K.E. Davies

1.4k total citations
18 papers, 998 citations indexed

About

K.E. Davies is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, K.E. Davies has authored 18 papers receiving a total of 998 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Genetics. Recurrent topics in K.E. Davies's work include RNA Research and Splicing (5 papers), RNA modifications and cancer (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). K.E. Davies is often cited by papers focused on RNA Research and Splicing (5 papers), RNA modifications and cancer (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). K.E. Davies collaborates with scholars based in United Kingdom, United States and India. K.E. Davies's co-authors include Victor Dubowitz, R.J. Daniels, I Hausmanowa-Pétrusewicz, Jürg Ott, Thomas Lehner, Klaus Zerres, Linda M. Brzustowicz, Lucio H. Castilla, F. A. Ziter and David Wood and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

K.E. Davies

18 papers receiving 952 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K.E. Davies United Kingdom	13	758	473	257	175	71	18	998
Li‐Chen Wu United States	8	1.2k 1.6×	380 0.8×	188 0.7×	190 1.1×	184 2.6×	15	1.6k
Pagon Ra United States	6	450 0.6×	70 0.1×	260 1.0×	55 0.3×	52 0.7×	291	791
Luitgard Graul‐Neumann Germany	19	539 0.7×	128 0.3×	457 1.8×	97 0.6×	13 0.2×	46	884
Sumita Danda India	16	489 0.6×	59 0.1×	269 1.0×	70 0.4×	36 0.5×	122	1.0k
Patrizia Ciscato Italy	17	826 1.1×	181 0.4×	104 0.4×	110 0.6×	21 0.3×	47	1.1k
Zehra Oya Uyguner Türkiye	20	823 1.1×	86 0.2×	398 1.5×	66 0.4×	14 0.2×	107	1.2k
Dominique Récan France	20	1.3k 1.7×	107 0.2×	700 2.7×	69 0.4×	15 0.2×	33	1.6k
Katja Eggermann Germany	20	703 0.9×	399 0.8×	527 2.1×	239 1.4×	5 0.1×	44	1.2k
Jeroen Schoots Netherlands	11	451 0.6×	244 0.5×	281 1.1×	120 0.7×	4 0.1×	14	854
Valentina Saccone Italy	16	1.4k 1.8×	251 0.5×	192 0.7×	248 1.4×	9 0.1×	28	1.6k

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

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18 of 18 papers shown

Francis, Michael J., M. Andrew Nesbit, Aspasia Theodosiou, et al.. (1995). Mapping of Retrotransposon Sequences in the Unstable Region Surrounding the Spinal Muscular Atrophy Locus in 5q13. Genomics. 27(2). 366–369. 24 indexed citations

Partridge, T. & K.E. Davies. (1995). Myoblast-based gene therapies. British Medical Bulletin. 51(1). 123–137. 54 indexed citations

Morrison, Karen, R.J. Daniels, G K Suthers, et al.. (1993). Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA). Human Genetics. 92(2). 133–8. 9 indexed citations

Good, Peter, Michel P. Coleman, M. Giles, et al.. (1993). Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.. Journal of Medical Genetics. 30(12). 1044–1050. 27 indexed citations

Hirst, Mark C., J. H. Duncan Bassett, A. Roche, & K.E. Davies. (1992). Preparation of radiolabelled hybridization probes by STS labelling. Trends in Genetics. 8(1). 6–7. 6 indexed citations

Sims, Katherine B., Michel P. Coleman, D Donnai, et al.. (1992). Characterization of a YAC containing part or all of the Norrie disease locus. Human Molecular Genetics. 1(3). 161–164. 12 indexed citations

Wells, Dominic J., Kim E. Wells, Frank S. Walsh, et al.. (1992). Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice. Human Molecular Genetics. 1(1). 35–40. 57 indexed citations

Hirst, Mark C., Katrina Rack, Yutaka Nakahori, et al.. (1991). A YAC contig across the fragile X site defines the region of fragility. Nucleic Acids Research. 19(12). 3283–3288. 35 indexed citations

Thakker, Rajesh V., K.E. Davies, Andrew Read, et al.. (1990). Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families. Genomics. 8(2). 189–193. 18 indexed citations

10.

Brzustowicz, Linda M., Thomas Lehner, Lucio H. Castilla, et al.. (1990). Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3. Nature. 344(6266). 540–541. 449 indexed citations

11.

Bell, M.V., J.F. Bloomfield, Michael J. McKinley, et al.. (1989). Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.. PubMed. 45(6). 883–8. 35 indexed citations

12.

Robbins, Timothy P., Peter Scambler, K.E. Davies, & R. Williamson. (1987). An anonymous clone E9pl (D4S112) localised to 4q26-qter detects and Msp I RFLP. Nucleic Acids Research. 15(19). 8122–8122. 1 indexed citations

13.

Read, Andrew, Rajesh V. Thakker, K.E. Davies, et al.. (1986). Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis. Human Genetics. 73(3). 267–270. 53 indexed citations

14.

Old, Julie M., Stuart Purvis‐Smith, Bridget Wilcken, et al.. (1985). PRENATAL EXCLUSION OF ORNITHINE TRANSCARBAMYLASE DEFICIENCY BY DIRECT GENE ANALYSIS. The Lancet. 325(8420). 73–75. 49 indexed citations

15.

Scambler, Peter, Timothy P. Robbins, Conrad Gilliam, et al.. (1985). Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Human Genetics. 69(3). 250–254. 11 indexed citations

16.

Harper, Katherine L., Marcus Pembrey, K.E. Davies, et al.. (1984). A CLINICALLY USEFUL DNA PROBE CLOSELY LINKED TO HAEMOPHILIA A. The Lancet. 324(8393). 6–8. 83 indexed citations

17.

Rappold, Gudrun, et al.. (1984). Sex chromosome positions in human interphase nuclei as studied by in situ hybridization with chromosome specific DNA probes. Human Genetics. 67(3). 317–325. 73 indexed citations

18.

Davies, K.E.. (1982). Principles of Gene Manipulation. An Introduction to Genetic Engineering. Journal of Medical Genetics. 19(5). 397.2–398. 2 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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