Klaus Rohrschneider

Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer et al. · The American Journal of Human Genetics · 2006 · 670 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7

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 · 361 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +10

Mutations in the ABCA4 (ABCR) Gene Are the Major Cause of Autosomal Recessive Cone-Rod Dystrophy

Alessandra Maugeri, B. Jeroen Klevering, Klaus Rohrschneider et al. · The American Journal of Human Genetics · 2000 · 343 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

Multilayer amniotic membrane transplantation for reconstruction of deep corneal ulcers

Friedrich E. Kruse, Klaus Rohrschneider, Hans E. Völcker · Ophthalmology · 1999 · 313 citations

Transplantation Surgery, Ophthalmology, Corneal Dystrophy +7

The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Stargardt Disease

Alessandra Maugeri, Marc A. van Driel, Dorien J.R. van de Pol et al. · The American Journal of Human Genetics · 1999 · 259 citations · Full text

Mendelian Disorder, Genetic Disorder, Abcr Gene +10