.. (2014). A novel Cd8-cis-regulatory element preferentially directs expression in CD44hiCD62L+ CD8+ T cells and in CD8αα+ dendritic cells. Journal of Leukocyte Biology. 97(4). 635–644. 8 indexed citations
13.
Sakaguchi, Shinya, Alexandra Schebesta, Nicole Boucheron, et al.. (2013). The Transcription Factor MAZR Preferentially Acts as a Transcriptional Repressor in Mast Cells and Plays a Minor Role in the Regulation of Effector Functions in Response to FcεRI Stimulation. PLoS ONE. 8(10). e77677–e77677. 8 indexed citations
14.
Sakaguchi, Shinya, Ivan Bilić, Yoshinori Naoe, et al.. (2010). The zinc-finger protein MAZR is part of the transcription factor network that controls the CD4 versus CD8 lineage fate of double-positive thymocytes. Nature Immunology. 11(5). 442–448. 83 indexed citations
15.
Negishi, Hideo, Xinshou Ouyang, Shinya Sakaguchi, et al.. (2008). A critical link between Toll-like receptor 3 and type II interferon signaling pathways in antiviral innate immunity. Proceedings of the National Academy of Sciences. 105(51). 20446–20451. 173 indexed citations
16.
Shinohara, Masahiro, Takako Koga, Kazuo Okamoto, et al.. (2008). Tyrosine Kinases Btk and Tec Regulate Osteoclast Differentiation by Linking RANK and ITAM Signals. Cell. 132(5). 794–806. 249 indexed citations
17.
Negishi, Hideo, Yasuyuki Fujita, Hideyuki Yanai, et al.. (2006). Evidence for licensing of IFN-γ-induced IFN regulatory factor 1 transcription factor by MyD88 in Toll-like receptor-dependent gene induction program. Proceedings of the National Academy of Sciences. 103(41). 15136–15141. 260 indexed citations
18.
Kurusu, Shiro, Shinya Sakaguchi, & Mitsumori Kawaminami. (2006). Regulation of luteal prostaglandin F2α production and its relevance to cell death: An in vitro study using rat dispersed luteal cells. Prostaglandins & Other Lipid Mediators. 83(4). 250–256. 5 indexed citations
19.
Ogasawara, Kouetsu, Shigeaki Hida, Akio Saiura, et al.. (2002). Requirement of the IFN‐α/β‐induced CXCR3 chemokine signalling for CD8+ T cell activation. Genes to Cells. 7(3). 309–320. 57 indexed citations
20.
Kurusu, Shiro, Shinya Sakaguchi, Mitsumori Kawaminami, & Inoru HASHIMOTO. (2001). Sustained Activity of Luteal Cytosolic Phospholipase A<sub>2</sub> During Luteolysis in Pseudopregnant Rats: Its Possible Implication in Tissue Involution. Endocrine. 14(3). 337–342. 18 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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