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Nutrition Journal|September 2, 2006
A randomised controlled trial investigating the effect of n-3 long-chain polyunsaturated fatty acid supplementation on cognitive and retinal function in cognitively healthy older people: the Older People And n-3 Long-chain polyunsaturated fatty acids (OPAL) study protocol [ISRCTN72331636]Alan D Dangour, Felicity Clemens, Diana Elbourne, et al.
The British Journal of Ophthalmology|March 20, 2004
An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 geneS S Dandekar, N D Ebenezer, C Grayson, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophyRobert H Henderson, Naushin Waseem, Rowan Searle, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Ophthalmology|February 1, 2014
Detailed phenotypic and genotypic characterization of bietti crystalline dystrophyStephanie Halford, Gerald Liew, Donna S Mackay, et al.
Stem Cell Research & Therapy|July 28, 2021
Submacular integration of hESC-RPE monolayer xenografts in a surgical non-human primate modelZengping Liu, Tanja Ilmarinen, Gavin S W Tan, et al.
American Journal of Ophthalmology|August 20, 2013
Clinical and molecular analysis of Stargardt disease with preserved foveal structure and functionKaoru Fujinami, Panagiotis I Sergouniotis, Alice E Davidson, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
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