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Publications by Fritsche, L G

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Number of items: 7.


Keilhauer, C N, Fritsche, L G, Guthoff, R, Haubitz, I and 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), pp. 72-79. Fulltext not available.


Baas, D C, Ho, L, Tanck, M W, Fritsche, L G, Merriam, J E, van het Slot, R, Koeleman, B P, Gorgels, T G, van Duijn, C M, Uitterlinden, A G, de Jong, P T, Hofman, A, ten Brink, J B, Vingerling, J R, Klaver, C C, Dean, M, Weber, Bernhard H. F. and et al, . (2012) Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration. Molecular vision 18, pp. 657-674.


Keilhauer, C N, Fritsche, L G and Weber, Bernhard H. F. (2011) Age-related macular degeneration with discordant late stage phenotypes in monozygotic twins. Ophthalmic Genetics 32, pp. 237-244. Fulltext not available.


Scholl, H P, Fleckenstein, M, Fritsche, L G, Schmitz-Valckenberg, S, Göbel, A, Adrion, C, Herold, C, Keilhauer, C N, Mackensen, F, Mössner, A, Pauleikhoff, D, Weinberger, A W, Mansmann, U, Holz, F G, Becker, T and Weber, Bernhard H. F. (2009) CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMD. PLoS one 4 (10), e7418.


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. and 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 and 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), pp. 576-578. Fulltext not available.

Fisher, S A, Rivera, A, Fritsche, L G, Keilhauer, C N, Lichtner, P, Meitinger, T, Rudolph, G and Weber, Bernhard H. F. (2007) Case–control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD). Human Mutation 28 (4), pp. 406-413. Fulltext not available.

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