Genetic Etiology and Clinical Consequences of Complete and Incomplete Achromatopsia von Thiadens, Alberta A.H.J., MD, Slingerland, Niki W.R., MD, Roosing, Susanne, Ing, van Schooneveld, Mary J., MD, PhD, van Lith-Verhoeven, Janneke J.C., MD, PhD, van Moll-Ramirez, Norka, MD, van den Born, L. Ingeborgh, MD, PhD, Hoyng, Carel B., MD, PhD, Cremers, Frans P.M., PhD, Klaver, Caroline C.W., MD, PhD

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Uveitis causes according to immune status of patients von Rothova, Aniki, Hajjaj, Anass, Hoog, Joeri, Thiadens, Alberta A.H.J., Dalm, Virgil A.S.H.

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Endophthalmitis after strabismus surgery: incidence and outcome in relation to age, operated eye muscle, surgical technique, scleral perforation and immune state von Simonsz, Huibert J., Rutar, Tina, Kraft, Stephen, Thiadens, Alberta A.H.J., Batstra, Manou R., Verdijk, Robert M., Loeffler, Karin U., Kommerell, Guntram, Berg, Mariette Swart‐van den, Schooneveld, Mary J, Drunen, Lamberdina C.J.W, Missotten, Luc, Kolling, Gerold H, Tusscher, Marcel P.M., Morad, Yair, Nucci, Paolo, Olitsky, Scott E, Kowal, Lionel, Eppinga, Hessel G, Duivenboden, Frank, Schalij, Nicoline E, Malacara Hernandez, José J.

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Clinical Course, Genetic Etiology, and Visual Outcome in Cone and Cone–Rod Dystrophy von Thiadens, Alberta A.H.J., MD, PhD, Phan, T. My Lan, MD, Zekveld-Vroon, Renate C., MD, Leroy, Bart P., MD, PhD, van den Born, L. Ingeborgh, MD, PhD, Hoyng, Carel B., MD, PhD, Klaver, Caroline C.W., MD, PhD, Roosing, Susanne, Pott, Jan-Willem R, van Schooneveld, Mary J, van Moll-Ramirez, Norka, van Genderen, Maria M, Boon, Camiel J.F, den Hollander, Anneke I, Bergen, Arthur A.B, De Baere, Elfride, Cremers, Frans P.M, Lotery, Andrew J

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Maternal Uniparental Isodisomy of Chromosome 6 Reveals a TULP1 Mutation as a Novel Cause of Cone Dysfunction von Roosing, Susanne, BSc, van den Born, L. Ingeborgh, MD, PhD, Hoyng, Carel B., MD, PhD, Thiadens, Alberta A.H.J., MD, PhD, de Baere, Elfride, MD, PhD, Collin, Rob W.J., PhD, Koenekoop, Robert K., MD, PhD, Leroy, Bart P., MD, PhD, van Moll-Ramirez, Norka, MD, Venselaar, Hanka, PhD, Riemslag, Frans C.C., PhD, Cremers, Frans P.M., PhD, Klaver, Caroline C.W., MD, PhD, den Hollander, Anneke I., PhD

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Progression Rate of Macular Retinal Pigment Epithelium Atrophy in Geographic Atrophy and Selected Inherited Retinal Dystrophies. A Systematic Review and Meta-Analysis von Bassil, Fabiana L., Colijn, Johanna M., Thiadens, Alberta A.H.J., Biarnés, Marc

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Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides von Sangermano, Riccardo, Garanto, Alejandro, Khan, Mubeen, Runhart, Esmee H., Bauwens, Miriam, Bax, Nathalie M., van den Born, L. Ingeborgh, Khan, Muhammad Imran, Cornelis, Stéphanie S., Verheij, Joke B. G. M., Pott, Jan-Willem R., Thiadens, Alberta A. H. J., Klaver, Caroline C. W., Puech, Bernard, Meunier, Isabelle, Naessens, Sarah, Arno, Gavin, Fakin, Ana, Carss, Keren J., Raymond, F. Lucy, Webster, Andrew R., Dhaenens, Claire-Marie, Stöhr, Heidi, Grassmann, Felix, Weber, Bernhard H. F., Hoyng, Carel B., De Baere, Elfride, Albert, Silvia, Collin, Rob W. J., Cremers, Frans P. M.

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Causes and consequences of inherited cone disorders von Roosing, Susanne, Thiadens, Alberta A.H.J., Hoyng, Carel B., Klaver, Caroline C.W., den Hollander, Anneke I., Cremers, Frans P.M.

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Whole exome sequencing of known eye genes reveals genetic causes for high myopia von Haarman, Annechien E G, Thiadens, Alberta A H J, van Tienhoven, Marianne, Loudon, Sjoukje E, de Klein, J E M M Annelies, Brosens, Erwin, Polling, Jan Roelof, van der Schoot, Vyne, Bouman, Arjan, Kievit, Anneke J A, Hoefsloot, Lies H, Klaver, Caroline C W, Verhoeven, Virginie J M

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The Common ABCA4 Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present in trans With Severe Variants von Runhart, Esmee H, Sangermano, Riccardo, Cornelis, Stéphanie S, Verheij, Joke B G M, Plomp, Astrid S, Boon, Camiel J F, Lugtenberg, Dorien, Roosing, Susanne, Bax, Nathalie M, Blokland, Ellen A W, Jacobs-Camps, Marlie H M, van der Velde-Visser, Saskia D, Pott, Jan-Willem R, Rohrschneider, Klaus, Thiadens, Alberta A H J, Klaver, Caroline C W, van den Born, L Ingeborgh, Hoyng, Carel B, Cremers, Frans P M

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Early onset X‐linked female limited high myopia in three multigenerational families caused by novel mutations in the ARR3 gene von Mazijk, Ralph, Haarman, Annechien E.G., Hoefsloot, Lies H., Polling, Jan R., Tienhoven, Marianne, Klaver, Caroline C.W., Verhoeven, Virginie J.M., Loudon, Sjoukje E., Thiadens, Alberta A.H.J., Kievit, Anneke J.A.

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Long-Term Follow-up of Patients With Uveitis Treated With Adalimumab: Response Rates and Reasons for Discontinuation of Therapy von Eurelings, Laura E.M., Missotten, Tom O.A.R., van Velthoven, Mirjam E.J., van Daele, Paul L.A., van Laar, Jan A.M., van Hagen, P. Martin, Thiadens, Alberta A.H.J., Rombach, Saskia M.

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Outcome of Cataract Surgery in Patients With Retinitis Pigmentosa von Nguyen, Xuan-Thanh-An, Thiadens, Alberta A.H.J., Fiocco, Marta, Tan, Weijen, McKibbin, Martin, Klaver, Caroline C.W., Meester-Smoor, Magda A., Van Cauwenbergh, Caroline, Strubbe, Ine, Vergaro, Andrea, Pott, Jan-Willem R., Hoyng, Carel B., Leroy, Bart P., Zemaitiene, Reda, Khan, Kamron N., Boon, Camiel J.F.

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Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis von de Groot, Evianne L, Ossewaarde–van Norel, Jeannette, de Boer, Joke H, Hiddingh, Sanne, Bakker, Bjorn, van Huet, Ramon A. C, ten Dam–van Loon, Ninette H, Thiadens, Alberta A. H. J, Meester-Smoor, Magda A, de Jong–Hesse, Yvonne, Los, Leonoor I, den Hollander, Anneke I, Boon, Camiel J. F, Kiemeney, Lambertus A, van Eijk, Kristel R, Bakker, Mark K, Hoyng, Carel B, Kuiper, Jonas J. W

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CRB1-Associated Retinal Dystrophies: A Prospective Natural History Study in Anticipation of Future Clinical Trials von Nguyen, Xuan-Thanh-An, Talib, Mays, van Schooneveld, Mary J., Wijnholds, Jan, van Genderen, Maria M., Schalij-Delfos, Nicoline E., Klaver, Caroline C.W., Talsma, Herman E., Fiocco, Marta, Florijn, Ralph J., ten Brink, Jacoline B., Cremers, Frans P.M., Meester-Smoor, Magda A., van den Born, L. Ingeborgh, Hoyng, Carel B., Thiadens, Alberta A.H.J., Bergen, Arthur A., Boon, Camiel J.F.

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Progressive loss of cones in achromatopsia: an imaging study using spectral-domain optical coherence tomography von Thiadens, Alberta A H J, Somervuo, Ville, van den Born, L Ingeborgh, Roosing, Susanne, van Schooneveld, Mary J, Kuijpers, Robert W A M, van Moll-Ramirez, Norka, Cremers, Frans P M, Hoyng, Carel B, Klaver, Caroline C W

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Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium von Heutinck, Pam A.T, van den Born, L. Ingeborgh, Vermeer, Maikel, Iglesias Gonzales, Adriana I, Hoyng, Carel B, Pott, Jan Willem R, Kroes, Hester Y, van Schooneveld, Mary J, Boon, Camiel J.F, van Genderen, Maria M, Plomp, Astrid S, de Jong-Hesse, Yvonne, van Egmond-Ebbeling, Michelle B, Hoefsloot, Lies H, A Bergen, Arthur, Klaver, Caroline C.W, Meester-Smoor, Magda A, Thiadens, Alberta A.H.J, Verhoeven, Virginie J.M

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Vitamin A for Children With Retinitis Pigmentosa: An Unresolved Mystery von Klaver, Caroline C. W, Thiadens, Alberta A. H. J

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Heterozygous Deep-Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant von Bax, Nathalie M., Sangermano, Riccardo, Roosing, Susanne, Thiadens, Alberta A.H.J., Hoefsloot, Lies H., van den Born, L. Ingeborgh, Phan, Milan, Klevering, B. Jeroen, Westeneng-van Haaften, Carla, Braun, Terry A., Zonneveld-Vrieling, Marijke N., de Wijs, Ilse, Mutlu, Merve, Stone, Edwin M., den Hollander, Anneke I., Klaver, Caroline C.W., Hoyng, Carel B., Cremers, Frans P.M.

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Extending the Spectrum of EYS-Associated Retinal Disease to Macular Dystrophy von Pierrache, Laurence H M, Messchaert, Muriël, Thiadens, Alberta A H J, Haer-Wigman, Lonneke, de Jong-Hesse, Yvonne, van Zelst-Stams, Wendy A G, Collin, Rob W J, Klaver, Caroline C W, van den Born, L Ingeborgh

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