Steven Hooper

18.8k total citations · 3 hit papers
36 papers, 6.1k citations indexed

About

Steven Hooper is a scholar working on Molecular Biology, Oncology and Cell Biology. According to data from OpenAlex, Steven Hooper has authored 36 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Oncology and 17 papers in Cell Biology. Recurrent topics in Steven Hooper's work include Cellular Mechanics and Interactions (14 papers), Cancer Cells and Metastasis (12 papers) and Hippo pathway signaling and YAP/TAZ (7 papers). Steven Hooper is often cited by papers focused on Cellular Mechanics and Interactions (14 papers), Cancer Cells and Metastasis (12 papers) and Hippo pathway signaling and YAP/TAZ (7 papers). Steven Hooper collaborates with scholars based in United Kingdom, United States and Japan. Steven Hooper's co-authors include Erik Sahai, Kevin J. Harrington, Cédric Gaggioli, Cristina Hidalgo-Carcedo, John F. Marshall, Robert Grosse, Robert P. Jenkins, Peter Williamson, Fernando Calvo and Nil Ege and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Steven Hooper

35 papers receiving 6.1k citations

Hit Papers

Fibroblast-led collective invasion of carcinoma cells wit... 2007 2026 2013 2019 2007 2013 2015 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven Hooper United Kingdom 28 3.0k 2.6k 2.5k 1.0k 839 36 6.1k
Paul Timpson Australia 49 3.8k 1.3× 2.5k 1.0× 2.0k 0.8× 1.3k 1.2× 825 1.0× 112 7.1k
Gregory D. Longmore United States 54 4.3k 1.4× 2.7k 1.0× 2.7k 1.1× 988 0.9× 923 1.1× 133 8.6k
Cédric Gaggioli France 26 2.2k 0.7× 2.0k 0.8× 1.4k 0.6× 959 0.9× 501 0.6× 37 4.4k
Andreas Friedl United States 37 2.1k 0.7× 1.6k 0.6× 1.6k 0.7× 825 0.8× 876 1.0× 63 4.9k
Victoria Sanz‐Moreno United Kingdom 35 2.7k 0.9× 1.6k 0.6× 1.6k 0.7× 762 0.7× 423 0.5× 63 4.7k
Senthil K. Muthuswamy United States 46 6.3k 2.1× 4.4k 1.7× 2.3k 0.9× 1.4k 1.3× 700 0.8× 91 9.7k
Erik H.J. Danen Netherlands 42 3.4k 1.1× 1.4k 0.5× 2.2k 0.9× 1.0k 1.0× 691 0.8× 120 6.7k
Paraic A. Kenny United States 31 2.6k 0.9× 2.1k 0.8× 854 0.3× 900 0.9× 934 1.1× 85 5.2k
Johnathon N. Lakins United States 24 3.5k 1.2× 3.5k 1.3× 4.6k 1.9× 1.1k 1.0× 2.8k 3.4× 30 9.3k
Katia Manova‐Todorova United States 27 3.9k 1.3× 2.8k 1.1× 811 0.3× 1.2k 1.2× 633 0.8× 48 6.8k

Countries citing papers authored by Steven Hooper

Since Specialization
Citations

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

Fields of papers citing papers by Steven Hooper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Steven Hooper

This figure shows the co-authorship network connecting the top 25 collaborators of Steven Hooper. A scholar is included among the top collaborators of Steven Hooper 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 Steven Hooper. Steven Hooper 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.
Rullan, Antonio, Yutaka Naito, Dhruva Biswas, et al.. (2024). Cancer cell – Fibroblast crosstalk via HB-EGF, EGFR, and MAPK signaling promotes the expression of macrophage chemo-attractants in squamous cell carcinoma. iScience. 27(9). 110635–110635. 4 indexed citations
2.
Kato, Takuya, Robert P. Jenkins, Stefanie Derzsi, et al.. (2023). Interplay of adherens junctions and matrix proteolysis determines the invasive pattern and growth of squamous cell carcinoma. eLife. 12. 6 indexed citations
3.
Romani, Patrizia, Probir Chakravarty, Colin D.H. Ratcliffe, et al.. (2021). EphB6 Regulates TFEB-Lysosomal Pathway and Survival of Disseminated Indolent Breast Cancer Cells. Cancers. 13(5). 1079–1079. 16 indexed citations
4.
Arwert, Esther N., Antonio Rullan, Stefanie Derzsi, et al.. (2020). STING and IRF3 in stromal fibroblasts enable sensing of genomic stress in cancer cells to undermine oncolytic viral therapy. Nature Cell Biology. 22(7). 758–766. 72 indexed citations
5.
Ege, Nil, Anna M. Dowbaj, Ming Jiang, et al.. (2018). Quantitative Analysis Reveals that Actin and Src-Family Kinases Regulate Nuclear YAP1 and Its Export. Cell Systems. 6(6). 692–708.e13. 100 indexed citations
6.
Sadok, Amine, Afshan McCarthy, John Caldwell, et al.. (2015). Rho Kinase Inhibitors Block Melanoma Cell Migration and Inhibit Metastasis. Cancer Research. 75(11). 2272–2284. 99 indexed citations
7.
Calvo, Fernando, Romana Ranftl, Steven Hooper, et al.. (2015). Cdc42EP3/BORG2 and Septin Network Enables Mechano-transduction and the Emergence of Cancer-Associated Fibroblasts. Cell Reports. 13(12). 2699–2714. 102 indexed citations
8.
Acton, Sophie E., Aaron J. Farrugia, Jillian L. Astarita, et al.. (2014). Dendritic cells control fibroblastic reticular network tension and lymph node expansion. Nature. 514(7523). 498–502. 214 indexed citations
9.
Calvo, Fernando, Nil Ege, A. Grande-García, et al.. (2013). Mechanotransduction and YAP-dependent matrix remodelling is required for the generation and maintenance of cancer-associated fibroblasts. Nature Cell Biology. 15(6). 637–646. 1076 indexed citations breakdown →
11.
Hidalgo-Carcedo, Cristina, Steven Hooper, Peter Williamson, et al.. (2010). Collective cell migration requires suppression of actomyosin at cell–cell contacts mediated by DDR1 and the cell polarity regulators Par3 and Par6. Nature Cell Biology. 13(1). 49–59. 287 indexed citations
12.
Hooper, Steven, Cédric Gaggioli, & Erik Sahai. (2009). A chemical biology screen reveals a role for Rab21-mediated control of actomyosin contractility in fibroblast-driven cancer invasion. British Journal of Cancer. 102(2). 392–402. 61 indexed citations
13.
Giampieri, Silvia, Cerys Manning, Steven Hooper, et al.. (2009). Localized and reversible TGFβ signalling switches breast cancer cells from cohesive to single cell motility. Nature Cell Biology. 11(11). 1287–1296. 489 indexed citations
14.
Hooper, Steven, et al.. (2008). La collecte comme iconoclasme. Gradhiva. 120–133.
15.
Macpherson, Iain R., Steven Hooper, Alan Serrels, et al.. (2007). p120-catenin is required for the collective invasion of squamous cell carcinoma cells via a phosphorylation-independent mechanism. Oncogene. 26(36). 5214–5228. 51 indexed citations
16.
Gaggioli, Cédric, Steven Hooper, Cristina Hidalgo-Carcedo, et al.. (2007). Fibroblast-led collective invasion of carcinoma cells with differing roles for RhoGTPases in leading and following cells. Nature Cell Biology. 9(12). 1392–1400. 1191 indexed citations breakdown →
17.
Hooper, Steven, John F. Marshall, & Erik Sahai. (2006). Tumor Cell Migration in Three Dimensions. Methods in enzymology on CD-ROM/Methods in enzymology. 406. 625–643. 53 indexed citations
18.
Hooper, Steven, Arnold Hill, Susan Kennedy, et al.. (2002). Tamoxifen as the primary treatment in elderly patients with breast cancer. Irish Journal of Medical Science (1971 -). 171(1). 28–30. 7 indexed citations
19.
Xavier, Gabriela da Silva, et al.. (2000). Glucose-stimulated Preproinsulin Gene Expression and Nucleartrans-Location of Pancreatic Duodenum Homeobox-1 Require Activation of Phosphatidylinositol 3-Kinase but Not p38 MAPK/SAPK2. Journal of Biological Chemistry. 275(21). 15977–15984. 97 indexed citations
20.
Ben-Levy, R, et al.. (1998). Nuclear export of the stress-activated protein kinase p38 mediated by its substrate MAPKAP kinase-2. Current Biology. 8(19). 1049–1057. 286 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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