Geoffrey Woodruff

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

The Prevalence of Nystagmus: The Leicestershire Nystagmus Survey

Nagini Sarvananthan, Mylvaganam Surendran, E.O. Roberts et al. · Investigative Ophthalmology & Visual Science · 2009 · 216 citations

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

Patrick Tarpey, Shery Thomas, Nagini Sarvananthan et al. · Nature Genetics · 2006 · 211 citations · Full text

Developmental Anomaly, Mendelian Disorder, Genetic Disorder +6

Factors affecting the outcome of children treated for amblyopia

Geoffrey Woodruff, F Hiscox, John R. Thompson et al. · Eye · 1994 · 203 citations · Full text

Oculoplastics, Pediatric Ophthalmology, Pediatrics +1

Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7

Shery Thomas, Frank A. Proudlock, Nagini Sarvananthan et al. · Brain · 2008 · 117 citations

Ocular Disease, Frmd7 Mutation, Pathology +16