David Waugh

6.7k total citations · 1 hit paper
90 papers, 5.0k citations indexed

About

David Waugh is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, David Waugh has authored 90 papers receiving a total of 5.0k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 28 papers in Oncology and 28 papers in Cancer Research. Recurrent topics in David Waugh's work include Prostate Cancer Treatment and Research (16 papers), Chemokine receptors and signaling (14 papers) and Receptor Mechanisms and Signaling (14 papers). David Waugh is often cited by papers focused on Prostate Cancer Treatment and Research (16 papers), Chemokine receptors and signaling (14 papers) and Receptor Mechanisms and Signaling (14 papers). David Waugh collaborates with scholars based in United Kingdom, United States and Australia. David Waugh's co-authors include Catherine Wilson, Patrick G. Johnston, Pamela Maxwell, A Hill, Suzanne McFarlane, J. Michael Conlon, Angela Seaton, Dianne M. Perez, Joe M. O’Sullivan and Manuel Salto‐Tellez and has published in prestigious journals such as Journal of Biological Chemistry, Nature Medicine and Journal of Clinical Oncology.

In The Last Decade

David Waugh

87 papers receiving 4.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Interleukin-8 Pathway in Cancer

2008 1.7k citations David Waugh, Catherine Wilson Clinical Cancer Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Waugh United Kingdom	33	2.1k	2.0k	1.3k	914	672	90	5.0k
Ramesh K. Ganju United States	50	2.7k 1.3×	2.1k 1.0×	1.9k 1.5×	813 0.9×	322 0.5×	127	6.6k
Bernd Baumann Germany	39	3.1k 1.5×	1.5k 0.8×	1.2k 0.9×	1.7k 1.9×	260 0.4×	84	5.7k
Xin Hong China	43	2.6k 1.2×	1.9k 1.0×	2.0k 1.6×	942 1.0×	459 0.7×	142	6.2k
Vincent Castronovo Belgium	49	4.2k 2.0×	1.6k 0.8×	1.6k 1.3×	995 1.1×	489 0.7×	117	6.7k
Kathleen Kelly United States	44	3.6k 1.7×	1.2k 0.6×	907 0.7×	894 1.0×	684 1.0×	88	5.9k
Stéphane Garcia France	36	1.9k 0.9×	1.3k 0.7×	422 0.3×	858 0.9×	477 0.7×	87	4.4k
Carl J. Kozlosky United States	18	3.1k 1.5×	2.0k 1.0×	2.1k 1.7×	1.2k 1.3×	258 0.4×	20	6.8k
Beverly J. Castner United States	13	2.5k 1.2×	1.8k 0.9×	1.3k 1.0×	1.2k 1.3×	211 0.3×	18	5.8k
Frédéric Hollande Australia	37	1.9k 0.9×	1.5k 0.8×	678 0.5×	732 0.8×	365 0.5×	97	4.1k
Jianjun Shen United States	45	4.4k 2.1×	1.4k 0.7×	610 0.5×	1.3k 1.4×	635 0.9×	151	6.6k

Countries citing papers authored by David Waugh

Since Specialization

Citations

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

Fields of papers citing papers by David Waugh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Waugh

This figure shows the co-authorship network connecting the top 25 collaborators of David Waugh. A scholar is included among the top collaborators of David Waugh 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 David Waugh. David Waugh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Savi, Flávia Medeiros, Jennifer H. Gunter, Shahrouz Amini, et al.. (2024). Humanized In Vivo Bone Tissue Engineering: In Vitro Preculture Conditions Control the Structural, Cellular, and Matrix Composition of Humanized Bone Organs. Advanced Healthcare Materials. 14(2). e2401939–e2401939. 6 indexed citations

Ravichandran, Akhilandeshwari, Christoph Meinert, David Waugh, et al.. (2024). ECM-mimicking hydrogel models of human adipose tissue identify deregulated lipid metabolism in the prostate cancer-adipocyte crosstalk under antiandrogen therapy. Materials Today Bio. 30. 101424–101424. 2 indexed citations

Savage, Kienan I., Paul G. O’Reilly, Philip D. Dunne, et al.. (2019). ACE: A Workbench Using Evolutionary Genetic Algorithms for Analyzing Association in TCGA. Cancer Research. 79(8). 2072–2075. 6 indexed citations

McCann, Christopher, Nyree Crawford, Joanna Majkut, et al.. (2018). Cytoplasmic FLIP(S) and nuclear FLIP(L) mediate resistance of castrate-resistant prostate cancer to apoptosis induced by IAP antagonists. Cell Death and Disease. 9(11). 1081–1081. 12 indexed citations

Dunne, Philip D., Darragh G. McArt, Conor A. Bradley, et al.. (2016). Challenging the Cancer Molecular Stratification Dogma: Intratumoral Heterogeneity Undermines Consensus Molecular Subtypes and Potential Diagnostic Value in Colorectal Cancer. Clinical Cancer Research. 22(16). 4095–4104. 103 indexed citations

Maxwell, Pamela, Chee Wee Ong, Kelly M. Redmond, et al.. (2016). PTEN deficiency promotes macrophage infiltration and hypersensitivity of prostate cancer to IAP antagonist/radiation combination therapy. Oncotarget. 7(7). 7885–7898. 32 indexed citations

McArt, Darragh G., Ken Mills, Mark Catherwood, et al.. (2013). Validation of Next Generation Sequencing Technologies in Comparison to Current Diagnostic Gold Standards for BRAF, EGFR and KRAS Mutational Analysis. PLoS ONE. 8(7). e69604–e69604. 85 indexed citations

Crawford, Nyree, Caitriona Holohan, Joanna Majkut, et al.. (2013). SAHA overcomes FLIP-mediated inhibition of SMAC mimetic-induced apoptosis in mesothelioma. Cell Death and Disease. 4(7). e733–e733. 31 indexed citations

Maxwell, Pamela, Roberta Mazzucchelli, Rodolfo Montironi, et al.. (2012). Elevation of c-FLIP in Castrate-Resistant Prostate Cancer Antagonizes Therapeutic Response to Androgen Receptor–Targeted Therapy. Clinical Cancer Research. 18(14). 3822–3833. 51 indexed citations

10.

Byrne, Niall M., et al.. (2012). Androgen deprivation results in time‐dependent hypoxia in LNCaP prostate tumours: Informed scheduling of the bioreductive drug AQ4N improves treatment response. International Journal of Cancer. 132(6). 1323–1332. 37 indexed citations

11.

Valentine, Andrea, Martin O’Rourke, Anita Yakkundi, et al.. (2011). FKBPL and Peptide Derivatives: Novel Biological Agents That Inhibit Angiogenesis by a CD44-Dependent Mechanism. Clinical Cancer Research. 17(5). 1044–1056. 44 indexed citations

12.

Seaton, Angela, P Maxwell, A Hill, et al.. (2009). Inhibition of constitutive and cxc-chemokine-induced NF-κB activity potentiates ansamycin-based HSP90-inhibitor cytotoxicity in castrate-resistant prostate cancer cells. British Journal of Cancer. 101(9). 1620–1629. 10 indexed citations

13.

Waugh, David & Catherine Wilson. (2008). The Interleukin-8 Pathway in Cancer. Clinical Cancer Research. 14(21). 6735–6741. 1701 indexed citations breakdown →

14.

Wilson, Catherine, Timothy R. Wilson, Patrick Johnston, Daniel B. Longley, & David Waugh. (2007). Interleukin-8/CXCR2 signaling plays an important role in conferring resistance of prostate cancer cells to chemotherapy. Molecular Cancer Therapeutics. 6. 2 indexed citations

15.

Maxwell, P, Ryan S. Gallagher, Angela Seaton, et al.. (2007). HIF-1 and NF-κB-mediated upregulation of CXCR1 and CXCR2 expression promotes cell survival in hypoxic prostate cancer cells. Oncogene. 26(52). 7333–7345. 169 indexed citations

16.

Seaton, Angela, et al.. (2006). CXCR2/NF-kappaB/Bcl-2-survivin signalling pathway promotes resistance to oxaliplatin in metastatic prostate cancer cells. Cancer Research. 66. 880–880. 2 indexed citations

17.

Hill, A, et al.. (2003). CD44 Expression on prostate cancer cells correlates with adhesion to bone marrow endothelial cells.. Clinical Cancer Research. 9(16). 1 indexed citations

18.

Zuscik, Michael J., Scott A. Sands, Sean Ross, et al.. (2000). Overexpression of the α1B-adrenergic receptor causes apoptotic neurodegeneration: Multiple system atrophy. Nature Medicine. 6(12). 1388–1394. 104 indexed citations

19.

McCune, Dan F., Stephanie E. Edelmann, Ginell R. Post, et al.. (2000). Regulation of the Cellular Localization and Signaling Properties of the α_1B- and α_1D-Adrenoceptors by Agonists and Inverse Agonists. Molecular Pharmacology. 57(4). 659–666. 90 indexed citations

20.

Saha, Shubhayu, David Waugh, Peipei Zhao, Peter W. Abel, & David Smith. (1998). Role of conformational constraints of position 7 of the disulphide bridge of h‐α‐CGRP derivatives in their agonist versus antagonist properties. Journal of Peptide Research. 52(2). 112–120. 13 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.

Explore authors with similar magnitude of impact