Elisabeth M. Bleeker‐Wagemakers

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)

Anneke I. den Hollander, Jacoline B. ten Brink, Yvette J.M. de Kok et al. · Nature Genetics · 1999 · 473 citations

Medicine, Genetics, Molecular Genetics +9

Autosomal Recessive Retinitis Pigmentosa With Preserved Para-arteriolar Retinal Pigment Epithelium

L. Ingeborgh van den Born, S. van Soest, Mary J. van Schooneveld et al. · American Journal of Ophthalmology · 1994 · 42 citations

Medicine, Genetics, Ophthalmology +14

Two different genes for X-linked retinitis pigmentosa

Brunhilde Wirth, Michael J. Denton, Jia-De Chen et al. · Genomics · 1988 · 40 citations

Medicine, Genetics, Molecular Genetics +7

Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation

Roelof‐Jan Oostra, Pieter A. Bolhuis, Ina Zorn-Ende et al. · Human Genetics · 1994 · 34 citations

Life Sciences, Genetics, Neurology +15

Stable and Progressive Hearing Loss in Type 2A Usher's Syndrome

A. van Aarem, A. Pinckers, William J. Kimberling et al. · Annals of Otology Rhinology & Laryngology · 1996 · 26 citations

Health Professions, Audiology, Genetics +17