Vernon Long

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Kinga M. Bujakowska, Elise Orhan et al. · The American Journal of Human Genetics · 2012 · 132 citations · Full text

Ocular Disease, Developmental Biology, Mendelian Disorder +6

Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at risk

Gillian Adams, Catey Bunce, Wen Xing et al. · BMJ Open · 2017 · 82 citations · Full text

Recessive Mutations in<i>TSPAN12</i>Cause Retinal Dysplasia and Severe Familial Exudative Vitreoretinopathy (FEVR)

James A. Poulter, Alice E. Davidson, Manir Ali et al. · Investigative Ophthalmology & Visual Science · 2012 · 71 citations

Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study

Lucinda Teoh, Ameenat Lola Solebo, Jugnoo S. Rahi et al. · The Lancet Child & Adolescent Health · 2021 · 67 citations · Full text

Ophthalmology, National Observational Study, Medicine +5

Outcome of zone 1 retinopathy of prematurity

Michael O’Keefe, Bernadette Lanigan, Vernon Long · Acta Ophthalmologica Scandinavica · 2003 · 46 citations · Full text