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Publications by Gehrig, A

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Number of items: 13.

Article

Kast, K, Rhiem, K, Wappenschmidt, B, Hahnen, E, Hauke, J, Bluemcke, B, Zarghooni, V, Herold, N, Ditsch, N, Kiechle, M, Braun, M, Fischer, C, Dikow, N, Schott, S, Rahner, N, Niederacher, D, Fehm, T, Gehrig, A, Mueller-Reible, C, Arnold, N, Maass, N, Borck, G, de Gregorio, N, Scholz, C, Auber, B, Varon-Manteeva, R, Speiser, D, Horvath, J, Lichey, N, Wimberger, P, Stark, S, Faust, U, Weber, Bernhard H. F. , Emons, G, Zachariae, S, Meindl, A, Schmutzler, R K, Engel, C and German Consortium for Hereditary Breast and Ovarian Cancer, (GC-HBOC) (2016) Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer. Journal of Medical Genetics 53 (7), pp. 465-471. Fulltext not available.

Gehrig, A, Langmann, T, Horling, F, Janssen, A, Bonin, M, Walter, M, Poths, S and Weber, Bernhard H. F. (2007) Genome-wide expression profiling of the retinoschisin-deficient retina in early postnatal mouse development. Investigative ophthalmology and visual science 48 (2), pp. 891-900.

Schulz, H, Rahman, F. A, Fadl El Moula, F M, Stojic, J, Gehrig, A and Weber, Bernhard H. F. (2004) Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization. Cytogenetic and Genome Research 106 (1), pp. 74-81. Fulltext not available.

Wappenschmidt, B, Wardelmann, E, Gehrig, A, Schondorf, T, Maass, N, Bonatz, G, Gassel, A M, Pietsch, T, Mallmann, P, Weber, Bernhard H. F. and Schmutzler, R K (2004) PTEN mutations do not cause nuclear beta-catenin accumulation in endometrial carcinomas. Human Pathology 35 (10), pp. 1260-1265. Fulltext not available.

Weber, Bernhard H. F. , Schrewe, H, Molday, L L, Gehrig, A, White, K L, Seeliger, M W, Jaissle, G B, Friedburg, C, Tamm, E and Molday, R S (2002) Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure. Proceedings of the National Academy of Sciences of the United States of America : PNAS 99 (9), pp. 6222-6227.

Stöhr, H, Mah, N, Schulz, H L, Gehrig, A, Fröhlich, S and Weber, Bernhard H. F. (2000) EST mining of the UniGene dataset to identify retina-specific genes. Cytogenetics and cell genetics 91, pp. 267-277. Fulltext not available.

Krämer, F, White, K, Pauleikhoff, D, Gehrig, A, Passmore, L, Rivera, A, Rudolph, G, Kellner, U, Andrassi, M, Lorenz, B, Rohrschneider, K, Blankenagel, A, Jurklies, B, Schilling, H, Schütt, F, Holz, F G and Weber, Bernhard H. F. (2000) Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. European Journal of Human Genetics 8 (4), pp. 286-292. Fulltext not available.

Stöhr, H, Klein, J, Gehrig, A, Koehler, M R, Jurklies, B, Kellner, U, Leo-Kottler, B, Schmid, M and Weber, Bernhard H. F. (1999) Mapping and genomic characterization of the gene encoding diacylglycerol kinase γ (DAGK3): assessment of its role in dominant optic atrophy (OPA1). Human Genetics 104 (1), pp. 99-105. Fulltext not available.

Gehrig, A, Lorenz, B, Andrassi, M and Weber, Bernhard H. F. (1999) First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis. Journal of Medical Genetics 36 (12), pp. 933-934. Fulltext not available.

Gehrig, A, Felbor, U, Kelsell, R E, Hunt, D M, Maumenee, I H and Weber, Bernhard H. F. (1998) Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1). Journal of Medical Genetics 35 (8), pp. 641-645. Fulltext not available.

Felbor, U, Gehrig, A, Sauer, C G, Marquardt, A, Köhler, M, Schmid, M and Weber, Bernhard H. F. (1998) Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies. Cytogenetics and cell genetics 81, pp. 12-17. Fulltext not available.

Warneke-Wittstock, R, Marquardt, A, Gehrig, A, Sauer, C G, Gessler, M and Weber, Bernhard H. F. (1998) Transcript Map of a 900-kb Genomic Region in Xp22.1–p22.2: Identification of 12 Novel Genes. Genomics 51 (1), pp. 59-67. Fulltext not available.

Sauer, G S, Gehrig, A, Warneke-Wittstock, R, Marquardt, A, Ewing, C C, Gibson, A, Lorenz, B, Jurklies, B and Weber, Bernhard H. F. (1997) Positional cloning of the gene associated with X-linked juvenile retinoschisis. Nature Genetics 17, pp. 164-170. Fulltext not available.

This list was generated on Fri Oct 18 08:07:35 2019 CEST.
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