Einträge von Baird, Paul N. auf dem Publikationsserver

Biasella, Fabiola, Plössl, Karolina, Baird, Paul N. und Weber, Bernhard H. F. (2023) The extracellular microenvironment in immune dysregulation and inflammation in retinal disorders. Frontiers in Immunology 14. Volltext nicht vorhanden.

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.

Persad, Patrice J., Heid, Iris M., Weeks, Daniel E. , Baird, Paul N., de Jong, Eiko K. , Haines, Jonathan L., Pericak-Vance, Margaret A. und Scott, William K. (2017) Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Investigative Opthalmology & Visual Science 58 (10), S. 4027. 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.