Refractive Error in Inherited Retinal Disease

This publication has 39 references indexed in Scilit:

• Shedding light on myopia by studying complete congenital stationary night blindness
  Progress in Retinal and Eye Research, 2023
• CRB1-Associated Retinal Dystrophies: Genetics, Clinical Characteristics, and Natural History
  American Journal of Ophthalmology, 2022
• Inherited retinal diseases are the most common cause of blindness in the working-age population in Australia
  Ophthalmic Genetics, 2021
• Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 Mutations
  American Journal of Ophthalmology, 2021
• Development of Refractive Errors—What Can We Learn From Inherited Retinal Dystrophies?
  American Journal of Ophthalmology, 2017
• Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
  Genetics in Medicine, 2015
• Emmetropisation and the aetiology of refractive errors
  Eye, 2014
• Education influences the role of genetics in myopia
  European Journal of Epidemiology, 2013
• Atropine for the Treatment of Childhood Myopia
  Ophthalmology, 2006
• CSNB1 in Chinese families associated with novel mutations in NYX
  Journal of Human Genetics, 2006