W. I. Davies

Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease

John Broxholme, Jiannis Ragoussis, Mark W Hankins, 2012, European Journal of Human Genetics.

De novo point mutations in patients diagnosed with ataxic cerebral palsy

J. Ragoussis, S. Tucker, P. Skehel, 2015, Brain : a journal of neurology.

Challenges using diagnostic next-generation sequencing in the clinical environment for inherited retinal disorders.

W. I. Davies, Wayne I. L. Davies, 2014, Personalized medicine.

Mortality in neurofibromatosis 1: in North West England: an assessment of actuarial survival in a region of the UK since 1989

J. Ragoussis, R. Copley, D. Evans, 2013, European Journal of Human Genetics.