Caroline Wheeler‐Jones

4.7k total citations
131 papers, 3.9k citations indexed

About

Caroline Wheeler‐Jones is a scholar working on Molecular Biology, Surgery and Pharmacology. According to data from OpenAlex, Caroline Wheeler‐Jones has authored 131 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 20 papers in Surgery and 20 papers in Pharmacology. Recurrent topics in Caroline Wheeler‐Jones's work include Angiogenesis and VEGF in Cancer (17 papers), Protein Kinase Regulation and GTPase Signaling (14 papers) and Inflammatory mediators and NSAID effects (12 papers). Caroline Wheeler‐Jones is often cited by papers focused on Angiogenesis and VEGF in Cancer (17 papers), Protein Kinase Regulation and GTPase Signaling (14 papers) and Inflammatory mediators and NSAID effects (12 papers). Caroline Wheeler‐Jones collaborates with scholars based in United Kingdom, United States and Australia. Caroline Wheeler‐Jones's co-authors include Rebecca A. Houliston, Kathleen M. Botham, Andrew A. Pitsillides, Jeremy D. Pearson, Ian Zachary, Robin ABU-GHAZALEH, Jonathan Elliott, Claire Clarkin, Michael J. May and John F. Martin and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Caroline Wheeler‐Jones

129 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caroline Wheeler‐Jones United Kingdom 37 1.5k 558 484 466 413 131 3.9k
Hui Liao China 36 1.5k 1.0× 821 1.5× 728 1.5× 502 1.1× 392 0.9× 107 4.6k
Janice Russell United States 39 1.4k 0.9× 702 1.3× 903 1.9× 445 1.0× 518 1.3× 109 4.2k
Sean Alber United States 33 1.3k 0.9× 488 0.9× 1.0k 2.1× 292 0.6× 366 0.9× 55 3.7k
Satoshi Fujii Japan 35 1.9k 1.2× 417 0.7× 673 1.4× 333 0.7× 604 1.5× 149 4.5k
Mariano Sánchez Crespo Spain 38 1.4k 0.9× 362 0.6× 1.3k 2.7× 481 1.0× 464 1.1× 140 4.0k
Izumi Hayashi Japan 40 1.9k 1.2× 576 1.0× 619 1.3× 500 1.1× 268 0.6× 152 5.0k
Kei Satoh Japan 38 1.4k 0.9× 555 1.0× 1.5k 3.0× 446 1.0× 561 1.4× 169 4.5k
Kirk M. Druey United States 37 2.8k 1.8× 836 1.5× 769 1.6× 553 1.2× 191 0.5× 98 5.2k
Timothy A. McCaffrey United States 35 2.1k 1.3× 386 0.7× 547 1.1× 230 0.5× 373 0.9× 88 4.0k
Tetsuaki Hirase Japan 27 3.0k 2.0× 597 1.1× 620 1.3× 844 1.8× 389 0.9× 57 6.1k

Countries citing papers authored by Caroline Wheeler‐Jones

Since Specialization
Citations

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

Fields of papers citing papers by Caroline Wheeler‐Jones

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Caroline Wheeler‐Jones. 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 Caroline Wheeler‐Jones. The network helps show where Caroline Wheeler‐Jones may publish in the future.

Co-authorship network of co-authors of Caroline Wheeler‐Jones

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline Wheeler‐Jones. A scholar is included among the top collaborators of Caroline Wheeler‐Jones 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 Caroline Wheeler‐Jones. Caroline Wheeler‐Jones 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.
Wheeler‐Jones, Caroline, et al.. (2024). Endothelial dysfunction in neurodegenerative disease: Is endothelial inflammation an overlooked druggable target?. Journal of Neuroimmunology. 391. 578363–578363. 6 indexed citations
2.
Lynam, Eleanor, et al.. (2022). Simultaneous Measurement of Endothelial Cell Proliferation and Cell Cycle Stage Using Flow Cytometry. Methods in molecular biology. 2475. 223–228. 1 indexed citations
3.
Mirczuk, Samantha, Christopher Scudder, Jordan E. Read, et al.. (2021). Natriuretic Peptide Expression and Function in GH3 Somatolactotropes and Feline Somatotrope Pituitary Tumours. International Journal of Molecular Sciences. 22(3). 1076–1076. 1 indexed citations
4.
Patel, Jessal J., Ellen Neven, Anja Verhulst, et al.. (2021). N‐acetylcysteine (NAC) differentially affects arterial medial calcification and bone formation: The role ofl‐cysteine and hydrogen sulphide. Journal of Cellular Physiology. 237(1). 1070–1086. 9 indexed citations
5.
Faulkner, Ashton, Eleanor Lynam, Robert H. Purcell, et al.. (2020). Context-dependent regulation of endothelial cell metabolism: differential effects of the PPARβ/δ agonist GW0742 and VEGF-A. Scientific Reports. 10(1). 7849–7849. 18 indexed citations
6.
Patel, Jessal J., José Luís Millán, Timothy R. Arnett, et al.. (2019). Inhibition of vascular smooth muscle cell calcification by ATP analogues. Purinergic Signalling. 15(3). 315–326. 10 indexed citations
7.
Vara, Dina, Matthew Burgess, Kate Wicks, et al.. (2017). Direct Activation of NADPH Oxidase 2 by 2-Deoxyribose-1-Phosphate Triggers Nuclear Factor Kappa B-Dependent Angiogenesis. Antioxidants and Redox Signaling. 28(2). 110–130. 31 indexed citations
8.
Patel, Jessal J., Dongxing Zhu, Britt Opdebeeck, et al.. (2017). Inhibition of arterial medial calcification and bone mineralization by extracellular nucleotides: The same functional effect mediated by different cellular mechanisms. Journal of Cellular Physiology. 233(4). 3230–3243. 37 indexed citations
9.
Bishop‐Bailey, David, et al.. (2014). Lipid-Metabolizing CYPs in the Regulation and Dysregulation of Metabolism. Annual Review of Nutrition. 34(1). 261–279. 52 indexed citations
10.
Tivers, Mickey, Arthur House, Ken Smith, Caroline Wheeler‐Jones, & Victoria J. Lipscomb. (2014). Markers of Angiogenesis Associated with Surgical Attenuation of Congenital Portosystemic Shunts in Dogs. Journal of Veterinary Internal Medicine. 28(5). 1424–1432. 3 indexed citations
11.
Wheeler‐Jones, Caroline, et al.. (2012). Saturated fatty acid-activated macrophage-conditioned medium activates MAP kinases and impairs insulin sensitivity in C2C12 myotubes. 28. 1 indexed citations
12.
13.
Maggio, Paola, et al.. (2010). Inhibition of macrophage inflammatory cytokine secretion by chylomicron remnants is dependent on their uptake by the low density lipoprotein receptor. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1811(3). 209–220. 7 indexed citations
14.
Thompson, Iain, Kim Jonas, Jacky M. Burrin, et al.. (2009). Molecular characterisation and functional interrogation of a local natriuretic peptide system in rodent pituitaries, αT3-1 and LβT2 gonadotroph cells. Journal of Endocrinology. 203(2). 215–229. 21 indexed citations
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Saka, Masako, Christopher MacKenzie, Robert J. Drummond, et al.. (2007). Cytokine upregulation of proteinase‐activated‐receptors 2 and 4 expression mediated by p38 MAP kinase and inhibitory kappa B kinaseβin human endothelial cells. British Journal of Pharmacology. 150(8). 1044–1054. 69 indexed citations
18.
Bailey, Simon, Caroline Wheeler‐Jones, & Jonathan Elliott. (2003). Uptake of 5‐hydroxytryptamine by equine digital vein endothelial cells: inhibition by amines found in the equine caecum. Equine Veterinary Journal. 35(2). 164–169. 25 indexed citations
19.
Wyatt, Amanda W., Joern R. Steinert, Caroline Wheeler‐Jones, et al.. (2002). Early activation of the p42/p44 MAPK pathway mediates adenosine‐induced nitric oxide production in human endothelial cells: a novel calcium‐insensitive mechanism. The FASEB Journal. 16(12). 1584–1594. 115 indexed citations
20.
Persaud, Shanta J., Paul E. Squires, David Sugden, et al.. (2002). A Key Role for β-Cell Cytosolic Phospholipase A2 in the Maintenance of Insulin Stores But Not in the Initiation of Insulin Secretion. Diabetes. 51(1). 98–104. 39 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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