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2017
Schellevis, R. L., van Dijk, E. H. C., van Bergen, M. G. J. M., Breukink, M. B., Altay, L., Scholz, P., Fauser, S., Meijer, O. C., Hoyng, C. B., den Hollander, A. I., Boon, C. J. F. and de Jong, E. K. (2017). A genetic variant in the NR3C2 gene, encoding the mineralocorticoid receptor, is associated with chronic central serous chorioretinopathy. Acta Ophthalmol., 95. S. 21 - 22. HOBOKEN: WILEY. ISSN 1755-3768
2016
Ersoy, L., Schick, T., de Graft, D., Felsch, M., Hoyng, C. B., den Hollander, A. I., Kirchhof, B., Fauser, S. and Liakopoulos, S. (2016). Extramacular drusen are highly associated with age-related macular degeneration, but not with CFH and ARMS2 genotypes. Br. J. Ophthalmol., 100 (8). S. 1047 - 1052. LONDON: BMJ PUBLISHING GROUP. ISSN 1468-2079
2013
van de Ven, J. P. H., Nilsson, S. C., Tan, P. L., Buitendijk, G., Ristau, T., Mohlin, F. C., Nabuurs, S. B., Schoenmaker-Koller, F. E., Smailhodzic, D., Campochiarro, P. A., Zack, D. J., Duvvari, M. R., Bakker, B., Paun, C. C., Boon, C. J. F., Uitterlinden, A. G., Liakopoulos, S., Klevering, B. J., Fauser, S., Daha, M. R., Katsanis, N., Klaver, C. C. W., Blom, A. M., Hoyng, C. B. and den Hollander, A. I. (2013). A functional variant in the CFI gene confers a high risk of age-related macular degeneration. Mol. Immunol., 56 (3). S. 247 - 249. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0161-5890