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Publications by Fritsche, L. G.

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Number of items: 7.


Fritsche, L. G., Igl, W., Bailey, J. N., Grassmann, Felix and Weber, Bernhard H. F. (2016) A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics 48, pp. 134-143. Fulltext not available.


Fritsche, L. G., Fleckenstein, M., Fiebig, B. S. and Weber, Bernhard H. F. (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, pp. 2112-2118. Fulltext not available.


Friedrich, U., Myers, C. A., Fritsche, L. G., Milenkovic, Andrea, Wolf, A., Corbo, J. C. and 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, pp. 1387-1399. Fulltext not available.

McKay, G. J., Silvestri, G., Chakravarthy, U., Dasari, S., Fritsche, L. G., Weber, Bernhard H. F. and et al, . (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), pp. 1357-1364. Fulltext not available.


Fritsche, L. G., Freitag-Wolf, S., Bettecken, T., Meitinger, T., Keilhauer, C. N., Krawczak, Michael and Weber, Bernhard H. F. (2009) Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene. Human Mutation 30, pp. 1048-1053. Fulltext not available.


Fritsche, L. G., Loenhardt, T., Janssen, A., Fisher, S. A., Rivera, A., Keilhauer, C. N. and Weber, Bernhard H. F. (2008) Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA. Nature Genetics 40, pp. 892-896. Fulltext not available.


Rivera, A., Fisher, Sheila A., Fritsche, L. G., Keilhauer, Claudia N., Lichtner, Peter, Meitinger, Thomas and 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, pp. 3227-3236. Fulltext not available.

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