Kay E. Davies

33.1k citations

380 papers · 24.4k indexed · 4 hit papers · h-index 79

Impact in

Genetics top 0.1%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Virus-based gene therapy research
Rehabilitation top 0.05%
- Exercise and Physiological Responses

Papers in

Rehabilitation 37
- Exercise and Physiological Responses 37
Genetics 54
- Genetics and Neurodevelopmental Disorders 63
- Neurogenetic and Muscular Disorders Research 51
- Virus-based gene therapy research 28

Co-authors: Jonathon M. Tinsley Derek J. Blake Peter L. Oliver Sarah E. Newey Theodore L. Munsat Donald R. Love Kristen L. Nowak Allyson C. Potter
Journals: Human Molecular Genetics (29 papers)Human Genetics (23 papers)Neuromuscular Disorders (23 papers)Journal of Medical Genetics (18 papers)Genomics (15 papers)
Partner nations: United Kingdom United States India

In The Last Decade

Kay E. Davies

375 papers receiving 23.8k citations

Hit Papers

align trajectories log scale

Function and Genetics of Dystrophin and Dystrophin-Related Proteins in Muscle 2002 · 907 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2002 Physiological Reviews
1997 Cell
1992 Neuromuscular Disorders
1985 Nature

Peers

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

The 25 scholars most cited alongside Kay E. Davies, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kay E. Davies Line = papers co-authored together Kay E. Davies links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cues Translational Psychiatry ·Norma Vivas, Laurence A. Brown, Shu K. E. Tam, Kay E. Davies, F. Foster, Paul J. Harrison, Rolf Sprengel, Vladyslav V. Vyazovskiy, Peter L. Oliver, David M. Bannerman, Stuart N. Peirson	2021	20
2	Discovery and mechanism of action studies of 4,6-diphenylpyrimidine-2-carbohydrazides as utrophin modulators for the treatment of Duchenne muscular dystrophy European Journal of Medicinal Chemistry ·Joanna Andonov, Fang Shiman, Maria Chatzopoulou, Ben Edwards, Sarah Squire, Rebecca J. Fairclough, Sacramentos, Carlos Morell, Daniel Conole, James R. Donald, Yun Daniel Park, Nicky J. Willis, R. Fernando Martínez, Francis X. Wilson, Graham M. Wynne, Stephen G. Davies, Kay E. Davies, Angela J. Russell	2021	10
3	Functional correction in mouse models of muscular dystrophy using exon-skipping tricyclo-DNA oligomers Nature Medicine ·Aurélie Goyenvalle, Graziella Griffith, Arran Babbs, Samir EL Andaloussi, Kariem Ezzat, Francisco Araujo-Feriera, Branislav Dugovič, Rémi Chaussenot, Arnaud Ferry, Thomas Voït, Helge Amthor, Claudia Bühr, Stefan Schürch, Matthew J. A. Wood, Kay E. Davies, Cyrille Vaillend, Christian J. Leumann, Luis Garcı́a	2015	240
4	A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse Proceedings of the National Academy of Sciences ·Alexander Jeans, Peter L. Oliver, Reuben Johnson, Marco Capogna, Jenny Vikman, Zoltán Molnár, Arran Babbs, Christopher J. Partridge, Albert Salehi, Martin Bengtsson, Lena Eliasson, Patrik Rorsman, Kay E. Davies	2007	95
5	MLP Accumulation and Remodelling in the Infarcted Rat Heart European Journal of Heart Failure ·Génesis Rivera Moncayo, Craig A. Lygate, Kay E. Davies, Stefan Neubauer, Kieran Clarke	2005	6
6	The role of utrophin in the potential therapy of Duchenne muscular dystrophy Neuromuscular Disorders ·Kelly J. Perkins, Kay E. Davies	2002	53
7	Evaluation of neurological mouse mutants caused by ENU mutagenesis European Journal of Neuroscience ·S. B. Gashkov, Allyson C. Potter, Gerald Rott, Lucie Vizor, Phillip Oliver, Kay E. Davies, Joseph E. Peters, Patrick M. Nolan, JR Schreiber, F S Walsh, B. Santich, A. Jackie Hunter	2000	9
8	Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressingFRAXE American Journal of Medical Genetics ·Michael T. Abrams, Kimberly F. Doheny, Michèle M. M. Mazzocco, Samantha J.L. Knight, Thomas L. Baumgardner, Lisa S. Freund, Kay E. Davies, Allan L. Reiss	1997	27
9	Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome. Journal of Medical Genetics ·John MacPherson, Sylvia L. Ivory, John A. Crolla, N R Dennis, Barbara R. Migeon, Prabhjit K. Grewal, Mark C. Hirst, Kay E. Davies, P. A. Jacobs	1995	21
10	Gene expression and its control Kay E. Davies, Shirley M. Tilghman	1991	7
11	Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies. Journal of Clinical Investigation ·Rajesh V. Thakker, Kay E. Davies, Michael P. Whyte, C Wooding, J. L. H. O’Riordan	1990	45
12	Molecular Analysis and Diagnosis of Duchenne Muscular Dystrophy Journal of the Royal College of Physicians of London ·S. M. Forrest, Terry Smith, Gareth Cross, Susan Kenwrick, Sarah England, Tracey Flint, Kay E. Davies	1988	0
13	Molecular basis of inherited diseases Kay E. Davies, Dr K. J. Gupta	1988	6
14	Physical mapping studies on the human X chromosome in the region Xq27-Xqter Genomics ·Mark Patterson, Charles E. Schwartz, M Bell, V. Tscholl, Marten H. Hofker, Barbara J. Trask, Ger van den Engh, Kay E. Davies	1987	52
15	Linkage analysis using nine dna polymorphisms along the length of the x chromosome locates the gene for emery dreifuss muscular dystrophy to distal xq Journal of Medical Genetics ·SV Hodgson, Alan BainGerry Swan, A.P. Walker, Martin Bobrow, Kay E. Davies, Victor Dubowitz, كعبار جمال, Luciano Merlini	1986	3
16	Molecular analysis of X-linked diseases. PubMed ·Kay E. Davies, Sarah Ball, Huw Dorkins, S. M. Forrest, Susan Kenwrick, Mark Patterson, Terry Smith, Julie M. Old, Andrew King, Rajesh V. Thakker	1986	1
17	Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16. BMJ ·Stephen T. Reeders, M.H. Breuning, G. CORNEY, S.J. Jeremiah, P. Meera Khan, Kay E. Davies, D. A. HOPKINSON, P. Pearson, D. J. Weatherall	1986	74
18	Cystic fibrosis linkage exclusion data Cytogenetic and Genome Research ·Peter Scambler, G. Bell, Eila Watson, Martin Farrall, Gillian P. Bates, Kay E. Davies, Nicholas Lench, Yogendra Jagatsinh, R. Williamson, P. Tippett, Brandon J. Wainwright	1986	7
19	Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. PubMed ·Peter Wieacker, Kay E. Davies, Howard J. Cooke, P. Pearson, R. Williamson, S.S. Bhattacharya, J. Zimmer, Hans‐Hilger Ropers	1984	137
20	The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy. Journal of Medical Genetics ·Peter S. Harper, T O'Brien, Jeffrey Murray, Kay E. Davies, P. Pearson, R. Williamson	1983	44

About Kay E. Davies

Kay E. Davies is a scholar working on Rehabilitation, Genetics, Genetics, Molecular Biology and Cellular and Molecular Neuroscience, having authored 380 papers that have together received 24.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (170 papers), Genetics and Neurodevelopmental Disorders (63 papers), Neurogenetic and Muscular Disorders Research (51 papers), RNA modifications and cancer (45 papers), RNA Research and Splicing (41 papers), Exercise and Physiological Responses (37 papers), Adipose Tissue and Metabolism (30 papers) and Virus-based gene therapy research (28 papers). The work is most often cited by research in Genetics (3.7k citations), Rehabilitation (2.0k citations), Molecular Biology (19.3k citations), Genetics (6.9k citations) and Cellular and Molecular Neuroscience (3.8k citations). Kay E. Davies has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Jonathon M. Tinsley, Derek J. Blake, Peter L. Oliver, Sarah E. Newey, Theodore L. Munsat, Donald R. Love, Kristen L. Nowak, Allyson C. Potter, Andrew Weir and Glenn E. Morris. Their work appears in journals such as Human Molecular Genetics, Human Genetics, Neuromuscular Disorders, Journal of Medical Genetics and Genomics.

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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