Publikationen von 0000-0002-2110-1690
(ORCID: 0000-0002-2110-1690)

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.

Fan, Qiao, Maranville, Joseph C., Fritsche, Lars , Sim, Xueling, Cheung, Chui Ming Gemmy, Chen, Li Jia, Gorski, Mathias, Yamashiro, Kenji , Ahn, Jeeyun, Laude, Augustinus, Dorajoo, Rajkumar, Lim, Tock Han, Teo, Yik-Ying, Blaustein, Robert O., Yoshimura, Nagahisa, Park, Kyu-Hyung, Pang, Chi Pui, Tai, E. Shyong, Khor, Chiea Chuen, Wong, Tien Yin, Runz, Heiko und Cheng, Ching-Yu (2017) HDL-cholesterol levels and risk of age-related macular degeneration: a multiethnic genetic study using Mendelian randomization. International Journal of Epidemiology 46 (6), S. 1891-1902. Volltext nicht vorhanden.

Fritsche, L. G. , Igl, Wilmar, Bailey, J. N., Grassmann, Felix , Sengupta, Sebanti, Bragg-Gresham, Jennifer L., Burdon, Kathryn P., Hebbring, Scott J., Weber, Bernhard H. F. und Heid, Iris M. (2016) A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics 48, S. 134-143. 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.

Keilhauer, C. N., Fritsche, L. G. , Guthoff, R., Haubitz, I. und Weber, Bernhard H. F. (2013) Age-related macular degeneration and coronary heart disease: Evaluation of genetic and environmental associations. European journal of medical genetics 56 (2), S. 72-79. 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, L. G. , Fleckenstein, M. , Fiebig, B. S., Weber, Bernhard H. F., make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference (2012) A Subgroup of Age-Related Macular Degeneration is Associated With Mono-Allelic Sequence Variants in the ABCA4 Gene. Investigative Ophthalmology & Visual Science (IOVS) 53, S. 2112-2118. Volltext nicht vorhanden.

Sofat, R., Casas, J. P., Webster, A. R., Bird, A. C., Mann, S. S., Yates, J. R., Moore, A. T., Sepp, T., Cipriani, V. , Bunce, C. , Khan, J. C., Shahid, H., Swaroop, A. , Abecasis, G. , Branham, K. E., Zareparsi, S., Bergen, A. A., Klaver, C. C. , Baas, D. C., Zhang, K., Chen, Y., Gibbs, D., Weber, Bernhard H. F. , et, al., make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference und make_name_string expected hash reference (2012) Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International Journal of Epidemiology 41 (1), S. 250-262. Volltext nicht vorhanden.

Keilhauer, C. N., Fritsche, L. G. und Weber, Bernhard H. F. (2011) Age-related macular degeneration with discordant late stage phenotypes in monozygotic twins. Ophthalmic Genetics 32, S. 237-244. Volltext nicht vorhanden.

McKay, G. J. , Patterson, C. C., Chakravarthy, U. , Dasari, S., Klaver, C. C. , Vingerling, J. R., Ho, L., de Jong, P. T., Fletcher, A. E., Young, I. S. , Seland, J. H., Rahu, M., Soubrane, G., Tomazzoli, L., Topouzis, F. , Vioque, J. , Weber, Bernhard H. F., et, al., make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference und make_name_string expected hash reference (2011) Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies. Human Mutation 32 (12), S. 1407-1416. Volltext nicht vorhanden.

Friedrich, U., Myers, C. A., Fritsche, L. G. , Milenkovic, Andrea, Wolf, A., Corbo, J. C. und Weber, Bernhard H. F. (2011) Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency. Human Molecular Genetics 20, S. 1387-1399. Volltext nicht vorhanden.

McKay, G. J. , Silvestri, G., Chakravarthy, U. , Dasari, S., Fritsche, L. G. , Weber, Bernhard H. F. , et, al., make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference, make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference , make_name_string expected hash reference und make_name_string expected hash reference (2011) Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. American Journal of Epidemiology 173 (12), S. 1357-1364. Volltext nicht vorhanden.

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.

Fritsche, L. G. , Freitag-Wolf, S., Bettecken, T., Meitinger, T. , Keilhauer, C. N., Krawczak, Michael und Weber, Bernhard H. F. (2009) Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene. Human Mutation 30, S. 1048-1053. Volltext nicht vorhanden.

Fritsche, L. G. , Loenhardt, T., Janssen, A., Fisher, S. A., Rivera, A., Keilhauer, C. N. und Weber, Bernhard H. F. (2008) Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA. Nature Genetics 40, S. 892-896. Volltext nicht vorhanden.

Scholl, H. P., Charbel Issa, P., Walier, M., Janzer, S., Pollok-Kopp, B., Börncke, F., Fritsche, L. G. , Chong, N. V. , Fimmers, R., Wienker, T., Holz, F. G., Weber, Bernhard H. F. und Oppermann, M. (2008) Systemic complement activation in age-related macular degeneration. PLoS one 3 (7), e2593.

Fisher, S. A., Rivera, A., Fritsche, L. G. , Babadjanova, G., Petrov, S. und Weber, Bernhard H. F. (2007) Assessment of the contribution of CFH and chromosome 10q26 AMD susceptibility loci in a Russian population isolate. British Journal of Ophthalmology 91 (5), S. 576-578. Volltext nicht vorhanden.

Skerka, C., Lauer, N., Weinberger, A. W. A., Keilhauer, C. N., Sühnel, J., Smith, R. , Schlötzer-Schrehardt, U., Fritsche, L. , Heinen, S. , Hartmann, A., Weber, Bernhard H. F. und Zipfel, P. F. (2007) Defective complement control of Factor H (Y402H) and FHL-1 in age-related macular degeneration. Molecular Immunology 44 (13), S. 3398-3406. Volltext nicht vorhanden.

Rivera, A., Fisher, Sheila A., Fritsche, L. G. , Keilhauer, Claudia N., Lichtner, Peter, Meitinger, Thomas und Weber, Bernhard H. F. (2005) Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk. Human Molecular Genetics 14, S. 3227-3236. Volltext nicht vorhanden.