Deborah Clarke

2.2k total citations
32 papers, 1.7k citations indexed

About

Deborah Clarke is a scholar working on Pulmonary and Respiratory Medicine, Physiology and Immunology. According to data from OpenAlex, Deborah Clarke has authored 32 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pulmonary and Respiratory Medicine, 14 papers in Physiology and 12 papers in Immunology. Recurrent topics in Deborah Clarke's work include Asthma and respiratory diseases (13 papers), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (10 papers) and Immune Response and Inflammation (6 papers). Deborah Clarke is often cited by papers focused on Asthma and respiratory diseases (13 papers), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (10 papers) and Immune Response and Inflammation (6 papers). Deborah Clarke collaborates with scholars based in United Kingdom, United States and Canada. Deborah Clarke's co-authors include Maria G. Belvisi, Nathan W. Bartlett, Sebastian L. Johnston, Michael R. Edwards, Mark A. Birrell, Matthew A. Sleeman, Tomas Mustelin, Alan J. Knox, Lynne A. Murray and Lisa Corbett and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Immunology and Scientific Reports.

In The Last Decade

Deborah Clarke

30 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah Clarke United Kingdom 22 591 551 500 444 218 32 1.7k
Liboria Siena Italy 27 515 0.9× 744 1.4× 784 1.6× 527 1.2× 122 0.6× 58 2.0k
Neil S. Holden Canada 25 523 0.9× 325 0.6× 499 1.0× 582 1.3× 140 0.6× 31 1.6k
Gye Young Park United States 23 689 1.2× 271 0.5× 316 0.6× 608 1.4× 167 0.8× 55 1.6k
Matthew C. Catley United Kingdom 24 556 0.9× 324 0.6× 416 0.8× 698 1.6× 99 0.5× 36 1.7k
Giuseppina Chiappara Italy 23 546 0.9× 882 1.6× 1.0k 2.0× 429 1.0× 113 0.5× 50 2.0k
Hsin Tai Canada 12 338 0.6× 891 1.6× 513 1.0× 453 1.0× 90 0.4× 16 1.8k
Bruno L. Diaz Brazil 28 531 0.9× 480 0.9× 483 1.0× 669 1.5× 151 0.7× 68 2.1k
Manminder Kaur United Kingdom 18 358 0.6× 383 0.7× 432 0.9× 368 0.8× 81 0.4× 29 1.1k
Osamu Kaminuma Japan 24 931 1.6× 213 0.4× 826 1.7× 571 1.3× 75 0.3× 149 2.0k
Masayuki Ii Japan 12 1.1k 1.8× 191 0.3× 251 0.5× 575 1.3× 396 1.8× 17 2.0k

Countries citing papers authored by Deborah Clarke

Since Specialization
Citations

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

Fields of papers citing papers by Deborah Clarke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deborah Clarke

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah Clarke. A scholar is included among the top collaborators of Deborah Clarke 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 Deborah Clarke. Deborah Clarke 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.
Feleszko, Wojciech, Marco Caminati, Sebastian L. Johnston, et al.. (2025). Effect of tezepelumab on asthma exacerbations co-occurring with infection-attributed acute respiratory illnesses. Annals of Allergy Asthma & Immunology. 136(1). 61–65.e1.
2.
Miranda, Elena, Rebecca Dunmore, Doris M. Rassl, et al.. (2020). Inhibition of mast cells: a novel mechanism by which nintedanib may elicit anti-fibrotic effects. Thorax. 75(9). 754–763. 30 indexed citations
3.
Watson, Julie K., Philip N. Sanders, Rebecca Dunmore, et al.. (2020). Distal lung epithelial progenitor cell function declines with age. Scientific Reports. 10(1). 10490–10490. 34 indexed citations
4.
Gayle, Alicia, Nils Schoof, Margarida Alves, et al.. (2020). Healthcare Resource Utilization Among Patients in England with Systemic Sclerosis-Associated Interstitial Lung Disease: A Retrospective Database Analysis. Advances in Therapy. 37(5). 2460–2476. 10 indexed citations
5.
Roux, Benoît, Eszter Csomor, Carol Feghali‐Bostwick, et al.. (2019). Long intergenic non-coding RNAs regulate human lung fibroblast function: Implications for idiopathic pulmonary fibrosis. Scientific Reports. 9(1). 6020–6020. 20 indexed citations
6.
Sleeman, Matthew A., et al.. (2014). The epithelium in idiopathic pulmonary fibrosis: breaking the barrier. Frontiers in Pharmacology. 4. 173–173. 186 indexed citations
7.
Vousden, Katherine A., et al.. (2013). Engineering Approaches to Develop the Next Generation of Antibodies to Respiratory Targets. Inflammation & Allergy - Drug Targets. 12(2). 99–108. 2 indexed citations
8.
Clarke, Deborah, Alan Carruthers, Tomas Mustelin, & Lynne A. Murray. (2013). Matrix regulation of idiopathic pulmonary fibrosis: the role of enzymes. PubMed. 6(1). 20–20. 86 indexed citations
9.
Bartlett, Nathan W., Jennifer Haas, Jie Zhu, et al.. (2012). Correction: Co-ordinated Role of TLR3, RIG-I and MDA5 in the Innate Response to Rhinovirus in Bronchial Epithelium. PLoS Pathogens. 8(4). 2 indexed citations
10.
Slater, Louise, Nathan W. Bartlett, Jennifer Haas, et al.. (2010). Co-ordinated Role of TLR3, RIG-I and MDA5 in the Innate Response to Rhinovirus in Bronchial Epithelium. PLoS Pathogens. 6(11). e1001178–e1001178. 245 indexed citations
11.
Clarke, Deborah, Gautam Damera, Maria B. Sukkar, & Omar Tliba. (2009). Transcriptional regulation of cytokine function in airway smooth muscle cells. Pulmonary Pharmacology & Therapeutics. 22(5). 436–445. 32 indexed citations
12.
Sutcliffe, Amy, et al.. (2009). Transcriptional regulation of monocyte chemotactic protein‐1 release by endothelin‐1 in human airway smooth muscle cells involves NF‐κB and AP‐1. British Journal of Pharmacology. 157(3). 436–450. 45 indexed citations
13.
Birrell, Mark A., Jorge De Alba, Matthew C. Catley, et al.. (2008). Liver X Receptor Agonists Increase Airway Reactivity in a Model of Asthma via Increasing Airway Smooth Muscle Growth. The Journal of Immunology. 181(6). 4265–4271. 23 indexed citations
14.
Clarke, Deborah, Amy Sutcliffe, Karl Deacon, et al.. (2008). PKCβΙΙ Augments NF-κB-Dependent Transcription at the CCL11 Promoter via p300/CBP-Associated Factor Recruitment and Histone H4 Acetylation. The Journal of Immunology. 181(5). 3503–3514. 39 indexed citations
15.
Clarke, Deborah, et al.. (2008). Lipid metabolites as regulators of airway smooth muscle function. Pulmonary Pharmacology & Therapeutics. 22(5). 426–435. 31 indexed citations
16.
Riley, M I, Deborah Clarke, Amanda L. Tatler, et al.. (2007). β-Tryptase Regulates IL-8 Expression in Airway Smooth Muscle Cells by a PAR-2–Independent Mechanism. American Journal of Respiratory Cell and Molecular Biology. 38(5). 600–608. 28 indexed citations
17.
Bradbury, Dawn A., Deborah Clarke, Claire Seedhouse, et al.. (2005). Vascular Endothelial Growth Factor Induction by Prostaglandin E2 in Human Airway Smooth Muscle Cells Is Mediated by E Prostanoid EP2/EP4 Receptors and SP-1 Transcription Factor Binding Sites. Journal of Biological Chemistry. 280(34). 29993–30000. 81 indexed citations
18.
Clarke, Deborah, Maria G. Belvisi, Matthew C. Catley, et al.. (2004). Identification in human airways smooth muscle cells of the prostanoid receptor and signalling pathway through which PGE2 inhibits the release of GM‐CSF. British Journal of Pharmacology. 141(7). 1141–1150. 41 indexed citations
19.
Clarke, Deborah, Maria G. Belvisi, Elizabeth Hardaker, Robert Newton, & Mark A. Giembycz. (2004). E-Ring 8-Isoprostanes Are Agonists at EP2- and EP4-Prostanoid Receptors on Human Airway Smooth Muscle Cells and Regulate the Release of Colony-Stimulating Factors by Activating cAMP-Dependent Protein Kinase. Molecular Pharmacology. 67(2). 383–393. 21 indexed citations
20.
Spicuzza, Lucia, El‐Bdaoui Haddad, Mark A. Birrell, et al.. (2000). Characterization of the effects of cannabinoids on guinea‐pig tracheal smooth muscle tone: role in the modulation of acetylcholine release from parasympathetic nerves. British Journal of Pharmacology. 130(7). 1720–1726. 19 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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