Rita E. Godfrey

832 total citations
23 papers, 641 citations indexed

About

Rita E. Godfrey is a scholar working on Molecular Biology, Genetics and Endocrinology. According to data from OpenAlex, Rita E. Godfrey has authored 23 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Endocrinology. Recurrent topics in Rita E. Godfrey's work include Bacterial Genetics and Biotechnology (10 papers), Escherichia coli research studies (6 papers) and Viral gastroenteritis research and epidemiology (3 papers). Rita E. Godfrey is often cited by papers focused on Bacterial Genetics and Biotechnology (10 papers), Escherichia coli research studies (6 papers) and Viral gastroenteritis research and epidemiology (3 papers). Rita E. Godfrey collaborates with scholars based in United Kingdom, Egypt and Japan. Rita E. Godfrey's co-authors include Francesco Michelangeli, Jonathan G. Bilmen, Alan Colman, James Shuttleworth, Stephen Busby, Laura L. Wootton, Oliver S. Smart, Douglas F. Browning, Stephen C. Tovey and Victoria Sabine and has published in prestigious journals such as Environmental Science & Technology, The EMBO Journal and Biochemical Journal.

In The Last Decade

Rita E. Godfrey

22 papers receiving 622 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rita E. Godfrey United Kingdom 12 332 179 110 57 50 23 641
David L. Greenman United States 18 338 1.0× 158 0.9× 164 1.5× 42 0.7× 6 0.1× 64 934
Riikka Pellinen Finland 17 586 1.8× 27 0.2× 172 1.6× 36 0.6× 31 0.6× 27 1.2k
Marc Dauplais France 11 492 1.5× 165 0.9× 216 2.0× 23 0.4× 9 0.2× 15 885
Stephan Jung Germany 13 459 1.4× 13 0.1× 38 0.3× 87 1.5× 35 0.7× 26 827
Alexander Miller United States 14 341 1.0× 22 0.1× 184 1.7× 45 0.8× 8 0.2× 26 635
Hong Wu China 13 180 0.5× 46 0.3× 77 0.7× 13 0.2× 5 0.1× 43 484
Michèle Minét France 12 1.3k 3.8× 30 0.2× 42 0.4× 67 1.2× 24 0.5× 14 1.8k
Aı̈da Abou-Haı̈la France 13 227 0.7× 19 0.1× 138 1.3× 62 1.1× 9 0.2× 31 735
J.W.G.M. Wilmer Netherlands 14 126 0.4× 188 1.1× 46 0.4× 16 0.3× 38 0.8× 26 542
Jun Ling United States 13 222 0.7× 25 0.1× 79 0.7× 41 0.7× 5 0.1× 25 567

Countries citing papers authored by Rita E. Godfrey

Since Specialization
Citations

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

Fields of papers citing papers by Rita E. Godfrey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rita E. Godfrey. 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 Rita E. Godfrey. The network helps show where Rita E. Godfrey may publish in the future.

Co-authorship network of co-authors of Rita E. Godfrey

This figure shows the co-authorship network connecting the top 25 collaborators of Rita E. Godfrey. A scholar is included among the top collaborators of Rita E. Godfrey 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 Rita E. Godfrey. Rita E. Godfrey 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.
Hothersall, Joanne, Rita E. Godfrey, Colin Robinson, et al.. (2022). Inexpensive protein overexpression driven by the NarL transcription activator protein. Biotechnology and Bioengineering. 119(6). 1614–1623. 7 indexed citations
2.
Hothersall, Joanne, et al.. (2022). New vectors for urea-inducible recombinant protein production. New Biotechnology. 72. 89–96. 5 indexed citations
3.
Godfrey, Rita E., et al.. (2022). Novel organisation and regulation of the pic promoter from enteroaggregative and uropathogenic Escherichia coli. Virulence. 13(1). 1393–1406. 1 indexed citations
4.
Hothersall, Joanne, et al.. (2021). The PAR promoter expression system: Modified lac promoters for controlled recombinant protein production in Escherichia coli. New Biotechnology. 64. 1–8. 9 indexed citations
5.
Hothersall, Joanne, et al.. (2020). Activation by NarL at the Escherichia coli ogt promoter. Biochemical Journal. 477(15). 2807–2820. 9 indexed citations
6.
Browning, Douglas F., et al.. (2019). Exploitation of the Escherichia coli lac operon promoter for controlled recombinant protein production. Biochemical Society Transactions. 47(2). 755–763. 31 indexed citations
7.
Rossiter, Amanda E., Rita E. Godfrey, Jack A. Connolly, et al.. (2014). Expression of different bacterial cytotoxins is controlled by two global transcription factors, CRP and Fis, that co-operate in a shared-recruitment mechanism. Biochemical Journal. 466(2). 323–335. 14 indexed citations
8.
Rossiter, Amanda E., Douglas F. Browning, Denisse L. Leyton, et al.. (2011). Transcription of the plasmid‐encoded toxin gene from Enteroaggregative Escherichia coli is regulated by a novel co‐activation mechanism involving CRP and Fis. Molecular Microbiology. 81(1). 179–191. 27 indexed citations
9.
Lloyd, Georgina S., Rita E. Godfrey, & Stephen Busby. (2010). Targets for the MalI repressor at the divergent Escherichia coli K-12 malX-malI promoters. FEMS Microbiology Letters. 305(1). 28–34. 3 indexed citations
10.
Lloyd, Georgina S., et al.. (2008). Transcription initiation in theEscherichia coliK-12malIâmalXintergenic region and the role of the cyclic AMP receptor protein. FEMS Microbiology Letters. 288(2). 250–257. 9 indexed citations
11.
Williams, Tim, Fernando Ortega, Victoria Sabine, et al.. (2008). Transcriptomic responses of European flounder (Platichthys flesus) to model toxicants. Aquatic Toxicology. 90(2). 83–91. 49 indexed citations
12.
Williams, Tim, Amer M. Diab, Stephen G. George, et al.. (2006). Development of the GENIPOL European Flounder (Platichthys flesus) Microarray and Determination of Temporal Transcriptional Responses to Cadmium at Low Dose.. Environmental Science & Technology. 40(20). 6479–6488. 73 indexed citations
13.
14.
Bilmen, Jonathan G., Laura L. Wootton, Rita E. Godfrey, Oliver S. Smart, & Francesco Michelangeli. (2002). Inhibition of SERCA Ca2+ pumps by 2‐aminoethoxydiphenyl borate (2‐APB). European Journal of Biochemistry. 269(15). 3678–3687. 105 indexed citations
15.
Hughes, Philip, Damon A. Lowes, Jonathan G. Bilmen, et al.. (2000). Estrogenic Alkylphenols Induce Cell Death by Inhibiting Testis Endoplasmic Reticulum Ca2+ Pumps. Biochemical and Biophysical Research Communications. 277(3). 568–574. 140 indexed citations
16.
Tovey, Stephen C., et al.. (2000). Subtype identification and functional properties of inositol 1,4,5-trisphosphate receptors in heart and aorta. Pharmacological Research. 42(6). 581–590. 11 indexed citations
17.
Tovey, Stephen C., Rita E. Godfrey, Mokdad Mezna, et al.. (1997). Identification and characterization of inositol 1,4,5-trisphosphate receptors in rat testis. Cell Calcium. 21(4). 311–319. 18 indexed citations
18.
19.
Godfrey, Rita E. & John Davey. (1996). Isolation of ptb1, a gene for the β-subunit of a prenyltransferase from fission yeast. Biochemical Society Transactions. 24(3). 432S–432S.
20.
Shuttleworth, James, Rita E. Godfrey, & Alan Colman. (1990). p40MO15, a cdc2-related protein kinase involved in negative regulation of meiotic maturation of Xenopus oocytes.. The EMBO Journal. 9(10). 3233–3240. 84 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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