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Cornea|March 31, 2011
Epibulbar molluscum contagiosum lesions in multiple myelomaPhillip Moradi, Mani Bhogal, Caroline Thaung, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 28, 2008
Electrophysiological monitoring in a patient with an optic nerve gliomaPhillip Moradi, Anthony G Robson, Geoffrey E Rose, et al.
The British Journal of Ophthalmology|February 8, 2007
Teenagers' perceptions of blindness related to smoking: a novel message to a vulnerable groupPhillip Moradi, Judith Thornton, Richard Edwards, et al.
Ophthalmology|February 6, 2018
Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel TherapiesLeo Sheck, Wayne I L Davies, Phillip Moradi, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
The British Journal of Ophthalmology|October 20, 2010
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1Robert H Henderson, Donna S Mackay, Zheng Li, et al.
Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
Molecular Vision|March 20, 2010
Novel mutations in MERTK associated with childhood onset rod-cone dystrophyDonna S Mackay, Robert H Henderson, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
Plos One|March 14, 2012
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapyMei Hong Tan, Donna S Mackay, Jill Cowing, et al.
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