K E Davies

1.2k total citations
40 papers, 1.0k citations indexed

About

K E Davies is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, K E Davies has authored 40 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Cognitive Neuroscience. Recurrent topics in K E Davies's work include Muscle Physiology and Disorders (9 papers), Neurobiology of Language and Bilingualism (5 papers) and Biotin and Related Studies (3 papers). K E Davies is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Neurobiology of Language and Bilingualism (5 papers) and Biotin and Related Studies (3 papers). K E Davies collaborates with scholars based in United Kingdom, Canada and Germany. K E Davies's co-authors include C R Cantor, Cassandra L. Smith, Karl J. A. McCullagh, RA Hirst, J. Weissenbach, Lucy Bowden, Wendy Dean, Wolf Reik, Jörn Walter and David R. Cox and has published in prestigious journals such as Science, Nucleic Acids Research and Circulation.

In The Last Decade

K E Davies

38 papers receiving 990 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	15	613	405	101	94	64	40	1.0k
Raffaella Meneveri Italy	25	747 1.2×	373 0.9×	207 2.0×	47 0.5×	124 1.9×	64	1.6k
Gabriel Minárik Slovakia	23	688 1.1×	198 0.5×	55 0.5×	142 1.5×	40 0.6×	123	1.5k
Shigeru Makino Japan	18	810 1.3×	296 0.7×	255 2.5×	32 0.3×	28 0.4×	37	1.5k
Toshio Inaba Japan	25	525 0.9×	470 1.2×	58 0.6×	37 0.4×	25 0.4×	163	2.0k
Fujio Umehara Japan	31	752 1.2×	207 0.5×	39 0.4×	47 0.5×	37 0.6×	102	2.6k
Ines Müller Germany	21	582 0.9×	342 0.8×	197 2.0×	87 0.9×	15 0.2×	34	1.3k
Jacques G. Lussier Canada	27	692 1.1×	1.1k 2.7×	41 0.4×	62 0.7×	42 0.7×	89	2.4k
Karen Rice United States	19	746 1.2×	687 1.7×	40 0.4×	106 1.1×	25 0.4×	37	1.5k
Rujuan Dai United States	25	953 1.6×	190 0.5×	77 0.8×	23 0.2×	40 0.6×	52	2.0k
Garry N. Hannan Australia	17	424 0.7×	208 0.5×	43 0.4×	40 0.4×	31 0.5×	39	1.0k

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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20 of 20 papers shown

Davies, K E, Tami Howe, Jeff Small, & Ging‐Yuek Robin Hsiung. (2024). ‛It's all communication’: Family members’ perspectives on the communication needs for themselves and their relatives with primary progressive aphasia. International Journal of Language & Communication Disorders. 59(5). 1946–1965. 2 indexed citations

Davies, K E, Tami Howe, Jeff Small, & Ging‐Yuek Robin Hsiung. (2024). “ Staying connected ” : Speech-language pathologists’ perspectives on the communication needs of people with primary progressive aphasia and their family members. International Journal of Speech-Language Pathology. 27(3). 423–439. 2 indexed citations

Davies, K E, Tami Howe, Jeff Small, & Ging‐Yuek Robin Hsiung. (2024). “I used to be a storyteller” : the perspectives of people with primary progressive aphasia on the communication needs for themselves and their family members. Aphasiology. 39(5). 710–731. 4 indexed citations

Davies, K E & Tami Howe. (2019). Experiences of Living With Primary Progressive Aphasia: A Scoping Review of Qualitative Studies. American Journal of Alzheimer s Disease & Other Dementias®. 35. 1310312330–1310312330. 18 indexed citations

Ilkovski, Biljana, Kristen L. Nowak, Ana Domazetovska, et al.. (2004). Mutant actins that cause congenital myopathy affect sarcomeric protein expression in patient muscle and produce intranuclear and cytoplasmic aggregates in cultured myoblasts. Neuromuscular Disorders. 14. 562–562. 3 indexed citations

Davies, K E, et al.. (2003). Functional studies of Af4 in the robotic mouse.. The American Journal of Human Genetics. 73. 179–179. 3 indexed citations

Herpers, Bram, Andrew T. McKie, Sarah Gledhill, et al.. (2003). Stromal cell-derived receptor 2 and cytochrome b561 are functional ferric reductases. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1651(1-2). 116–123. 73 indexed citations

Owen, Nicholas, et al.. (2001). Analysis of mutations in Survival of Motor Neuron (SMN1) gene through model systems.. The American Journal of Human Genetics. 69. 368–368. 1 indexed citations

Rybakova, Inna N., et al.. (2001). Dystrophin and utrophin are functionally homologous actin binding proteins but act through distinct modes of filament association. Molecular Biology of the Cell. 12. 1 indexed citations

10.

Davies, K E, et al.. (2001). Increased muscle lim protein expression associated with mild muscular dystrophy and with exercise. Circulation. 104. 165–165. 6 indexed citations

11.

Cullen, Michael J., Jason Walsh, Jonathon M. Tinsley, Rosie Fisher, & K E Davies. (2001). Confirmation by immunogold labeling that utrophin is localised to the normal position of dystrophin in dystrophin-negative transgenic mouse muscle. Neuromuscular Disorders. 11. 666–666. 2 indexed citations

12.

Fisher, Rosie, et al.. (2000). Non-toxic ubiquitous overexpression of utrophin in the mdx mouse.. The American Journal of Human Genetics. 67. 428–428. 2 indexed citations

13.

Perkins, Kelly J., Edward A. Burton, Allyson C. Potter, & K E Davies. (2000). Analysis of the transcriptional control of utrophin promoters as a therapeutic strategy for Duchenne muscular dystrophy (DMD).. The American Journal of Human Genetics. 67. 192–192. 1 indexed citations

14.

Paulsen, Martina, Lucy Bowden, Angela J. Villar, et al.. (1998). Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5. Human Molecular Genetics. 7(7). 1149–1159. 92 indexed citations

15.

Warren, Stephen T., K E Davies, & S M Tilghman. (1995). Genome rearrangement and stability. The American Journal of Human Genetics. 56(5). 6 indexed citations

16.

Davies, K E & Shirley M. Tilghman. (1993). Genome maps and neurological disorders. 5 indexed citations

17.

Murray, Joseph A., et al.. (1991). GENETIC AND PHYSICAL MAPPING AROUND THE RETINITIS-PIGMENTOSA (RP2) LOCUS IN XP11.23. UCL Discovery (University College London). 1 indexed citations

18.

Suthers, Graeme, K E Davies, Elizabeth Baker, & G.R. Sutherland. (1989). TaqI RFLP identified by probe 1A1 [DXS374] at Xq28. Nucleic Acids Research. 17(21). 8901–8901. 2 indexed citations

19.

Davies, K E. (1986). Human genetic diseases : a practical approach. 83 indexed citations

20.

Thakker, Rajesh V., Melanie J. Davies, K E Davies, et al.. (1986). LOCALIZATION OF THE GENE CAUSING X-LINKED HYPOPHOSPHATEMIC RICKETS. QJM. 61. 1071–1072. 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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