K. E. Davies

1.6k total citations
38 papers, 1.2k citations indexed

About

K. E. Davies is a scholar working on Molecular Biology, Radiological and Ultrasound Technology and Cell Biology. According to data from OpenAlex, K. E. Davies has authored 38 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Radiological and Ultrasound Technology and 4 papers in Cell Biology. Recurrent topics in K. E. Davies's work include Muscle Physiology and Disorders (10 papers), Nuclear Structure and Function (6 papers) and Family and Patient Care in Intensive Care Units (5 papers). K. E. Davies is often cited by papers focused on Muscle Physiology and Disorders (10 papers), Nuclear Structure and Function (6 papers) and Family and Patient Care in Intensive Care Units (5 papers). K. E. Davies collaborates with scholars based in United Kingdom, Australia and United States. K. E. Davies's co-authors include S. M. Forrest, Andreas Speer, Gareth Cross, Tracey Flint, Britta S. von Ungern‐Sternberg, Mary Hegarty, Kathryn Robson, D. Gardner‐Medwin, John Burn and Andrew Read and has published in prestigious journals such as Nature, The Lancet and Journal of Biological Chemistry.

In The Last Decade

K. E. Davies

38 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K. E. Davies United Kingdom 19 796 222 191 175 175 38 1.2k
Vincent Laugel France 26 1.7k 2.1× 475 2.1× 184 1.0× 171 1.0× 123 0.7× 88 2.3k
M. H. K. Shokeir Canada 19 557 0.7× 355 1.6× 70 0.4× 175 1.0× 60 0.3× 48 1.3k
Gloria Galloway United States 11 731 0.9× 463 2.1× 214 1.1× 126 0.7× 58 0.3× 21 1.2k
Harold F. Falls United States 24 1.0k 1.3× 478 2.2× 30 0.2× 67 0.4× 122 0.7× 50 2.0k
Leslie Acakpo‐Satchivi United States 13 337 0.4× 108 0.5× 129 0.7× 38 0.2× 47 0.3× 28 742
Meinhard Robinow United States 21 781 1.0× 599 2.7× 62 0.3× 116 0.7× 128 0.7× 70 1.7k
Preethi Ramachandran United States 13 514 0.6× 85 0.4× 18 0.1× 60 0.3× 47 0.3× 50 1.1k
Jacov Levy Israel 17 169 0.2× 120 0.5× 20 0.1× 93 0.5× 160 0.9× 42 909
Fung-Yee Chan Australia 12 455 0.6× 79 0.4× 52 0.3× 67 0.4× 93 0.5× 25 1.1k
Michael Niehaus Germany 19 167 0.2× 48 0.2× 624 3.3× 63 0.4× 58 0.3× 62 1.1k

Countries citing papers authored by K. E. Davies

Since Specialization
Citations

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

Fields of papers citing papers by K. E. Davies

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. E. Davies

This figure shows the co-authorship network connecting the top 25 collaborators of K. E. Davies. A scholar is included among the top collaborators of K. E. Davies 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 K. E. Davies. K. E. Davies 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.
Dimech, Wayne, et al.. (2020). Validation of Dried Tube Sample Format Quality Controls for the Monitoring of Viral Load and Blood Screening Assays. Journal of Virological Methods. 285. 113957–113957. 3 indexed citations
2.
Davies, K. E., Max Bulsara, Anne‐Sylvie Ramelet, & Leanne Monterosso. (2017). Content validity testing of the ESAT©: A decision aid tool for performing endotracheal suction in children. Australian Critical Care. 31(1). 23–30. 7 indexed citations
3.
Davies, K. E., Leanne Monterosso, Max Bulsara, & Anne‐Sylvie Ramelet. (2014). Clinical indicators for the initiation of endotracheal suction in children: An integrative review. Australian Critical Care. 28(1). 11–18. 18 indexed citations
4.
Ungern‐Sternberg, Britta S. von, K. E. Davies, Mary Hegarty, Thomas O. Erb, & Walid Habre. (2013). The effect of deep vs. awake extubation on respiratory complications in high-risk children undergoing adenotonsillectomy. European Journal of Anaesthesiology. 30(9). 529–536. 52 indexed citations
5.
Ravenscroft, Gianina, J. M. Papadimitriou, Edna C. Hardeman, et al.. (2013). Cardiac  -actin over-expression therapy in dominant ACTA1 disease. Human Molecular Genetics. 22(19). 3987–3997. 18 indexed citations
6.
7.
8.
Davies, K. E., Leanne Monterosso, & Gavin Leslie. (2011). Determining standard criteria for endotracheal suctioning in the paediatric intensive care patient: An exploratory study. Intensive and Critical Care Nursing. 27(2). 85–93. 13 indexed citations
9.
Davies, K. E.. (1993). Human genetic disease analysis: a practical approach. 18 indexed citations
10.
Knox-Macaulay, Huxley, Layla Bashawri, & K. E. Davies. (1993). X linked recessive thrombocytopenia.. Journal of Medical Genetics. 30(11). 968–969. 11 indexed citations
11.
Hirst, Mark C., A. Roche, Tracey Flint, et al.. (1991). Linear order of new and established DNA markers around the fragile site at Xq27.3. Genomics. 10(1). 243–249. 23 indexed citations
12.
Read, Andrew & K. E. Davies. (1989). Molecular basis of inherited disease. 9 indexed citations
13.
Read, Andrew, R. Mountford, S. M. Forrest, et al.. (1988). Patterns of exon deletions in Duchenne and Becker muscular dystrophy. Human Genetics. 80(2). 152–156. 36 indexed citations
14.
Davies, K. E., Mark Patterson, Susan Kenwrick, et al.. (1988). Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome. American Journal of Medical Genetics. 29(3). 557–564. 21 indexed citations
15.
Forrest, S. M., Gareth Cross, Tracey Flint, et al.. (1988). Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies. Genomics. 2(2). 109–114. 147 indexed citations
16.
Coulson, Alan, J.E. Sulston, & K. E. Davies. (1988). Genome mapping by restriction fingerprinting.. 19–39. 18 indexed citations
17.
Davies, K. E., et al.. (1988). Report of the committee on the genetic constitution of the X chromosome. Cytogenetic and Genome Research. 49(1-3). 107–128. 18 indexed citations
18.
Forrest, S. M., Gareth Cross, Andreas Speer, et al.. (1987). Preferential deletion of exons in Duchenne and Becker muscular dystrophies. Nature. 329(6140). 638–640. 164 indexed citations
19.
Davies, K. E. & Kathryn Robson. (1987). Molecular analysis of human monogenic diseases. BioEssays. 6(6). 247–253. 10 indexed citations
20.
Davies, K. E.. (1983). Genetic Recombination. Understanding the Mechanisms. Journal of Medical Genetics. 20(4). 317.3–318. 65 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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