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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
Riaz, Moeen, Lores-Motta, Laura ORCID: 0000-0002-2423-9126, Richardson, Andrea J., Lu, Yi ORCID: 0000-0001-9933-3654, Montgomery, Grant, Omar, Amer ORCID: 0000-0003-1520-392X, Koenekoop, Robert K., Chen, John, Muether, Philipp, Altay, Lebriz, Schick, Tina, Fauser, Sascha, Smailhodzic, Dzenita, van Asten, Freekje ORCID: 0000-0002-8141-4234, de Jong, Eiko K., Hoyng, Carel B., Burdon, Kathryn P., MacGregor, Stuart, Guymer, Robyn H., den Hollander, Anneke I. and Baird, Paul N. (2016). GWAS study using DNA pooling strategy identifies association of variant rs4910623 in OR52B4 gene with anti-VEGF treatment response in age-related macular degeneration. Sci Rep, 6. LONDON: NATURE PUBLISHING GROUP. ISSN 2045-2322
Lores-Motta, Laura ORCID: 0000-0002-2423-9126, van Asten, Freekje ORCID: 0000-0002-8141-4234, Muether, Philipp S., Smailhodzic, Dzenita, Groenewoud, Joannes M., Omar, Amer ORCID: 0000-0003-1520-392X, Chen, John, Koenekoop, Robert K., Fauser, Sascha, Hoyng, Carel B., den Hollander, Anneke I. and de Jong, Eiko K. (2016). A genetic variant in NRP1 is associated with worse response to ranibizumab treatment in neovascular age-related macular degeneration. Pharmacogenet. Genomics, 26 (1). S. 20 - 28. PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1744-6880