Kevin Gregory-Evans

Mutations in LRP5 or FZD4 Underlie the Common Familial Exudative Vitreoretinopathy Locus on Chromosome 11q

Carmel Toomes, H.M. Bottomley, Richard M. Jackson et al. · The American Journal of Human Genetics · 2004 · 370 citations · Full text

Fzd4 Underlie, Chromosome 11Q, Mendelian Disorder +8

Short-Wavelength Light Sensitivity of Circadian, Pupillary, and Visual Awareness in Humans Lacking an Outer Retina

F H Zaidi, Joseph T. Hull, Stuart N. Peirson et al. · Current Biology · 2007 · 360 citations · Full text

Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy

Rosemary E. Kelsell, Kevin Gregory-Evans, Annette Payne et al. · Human Molecular Genetics · 1998 · 232 citations

Focused Magnetic Stem Cell Targeting to the Retina Using Superparamagnetic Iron Oxide Nanoparticles

Anat Yanai, Urs O. Häfeli, Andrew Metcalfe et al. · Cell Transplantation · 2012 · 146 citations · Full text

Nanoparticles, Engineering, Magnetic Resonance +21

Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

Kevin Gregory-Evans, Alan Fryer, C.F. Inglehearn et al. · Nature Genetics · 1994 · 121 citations

Retina, Ophthalmology, Genetic Disorder +6