Maria M. van Genderen

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 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

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

Hydrological properties of the epiphyte mass of a montane tropical rain forest, Colombia

Erik J. Veneklaas, Roderick Zagt, Andrea van Leerdam et al. · Plant Ecology · 1990 · 136 citations

Epiphyte Mass, Engineering, Forest Hydrology +7

Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy

Alberta A. H. J. Thiadens, T. My Lan Phan, Renate C. Zekveld-Vroon et al. · Ophthalmology · 2012 · 136 citations

Clinical Course, Ophthalmology, Degenerative Disease +5