B. Jeroen Klevering

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

Next‐generation genetic testing for retinitis pigmentosa

Kornelia Neveling, Rob W.J. Collin, Christian Gilissen et al. · Human Mutation · 2012 · 284 citations · Full text

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

A functional variant in the CFI gene confers a high risk of age-related macular degeneration

Johannes P. H. van de Ven, Sara C. Nilsson, Perciliz L. Tan et al. · Nature Genetics · 2013 · 185 citations

Ocular Disease, Ophthalmology, Genetics +9

Identification of a 2 Mb Human Ortholog of Drosophila eyes shut/spacemaker that Is Mutated in Patients with Retinitis Pigmentosa

Rob W.J. Collin, Karin W. Littink, B. Jeroen Klevering et al. · The American Journal of Human Genetics · 2008 · 164 citations · Full text

Ocular Disease, Developmental Biology, Retina +9