Fingert JH - Search Results

1

Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape.

Tang L, Scheetz TE, Mackey DA, Hewitt AW, Fingert JH, Kwon YH, Quellec G, Reinhardt JM, Abràmoff MD. Tang L, et al. Among authors: fingert jh. Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5870-7. doi: 10.1167/iovs.10-5527. Epub 2010 May 26. Invest Ophthalmol Vis Sci. 2010. PMID: 20505201 Free PMC article.

2

Identification of a gene that causes primary open angle glaucoma.

Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Stone EM, et al. Among authors: fingert jh. Science. 1997 Jan 31;275(5300):668-70. doi: 10.1126/science.275.5300.668. Science. 1997. PMID: 9005853

3

Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A).

Alward WL, Fingert JH, Coote MA, Johnson AT, Lerner SF, Junqua D, Durcan FJ, McCartney PJ, Mackey DA, Sheffield VC, Stone EM. Alward WL, et al. Among authors: fingert jh. N Engl J Med. 1998 Apr 9;338(15):1022-7. doi: 10.1056/NEJM199804093381503. N Engl J Med. 1998. PMID: 9535666 Free article.

4

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

5

Localization of MYOC transcripts in human eye and optic nerve by in situ hybridization.

Swiderski RE, Ross JL, Fingert JH, Clark AF, Alward WL, Stone EM, Sheffield VC. Swiderski RE, et al. Among authors: fingert jh. Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3420-8. Invest Ophthalmol Vis Sci. 2000. PMID: 11006234

6

Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension.

Fingert JH, Clark AF, Craig JE, Alward WL, Snibson GR, McLaughlin M, Tuttle L, Mackey DA, Sheffield VC, Stone EM. Fingert JH, et al. Invest Ophthalmol Vis Sci. 2001 Jan;42(1):145-52. Invest Ophthalmol Vis Sci. 2001. PMID: 11133859

7

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

8

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

9

Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus.

Mackey DA, Fingert JH, Luzhansky JZ, McCluskey PJ, Howell N, Hall AJ, Pierce AB, Hoy JF. Mackey DA, et al. Among authors: fingert jh. Eye (Lond). 2003 Apr;17(3):312-7. doi: 10.1038/sj.eye.6700362. Eye (Lond). 2003. PMID: 12724691

10

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

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