Universität zu Köln

Journal Article

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

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

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

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