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A decade in search of myopia genes.
Jacobi FK, Pusch CM. Jacobi FK, et al. Front Biosci (Landmark Ed). 2010 Jan 1;15:359-72. doi: 10.2741/3625. Front Biosci (Landmark Ed). 2010. PMID: 20036825 Review.
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.
Nürnberg G, Jacobi FK, Broghammer M, Becker C, Blin N, Nürnberg P, Stephani U, Pusch CM. Nürnberg G, et al. Among authors: jacobi fk. Int J Mol Med. 2008 Apr;21(4):429-38. Int J Mol Med. 2008. PMID: 18360688
Pseudophakic retinal detachment in high axial myopia.
Jacobi FK, Hessemer V. Jacobi FK, et al. J Cataract Refract Surg. 1997 Sep;23(7):1095-102. doi: 10.1016/s0886-3350(97)80087-9. J Cataract Refract Surg. 1997. PMID: 9379384
A genetic perspective on myopia.
Jacobi FK, Zrenner E, Broghammer M, Pusch CM. Jacobi FK, et al. Cell Mol Life Sci. 2005 Apr;62(7-8):800-8. doi: 10.1007/s00018-004-4353-z. Cell Mol Life Sci. 2005. PMID: 15868405 Review.
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene.
Jacobi FK, Andréasson S, Langrova H, Meindl A, Zrenner E, Apfelstedt-Sylla E, Pusch CM. Jacobi FK, et al. Graefes Arch Clin Exp Ophthalmol. 2002 Oct;240(10):822-8. doi: 10.1007/s00417-002-0562-z. Epub 2002 Sep 21. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 12397430
Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders.
Karra D, Jacobi FK, Broghammer M, Blin N, Pusch CM. Karra D, et al. Among authors: jacobi fk. Mol Diagn Ther. 2006;10(2):115-23. doi: 10.1007/BF03256451. Mol Diagn Ther. 2006. PMID: 16669610
[Twilight vision and glare sensitivity in monofocal and multifocal pseudophakia].
Grosskopf U, Wagner R, Jacobi FK, Krzizok T. Grosskopf U, et al. Ophthalmologe. 1998 Jun;95(6):432-7. doi: 10.1007/s003470050293. Ophthalmologe. 1998. PMID: 9703724 German.
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders.
Pesch K, Tomiuk J, Broghammer M, Zrenner E, Apfelstedt-Sylla E, Jacobi FK, Wissinger B, Pusch CM. Pesch K, et al. Int J Mol Med. 2001 Jul;8(1):53-8. doi: 10.3892/ijmm.8.1.53. Int J Mol Med. 2001. PMID: 11408949
Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity.
Pusch CM, Maurer J, Ramser J, Tomiuk J, Achatz H, Pesch K, Lichtner P, Apfelstedt-Sylla E, Jacobi FK, Berger W, Meindl A, Wissinger B. Pusch CM, et al. Int J Mol Med. 2001 Feb;7(2):155-61. doi: 10.3892/ijmm.7.2.155. Int J Mol Med. 2001. PMID: 11172618
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