Fingert JH - Search Results

1

Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy.

Rosenberg T, Roos B, Johnsen T, Bech N, Scheetz TE, Larsen M, Stone EM, Fingert JH. Rosenberg T, et al. Among authors: fingert jh. Mol Vis. 2010 Dec 9;16:2659-68. Mol Vis. 2010. PMID: 21179233 Free PMC article.

2

Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1).

Brown J Jr, Fingert JH, Taylor CM, Lake M, Sheffield VC, Stone EM. Brown J Jr, et al. Among authors: fingert jh. Arch Ophthalmol. 1997 Jan;115(1):95-9. doi: 10.1001/archopht.1997.01100150097016. Arch Ophthalmol. 1997. PMID: 9006432

3

Clinical and molecular characterization of a family affected with X-linked ocular albinism (OA1).

Lam BL, Fingert JH, Shutt BC, Singleton EM, Merin LM, Brown HH, Sheffield VC, Stone EM. Lam BL, et al. Among authors: fingert jh. Ophthalmic Genet. 1997 Dec;18(4):175-84. doi: 10.3109/13816819709041432. Ophthalmic Genet. 1997. PMID: 9457748

4

Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomaly.

Mellott ML, Brown J Jr, Fingert JH, Taylor CM, Keech RV, Sheffield VC, Stone EM. Mellott ML, et al. Among authors: fingert jh. Arch Ophthalmol. 1999 Dec;117(12):1630-3. doi: 10.1001/archopht.117.12.1630. Arch Ophthalmol. 1999. PMID: 10604668

5

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier.

Craig JE, Baird PN, Healey DL, McNaught AI, McCartney PJ, Rait JL, Dickinson JL, Roe L, Fingert JH, Stone EM, Mackey DA. Craig JE, et al. Among authors: fingert jh. Ophthalmology. 2001 Sep;108(9):1607-20. doi: 10.1016/s0161-6420(01)00654-6. Ophthalmology. 2001. PMID: 11535458

6

Myocilin glaucoma.

Fingert JH, Stone EM, Sheffield VC, Alward WL. Fingert JH, et al. Surv Ophthalmol. 2002 Nov-Dec;47(6):547-61. doi: 10.1016/s0039-6257(02)00353-3. Surv Ophthalmol. 2002. PMID: 12504739 Review.

7

Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation.

Mackey DA, Healey DL, Fingert JH, Coote MA, Wong TL, Wilkinson CH, McCartney PJ, Rait JL, de Graaf AP, Stone EM, Craig JE. Mackey DA, et al. Among authors: fingert jh. Arch Ophthalmol. 2003 Aug;121(8):1172-80. doi: 10.1001/archopht.121.8.1172. Arch Ophthalmol. 2003. PMID: 12912696

8

Case of Stargardt disease caused by uniparental isodisomy.

Fingert JH, Eliason DA, Phillips NC, Lotery AJ, Sheffield VC, Stone EM. Fingert JH, et al. Arch Ophthalmol. 2006 May;124(5):744-5. doi: 10.1001/archopht.124.5.744. Arch Ophthalmol. 2006. PMID: 16682602 No abstract available.

9

Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His.

Grassi MA, Fingert JH, Scheetz TE, Roos BR, Ritch R, West SK, Kawase K, Shire AM, Mullins RF, Stone EM. Grassi MA, et al. Among authors: fingert jh. Hum Mutat. 2006 Sep;27(9):921-5. doi: 10.1002/humu.20359. Hum Mutat. 2006. PMID: 16865697

10

The optic nerve head in myocilin glaucoma.

Hewitt AW, Bennett SL, Fingert JH, Cooper RL, Stone EM, Craig JE, Mackey DA. Hewitt AW, et al. Among authors: fingert jh. Invest Ophthalmol Vis Sci. 2007 Jan;48(1):238-43. doi: 10.1167/iovs.06-0611. Invest Ophthalmol Vis Sci. 2007. PMID: 17197538

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