K. E. Davies

1.5k citations

37 papers · 1.1k · h-index 19

Impact in

Genetics top 5%
- Neurogenetic and Muscular Disorders Research
Anesthesiology and Pain Medicine top 5%

Papers in

Molecular Biology 14
- Muscle Physiology and Disorders 10
- Nuclear Structure and Function 6
Critical Care and Intensive Care Medicine 4
- Nosocomial Infections in ICU 4

Co-authors: S. M. Forrest (6 shared papers)Andreas Speer (5 shared papers)Gareth Cross (4 shared papers)Tracey Flint (4 shared papers)Britta S. von Ungern‐Sternberg (4 shared papers)Mary Hegarty (4 shared papers)Kathryn Robson (2 shared papers)John Burn (1 shared paper)
Journals: Pediatric Anesthesia (3 papers)Journal of Medical Genetics (3 papers)Human Genetics (2 papers)Genomics (2 papers)Australian Critical Care (2 papers)
Partner nations: United Kingdom Australia United States

In The Last Decade

K. E. Davies

36 papers receiving 1.1k citations

Peers

Replace Michael E. Nemergut with:

Michael E. Nemergut United States

Austin T. Smith United States

Seby Edassery United States

Douglas F. Hacking Australia

Fung-Yee Chan Australia

Valentina Cetica Italy

Cecilia Riquelme Chile

Richard N. Yu United States

Weihong Zhao China

A L Beaudet United States

K. E. Davies relative to Michael E. Nemergut United States Michael E. Nemergut's profile →

Citations per field

00.5×5×10.7×

Michael E. Nemergut · 1×

×11 160/15

GENET

×1.5 56/38

APM

×1.4 729/538

MB

×1.2 41/35

CCICM

×3.3 173/52

CCM

Citations per year

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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-authors

The 25 scholars most cited alongside K. 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 K. E. Davies Line = papers co-authored together K. E. Davies links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Preferential deletion of exons in Duchenne and Becker muscular dystrophies Nature ·S. M. Forrest, Gareth Cross, Andreas Speer, D. Gardner‐Medwin, John Burn, K. E. Davies	1987	164
2	Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies Genomics ·S. M. Forrest, Gareth Cross, Tracey Flint, Andreas Speer, Kathryn Robson, K. E. Davies	1988	147
3	Immunological studies of yeast nuclear RNA polymerases at the subunit level. Journal of Biological Chemistry ·Jean‐Marie Buhler, Janine Huet, K. E. Davies, André Sentenac, P. Fromageot	1980	108
4	Postoperative pain, nausea and vomiting following adeno‐tonsillectomy – a long‐term follow‐up Pediatric Anesthesia ·Dana Stanko, R. Bergesio, K. E. Davies, Mary Hegarty, Britta S. von Ungern‐Sternberg	2013	67
5	The effect of deep vs. awake extubation on respiratory complications in high-risk children undergoing adenotonsillectomy European Journal of Anaesthesiology ·Britta S. von Ungern‐Sternberg, K. E. Davies, Mary Hegarty, Thomas O. Erb, Walid Habre	2013	54
6	Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. Journal of Medical Genetics ·K. E. Davies, Terry Smith, Sarah Bundey, Andrew Read, Tracey Flint, M Bell, Andreas Speer	1988	49
7	Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families Human Genetics ·Huw Dorkins, C. Iunien, Jean‐Louis Mandel, Klaus Wrogemann, J. P. Moison, María Martínez, Julie M. Old, Sarah Bundey, M. Schwartz, Nancy J. Carpenter, D. Hill, Mikael Lindlöf, Albert de la Chapelle, P. Pearson, K. E. Davies	1985	43
8	Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients. The EMBO Journal ·Gareth Cross, Andreas Speer, A Rosenthal, S. M. Forrest, Terry Smith, Yvonne H. Edwards, Tracey Flint, D. Hill, K. E. Davies	1987	41
9	EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY The Lancet ·S. M. Forrest, Gareth Cross, Nick Thomas, Peter S. Harper, Terry Smith, Andrew Read, R. Mountford, R.T. Geirsson, K. E. Davies	1987	40
10	Patterns of exon deletions in Duchenne and Becker muscular dystrophy Human Genetics ·Andrew Read, R. Mountford, S. M. Forrest, Susan Kenwrick, K. E. Davies, R Harris	1988	36
11	Molecular biology of the W and steel loci. A. D. Reith, Alan Bernstein, K. E. Davies, S M Tilghman	1991	32
12	Does take‐home analgesia improve postoperative pain after elective day case surgery? A comparison of hospital vs parent‐supplied analgesia Pediatric Anesthesia ·Mary Hegarty, Alyson Calder, K. E. Davies, Margaret Shave, Elaine Christiansen, Tessa Meyer, Britta S. von Ungern‐Sternberg	2012	27
13	Utrophin, the autosomal homologue of dystrophin, is widely‐expressed and membrane‐associated in cultured cell lines FEBS Letters ·Nguyen thi Mân, LeThiet Thanh, David J. Blake, K. E. Davies, Glenn E. Morris	1992	26
14	Linear order of new and established DNA markers around the fragile site at Xq27.3 Genomics ·Mark C. Hirst, A. Roche, Tracey Flint, Ruth N. MacKinnon, J. H. Duncan Bassett, Yutaka Nakahori, J. E. Vivienne Watson, M.V. Bell, Mark Patterson, Yvonne Boyd, Nick Thomas, Samantha J.L. Knight, Stephen T. Warren, M. C. Hors‐Cayla, Malgorzata Schmidt, G.R. Sutherland, K. E. Davies	1991	23
15	Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome American Journal of Medical Genetics ·K. E. Davies, Mark Patterson, Susan Kenwrick, M.V. Bell, Howard R. Sloan, Judith A. Westman, Louis J. Elsas, John D. Mahan, John M. Optiz, James F. Reynolds	1988	21
16	Cardiac -actin over-expression therapy in dominant ACTA1 disease Human Molecular Genetics ·Gianina Ravenscroft, E. McNamara, Lisa M. Griffiths, J. M. Papadimitriou, Edna C. Hardeman, Anthony J. Bakker, K. E. Davies, Nigel G. Laing, Kamila Nowak	2013	19
17	Human genetic disease analysis: a practical approach K. E. Davies	1993	18
18	Clinical indicators for the initiation of endotracheal suction in children: An integrative review Australian Critical Care ·K. E. Davies, Leanne Monterosso, Max Bulsara, Anne‐Sylvie Ramelet	2014	18
19	Genome mapping by restriction fingerprinting. Alan Coulson, J.E. Sulston, K. E. Davies	1988	18
20	Development of a Population Pharmacokinetic Model for Parecoxib and Its Active Metabolite Valdecoxib after Parenteral Parecoxib Administration in Children Anesthesiology ·Bruce Hullett, Sam Salman, Sean O’Halloran, Deborah Peirce, K. E. Davies, Kenneth F. Ilett	2012	15

About K. E. Davies

K. E. Davies is a scholar working on Molecular Biology, Critical Care and Intensive Care Medicine, Cell Biology, Genetics and Genetics, having authored 37 papers that have together received 1.1k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Nuclear Structure and Function (6 papers), Nosocomial Infections in ICU (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Animal Genetics and Reproduction (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Biotin and Related Studies (2 papers). The work is most often cited by research in Genetics (160 citations), Anesthesiology and Pain Medicine (56 citations), Molecular Biology (729 citations), Critical Care and Intensive Care Medicine (41 citations) and Cardiology and Cardiovascular Medicine (173 citations). K. E. Davies has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include S. M. Forrest, Andreas Speer, Gareth Cross, Tracey Flint, Britta S. von Ungern‐Sternberg, Mary Hegarty, Kathryn Robson, John Burn, D. Gardner‐Medwin and André Sentenac. Their work appears in journals such as Pediatric Anesthesia, Journal of Medical Genetics, Human Genetics, Genomics and Australian Critical Care.

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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