Foo Y. Liew

35.1k total citations · 8 hit papers
232 papers, 28.9k citations indexed

About

Foo Y. Liew is a scholar working on Immunology, Epidemiology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Foo Y. Liew has authored 232 papers receiving a total of 28.9k indexed citations (citations by other indexed papers that have themselves been cited), including 151 papers in Immunology, 46 papers in Epidemiology and 41 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Foo Y. Liew's work include Immune Cell Function and Interaction (62 papers), IL-33, ST2, and ILC Pathways (49 papers) and Research on Leishmaniasis Studies (37 papers). Foo Y. Liew is often cited by papers focused on Immune Cell Function and Interaction (62 papers), IL-33, ST2, and ILC Pathways (49 papers) and Research on Leishmaniasis Studies (37 papers). Foo Y. Liew collaborates with scholars based in United Kingdom, Brazil and United States. Foo Y. Liew's co-authors include Iain B. McInnes, Damo Xu, Bernard P. Leung, Damo Xu, Fernando Q. Cunha, Salvador Moncada, Nick Pitman, Luke O'neill, Elizabeth Brint and Xiaoqing Wei and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Foo Y. Liew

232 papers receiving 28.3k citations

Hit Papers

Negative regulation of Toll-like receptor-mediated... 1990 2026 2002 2014 2005 2016 2010 1990 2009 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
Foo Y. Liew United Kingdom 96 17.1k 5.4k 5.3k 4.7k 4.0k 232 28.9k
Sergio Romagnani Italy 95 20.6k 1.2× 4.7k 0.9× 3.2k 0.6× 6.2k 1.3× 3.7k 0.9× 350 36.0k
Fred D. Finkelman United States 87 15.8k 0.9× 3.5k 0.6× 2.4k 0.4× 6.1k 1.3× 1.7k 0.4× 380 26.9k
Bernhard Ryffel France 88 14.1k 0.8× 7.5k 1.4× 2.6k 0.5× 2.5k 0.5× 4.3k 1.1× 438 27.8k
René de Waal Malefyt United States 70 25.5k 1.5× 4.5k 0.8× 2.2k 0.4× 4.8k 1.0× 4.8k 1.2× 150 38.3k
Sharon M. Wahl United States 87 15.0k 0.9× 7.9k 1.5× 2.5k 0.5× 2.7k 0.6× 3.1k 0.8× 277 31.6k
Steven L. Kunkel United States 113 21.6k 1.3× 9.7k 1.8× 4.7k 0.9× 5.3k 1.1× 6.3k 1.6× 528 48.1k
Andrew N. J. McKenzie United Kingdom 100 25.4k 1.5× 4.1k 0.8× 12.2k 2.3× 8.7k 1.9× 2.6k 0.7× 237 35.4k
William E. Paul United States 98 30.2k 1.8× 8.2k 1.5× 2.8k 0.5× 4.7k 1.0× 3.4k 0.8× 344 42.5k
Anthony J. Coyle United States 84 19.8k 1.2× 7.7k 1.4× 3.1k 0.6× 6.6k 1.4× 2.7k 0.7× 209 30.3k
Enrico Maggi Italy 83 15.6k 0.9× 3.6k 0.7× 2.1k 0.4× 4.5k 1.0× 2.6k 0.6× 367 27.2k

Countries citing papers authored by Foo Y. Liew

Since Specialization
Citations

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

Fields of papers citing papers by Foo Y. Liew

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Foo Y. Liew. 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 Foo Y. Liew. The network helps show where Foo Y. Liew may publish in the future.

Co-authorship network of co-authors of Foo Y. Liew

This figure shows the co-authorship network connecting the top 25 collaborators of Foo Y. Liew. A scholar is included among the top collaborators of Foo Y. Liew 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 Foo Y. Liew. Foo Y. Liew 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.
Donate, Paula B., Kalil Alves de Lima, Raphael Sanches Peres, et al.. (2020). Cigarette smoke induces miR-132 in Th17 cells that enhance osteoclastogenesis in inflammatory arthritis. Proceedings of the National Academy of Sciences. 118(1). 43 indexed citations
2.
Akbar, Moeed, Emma García-Melchor, Sabarinadh Chilaka, et al.. (2020). Attenuation of Dupuytren’s fibrosis via targeting of the STAT1 modulated IL-13Rα1 response. Science Advances. 6(28). eaaz8272–eaaz8272. 19 indexed citations
3.
Fu, Amy K.Y., Xiaopu Zhou, D.S.Y. Mak, et al.. (2016). IL-33 ameliorates Alzheimer’s disease-like pathology and cognitive decline. Proceedings of the National Academy of Sciences. 113(19). E2705–13. 294 indexed citations
4.
Mirchandani, Ananda S., Anne‐Gaëlle Besnard, Charlotte L. Scott, et al.. (2014). Type 2 Innate Lymphoid Cells Drive CD4+ Th2 Cell Responses. The Journal of Immunology. 192(5). 2442–2448. 259 indexed citations
5.
Kurowska‐Stolarska, Mariola, Stefano Alivernini, L. Ballantine, et al.. (2011). MicroRNA-155 as a proinflammatory regulator in clinical and experimental arthritis. Proceedings of the National Academy of Sciences. 108(27). 11193–11198. 503 indexed citations breakdown →
6.
Asquith, Darren L., Ashley M. Miller, Axel J. Hueber, et al.. (2010). Apolipoprotein E–deficient mice are resistant to the development of collagen‐induced arthritis. Arthritis & Rheumatism. 62(2). 472–477. 14 indexed citations
7.
Kurowska‐Stolarska, Mariola, Bartosz Stolarski, Peter Kewin, et al.. (2009). IL-33 Amplifies the Polarization of Alternatively Activated Macrophages That Contribute to Airway Inflammation. The Journal of Immunology. 183(10). 6469–6477. 579 indexed citations breakdown →
8.
Xu, Damo, Hui‐Rong Jiang, Peter Kewin, et al.. (2008). IL-33 exacerbates antigen-induced arthritis by activating mast cells. Proceedings of the National Academy of Sciences. 105(31). 10913–10918. 396 indexed citations
9.
Trieu, Angela, Nilesh J. Bokil, Jasmyn A. Dunn, et al.. (2008). TLR9‐independent effects of inhibitory oligonucleotides on macrophage responses to S. typhimurium. Immunology and Cell Biology. 87(3). 218–225. 12 indexed citations
10.
Liu, Haiying, Mousa Komai‐Koma, Damo Xu, & Foo Y. Liew. (2006). Toll-like receptor 2 signaling modulates the functions of CD4 + CD25 + regulatory T cells. Proceedings of the National Academy of Sciences. 103(18). 7048–7053. 379 indexed citations
11.
Komai‐Koma, Mousa, Louise Jones, Graham S. Ogg, Damo Xu, & Foo Y. Liew. (2004). TLR2 is expressed on activated T cells as a costimulatory receptor. Proceedings of the National Academy of Sciences. 101(9). 3029–3034. 408 indexed citations
12.
Leung, Bernard P., Naveed Sattar, Anne Crilly, et al.. (2003). A Novel Anti-Inflammatory Role for Simvastatin in Inflammatory Arthritis. The Journal of Immunology. 170(3). 1524–1530. 361 indexed citations
13.
Shinozaki, Michiya, Junichi Hirahashi, Tatiana Lebedeva, et al.. (2002). IL-15, a survival factor for kidney epithelial cells, counteracts apoptosis and inflammation during nephritis. Journal of Clinical Investigation. 109(7). 951–960. 7 indexed citations
14.
Shinozaki, Michiya, Junichi Hirahashi, Tatiana Lebedeva, et al.. (2002). IL-15, a survival factor for kidney epithelial cells, counteracts apoptosis and inflammation during nephritis. Journal of Clinical Investigation. 109(7). 951–960. 64 indexed citations
15.
Gri, Giorgia, Claudia Chiodoni, Elena Gallo, et al.. (2002). Antitumor effect of interleukin (IL)-12 in the absence of endogenous IFN-gamma: a role for intrinsic tumor immunogenicity and IL-15.. Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna). 62(15). 4390–7. 27 indexed citations
16.
Goodridge, Helen S., Emma H. Wilson, William Harnett, et al.. (2001). Modulation of Macrophage Cytokine Production by ES-62, a Secreted Product of the Filarial Nematode Acanthocheilonema viteae. The Journal of Immunology. 167(2). 940–945. 99 indexed citations
17.
Wei, Xiaoqing, J. Alastair Gracie, Bernard P. Leung, et al.. (2001). The Sushi Domain of Soluble IL-15 Receptor α Is Essential for Binding IL-15 and Inhibiting Inflammatory and Allogenic Responses In Vitro and In Vivo. The Journal of Immunology. 167(1). 277–282. 79 indexed citations
18.
Esfandiari, Ehsanollah, Iain B. McInnes, George B.M. Lindop, et al.. (2001). A Proinflammatory Role of IL-18 in the Development of Spontaneous Autoimmune Disease. The Journal of Immunology. 167(9). 5338–5347. 103 indexed citations
19.
McInnes, Iain B., et al.. (1998). Septic Arthritis Following Staphylococcus aureus Infection in Mice Lacking Inducible Nitric Oxide Synthase. The Journal of Immunology. 160(1). 308–315. 82 indexed citations
20.
Huang, Fang‐Ping, et al.. (1998). Mice defective in Fas are highly susceptible to Leishmania major infection despite elevated IL-12 synthesis, strong Th1 responses, and enhanced nitric oxide production.. ORCA Online Research @Cardiff. 160(9). 4143–7. 77 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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