Maria van Genderen

GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

Neal S. Peachey, Thomas A. Ray, Ralph Florijn et al. · The American Journal of Human Genetics · 2012 · 158 citations · Full text

Is Mutated, Bipolar Cell Function, Photoreceptor Cell +7

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

Changes in causes of low vision between 1988 and 2009 in a Dutch population of children

Nienke Boonstra, Hans Limburg, Nel Tijmes et al. · Acta Ophthalmologica · 2011 · 87 citations · Full text

Diagnosing Cerebral Visual Impairment in Children with Good Visual Acuity

Maria van Genderen, Marjoke J. Dekker, Florine Pilon et al. · Strabismus · 2012 · 87 citations

Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome

Karin W. Littink, Patricia Stappers, Frans C. C. Riemslag et al. · Genes · 2018 · 43 citations · Full text