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Publications by Gramer, E

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Jump to: 2014 | 2011 | 2010 | 2009
Number of items: 6.

2014

Gramer, G, Weber, Bernhard H. F. and Gramer, E (2014) Results of a patient-directed survey on frequency of family history of glaucoma in 2170 patients. Investigative ophthalmology and visual science 55 (1), pp. 259-264.

2011

Fernández-Martínez, L, Letteboer, S, Mardin, C Y, Weisschuh, N, Gramer, E, Weber, Bernhard H. F. , Rautenstrauss, B, Ferreira, P A, Kruse, F E, Reis, A, Roepman, R and Pasutto, F (2011) Evidence for RPGRIP1 gene as risk factor for primary open angle glaucoma. European Journal of Human Genetics 19 (4), pp. 445-451. Fulltext not available.

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.

Pasutto, F, Matsumoto, T, Mardin, C Y, Sticht, H, Brandstätter, J H, Michels-Rautenstrauss, K, Weisschuh, N, Gramer, E, Ramdas, W D, van Koolwijk, L M, Klaver, C C, Vingerling, J R, Weber, Bernhard H. F. , Kruse, F E, Rautenstrauss, B, Barde, Y-A and Reis, A (2009) Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma. The American Journal of Human Genetics 85 (4), pp. 447-456. Fulltext not available.

This list was generated on Sat Sep 21 07:02:50 2019 CEST.
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