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

Duvvari, Maheswara R., van de Ven, Johannes P. H., Geerlings, Maartje J., Saksens, Nicole T. M., Bakker, Bjorn, Henkes, Arjen, Neveling, Kornelia, del Rosario, Marisol, Westra, Dineke, van den Heuvel, Lambertus P. W. J., Schick, Tina, Fauser, Sascha, Boon, Camiel J. F., Hoyng, Carel B., de Jong, Eiko K. and den Hollander, Anneke I. (2016). Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration. PLoS One, 11 (3). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Geerlings, Maartje ORCID: 0000-0003-1164-3573, Saksens, Nicole T. M., Bakker, Bjorn, Schick, Tina, Fauser, Sascha, Boon, Camiel J. F., de Jong, Eiko, Hoyng, Carel C. B. and Den Hollander, Anneke I. (2015). Rare variants in complement genes associated with age-related macular degeneration result in a lower age at onset and higher familial occurrence. Invest. Ophthalmol. Vis. Sci., 56 (7). 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

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

Kremlitzka, Mariann, Geerlings, Maartje J., de Jong, Sarah, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M. (2018). Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration. Hum. Mol. Genet., 27 (15). S. 2678 - 2689. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2083

Kremlitzka, Mariann, de Jong, Sarah, Geerlings, Maartje ORCID: 0000-0003-1164-3573, Bakker, Bjorn, Nilsson, Sara C., Fauser, Sascha, Hoyng, Carel B., de Jong, Eiko K., den Hollander, Anneke I. and Blom, Anna M. (2017). Functional analysis of AMD-associated rare genetic variants in C9. Mol. Immunol., 89. S. 150 - 151. OXFORD: PERGAMON-ELSEVIER SCIENCE LTD. ISSN 0161-5890

Saksens, Nicole T. M., Geerlings, Maartje J., Bakker, Bjorn, Schick, Tina, Daha, Mohamed R., Fauser, Sascha, Boon, Camiel J. F., de Jong, Eiko K., Hoyng, Carel B. and den Hollander, Anneke I. (2016). Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration. JAMA Ophthalmol., 134 (3). S. 287 - 294. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6173

Schellevis, Rosa, Van Dijk, Elon H., Breukink, Myrte, Altay, Lebriz, Bakker, Bjorn, Koeleman, Bobby, Kiemeney, Lambertus, Swinkels, Dorine, Keunen, Jan, Fauser, Sascha, Hoyng, Carel C. B., Den Hollander, Anneke I., Boon, Camiel and de Jong, Eiko (2018). Genome-wide association study underlines the role of the complement system in chronic central serous chorioretinopathy. Invest. Ophthalmol. Vis. Sci., 59 (9). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783

Schellevis, Rosa L., van Dijk, Elon H. C., Breukink, Myrte B., Altay, Lebuz, Bakker, Bjorn, Koeleman, Bobby P. C., Kiemeney, Lambertus A. ORCID: 0000-0002-2368-1326, Swinkels, Dorine W., Keunen, Jan E. E., Fauser, Sascha, Hoyng, Carel B., den Hollander, Anneke, I, Boon, Camiel J. F. and de Jong, Eiko K. (2018). Role of the Complement System in Chronic Central Serous Chorioretinopathy A Genome-Wide Association Study. JAMA Ophthalmol., 136 (10). S. 1128 - 1137. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6173

de Breuk, Anita ORCID: 0000-0001-7072-1928, Acar, Ilhan E., Kersten, Eveline, Schijvenaars, Mascha M. V. A. P., Colijn, Johanna M., Haer-Wigman, Lonneke, Bakker, Bjorn, de Jong, Sarah ORCID: 0000-0002-3705-3371, Meester-Smoor, Magda A., Verzijden, Timo, Missotten, Tom O. A. R., Mones, Jordi, Biarnes, Marc, Pauleikhoff, Daniel, Hense, Hans W., Silva, Rufino ORCID: 0000-0001-8676-0833, Nunes, Sandrina, Melo, Joana B., Fauser, Sascha, Hoyng, Carel B., Ueffing, Marius, Coenen, Marieke J. H., Klaver, Caroline C. W. and den Hollander, Anneke, I (2021). Development of a Genotype Assay for Age-Related Macular Degeneration The EYE-RISK Consortium. Ophthalmology, 128 (11). S. 1604 - 1618. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1549-4713

de Jong, Eiko K., Breukink, Myrte B., Schellevis, Rosa L., Bakker, Bjorn, Mohr, Jacqueline K., Fauser, Sascha, Keunen, Jan E. E., Hoyng, Carel B., den Hollander, Anneke I. and Boon, Camiel J. F. (2015). Chronic Central Serous Chorioretinopathy Is Associated with Genetic Variants Implicated in Age-Related Macular Degeneration. Ophthalmology, 122 (3). S. 562 - 571. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1549-4713

de Jong, Eiko K., Breukink, Myrte B., Schellevis, Rosa L., Bakker, Bjorn, Mohr, Jacqueline K., Fauser, Sascha, Keunen, Jan E. E., Hoyng, Carel B., den Hollander, Anneke I. and Boon, Camiel J. F. (2015). Chronic Central Serous Chorioretinopathy Is Associated with Genetic Variants Implicated in Age-Related Macular Degeneration. Ophthalmology, 122 (3). S. 562 - 571. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1549-4713

de Jong, Sarah ORCID: 0000-0002-3705-3371, de Breuk, Anita, Volokhina, Elena B., Bakker, Bjorn, Garanto, Alejandro ORCID: 0000-0001-5721-1560, Fauser, Sascha, Katti, Suresh, Hoyng, Carel B., Lechanteur, Yara T. E., van den Heuvel, Lambert P. and den Hollander, Anneke, I (2022). Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene. Hum. Mol. Genet., 31 (3). S. 455 - 471. OXFORD: OXFORD UNIV PRESS. ISSN 1460-2083

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