Frans C. C. Riemslag

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Maria M. van Genderen, Mieke M. C. Bijveld, Y. Claassen et al. · The American Journal of Human Genetics · 2009 · 237 citations · Full text

Developmental Biology, Ophthalmology, Genetic Disorder +3

A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14

Abbas M Solouki, Virginie J. M. Verhoeven, Cornelia M. van Duijn et al. · Nature Genetics · 2010 · 212 citations · Full text

Genome-wide Association Study, Genotype-phenotype Association, Genetic Disorder +7

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

Susanne Kohl, Frauke Coppieters, Françoise Meire et al. · The American Journal of Human Genetics · 2012 · 179 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +4

Mutations in<i>GRM6</i>Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram

Christina Zeitz, Maria van Genderen, John Neidhardt et al. · Investigative Ophthalmology & Visual Science · 2005 · 149 citations

Genotype and Phenotype of 101 Dutch Patients with Congenital Stationary Night Blindness

Mieke M. C. Bijveld, Ralph J. Florijn, Arthur A. Bergen et al. · Ophthalmology · 2013 · 147 citations

Sleep, Ocular Disease, Ophthalmology +4