Works by Hoyng, Carel B.

Results: 118
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    Genetic and environmental risk factors for extramacular drusen.

    Published in:
    Molecular Vision, 2020, v. 26, p. 661
    By:
    • Altay, Lebriz;
    • Subiras, Xavier;
    • de Motta, Laura Lorés;
    • Schick, Tina;
    • Berghold, Aileen;
    • Hoyng, Carel B.;
    • den Hollander, Anneke I.;
    • Fauser, Sascha;
    • Sadda, Srinivas R.;
    • Liakopoulos, Sandra
    Publication type:
    Article
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    Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis.

    Published in:
    JAMA Ophthalmology, 2023, v. 141, n. 8, p. 737, doi. 10.1001/jamaophthalmol.2023.2557
    By:
    • 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.
    Publication type:
    Article
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    Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.

    Published in:
    2020
    By:
    • Runhart, Esmee H.;
    • Khan, Mubeen;
    • Cornelis, Stéphanie S.;
    • Roosing, Susanne;
    • Del Pozo-Valero, Marta;
    • Lamey, Tina M.;
    • Liskova, Petra;
    • Roberts, Lisa;
    • Stöhr, Heidi;
    • Klaver, Caroline C. W.;
    • Hoyng, Carel B.;
    • Cremers, Frans P. M.;
    • Dhaenens, Claire-Marie;
    • ABCA4 Disease Consortium Study Group;
    • Disease Consortium Study Group
    Publication type:
    journal article
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    CNGB3 mutations account for 50%of all cases with autosomal recessive achromatopsia.

    Published in:
    European Journal of Human Genetics, 2005, v. 13, n. 3, p. 302, doi. 10.1038/sj.ejhg.5201269
    By:
    • Kohl, Susanne;
    • Varsanyi, Balazs;
    • Antunes, Gesine Abadin;
    • Baumann, Britta;
    • Hoyng, Carel B.;
    • Jägle, Herbert;
    • Rosenberg, Thomas;
    • Kellner, Ulrich;
    • Lorenz, Birgit;
    • Salati, Roberto;
    • Jurklies, Bernhard;
    • Farkas, Agnes;
    • Andreasson, Sten;
    • Weleber, Richard G.;
    • Jacobson, Samuel G.;
    • Rudolph, Günther;
    • Castellan, Claudio;
    • Dollfus, Helene;
    • Legius, Eric;
    • Anastasi, Mario
    Publication type:
    Article
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    The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East Europe.

    Published in:
    European Journal of Human Genetics, 2002, v. 10, n. 3, p. 197, doi. 10.1038/sj.ejhg.5200784
    By:
    • Maugeri, Alessandra;
    • Flothmann, Kris;
    • Hemmrich, Nadine;
    • Ingvast, Sofie;
    • Jorge, Paula;
    • Paloma, Eva;
    • Patel, Reshma;
    • Rozet, Jean-Michael;
    • Tammur, Jaana;
    • Testa, Francesco;
    • Balcells, Susana;
    • Bird, Alan C.;
    • Brunner, Han G.;
    • Hoyng, Carel B.;
    • Metspalu, Andres;
    • Simonelli, Francesca;
    • Allikmets, Rando;
    • Bhattacharya, Shomi S.;
    • D'Urso, Michele
    Publication type:
    Article
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    Quality of life in patients with CRB1‐associated retinal dystrophies: A longitudinal study.

    Published in:
    Acta Ophthalmologica (1755375X), 2024, v. 102, n. 4, p. 469, doi. 10.1111/aos.15769
    By:
    • Karuntu, Jessica S.;
    • Nguyen, Xuan‐Thanh‐An;
    • Talib, Mays;
    • van Schooneveld, Mary J.;
    • Wijnholds, Jan;
    • van Genderen, Maria M.;
    • Schalij‐Delfos, Nicoline E.;
    • Klaver, Caroline C. W.;
    • Meester‐Smoor, Magda A.;
    • van den Born, L. Ingeborgh;
    • Hoyng, Carel B.;
    • Thiadens, Alberta A. H. J.;
    • Bergen, Arthur A.;
    • van Nispen, Ruth M. A.;
    • Boon, Camiel J. F.
    Publication type:
    Article
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    Imaging diabetic retinal disease: clinical imaging requirements.

    Published in:
    Acta Ophthalmologica (1755375X), 2022, v. 100, n. 7, p. 752, doi. 10.1111/aos.15110
    By:
    • Schreur, Vivian;
    • Larsen, Morten B.;
    • Sobrin, Lucia;
    • Bhavsar, Abdhish R.;
    • den Hollander, Anneke I.;
    • Klevering, B. Jeroen;
    • Hoyng, Carel B.;
    • de Jong, Eiko K.;
    • Grauslund, Jakob;
    • Peto, Tunde
    Publication type:
    Article
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    Stargardt disease: monitoring incidence and diagnostic trends in the Netherlands using a nationwide disease registry.

    Published in:
    Acta Ophthalmologica (1755375X), 2022, v. 100, n. 4, p. 395, doi. 10.1111/aos.14996
    By:
    • Runhart, Esmee H.;
    • Dhooge, Patty;
    • Meester‐Smoor, Magda;
    • Pas, Jeroen;
    • Pott, Jan Willem R.;
    • van Leeuwen, Redmer;
    • Kroes, Hester Y.;
    • Bergen, Arthur A.;
    • de Jong‐Hesse, Yvonne;
    • Thiadens, Alberta A.;
    • van Schooneveld, Mary J.;
    • van Genderen, Maria;
    • Boon, Camiel;
    • Klaver, Caroline;
    • van den Born, L. Ingeborg;
    • Cremers, Frans P. M.;
    • Hoyng, Carel B.
    Publication type:
    Article
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    Defining inclusion criteria and endpoints for clinical trials: a prospective cross‐sectional study in CRB1‐associated retinal dystrophies.

    Published in:
    Acta Ophthalmologica (1755375X), 2021, v. 99, n. 3, p. e402, doi. 10.1111/aos.14597
    By:
    • Talib, Mays;
    • Schooneveld, Mary J.;
    • Wijnholds, Jan;
    • Genderen, Maria M.;
    • Schalij‐Delfos, Nicoline E.;
    • Talsma, Herman E.;
    • Florijn, Ralph J.;
    • Brink, Jacoline B.;
    • Cremers, Frans P.M.;
    • Thiadens, Alberta A.H.J.;
    • Born, L. Ingeborgh;
    • Hoyng, Carel B.;
    • Meester‐Smoor, Magda A.;
    • Bergen, Arthur A.;
    • Boon, Camiel J.F.
    Publication type:
    Article
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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.

    Published in:
    Acta Ophthalmologica (1755375X), 2015, v. 93, n. 2, p. 126, doi. 10.1111/aos.12610
    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.
    Publication type:
    Article
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    Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features.

    Published in:
    Acta Ophthalmologica (1755375X), 2015, v. 93, n. 1, p. 83, doi. 10.1111/aos.12500
    By:
    • Huet, Ramon A. C.;
    • Siemiatkowska, Anna M.;
    • Özgül, Riza K.;
    • Yücel, Didem;
    • Hoyng, Carel B.;
    • Banin, Eyal;
    • Blumenfeld, Anat;
    • Rotenstreich, Ygal;
    • Riemslag, Frans C. C.;
    • Hollander, Anneke I.;
    • Theelen, Thomas;
    • Collin, Rob W. J.;
    • Born, L. Ingeborgh;
    • Klevering, B. Jeroen
    Publication type:
    Article
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    Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).

    Published in:
    Nature Genetics, 1999, v. 23, n. 2, p. 217, doi. 10.1038/13848
    By:
    • den Hollander, Anneke I.;
    • ten Brink, Jacoline B.;
    • de Kok, Yvette J.M.;
    • van Soest, Simone;
    • van den Born, L. Ingeborgh;
    • van Driel, Marc A.;
    • van de Pol, Dorien J.R.;
    • Payne, Annette M.;
    • Bhattacharya, Shomi S.;
    • Kellner, Ulrich;
    • Hoyng, Carel B.;
    • Westerveld, Andries;
    • Brunner, Han G.;
    • Bleeker-Wagemakers, Elisabeth M.;
    • Deutman, August F.;
    • Heckenlively, John R.;
    • Cremers, Frans P.M.;
    • Bergen, Arthur A.B.
    Publication type:
    Article
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    Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy.

    Published in:
    Communications Biology, 2019, v. 2, n. 1, p. 1, doi. 10.1038/s42003-019-0712-z
    By:
    • Hosoda, Yoshikatsu;
    • Miyake, Masahiro;
    • Schellevis, Rosa L.;
    • Boon, Camiel J. F.;
    • Hoyng, Carel B.;
    • Miki, Akiko;
    • Meguro, Akira;
    • Sakurada, Yoichi;
    • Yoneyama, Seigo;
    • Takasago, Yukari;
    • Hata, Masayuki;
    • Muraoka, Yuki;
    • Nakanishi, Hideo;
    • Oishi, Akio;
    • Ooto, Sotaro;
    • Tamura, Hiroshi;
    • Uji, Akihito;
    • Miyata, Manabu;
    • Takahashi, Ayako;
    • Ueda-Arakawa, Naoko
    Publication type:
    Article
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    Semi-Quantitative Multiplex Profiling of the Complement System Identifies Associations of Complement Proteins with Genetic Variants and Metabolites in Age-Related Macular Degeneration.

    Published in:
    Journal of Personalized Medicine, 2021, v. 11, n. 12, p. 1256, doi. 10.3390/jpm11121256
    By:
    • Acar, I. Erkin;
    • Willems, Esther;
    • Kersten, Eveline;
    • Keizer-Garritsen, Jenneke;
    • Kragt, Else;
    • Bakker, Bjorn;
    • Galesloot, Tessel E.;
    • Hoyng, Carel B.;
    • Fauser, Sascha;
    • van Gool, Alain J.;
    • Lechanteur, Yara T. E.;
    • Koertvely, Elod;
    • Nogoceke, Everson;
    • Gloerich, Jolein;
    • de Jonge, Marien I.;
    • Lorés-Motta, Laura;
    • den Hollander, Anneke I.
    Publication type:
    Article