Achieving balance in the treatment and monitoring of neovascular age‐related macular degeneration in the real world: lessons from the Netherlands cohort of the AURA study by Asten, Freekje, Jong‐Hesse, Yvonne, Lith‐Verhoeven, Janneke J. C., Verbraak, Frank D., Vromans, Johannes G. F., Lau, Nga‐Chi, Altemark, Andreas, Hoyng, Carel B.

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Scrutinizing pathogenicity of the USH2A c.2276 G > T; p.(Cys759Phe) variant by Reurink, Janine, de Vrieze, Erik, Li, Catherina H. Z., van Berkel, Emma, Broekman, Sanne, Aben, Marco, Peters, Theo, Oostrik, Jaap, Neveling, Kornelia, Venselaar, Hanka, Ramos, Mariana Guimarães, Gilissen, Christian, Astuti, Galuh D. N., Galbany, Jordi Corominas, van Lith-Verhoeven, Janneke J. C., Ockeloen, Charlotte W., Haer-Wigman, Lonneke, Hoyng, Carel B., Cremers, Frans P. M., Kremer, Hannie, Roosing, Susanne, van Wijk, Erwin

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Homozygosity Mapping Reveals PDE6C Mutations in Patients with Early-Onset Cone Photoreceptor Disorders by Thiadens, Alberta A.H.J., den Hollander, Anneke I., Roosing, Susanne, Nabuurs, Sander B., Zekveld-Vroon, Renate C., Collin, Rob W.J., De Baere, Elfride, Koenekoop, Robert K., van Schooneveld, Mary J., Strom, Tim M., van Lith-Verhoeven, Janneke J.C., Lotery, Andrew J., van Moll-Ramirez, Norka, Leroy, Bart P., van den Born, L. Ingeborgh, Hoyng, Carel B., Cremers, Frans P.M., Klaver, Caroline C.W.

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A prospective, observational, open‐label, multicentre study to investigate the daily treatment practice of ranibizumab in patients with neovascular age‐related macular degeneration... by Asten, Freekje, Evers‐Birkenkamp, Kim U., Lith‐Verhoeven, Janneke J. C., Jong‐Hesse, Yvonne, Hoppenreijs, Vincent P. T., Hommersom, Richard F., Scholten, Agnes M., Hoyng, Carel B., Klaver, Johannes H. J.

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Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus by Boon, Camiel J F, van Schooneveld, Mary J, den Hollander, Anneke I, van Lith-Verhoeven, Janneke J C, Zonneveld-Vrieling, Marijke N, Theelen, Thomas, Cremers, Frans P M, Hoyng, Carel B, Klevering, B Jeroen

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Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13) by MCKIE, Arthur B, MCHALE, John C, MACKEY, David A, BHATTACHARYA, Shomi S, BIRD, Alan C, MARKHAM, Alexander F, INGLEHEARN, Chris F, KEEN, T. Jeffrey, TARTTELIN, Emma E, GOLIATH, Rene, VAN LITH-VERHOEVEN, Janneke J. C, GREENBERG, Jacquie, RAMESAR, Rajkumar S, HOYNG, Carel B, CREMERS, Frans P. M

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Genetic heterogeneity of butterfly-shaped pigment dystrophy of the fovea by van Lith-Verhoeven, Janneke J C, Cremers, Frans P M, van den Helm, Bellinda, Hoyng, Carel B, Deutman, August F

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Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGDi/fundus flavimaculatus by BOON, Camiel J. F, VAN SCHOONEVELD, Mary J, DEN HOLLANDER, Anneke I, VAN LITH-VERHOEVEN, Janneke J. C, ZONNEVELD-VRIELING, Marijke N, THEELEN, Thomas, CREMERS, Frans P. M, HOYNG, Carel B, KLEVERING, B. Jeroen

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