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Ophthalmology|October 1, 1998
Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigreeJ E Richards, R Ritch, P R Lichter, et al.Clinical Dysmorphology|August 28, 2025
Monoallelic variants in ACVR1 in a cohort of Egyptian individuals with fibrodysplasia ossificans progressivaRasha M Elhossini, Hala T El-Bassyouni, Engy A Ashaat, et al.Health Science Reports|April 25, 2025
Exploring Glucagon-Like Peptide-1 Receptor Agonists Usage Among Non-Diabetic Healthcare Providers: A Cross-Sectional Multi-Country StudyAbdulqadir J Nashwan, Hana J Abukhadijah, Vidusha Karavadi, et al.Plos Genetics|May 4, 2019
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in miceSarah J Garnai, Michelle L Brinkmeier, Ben Emery, et al.Nature Genetics|May 12, 2009
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathiesHemant Khanna, Erica E Davis, Carlos A Murga-Zamalloa, et al.Nature Genetics|December 23, 2015
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variantsLars G Fritsche, Wilmar Igl, Jessica N Cooke Bailey, et al.Nature Genetics|March 5, 2013
Seven new loci associated with age-related macular degenerationLars G Fritsche, Wei Chen, Matthew Schu, et al.Pageof 21