Quincy Prescott

Dominant cataract formation in association with a vimentin assembly disrupting mutation

Melanie Müller, Siladitya Bhattacharya, Tanya Moore et al. · Human Molecular Genetics · 2009 · 110 citations · Full text

Medicine, Genetics, Ophthalmology +15

Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular Retinal Pigment Epithelium Atrophy

Christina Chakarova, Myrto Papaioannou, Hemant Khanna et al. · The American Journal of Human Genetics · 2007 · 79 citations · Full text

Medicine, Genetics, Ophthalmology +12

Novel mutations in theZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy

Petra Lišková, Stephen J. Tuft, Rhian Gwilliam et al. · Human Mutation · 2007 · 75 citations · Full text

Medicine, Genetics, Molecular Genetics +16

British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene

Petra Lišková, Quincy Prescott, Shomi S. Bhattacharya et al. · British Journal of Ophthalmology · 2007 · 39 citations · Full text

Veterinary Medicine, Genetics, Ophthalmology +17

Characterisation of phosphoglycerate kinase genes in Leishmania major and evidence for the absence of a third closely related gene or isoenzyme1Note: Nucleotide sequence data reported in this paper are available in the EMBL, GenBank™ and DDJB data bases under the accession numbers L12520 (PGK gene B) and L12521 (PGK gene C).1

Godfrina McKoy, Quincy Prescott, H. Lux et al. · Molecular and Biochemical Parasitology · 1997 · 24 citations

Life Sciences, Biochemistry, Molecular Biology +12