Rosenberg T - Search Results

1

Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2).

Rosenberg T, Schwahn U, Feil S, Berger W. Rosenberg T, et al. Ophthalmic Genet. 1999 Sep;20(3):161-72. doi: 10.1076/opge.20.3.161.2278. Ophthalmic Genet. 1999. PMID: 10520237

2

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Schwahn U, Lenzner S, Dong J, Feil S, Hinzmann B, van Duijnhoven G, Kirschner R, Hemberger M, Bergen AA, Rosenberg T, Pinckers AJ, Fundele R, Rosenthal A, Cremers FP, Ropers HH, Berger W. Schwahn U, et al. Among authors: rosenberg t. Nat Genet. 1998 Aug;19(4):327-32. doi: 10.1038/1214. Nat Genet. 1998. PMID: 9697692

3

RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa.

Kirschner R, Rosenberg T, Schultz-Heienbrok R, Lenzner S, Feil S, Roepman R, Cremers FP, Ropers HH, Berger W. Kirschner R, et al. Among authors: rosenberg t. Hum Mol Genet. 1999 Aug;8(8):1571-8. doi: 10.1093/hmg/8.8.1571. Hum Mol Genet. 1999. PMID: 10401007

4

Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.

Neidhardt J, Glaus E, Lorenz B, Netzer C, Li Y, Schambeck M, Wittmer M, Feil S, Kirschner-Schwabe R, Rosenberg T, Cremers FP, Bergen AA, Barthelmes D, Baraki H, Schmid F, Tanner G, Fleischhauer J, Orth U, Becker C, Wegscheider E, Nürnberg G, Nürnberg P, Bolz HJ, Gal A, Berger W. Neidhardt J, et al. Among authors: rosenberg t. Mol Vis. 2008 Jun 6;14:1081-93. Mol Vis. 2008. PMID: 18552978 Free PMC article.

5

Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP).

Roepman R, Bauer D, Rosenberg T, van Duijnhoven G, van de Vosse E, Platzer M, Rosenthal A, Ropers HH, Cremers FP, Berger W. Roepman R, et al. Among authors: rosenberg t. Hum Mol Genet. 1996 Jun;5(6):827-33. doi: 10.1093/hmg/5.6.827. Hum Mol Genet. 1996. PMID: 8776599 Free article.

6

Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1.

Roepman R, van Duijnhoven G, Rosenberg T, Pinckers AJ, Bleeker-Wagemakers LM, Bergen AA, Post J, Beck A, Reinhardt R, Ropers HH, Cremers FP, Berger W. Roepman R, et al. Among authors: rosenberg t. Hum Mol Genet. 1996 Jul;5(7):1035-41. doi: 10.1093/hmg/5.7.1035. Hum Mol Genet. 1996. PMID: 8817343

7

A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa.

Banin E, Mizrahi-Meissonnier L, Neis R, Silverstein S, Magyar I, Abeliovich D, Roepman R, Berger W, Rosenberg T, Sharon D. Banin E, et al. Among authors: rosenberg t. Am J Med Genet A. 2007 Jun 1;143A(11):1150-8. doi: 10.1002/ajmg.a.31642. Am J Med Genet A. 2007. PMID: 17480003

8

Novel rhodopsin mutation (M216R) in a Danish family with autosomal dominant retinitis pigmentosa.

Haim M, Grundmann K, Gal A, Rosenberg T. Haim M, et al. Among authors: rosenberg t. Ophthalmic Genet. 1996 Dec;17(4):193-7. doi: 10.3109/13816819609057893. Ophthalmic Genet. 1996. PMID: 9010870

9

X-linked ocular albinism: prevalence and mutations--a national study.

Rosenberg T, Schwartz M. Rosenberg T, et al. Eur J Hum Genet. 1998 Nov-Dec;6(6):570-7. doi: 10.1038/sj.ejhg.5200226. Eur J Hum Genet. 1998. PMID: 9887374

10

The prevalence of Usher syndrome and other retinal dystrophy-hearing impairment associations.

Rosenberg T, Haim M, Hauch AM, Parving A. Rosenberg T, et al. Clin Genet. 1997 May;51(5):314-21. doi: 10.1111/j.1399-0004.1997.tb02480.x. Clin Genet. 1997. PMID: 9212179

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