M.G. Chambers

3.7k total citations · 1 hit paper
46 papers, 2.6k citations indexed

About

M.G. Chambers is a scholar working on Pharmacology, Rheumatology and Molecular Biology. According to data from OpenAlex, M.G. Chambers has authored 46 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pharmacology, 23 papers in Rheumatology and 14 papers in Molecular Biology. Recurrent topics in M.G. Chambers's work include Osteoarthritis Treatment and Mechanisms (22 papers), Inflammatory mediators and NSAID effects (22 papers) and Cell Adhesion Molecules Research (9 papers). M.G. Chambers is often cited by papers focused on Osteoarthritis Treatment and Mechanisms (22 papers), Inflammatory mediators and NSAID effects (22 papers) and Cell Adhesion Molecules Research (9 papers). M.G. Chambers collaborates with scholars based in United States, United Kingdom and Canada. M.G. Chambers's co-authors include W. B. Van Den Berg, Christopher B. Little, S.S. Glasson, Roger M. Mason, Michael T. Bayliss, J.L. Oskins, Kristen M. Clements, Chaohua Lin, A. Robin Poole and Denise M. Visco and has published in prestigious journals such as Analytical Biochemistry, Pain and Journal of Medicinal Chemistry.

In The Last Decade

M.G. Chambers

45 papers receiving 2.6k citations

Hit Papers

The OARSI histopathology initiative – recommendations for... 2010 2026 2015 2020 2010 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
M.G. Chambers United States 21 1.8k 952 749 450 426 46 2.6k
John Rediske United States 17 845 0.5× 490 0.5× 531 0.7× 182 0.4× 162 0.4× 28 1.9k
Shan‐Chi Liu Taiwan 30 712 0.4× 895 0.9× 291 0.4× 343 0.8× 143 0.3× 64 1.9k
Chen‐Ming Su Taiwan 25 329 0.2× 726 0.8× 127 0.2× 313 0.7× 98 0.2× 57 1.5k
Federica Ciregia Italy 22 327 0.2× 631 0.7× 104 0.1× 226 0.5× 237 0.6× 52 1.6k
Artur J. de Brum‐Fernandes Canada 24 356 0.2× 465 0.5× 281 0.4× 73 0.2× 84 0.2× 59 1.3k
I R Patel United States 8 305 0.2× 338 0.4× 405 0.5× 104 0.2× 65 0.2× 11 1.0k
J.R. Connor United States 16 322 0.2× 431 0.5× 135 0.2× 100 0.2× 67 0.2× 17 1.1k
Marsha L. Roach United States 13 87 0.0× 882 0.9× 483 0.6× 222 0.5× 613 1.4× 13 1.9k
Jean‐Michel Longpré Canada 21 83 0.0× 684 0.7× 347 0.5× 161 0.4× 325 0.8× 57 1.6k
Anna M. Gómèz‐Foix Spain 26 320 0.2× 1.7k 1.7× 66 0.1× 168 0.4× 734 1.7× 67 2.8k

Countries citing papers authored by M.G. Chambers

Since Specialization
Citations

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

Fields of papers citing papers by M.G. Chambers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.G. Chambers. 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 M.G. Chambers. The network helps show where M.G. Chambers may publish in the future.

Co-authorship network of co-authors of M.G. Chambers

This figure shows the co-authorship network connecting the top 25 collaborators of M.G. Chambers. A scholar is included among the top collaborators of M.G. Chambers 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 M.G. Chambers. M.G. Chambers 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.
Lesage, R, Nicole Kops, Niamh Fahy, et al.. (2024). A multi-model approach identifies ALW-II-41-27 as a promising therapy for osteoarthritis-associated inflammation and endochondral ossification. Heliyon. 10(23). e40871–e40871. 1 indexed citations
2.
Chandrasekhar, Srinivasan, Anita K. Harvey, J.L. Oskins, et al.. (2017). Analgesic and anti‐inflammatory properties of novel, selective, and potent EP4 receptor antagonists. Pharmacology Research & Perspectives. 5(3). e00316–e00316. 15 indexed citations
3.
Stuart, Kate, Alan Chan, J.L. Oskins, et al.. (2017). Sustained efficacy of intra-articular SB-061, a novel bioconjugate inspired by aggrecan, in a rat model of osteoarthritis. Osteoarthritis and Cartilage. 25. S415–S415. 2 indexed citations
4.
McDougall, Jason J., Niklas Schuelert, Chaohua Lin, et al.. (2016). Lysophosphatidic acid provides a missing link between osteoarthritis and joint neuropathic pain. Osteoarthritis and Cartilage. 25(6). 926–934. 54 indexed citations
5.
Chandrasekhar, S., Anita K. Harvey, M.G. Chambers, et al.. (2016). Identification and Characterization of Novel Microsomal Prostaglandin E Synthase-1 Inhibitors for Analgesia. Journal of Pharmacology and Experimental Therapeutics. 356(3). 635–644. 20 indexed citations
6.
Blanco, María‐Jesús, Tatiana Vetman, Srinivasan Chandrasekhar, et al.. (2016). Identification and biological activity of 6-alkyl-substituted 3-methyl-pyridine-2-carbonyl amino dimethyl-benzoic acid EP4 antagonists. Bioorganic & Medicinal Chemistry Letters. 26(9). 2303–2307. 10 indexed citations
7.
Benschop, Robert J., Emily C. Collins, Ryan J. Darling, et al.. (2014). Development of a novel antibody to calcitonin gene-related peptide for the treatment of osteoarthritis-related pain. Osteoarthritis and Cartilage. 22(4). 578–585. 100 indexed citations
8.
Norman, Bryan H., Andrew G. Geiser, M.G. Chambers, et al.. (2013). Selective RAR gamma antagonist LY2813631 protects against retinoid induced cartilage degradation in preclinical models of arthritis. Osteoarthritis and Cartilage. 21. S287–S288. 1 indexed citations
9.
Bar, Grégory, Paul Edwards, Reginald Brys, et al.. (2012). Discovery of a series of imidazopyrazine small molecule inhibitors of the kinase MAPKAPK5, that show activity using in vitro and in vivo models of rheumatoid arthritis. Bioorganic & Medicinal Chemistry Letters. 22(6). 2266–2270. 12 indexed citations
10.
Swearingen, Craig, M.G. Chambers, Chaohua Lin, et al.. (2010). A short-term pharmacodynamic model for monitoring aggrecanase activity: injection of monosodium iodoacetate (MIA) in rats and assessment of aggrecan neoepitope release in synovial fluid using novel ELISAs. Osteoarthritis and Cartilage. 18(9). 1159–1166. 21 indexed citations
11.
Glasson, S.S., M.G. Chambers, W. B. Van Den Berg, & Christopher B. Little. (2010). The OARSI histopathology initiative – recommendations for histological assessments of osteoarthritis in the mouse. Osteoarthritis and Cartilage. 18. S17–S23. 1292 indexed citations breakdown →
13.
Chambers, M.G., et al.. (2006). The role of adenosine in chondrocyte death in murine osteoarthritis and in a murine chondrocyte cell line. Osteoarthritis and Cartilage. 14(5). 486–495. 25 indexed citations
15.
Howard, Michael J., M.G. Chambers, Roger M. Mason, & Clare M. Isacke. (2003). Distribution of Endo180 receptor and ligand in developing articular cartilage. Osteoarthritis and Cartilage. 12(1). 74–82. 22 indexed citations
16.
Chambers, M.G., et al.. (2003). Chondrocyte death during murine osteoarthritis. Osteoarthritis and Cartilage. 12(2). 131–141. 76 indexed citations
19.
Chambers, M.G., et al.. (2002). Expression of collagen and aggrecan genes in normal and osteoarthritic murine knee joints. Osteoarthritis and Cartilage. 10(1). 51–61. 45 indexed citations
20.
Flannelly, J., M.G. Chambers, Jayesh Dudhia, et al.. (2002). Metalloproteinase and tissue inhibitor of metalloproteinase expression in the murine STR/ort model of osteoarthritis. Osteoarthritis and Cartilage. 10(9). 722–733. 64 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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