Alice E. Davidson

Missense Mutations in a Retinal Pigment Epithelium Protein, Bestrophin-1, Cause Retinitis Pigmentosa

Alice E. Davidson, I. D. Millar, Jill Urquhart et al. · The American Journal of Human Genetics · 2009 · 180 citations · Full text

Missense Mutations, Ocular Disease, Retina +6

Retinal Structure and Function in Achromatopsia

Venki Sundaram, Caroline Wilde, Jonathan Aboshiha et al. · Ophthalmology · 2013 · 174 citations · Full text

Retina, Ophthalmology, Retinal Structure +4

A Longitudinal Study of Stargardt Disease: Clinical and Electrophysiologic Assessment, Progression, and Genotype Correlations

Kaoru Fujinami, Noemi Lois, Alice E. Davidson et al. · American Journal of Ophthalmology · 2013 · 151 citations

Pathology, Genotype Correlations, Neuropathology +2

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Tom R. Webb, David A. Parfitt, J.C. Gardner et al. · Human Molecular Genetics · 2012 · 151 citations · Full text

Recessive Mutations in KCNJ13, Encoding an Inwardly Rectifying Potassium Channel Subunit, Cause Leber Congenital Amaurosis

Panagiotis I. Sergouniotis, Alice E. Davidson, Donna S. Mackay et al. · The American Journal of Human Genetics · 2011 · 140 citations · Full text

Molecular Neuroscience, Developmental Biology, Hyperpolarization (Biology) +8