Kay E. Davies

5.0k total citations
43 papers, 3.3k citations indexed

About

Kay E. Davies is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Kay E. Davies has authored 43 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 9 papers in Genetics. Recurrent topics in Kay E. Davies's work include Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Nerve injury and regeneration (6 papers). Kay E. Davies is often cited by papers focused on Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Nerve injury and regeneration (6 papers). Kay E. Davies collaborates with scholars based in United Kingdom, United States and Australia. Kay E. Davies's co-authors include Derek J. Blake, Jonathon M. Tinsley, Christopher Phillips, Chris P. Ponting, Klaus Zerres, Susan Kenwrick, Mark Patterson, Steve Arkinstall, Marco Muda and Alan Ashworth and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Kay E. Davies

43 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kay E. Davies United Kingdom 26 2.5k 553 477 459 416 43 3.3k
Gregory A. Cox United States 38 3.3k 1.3× 582 1.1× 891 1.9× 497 1.1× 617 1.5× 82 4.4k
Bettina Erdmann Germany 26 3.0k 1.2× 410 0.7× 496 1.0× 758 1.7× 165 0.4× 47 4.6k
Robert S. Krauss United States 36 3.3k 1.3× 948 1.7× 405 0.8× 515 1.1× 321 0.8× 94 4.0k
Sarah E. Newey United Kingdom 24 2.7k 1.1× 503 0.9× 1.4k 2.8× 896 2.0× 142 0.3× 32 4.0k
Iain W. McKinnell United Kingdom 22 1.7k 0.7× 272 0.5× 231 0.5× 344 0.7× 182 0.4× 29 2.1k
Scott Q. Harper United States 27 3.9k 1.5× 1.1k 2.0× 1.1k 2.3× 231 0.5× 413 1.0× 54 4.4k
Peter G. Noakes Australia 39 3.1k 1.2× 298 0.5× 1.7k 3.6× 925 2.0× 617 1.5× 102 5.6k
Stephan Kröger Germany 31 2.2k 0.9× 173 0.3× 1.0k 2.2× 962 2.1× 138 0.3× 63 3.5k
E. Bryan Crenshaw United States 32 4.0k 1.6× 1.3k 2.3× 544 1.1× 445 1.0× 207 0.5× 51 5.9k
Mario Soriano‐Navarro Spain 30 1.8k 0.7× 393 0.7× 899 1.9× 390 0.8× 612 1.5× 47 3.7k

Countries citing papers authored by Kay E. Davies

Since Specialization
Citations

This map shows the geographic impact of Kay 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 Kay 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 Kay E. Davies more than expected).

Fields of papers citing papers by Kay E. Davies

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Kay E. Davies. A scholar is included among the top collaborators of Kay 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 Kay E. Davies. Kay 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.
Moir, Lee, Sarah Hemming, Benjamin Edwards, et al.. (2017). Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle. Skeletal Muscle. 7(1). 22–22. 13 indexed citations
2.
Finelli, Mattéa J., Luis Sánchez‐Pulido, Kevin X. Liu, Kay E. Davies, & Peter L. Oliver. (2015). The Evolutionarily Conserved Tre2/Bub2/Cdc16 (TBC), Lysin Motif (LysM), Domain Catalytic (TLDc) Domain Is Neuroprotective against Oxidative Stress. Journal of Biological Chemistry. 291(6). 2751–2763. 51 indexed citations
3.
Tan, Suat Cheng, Carolyn A. Carr, Kar Kheng Yeoh, et al.. (2011). Identification of valid housekeeping genes for quantitative RT-PCR analysis of cardiosphere-derived cells preconditioned under hypoxia or with prolyl-4-hydroxylase inhibitors. Molecular Biology Reports. 39(4). 4857–4867. 67 indexed citations
4.
Pichavant, Christophe, Annemieke Aartsma‐Rus, Paula R. Clemens, et al.. (2011). Current Status of Pharmaceutical and Genetic Therapeutic Approaches to Treat DMD. Molecular Therapy. 19(5). 830–840. 140 indexed citations
5.
Edwards, Benjamin, Matthew Burgess, William T. Clarke, et al.. (2008). Syncoilin isoform organization and differential expression in murine striated muscle. Journal of Structural Biology. 165(3). 196–203. 10 indexed citations
6.
Oliver, Peter L., David A. Keays, & Kay E. Davies. (2007). Behavioural characterisation of the robotic mouse mutant. Behavioural Brain Research. 181(2). 239–247. 17 indexed citations
7.
Davies, Kay E. & Miranda D. Grounds. (2006). Treating Muscular Dystrophy with Stem Cells?. Cell. 127(7). 1304–1306. 27 indexed citations
8.
Anderson, Kirstie N., et al.. (2004). Isolation and culture of motor neurons from the newborn mouse spinal cord. Brain Research Protocols. 12(3). 132–136. 29 indexed citations
9.
Anderson, Kirstie N., Dilair Baban, Peter L. Oliver, Allyson C. Potter, & Kay E. Davies. (2004). Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit. Neuromuscular Disorders. 14(11). 711–722. 20 indexed citations
10.
Howman, Emily V., et al.. (2002). Syncoilin accumulation in two patients with desmin-related myopathy. Neuromuscular Disorders. 13(1). 42–48. 25 indexed citations
11.
Miguel‐Aliaga, Irene, et al.. (2000). Disruption of SMN function by ectopic expression of the human SMN gene in Drosophila. FEBS Letters. 486(2). 99–102. 53 indexed citations
12.
13.
Deconinck, Nicolas, Jonathon M. Tinsley, Fabienne De Backer, et al.. (1997). Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice. Nature Medicine. 3(11). 1216–1221. 212 indexed citations
14.
Muda, Marco, Aspasia Theodosiou, Nanda R. Rodrigues, et al.. (1996). The Dual Specificity Phosphatases M3/6 and MKP-3 Are Highly Selective for Inactivation of Distinct Mitogen-activated Protein Kinases. Journal of Biological Chemistry. 271(44). 27205–27208. 341 indexed citations
15.
Flannery, Angela V., Mark C. Hirst, Samantha J.L. Knight, Rachael J. Ritchie, & Kay E. Davies. (1995). The fragile X syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1271(2-3). 293–303. 8 indexed citations
16.
Schofield, Julian, Dariusz C. Górecki, Derek J. Blake, Kay E. Davies, & Yvonne H. Edwards. (1995). Dystroglycan mRNA expression during normal and mdx mouse embryogenesis: A comparison with utrophin and the apo‐dystrophins. Developmental Dynamics. 204(2). 178–185. 37 indexed citations
17.
Ritchie, Rachael J., Samantha J.L. Knight, Mark C. Hirst, et al.. (1994). The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter. Human Molecular Genetics. 3(12). 2115–2121. 59 indexed citations
18.
Walker, Ann P., Jamel Chelly, Donald R. Love, et al.. (1992). A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes. Human Molecular Genetics. 1(8). 579–585. 33 indexed citations
19.
Davies, Kay E., Neil H. Thomas, R.J. Daniels, & Victor Dubowitz. (1991). Molecular studies of spinal muscular atrophy. Neuromuscular Disorders. 1(2). 83–85. 4 indexed citations
20.
Passos‐Bueno, Maria Rita, Joseph D. Terwilliger, Jürg Ott, et al.. (1991). Linkage analysis in families with autosomal recessive limb‐girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin‐related sequence. American Journal of Medical Genetics. 38(1). 140–146. 8 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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