Keith Bradshaw

The<i>PROM1</i>Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

Michel Michaelides, Marie‐Claire Gaillard, Pascal Escher et al. · Investigative Ophthalmology & Visual Science · 2010 · 121 citations · Full text

Identification of Novel<i>RPGR</i>ORF15 Mutations in X-linked Progressive Cone-Rod Dystrophy (XLCORD) Families

Neil D. Ebenezer, Michel Michaelides, Sharon Jenkins et al. · Investigative Ophthalmology & Visual Science · 2005 · 112 citations

Infantile presentation of X linked retinoschisis.

N D George, John R. Yates, Keith Bradshaw et al. · British Journal of Ophthalmology · 1995 · 103 citations · Full text

Ocular Disease, Developmental Biology, Retina +13

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals

Michel Michaelides, S Johnson, Matthew P. Simunovic et al. · Eye · 2004 · 77 citations · Full text

Ophthalmology, Genetics, Cone Function +3

Cone–Rod Dystrophy, Intrafamilial Variability, and Incomplete Penetrance Associated with the R172W Mutation in the Peripherin/RDS Gene

Michel Michaelides, Graham E. Holder, Keith Bradshaw et al. · Ophthalmology · 2005 · 77 citations

R172w Mutation, Mendelian Disorder, Peripherin/rds Gene +9