I. D. Millar

Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans

Rosemary Burgess, I. D. Millar, Bart P. Leroy et al. · The American Journal of Human Genetics · 2008 · 307 citations · Full text

Ocular Disease, Ophthalmology, Genetic Disorder +7

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

Ion channel diversity, channel expression and function in the choroid plexuses

I. D. Millar, Jason I.E. Bruce, Peter de Nully Brown · Cerebrospinal Fluid Research · 2007 · 63 citations · Full text

Functional Characterization of Bestrophin-1 Missense Mutations Associated with Autosomal Recessive Bestrophinopathy

Alice E. Davidson, I. D. Millar, Rosemary Burgess-Mullan et al. · Investigative Ophthalmology & Visual Science · 2011 · 56 citations

Mammary Protein Synthesis Is Acutely Regulated by the Cellular Hydration State

I. D. Millar, MICHAEL C. BARBER, M. A. Lomax et al. · Biochemical and Biophysical Research Communications · 1997 · 53 citations

Protein Function, Protein Expression, Biochemistry +10