Einträge von Guymer, Robyn H. auf dem Publikationsserver

Lorés-Motta, Laura , Riaz, Moeen, Grunin, Michelle , Corominas, Jordi, van Asten, Freekje, Pauper, Marc , 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 , 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. und Chowers, Itay (2018) Association of Genetic Variants With Response to Anti–Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration. JAMA Ophthalmology 136 (8), S. 875. Volltext nicht vorhanden.

Cantsilieris, Stuart, Nelson, Bradley J., Huddleston, John, Baker, Carl, Harshman, Lana, Penewit, Kelsi, Munson, Katherine M. , Sorensen, Melanie , Welch, AnneMarie E., Dang, Vy, Grassmann, Felix , Richardson, Andrea J., Guymer, Robyn H. , Graves-Lindsay, Tina A., Wilson, Richard K., Weber, Bernhard H. F., Baird, Paul N., Allikmets, Rando und Eichler, Evan E. (2018) Recurrent structural variation, clustered sites of selection, and disease risk for the complement factor H (CFH) gene family. Proceedings of the National Academy of Sciences 115 (19), E4433-E4442. Volltext nicht vorhanden.

Weber, Bernhard H. F. , Grassmann, Felix, Cantsilieris, Stuart, Schulz-Kuhnt, Anja-Sabrina, White, Stefan J., Richardson, Andrea J., Hewitt, Alex W., Vote, Brendan J., Schmied, Denise , Guymer, Robyn H. und Baird, Paul N. (2016) Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD). Jornal of Neuroinflammation 13 (81), S. 1-9.