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 · 184 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Retinal Structure and Function in Achromatopsia

Venki Sundaram, Caroline Wilde, Jonathan Aboshiha et al. · Ophthalmology · 2013 · 179 citations · Full text

Medicine, Anatomy, Ophthalmology +12

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 · 155 citations

Life Sciences, Molecular Medicine, Human Genetics +6

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 · 152 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

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 · 142 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16