Kay E. Davies

1.2k total citations
15 papers, 977 citations indexed

About

Kay E. Davies is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Kay E. Davies has authored 15 papers receiving a total of 977 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Genetics. Recurrent topics in Kay E. Davies's work include Genetics and Neurodevelopmental Disorders (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA Research and Splicing (4 papers). Kay E. Davies is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA Research and Splicing (4 papers). Kay E. Davies collaborates with scholars based in United Kingdom, United States and France. Kay E. Davies's co-authors include R Elles, Robert Williamson, Bryan D. Young, Kevin Talbot, Maria Carmen Piñon, Zoltán Molnár, James Cleak, Victoria L. Harvey, Guoling Tian and David A. Keays and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Kay E. Davies

15 papers receiving 942 citations

Peers

Kay E. Davies

GENET

Adriano Flora Italy

M A Teillet France

Sylvia Dobrzeniecka Canada

Frank J. Probst United States

Jill Heemskerk United States

Michael J. McConnell United States

Marie Claude Vinet France

Ina Nüsslein Germany

Michael J. McConnell United States

Alexandra L. Bey United States

Adriano Flora Italy

Kay E. Davies

855 ×1.2

209 ×0.7

GENET

113 ×0.6

36 ×0.3

GENET

58 ×0.6

Citations per year, relative to Kay E. Davies Kay E. Davies (= 1×) peers Adriano Flora

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

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15 of 15 papers shown

Molnár, Zoltán, Anna Hoerder‐Suabedissen, Weizhi Wang, et al.. (2008). Genes Involved in the Formation of the Earliest Cortical Circuits. Novartis Foundation symposium. 288. 212–229. 7 indexed citations

Keays, David A., Guoling Tian, Karine Poirier, et al.. (2007). Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans. Cell. 128(1). 45–57. 322 indexed citations

Vernes, Sonja C., Jérôme Nicod, Fanny M. Elahi, et al.. (2006). Functional genetic analysis of mutations implicated in a human speech and language disorder. Human Molecular Genetics. 15(21). 3154–3167. 135 indexed citations

Trülzsch, Barbara, Kay E. Davies, & Matthew J. A. Wood. (2003). Characterisation of catalytic nucleic acids targeting the survival of motor neuron messenger RNA. Neuroscience Research Communications. 32(2). 95–106. 1 indexed citations

Skordis, L., Matthew G. Dunckley, Lydie Bürglen, et al.. (2001). Characterisation of novel point mutations in the survival motor neuron gene SMN , in three patients with SMA. Human Genetics. 108(4). 356–357. 19 indexed citations

Talbot, Kevin & Kay E. Davies. (2001). Spinal Muscular Atrophy. Seminars in Neurology. 21(2). 189–198. 65 indexed citations

Muda, Marco, Aspasia Theodosiou, Corine Gilliéron, et al.. (1998). The Mitogen-activated Protein Kinase Phosphatase-3 N-terminal Noncatalytic Region Is Responsible for Tight Substrate Binding and Enzymatic Specificity. Journal of Biological Chemistry. 273(15). 9323–9329. 133 indexed citations

Pook, Mark A., Brian Harding, David J. Porteous, et al.. (1996). EagI andNotI linking clones from human chromosomes 11 and Xp. Human Genetics. 97(6). 742–749. 3 indexed citations

Pook, Mark A., Brian Harding, David J. Porteous, et al.. (1996). Eag I and Not I linking clones from human chromosomes 11 and Xp. Human Genetics. 97(6). 742–749. 1 indexed citations

10.

Rodrigues, Nanda R., Kevin Talbot, & Kay E. Davies. (1996). Molecular Genetics of Autosomal Recessive Spinal Muscular Atrophy. Molecular Medicine. 2(4). 400–404. 3 indexed citations

11.

Clark, Jeremy, Sarah Ball, Sandra Gill, et al.. (1995). The human SB1.8 gene (DXS423E) encodes a putative chromosome segregation protein conserved in lower eukaryotes and prokaryotes. Human Molecular Genetics. 4(2). 243–249. 24 indexed citations

12.

Németh, Andrea H., Neil Hunter, Michel P. Coleman, et al.. (1993). Rescue of a single yeast artificial chromosome from a cotransformation event utilizing segregation at meiosis. Genetic Analysis Biomolecular Engineering. 10(6). 123–127. 3 indexed citations

13.

Hartley, David A., Kay E. Davies, Dennis Drayna, R. White, & R. Williamson. (1984). A cytological map of the human X chromosome - evidence for non-random recombination. Nucleic Acids Research. 12(13). 5277–5285. 43 indexed citations

14.

Davies, Kay E., et al.. (1983). Sex Chromosome-Specific DNA Sequences. 44–47. 1 indexed citations

15.

Davies, Kay E., et al.. (1981). Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry. Nature. 293(5831). 374–376. 217 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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