Vanita Berry

A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q

Alan Shiels, Donna S. Mackay, Alexander Ionides et al. · The American Journal of Human Genetics · 1998 · 382 citations · Full text

Chromosome 1Q, Ocular Disease, Ophthalmology +6

Connexin46 Mutations in Autosomal Dominant Congenital Cataract

Donna S. Mackay, Alexander Ionides, Zoha Kibar et al. · The American Journal of Human Genetics · 1999 · 299 citations · Full text

Ocular Disease, Cataract, Connexin46 Mutations +1

Functional impairment of lens aquaporin in two families with dominantly inherited cataracts

Peter J. Francis, Jean‐Ju Chung, Masayoshi Yasui et al. · Human Molecular Genetics · 2000 · 138 citations

Crystalline Lens, Developmental Biology, Signal Transduction +13

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin

Vanita Berry, Donna S. Mackay, Shagufta Khaliq et al. · Human Genetics · 1999 · 129 citations

Ocular Disease, Ophthalmology, Pulverulent Cataract +6

Clinical and genetic heterogeneity in autosomal dominant cataract

Alexander Ionides, Peter J. Francis, Vanita Berry et al. · British Journal of Ophthalmology · 1999 · 111 citations · Full text