K. E. Davies - Concepedia

Author

K. E. Davies

John Radcliffe Hospital ORCID

Also Known As

K E Davies, K. D. Davies, K. Davies, K. E. Davies, K.E. Davies, Kay E Davies, Kylie Davies, R. Damels

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

John Radcliffe Hospital Princess Margaret Hospital for Children The University of Western Australia University of Oxford St John of God Murdoch Hospital

About

K. E. Davies is an author at John Radcliffe Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	990
2	Engineering	2	2	39
3	Health Sciences	1	1	42
4	Natural Sciences	1	1	116
5	Public Health	1	1	56

K. E. Davies

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Preferential deletion of exons in Duchenne and Becker muscular dystrophies S. M. Forrest, Gareth Cross, Andreas Speer, Nature KinesiologyMedicineDegenerative DiseasePreferential DeletionNeuromuscular Pathology	1987	196
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies S. M. Forrest, Gareth Cross, Tracey Flint, Genomics Mendelian DisorderGenetic DisorderMedicineGeneticsDegenerative Disease	1988	178
Immunological studies of yeast nuclear RNA polymerases at the subunit level. Jean‐Marie Buhler, Janine Huet, K. E. Davies, Journal of Biological Chemistry GeneticsImmunologyMolecular BiologyMolecular GeneticsProtein Expression	1980	116
Genetic Recombination. Understanding the Mechanisms K. E. Davies Journal of Medical Genetics GeneticsMolecular BiologyGenetic MechanismMolecular GeneticsChromosomal Rearrangement	1983	94
Postoperative pain, nausea and vomiting following adeno‐tonsillectomy – a long‐term follow‐up Dana Stanko, R. Bergesio, K. E. Davies, Pediatric Anesthesia	2013	85
The effect of deep vs. awake extubation on respiratory complications in high-risk children undergoing adenotonsillectomy Britta S. von Ungern‐Sternberg, K. E. Davies, Mary Hegarty, European Journal of Anaesthesiology	2013	84
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome. K. E. Davies, Terry Smith, Sarah Bundey, Journal of Medical Genetics Mendelian DisorderDmd GeneMedicineGeneticsGenetic Disorder	1988	56
EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY S. M. Forrest, Gareth Cross, Nick Thomas, The Lancet Developmental BiologyMotor DevelopmentPediatricsMaternal HealthPreterm Birth	1987	53
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families Huw Dorkins, C. Iunien, Jean‐Louis Mandel, Human Genetics Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyMolecular Biology	1985	49
Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients. Gareth Cross, Andreas Speer, A Rosenthal, The EMBO Journal Muscle FunctionKinesiologySkeletal MuscleMedicineDegenerative Disease	1987	42

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