Derek Lacey

2.0k total citations
23 papers, 1.6k citations indexed

About

Derek Lacey is a scholar working on Immunology, Oncology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Derek Lacey has authored 23 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Immunology, 5 papers in Oncology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Derek Lacey's work include Immune cells in cancer (7 papers), Immune Response and Inflammation (5 papers) and Nuclear Receptors and Signaling (4 papers). Derek Lacey is often cited by papers focused on Immune cells in cancer (7 papers), Immune Response and Inflammation (5 papers) and Nuclear Receptors and Signaling (4 papers). Derek Lacey collaborates with scholars based in Australia, Germany and United Kingdom. Derek Lacey's co-authors include John A. Hamilton, Andrew D. Cook, Andrew J. Fleetwood, Stephen E. Graves, Paul J. Simmons, Adrian Achuthan, Eric F. Morand, Leilani L. Santos, Glen M. Scholz and Hang Thuy Dinh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and The Journal of Immunology.

In The Last Decade

Derek Lacey

23 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Derek Lacey Australia 16 845 351 236 218 168 23 1.6k
Mark Bodman‐Smith United Kingdom 19 755 0.9× 506 1.4× 318 1.3× 356 1.6× 111 0.7× 49 1.7k
Eko Raharjo Canada 13 582 0.7× 420 1.2× 93 0.4× 126 0.6× 86 0.5× 15 1.4k
Ram P. Singh United States 20 902 1.1× 467 1.3× 316 1.3× 191 0.9× 170 1.0× 44 1.7k
Ian Welch Canada 24 334 0.4× 701 2.0× 235 1.0× 241 1.1× 211 1.3× 56 1.8k
James T. Rosenbaum United States 29 701 0.8× 472 1.3× 484 2.1× 173 0.8× 76 0.5× 63 2.2k
S Eto Japan 26 757 0.9× 411 1.2× 145 0.6× 261 1.2× 320 1.9× 97 1.9k
Wassila Carpentier France 21 787 0.9× 685 2.0× 130 0.6× 146 0.7× 183 1.1× 32 2.0k
Francesca Cianfarani Italy 20 814 1.0× 680 1.9× 98 0.4× 415 1.9× 201 1.2× 34 2.4k
Yojiro Kawabe Japan 22 898 1.1× 520 1.5× 262 1.1× 247 1.1× 102 0.6× 51 1.8k
Hidetoshi Tanioka Japan 24 528 0.6× 423 1.2× 297 1.3× 178 0.8× 159 0.9× 48 2.2k

Countries citing papers authored by Derek Lacey

Since Specialization
Citations

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

Fields of papers citing papers by Derek Lacey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Derek Lacey

This figure shows the co-authorship network connecting the top 25 collaborators of Derek Lacey. A scholar is included among the top collaborators of Derek Lacey 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 Derek Lacey. Derek Lacey 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.
Kueh, Andrew J., et al.. (2020). Severe Impairment of TNF Post-transcriptional Regulation Leads to Embryonic Death. iScience. 23(11). 101726–101726. 8 indexed citations
2.
Cook, Andrew D., Ming-Chin Lee, Reem Saleh, et al.. (2018). TNF and granulocyte macrophage-colony stimulating factor interdependence mediates inflammation via CCL17. JCI Insight. 3(6). 44 indexed citations
3.
Seillet, Cyril, Derek Lacey, Michael D. Stutz, et al.. (2018). Constitutive overexpression of TNF in BPSM1 mice causes iBALT and bone marrow nodular lymphocytic hyperplasia. Immunology and Cell Biology. 97(1). 29–38. 1 indexed citations
4.
Achuthan, Adrian, Andrew D. Cook, Ming-Chin Lee, et al.. (2016). Granulocyte macrophage colony-stimulating factor induces CCL17 production via IRF4 to mediate inflammation. Journal of Clinical Investigation. 126(9). 3453–3466. 126 indexed citations
5.
Lacey, Derek & Philippe Bouillet. (2015). Deregulation of TNF expression can also cause heart valve disease. Cytokine. 77. 248–249. 4 indexed citations
6.
Lacey, Derek, Peter F. Hickey, Benedicta D. Arhatari, et al.. (2015). Spontaneous retrotransposon insertion into TNF 3′UTR causes heart valve disease and chronic polyarthritis. Proceedings of the National Academy of Sciences. 112(31). 9698–9703. 23 indexed citations
7.
Cook, Andrew D., et al.. (2014). 24. Cytokine. 70(1). 33–33. 2 indexed citations
8.
Lee, Ming-Chin, Andrew D. Cook, Derek Lacey, & John A. Hamilton. (2014). 109. Cytokine. 70(1). 54–54. 3 indexed citations
9.
Cook, Andrew D., Shannon Sarros, Stefan Steidl, et al.. (2012). Granulocyte-macrophage colony-stimulating factor is a key mediator in inflammatory and arthritic pain. Annals of the Rheumatic Diseases. 72(2). 265–270. 77 indexed citations
10.
Lacey, Derek, Adrian Achuthan, Andrew J. Fleetwood, et al.. (2012). Defining GM-CSF– and Macrophage-CSF–Dependent Macrophage Responses by In Vitro Models. The Journal of Immunology. 188(11). 5752–5765. 410 indexed citations
11.
Manuelpillai, Ursula, Dinushka Lourensz, Vijesh Vaghjiani, et al.. (2012). Human Amniotic Epithelial Cell Transplantation Induces Markers of Alternative Macrophage Activation and Reduces Established Hepatic Fibrosis. PLoS ONE. 7(6). e38631–e38631. 90 indexed citations
12.
Hamilton, John A., et al.. (2012). Hypoxia Enhances the Proliferative Response of Macrophages to CSF-1 and Their Pro-Survival Response to TNF. PLoS ONE. 7(9). e45853–e45853. 12 indexed citations
13.
Bailey, Mark, et al.. (2010). Extracellular proteomes of M‐CSF (CSF‐1) and GM‐CSF‐dependent macrophages. Immunology and Cell Biology. 89(2). 283–293. 20 indexed citations
14.
Lacey, Derek, Felix I. L. Clanchy, Mark Bailey, et al.. (2009). Low dose metal particles can induce monocyte/macrophage survival. Journal of Orthopaedic Research®. 27(11). 1481–1486. 12 indexed citations
15.
Lacey, Derek, Paul J. Simmons, Stephen E. Graves, & John A. Hamilton. (2008). Proinflammatory cytokines inhibit osteogenic differentiation from stem cells: implications for bone repair during inflammation. Osteoarthritis and Cartilage. 17(6). 735–742. 249 indexed citations
16.
Toh, Myew–Ling, Daniel Aeberli, Derek Lacey, et al.. (2006). Regulation of IL-1 and TNF Receptor Expression and Function by Endogenous Macrophage Migration Inhibitory Factor. The Journal of Immunology. 177(7). 4818–4825. 62 indexed citations
17.
Xue, Jin, Derek Lacey, Paul Hutchinson, et al.. (2005). Detection of the p53 regulator murine double-minute protein 2 in rheumatoid arthritis.. PubMed. 32(3). 424–9. 22 indexed citations
18.
Santos, Leilani L., et al.. (2004). Activation of synovial cell p38 MAP kinase by macrophage migration inhibitory factor.. PubMed. 31(6). 1038–43. 56 indexed citations
19.
Leech, Michelle, Derek Lacey, Jin Xue, et al.. (2003). Regulation of p53 by macrophage migration inhibitory factor in inflammatory arthritis. Arthritis & Rheumatism. 48(7). 1881–1889. 99 indexed citations
20.
Lacey, Derek, Robert A. Mitchell, Richard Bucala, et al.. (2003). Control of fibroblast‐like synoviocyte proliferation by macrophage migration inhibitory factor. Arthritis & Rheumatism. 48(1). 103–109. 100 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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