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 · 345 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Next‐generation genetic testing for retinitis pigmentosa

Kornelia Neveling, Rob W.J. Collin, Christian Gilissen et al. · Human Mutation · 2012 · 287 citations · Full text

Medicine, Genetics, Molecular Genetics +17

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 · 262 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

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 · 187 citations

Medicine, Genetics, Ophthalmology +13

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 · 169 citations · Full text

Medicine, Genetics, Molecular Genetics +11