Yvette J.M. de Kok

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

Association Between X-Linked Mixed Deafness and Mutations in the POU Domain Gene <i>POU3F4</i>

Yvette J.M. de Kok, Silvère M. van der Maarel, Maria Bitner‐Glindzicz et al. · Science · 1995 · 449 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Leber Congenital Amaurosis and Retinitis Pigmentosa with Coats-like Exudative Vasculopathy Are Associated with Mutations in the Crumbs Homologue 1 (CRB1) Gene

Anneke I. den Hollander, John R. Heckenlively, L. Ingeborgh van den Born et al. · The American Journal of Human Genetics · 2001 · 365 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Isolation of Crb1, a mouse homologue of Drosophila crumbs, and analysis of its expression pattern in eye and brain

Anneke I. den Hollander, Michela Ghiani, Yvette J.M. de Kok et al. · Mechanisms of Development · 2002 · 113 citations

Life Sciences, Genetics, Neuroscience +6

Further mutations in <i>Brain 4</i> (POU3F4) clarify the phenotype in the X-linked deafness, DFN3

Maria Bitner‐Glindzicz, Peter D. Turnpenny, Pia Höglund et al. · Human Molecular Genetics · 1995 · 84 citations

Life Sciences, Genetics, Molecular Genetics +9