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Publications by Schlötzer-Schrehardt, U

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Jump to: 2011 | 2010 | 2009 | 2008 | 2007
Number of items: 5.

2011

Krumbiegel, M, Pasutto, F, Schlötzer-Schrehardt, U, Uebe, S, Zenkel, M, Mardin, C Y, Weisschuh, N, Paoli, D, Gramer, E, Becker, C, Ekici, A B, Weber, Bernhard H. F. , Nürnberg, P, Kruse, F E and Reis, A (2011) Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. European Journal of Human Genetics 19 (2), pp. 186-193. Fulltext not available.

2010

Krumbiegel, M, Pasutto, F, Mardin, C Y, Weisschuh, N, Paoli, D, Gramer, E, Weber, Bernhard H. F. , Kruse, F E, Schlötzer-Schrehardt, U and Reis, A (2010) Apolipoprotein E genotypes in pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Journal of Glaucoma 19 (8), pp. 561-565. Fulltext not available.

2009

Krumbiegel, M, Pasutto, F, Mardin, C Y, Weisschuh, N, Paoli, D, Gramer, E, Zenkel, M, Weber, Bernhard H. F. , Kruse, F E, Schlötzer-Schrehardt, U and Reis, A (2009) Exploring functional candidate genes for genetic association in German patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Investigative ophthalmology and visual science 50 (6), pp. 2796-2801.

2008

Pasutto, F, Krumbiegel, M, Mardin, C Y, Paoli, D, Lämmer, R, Weber, Bernhard H. F. , Kruse, F E, Schlötzer-Schrehardt, U and Reis, A (2008) Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Investigative ophthalmology and visual science 49 (4), pp. 1459-1463.

2007

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. and Zipfel, P F (2007) Defective complement control of Factor H (Y402H) and FHL-1 in age-related macular degeneration. Molecular Immunology 44 (13), pp. 3398-3406. Fulltext not available.

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