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2018
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
2016
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
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
2015
de Motta, Laura Lores, Van Asten, Freekje, Muether, Philipp S., Smailhodzic, Dzenita, Chen, John C., Koenekoop, Robert K., Fauser, Sascha, Hoyng, Carel C. B., Den Hollander, Anneke I. and de Jong, Eiko (2015). A genetic variant in NRP1 is associated with worse response to ranibizumab treatment in neovascular age-related macular degeneration. Invest. Ophthalmol. Vis. Sci., 56 (7). ROCKVILLE: ASSOC RESEARCH VISION OPHTHALMOLOGY INC. ISSN 1552-5783
2012
Smailhodzic, Dzenita, Muether, Philipp S., Chen, John, Kwestro, Angela, Zhang, Alice Yang ORCID: 0000-0001-5194-5256, Omar, Amer ORCID: 0000-0003-1520-392X, Van de Ven, Johannes P. H., Keunen, Jan E. E., Kirchhof, Bernd, Hoyng, Carel B., Klevering, B. Jeroen, Koenekoop, Robert K., Fauser, Sascha and den Hollander, Anneke I.
(2012).
Cumulative Effect of Risk Alleles in CFH, ARMS2, and VEGFA on the Response to Ranibizumab Treatment in Age-related Macular Degeneration.
Ophthalmology, 119 (11).
S. 2304 - 2312.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1549-4713
2010
Otto, Edgar A., Hurd, Toby W., Airik, Rannar, Chaki, Moumita, Zhou, Weibin, Stoetzel, Corinne, Patil, Suresh B., Levy, Shawn ORCID: 0000-0002-1369-5740, Ghosh, Amiya K., Murga-Zamalloa, Carlos A., van Reeuwijk, Jeroen ORCID: 0000-0002-0658-4399, Letteboer, Stef J. F., Sang, Liyun, Giles, Rachel H., Liu, Qin, Coene, Karlien L. M., Estrada-Cuzcano, Alejandro ORCID: 0000-0001-9868-2465, Collin, Rob W. J., McLaughlin, Heather M., Held, Susanne, Kasanuki, Jennifer M., Ramaswami, Gokul, Conte, Jinny, Lopez, Irma, Washburn, Joseph, MacDonald, James, Hu, Jinghua, Yamashita, Yukiko ORCID: 0000-0001-5541-0216, Maher, Eamonn R., Guay-Woodford, Lisa M., Neumann, Hartmut P. H., Obermueller, Nicholas, Koenekoop, Robert K., Bergmann, Carsten, Bei, Xiaoshu ORCID: 0000-0003-1772-7161, Lewis, Richard A., Katsanis, Nicholas ORCID: 0000-0002-2480-0171, Lopes, Vanda, Williams, David S., Lyons, Robert H., Dang, Chi V., Brito, Daniela A., Dias, Monica Bettencourt, Zhang, Xinmin, Cavalcoli, James D., Nuernberg, Gudrun, Nuernberg, Peter, Pierce, Eric A., Jackson, Peter K., Antignac, Corinne, Saunier, Sophie ORCID: 0000-0002-1069-0047, Roepman, Ronald ORCID: 0000-0002-5178-8163, Dollfus, Helene, Khanna, Hemant and Hildebrandt, Friedhelm
(2010).
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy.
Nature Genet., 42 (10).
S. 840 - 853.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 1546-1718