Universität zu Köln

Journal Article

Corominas, Jordi, Colijn, Johanna M., Geerlings, Maartje J., Pauper, Marc ORCID: 0000-0001-6274-9891, Bakker, Bjorn, Amin, Najaf, Motta, Laura Lores, Kersten, Eveline, Garanto, Alejandro ORCID: 0000-0001-5721-1560, Verlouw, Joost A. M., van Rooij, Jeroen G. J., Kraaij, Robert, de Jong, Paulus T. V. M., Hofman, Albert, Vingerling, Johannes R., Schick, Tina, Fauser, Sascha, de Jong, Eiko K., van Duijn, Cornelia M., Hoyng, Carel B., Klaver, Caroline C. W. and den Hollander, Anneke I. (2018). Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane. Ophthalmology, 125 (9). S. 1433 - 1444. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1549-4713

Den Hollander, Anneke I., Corominas, Jordi, Colijn, Johanna Maria, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Fauser, Sascha, de Jong, Eiko, van Duijn, Cornelia, Hoyng, Carel C. B. and Klaver, Caroline C. W. (2018). Whole-exome sequencing in age-related macular degeneration identifies rare protein-altering variants in COL8A1, a component of Bruch's membrane. Invest. Ophthalmol. Vis. Sci., 59 (9). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783

Geerlings, Maartje J., Kremlitzka, Mariann, Bakker, Bjorn, Nilsson, Sara C., Saksens, Nicole T., Lechanteur, Yara T., Pauper, Marc ORCID: 0000-0001-6274-9891, Corominas, Jordi, Fauser, Sascha, Hoyng, Carel B., Blom, Anna M., de Jong, Eiko K. and den Hollander, Anneke I. (2017). The Functional Effect of Rare Variants in Complement Genes on C3b Degradation in Patients With Age-Related Macular Degeneration. JAMA Ophthalmol., 135 (1). S. 39 - 47. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6173

Grunin, Michelle ORCID: 0000-0002-3155-2858, Lores-Motta, Laura, Riaz, Moeen, Corominas, Jordi, Richardson, Andrea J., Fauser, Sascha, Guymer, Robyn H., de Jong, Eiko, Heid, Iris M., Hoyng, Carel C. B., Lotery, Andrew J., Mitchell, Paul, Baird, Paul N., Den Hollander, Anneke I. and Chowers, Itay (2017). Identification of a Novel Variant Associated with anti-VEGF Response in Age-related Macular Degeneration Using Exome Chip Analysis. Invest. Ophthalmol. Vis. Sci., 58 (8). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783

Kersten, Eveline, Geerlings, Maartje J., Pauper, Marc, Corominas, Jordi, Bakker, Bjorn, Altay, Lebriz, Fauser, Sascha, de Jong, Eiko K., Hoyng, Carel B. and den Hollander, Anneke I. (2018). Genetic screening for macular dystrophies in patients clinically diagnosed with dry age-related macular degeneration. Clin. Genet., 94 (6). S. 569 - 575. HOBOKEN: WILEY. ISSN 1399-0004

Lores-Motta, Laura ORCID: 0000-0002-2423-9126, Paun, Constantin C., Corominas, Jordi, Pauper, Marc ORCID: 0000-0001-6274-9891, Geerlings, Maartje J., Altay, Lebriz, Schick, Tina, Daha, Mohamed R., Fauser, Sascha, Hoyng, Carel B., den Hollander, Anneke I. and de Jong, Eiko K. (2018). Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation. Ophthalmology, 125 (7). S. 1064 - 1075. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1549-4713

Lores-Motta, Laura ORCID: 0000-0002-2423-9126, Riaz, Moeen, Grunin, Michelle ORCID: 0000-0002-3155-2858, Corominas, Jordi, van Asten, Freekje, Pauper, Marc ORCID: 0000-0001-6274-9891, Leenders, Mathieu, Richardson, Andrea J., Muether, Philipp, Cree, Angela J., Griffiths, Helen L., Pham, Connie, Belanger, Marie-Claude, Meester-Smoor, Magda A., Ali, Manir, Heid, Iris M., Fritsche, Lars G., Chakravarthy, Usha, Gale, Richard, McKibbin, Martin, Inglehearn, Chris F., Schlingemann, Reinier O., Omar, Amer ORCID: 0000-0003-1520-392X, Chen, John, Koenekoop, Robert K., Fauser, Sascha, Guymer, Robyn H., Hoyng, Carel B., de Jong, Eiko K., Lotery, Andrew J., Mitchell, Paul, den Hollander, Anneke I., Baird, Paul N. and Chowers, Itay (2018). Association of Genetic Variants With Response to Anti-Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration. JAMA Ophthalmol., 136 (8). S. 875 - 885. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6173

de Motta, Laura Lores, Paun, Constantin, Corominas, Jordi, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Altay, Lebriz, Schick, Tina, Bakker, Bjorn, Groenewoud, Joannes, Daha, Mohamed, Fauser, Sascha, Den Hollander, Anneke I. and de Jong, Eiko (2017). Towards precision medicine in AMD: Genome-wide association study reveals genetic variants in CFH and CFHR4 that are strongly associated with complement activation levels. Invest. Ophthalmol. Vis. Sci., 58 (8). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783