Fingert JH - Search Results

1

Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India.

Sundaresan P, Vijayalakshmi P, Thompson S, Ko AC, Fingert JH, Stone EM. Sundaresan P, et al. Among authors: fingert jh. Mol Vis. 2009 Sep 4;15:1781-7. Mol Vis. 2009. PMID: 19753312 Free PMC article.

2

Mitochondrial TXNRD2 and ME3 Genetic Risk Scores Are Associated with Specific Primary Open-Angle Glaucoma Phenotypes.

Aboobakar IF, Kinzy TG, Zhao Y, Fan B, Pasquale LR, Qassim A, Kolovos A, Schmidt JM, Craig JE, Cooke Bailey JN, Wiggs JL; NEIGHBORHOOD Consortium. Aboobakar IF, et al. Ophthalmology. 2023 Jul;130(7):756-763. doi: 10.1016/j.ophtha.2023.02.018. Epub 2023 Feb 20. Ophthalmology. 2023. PMID: 36813040 Free PMC article.

3

Familial normal tension glaucoma genetics.

Fox AR, Fingert JH. Fox AR, et al. Among authors: fingert jh. Prog Retin Eye Res. 2023 Sep;96:101191. doi: 10.1016/j.preteyeres.2023.101191. Epub 2023 Jun 22. Prog Retin Eye Res. 2023. PMID: 37353142 Review.

4

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

5

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

6

Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.

Fingert JH, Héon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey DA, Alward WL, Sheffield VC, Stone EM. Fingert JH, et al. Hum Mol Genet. 1999 May;8(5):899-905. doi: 10.1093/hmg/8.5.899. Hum Mol Genet. 1999. PMID: 10196380

7

The genetic aspects of adult-onset glaucoma: a perspective from the Greater Toronto area.

Williams-Lyn D, Flanagan J, Buys Y, Trope GE, Fingert J, Stone EM, Héon E. Williams-Lyn D, et al. Can J Ophthalmol. 2000 Feb;35(1):12-7. doi: 10.1016/s0008-4182(00)80103-9. Can J Ophthalmol. 2000. PMID: 10711378

8

Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humor.

Jacobson N, Andrews M, Shepard AR, Nishimura D, Searby C, Fingert JH, Hageman G, Mullins R, Davidson BL, Kwon YH, Alward WL, Stone EM, Clark AF, Sheffield VC. Jacobson N, et al. Among authors: fingert jh. Hum Mol Genet. 2001 Jan 15;10(2):117-25. doi: 10.1093/hmg/10.2.117. Hum Mol Genet. 2001. PMID: 11152659

9

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

10

Variations in the myocilin gene in patients with open-angle glaucoma.

Alward WL, Kwon YH, Khanna CL, Johnson AT, Hayreh SS, Zimmerman MB, Narkiewicz J, Andorf JL, Moore PA, Fingert JH, Sheffield VC, Stone EM. Alward WL, et al. Among authors: fingert jh. Arch Ophthalmol. 2002 Sep;120(9):1189-97. doi: 10.1001/archopht.120.9.1189. Arch Ophthalmol. 2002. PMID: 12215093

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