Amanda S. Coutts

2.2k total citations
44 papers, 1.6k citations indexed

About

Amanda S. Coutts is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Amanda S. Coutts has authored 44 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 20 papers in Oncology and 8 papers in Genetics. Recurrent topics in Amanda S. Coutts's work include Cancer-related Molecular Pathways (15 papers), Estrogen and related hormone effects (8 papers) and DNA Repair Mechanisms (6 papers). Amanda S. Coutts is often cited by papers focused on Cancer-related Molecular Pathways (15 papers), Estrogen and related hormone effects (8 papers) and DNA Repair Mechanisms (6 papers). Amanda S. Coutts collaborates with scholars based in United Kingdom, Canada and Sweden. Amanda S. Coutts's co-authors include Nicholas B. La Thangue, Leigh C. Murphy, Donald M. Black, Elen Griffith, Louise Weston, Helmut Dotzlaw, Deborah Douglas, Anne Graham, Etienne Leygue and Peter H. Watson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Amanda S. Coutts

43 papers receiving 1.6k citations

Peers

Amanda S. Coutts
Victor Stastny United States
Rina Plattner United States
Gonosuke Sonoda United States
Larisa Litovchick United States
Gretchen Argast United States
Steven J. Weintraub United States
Diep Nguyen United States
Victor Stastny United States
Amanda S. Coutts
Citations per year, relative to Amanda S. Coutts Amanda S. Coutts (= 1×) peers Victor Stastny

Countries citing papers authored by Amanda S. Coutts

Since Specialization
Citations

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

Fields of papers citing papers by Amanda S. Coutts

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amanda S. Coutts. 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 Amanda S. Coutts. The network helps show where Amanda S. Coutts may publish in the future.

Co-authorship network of co-authors of Amanda S. Coutts

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda S. Coutts. A scholar is included among the top collaborators of Amanda S. Coutts 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 Amanda S. Coutts. Amanda S. Coutts 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.
Boocock, David J., et al.. (2023). PARP1 mediated PARylation contributes to myogenic progression and glucocorticoid transcriptional response. Cell Death Discovery. 9(1). 133–133. 5 indexed citations
2.
Coutts, Amanda S. & Nicholas B. La Thangue. (2016). Regulation of actin nucleation and autophagosome formation. Cellular and Molecular Life Sciences. 73(17). 3249–3263. 32 indexed citations
3.
Coutts, Amanda S. & Nicholas B. La Thangue. (2015). Actin nucleation by WH2 domains at the autophagosome. Nature Communications. 6(1). 7888–7888. 66 indexed citations
4.
Adighibe, Omanma, Helen Turley, Russell Leek, et al.. (2014). JMY protein, a regulator of P53 and cytoplasmic actin filaments, is expressed in normal and neoplastic tissues. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 465(6). 715–722. 11 indexed citations
5.
New, Mark, Heidi Olzscha, Geng Liu, et al.. (2013). A regulatory circuit that involves HR23B and HDAC6 governs the biological response to HDAC inhibitors. Cell Death and Differentiation. 20(10). 1306–1316. 37 indexed citations
6.
Zheng, Shunsheng, Shonagh Munro, Geng Liu, et al.. (2012). Arginine methylation controls growth regulation by E2F‐1. The EMBO Journal. 31(7). 1785–1797. 174 indexed citations
7.
Coutts, Amanda S., Isabel M. Pires, Louise Weston, et al.. (2011). Hypoxia-driven cell motility reflects the interplay between JMY and HIF-1α. Oncogene. 30(48). 4835–4842. 32 indexed citations
8.
Coutts, Amanda S., et al.. (2010). E2F-1 regulation by an unusual DNA damage-responsive DP partner subunit. Cell Death and Differentiation. 18(1). 122–132. 22 indexed citations
9.
Coutts, Amanda S., Louise Weston, & Nicholas B. La Thangue. (2010). Actin nucleation by a transcription co-factor that links cytoskeletal events with the p53 response. Cell Cycle. 9(8). 1511–1515. 16 indexed citations
10.
Zalmas, Lykourgos‐Panagiotis, et al.. (2008). DNA‐damage response control of E2F7 and E2F8. EMBO Reports. 9(3). 252–259. 112 indexed citations
11.
Griffith, Elen, Amanda S. Coutts, & Donald M. Black. (2005). RNAi knockdown of the focal adhesion protein TES reveals its role in actin stress fibre organisation. Cell Motility and the Cytoskeleton. 60(3). 140–152. 45 indexed citations
12.
Coutts, Amanda S. & Nicholas B. La Thangue. (2005). The p53 response: Emerging levels of co-factor complexity. Biochemical and Biophysical Research Communications. 331(3). 778–785. 65 indexed citations
13.
Coutts, Amanda S., Etienne Leygue, & Leigh C. Murphy. (1999). Variant estrogen receptor-alpha messenger RNA expression in hormone-independent human breast cancer cells. Journal of Molecular Endocrinology. 23(3). 325–336. 5 indexed citations
14.
Spencer, Virginia A., Amanda S. Coutts, Shanti K. Samuel, Leigh C. Murphy, & James Davie. (1998). Estrogen Regulates the Association of Intermediate Filament Proteins with Nuclear DNA in Human Breast Cancer Cells. Journal of Biological Chemistry. 273(44). 29093–29097. 37 indexed citations
15.
Murphy, Leigh C., Helmut Dotzlaw, Etienne Leygue, Amanda S. Coutts, & Peter H. Watson. (1998). The pathophysiological role of estrogen receptor variants in human breast cancer. The Journal of Steroid Biochemistry and Molecular Biology. 65(1-6). 175–180. 40 indexed citations
16.
Murphy, Leigh C., Etienne Leygue, Helmut Dotzlaw, et al.. (1997). Oestrogen Receptor Variants and Mutations in Human Breast Cancer. Annals of Medicine. 29(3). 221–234. 25 indexed citations
17.
Holth, Laurel T., et al.. (1997). Estrogen Receptor Diminishes DNA-Binding Activities of Chicken GATA-1 and CACCC-Binding Proteins. DNA and Cell Biology. 16(12). 1477–1482. 3 indexed citations
18.
Miller, Teresa, Yan Jin, Jian-Min Sun, et al.. (1996). Analysis of human breast cancer nuclear proteins binding to the promoter elements of the c-myc gene. Journal of Cellular Biochemistry. 60(4). 560–571. 19 indexed citations
19.
Coutts, Amanda S., James Davie, Helmut Dotzlaw, & Leigh C. Murphy. (1996). Estrogen regulation of nuclear matrix-intermediate filament proteins in human breast cancer cells. Journal of Cellular Biochemistry. 63(2). 174–184. 37 indexed citations
20.
Murphy, Leigh C., et al.. (1994). Regulation of gene expression in T-47D human breast cancer cells by progestins and antiprogestins. Human Reproduction. 9(suppl 1). 174–180. 6 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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