Einträge von Fritsche, Lars G. auf dem Publikationsserver

Bouzigon, Emmanuelle, Ferreira, Manuel A. R. , Vonk, Judith M. , Baurecht, Hansjörg, Marenholz, Ingo , Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika , Ullemar, Vilhelmina, Lu, Yi, Grosche, Sarah, Rüschendorf, Franz , Granell, Raquel, Brumpton, Ben M., Fritsche, Lars G. , Bhatta, Laxmi, Gabrielsen, Maiken E., Nielsen, Jonas B., Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L. , Løset, Mari, Abecasis, Gonçalo R., Willer, Cristen J., Emami, Nima C., Cavazos, Taylor B., Witte, John S., Szwajda, Agnieszka, Hinds, David A., Hübner, Norbert, Weidinger, Stephan , Magnusson, Patrik K. E., Jorgenson, Eric, Karlsson, Robert, Paternoster, Lavinia, Boomsma, Dorret I., Almqvist, Catarina, Lee, Young-Ae und Koppelman, Gerard H. (2020) Age-of-onset information helps identify 76 genetic variants associated with allergic disease. PLOS Genetics 16 (6), e1008725. 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.

Roth, Helmut, Fritsche, Lars G. , Meier, Christoph, Pilz, P., Eigenthaler, M., Meyer-Marcotty, P., Stellzig-Eisenhauer, A., Proff, Peter, Kanno, C. M. und Weber, Bernhard H. F. (2014) Expanding the spectrum of PTH1R mutations in patients with primary failure of tooth eruption. Clinical Oral Investigations 18, S. 377-384. Volltext nicht vorhanden.

Fritsche, Lars G. , Chen, W., Schu, M., Weber, Bernhard H. F. und et, al. (2013) Seven new loci associated with age-related macular degeneration. Nature Genetics 45, S. 433-439. Volltext nicht vorhanden.

Grassmann, Felix , Fritsche, Lars G. , Keilhauer, Claudia N., Heid, Iris M. und Weber, Bernhard H. F. (2012) Modelling the Genetic Risk in Age-Related Macular Degeneration. PLoS ONE 7, e37979.

Fritsche, Lars G. , Lauer, N., Hartmann, Andrea, Stippa, S., Keilhauer, Claudia N., Oppermann, M., Pandey, M. K., Köhl, Jörg , Zipfel, P. F., Weber, Bernhard H. F. und make_name_string expected hash reference (2010) An imbalance of human complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age-related macular degeneration (AMD). Human Molecular Genetics 19, S. 4694-4704. Volltext nicht vorhanden.

Corbo, Joseph C. , Lawrence, Karen A. , Karlstetter, Marcus, Myers, Connie A., Abdelaziz, Musa, Dirkes, William, Weigelt, Karin, Seifert, Martin, Benes, Vladimir , Fritsche, Lars G. , Weber, Bernhard H. F. und Langmann, Thomas (2010) CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors. Genome research 20 (11), S. 1512-25. Volltext nicht vorhanden.

Lauer, Nadine, Fritsche, Lars G., Weber, Bernhard H.F., Hartmann, Andrea, Keilhauer, Claudia N., Hälbich, Steffi, Oppermann, Martin, Pandey, Manoij, Köhl, Jörg und Zipfel, Peter F. (2010) Imbalance of complement regulatory proteins CFHR1, CFHR3 and factor H influences risk for age related macular degeneration (AMD). Molecular Immunology 47 (13), S. 2211. Volltext nicht vorhanden.