Kay Elizabeth Davies - Genetic Mutations

Author Information

Kay Elizabeth Davies is a distinguished researcher affiliated with the Oxford Neuromuscular Centre, Department of Physiology, Anatomy and Genetics at the University of Oxford, Oxford, UK. Her extensive work in the field of genetics has significantly contributed to our understanding of neuromuscular disorders, particularly Duchenne muscular dystrophy.

Research Contributions

Kay Elizabeth Davies has made substantial contributions to the field of genetics, focusing on Duchenne muscular dystrophy and related neuromuscular disorders. Her research has explored novel genetic approaches and therapeutic strategies for these conditions, including the study of genetic modulators like utrophin. Her work also delves into the mechanisms of genetic disorders and the development of potential treatments, highlighting the translational aspect of her research from diagnosis to therapy. Additionally, she has contributed to the understanding of circadian rhythm disruptions and evolutionary genomics in Africa, showcasing the breadth of her research interests and impact.

Aliases

Throughout her career, Kay Elizabeth Davies has been published under various aliases including Kay E. Davies, Kay Davies, K. Davies, K. E. Davies, Kaye. Davies, K Davies, K. E Davies, Kay E Davies, and K E Davies. These variations may appear across different publications and databases.

Publication and Citation Metrics

Metric Value
Total Citation Count 31,409
h-index 86
Total Paper Count 627

Publications:

DOI: 10.1093/hmg/ddab030

Year: 2021

DOI: 10.1016/j.neulet.2020.135304

Year: 2020

DOI: 10.1201/9781003076933-3

Year: 2020

DOI: 10.1042/BST20190282

Year: 2020

DOI: 10.1146/annurev-genom-112019-083518

Year: 2020

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