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Ophthalmology|October 30, 2007
Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qGu Zhu, Alex W Hewitt, Jonathan B Ruddle, et al.
Nature Communications|October 22, 2024
Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysisSantiago Diaz-Torres, Samantha Sze-Yee Lee, Luis M García-Marín, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosaT Jeffrey Keen, Matthew M Hims, Arthur B McKie, et al.
Clinical & Experimental Ophthalmology|September 2, 2022
Low-concentration atropine eyedrops for myopia control in a multi-racial cohort of Australian children: A randomised clinical trialSamantha Sze-Yee Lee, Gareth Lingham, Magdalena Blaszkowska, et al.
Molecular Vision|April 10, 2007
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgroundsAlex W Hewitt, John R Samples, R Rand Allingham, et al.
Investigative Ophthalmology & Visual Science|February 21, 2013
Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2Felicia Hawthorne, Sheng Feng, Ravikanth Metlapally, et al.
Scientific Reports|June 1, 2016
Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degenerationGabriel Cuellar-Partida, Jamie E Craig, Kathryn P Burdon, et al.
G3 (Bethesda, Md.)|August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern AustraliaShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Investigative Ophthalmology & Visual Science|June 15, 2022
Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal DiseasesKatie M Williams, Michalis Georgiou, Angelos Kalitzeos, et al.
American Journal of Human Genetics|October 20, 2021
Establishing risk of vision loss in Leber hereditary optic neuropathyM Isabel G Lopez Sanchez, Lisa S Kearns, Sandra E Staffieri, et al.
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