J H Fingert
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Explore the profile of J H Fingert including associated specialties, affiliations and a list of published articles.
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20
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1392
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Recent Articles
11.
Swiderski R, Ross J, Fingert J, Clark A, Alward W, Stone E, et al.
Invest Ophthalmol Vis Sci
. 2000 Sep;
41(11):3420-8.
PMID: 11006234
Purpose: To evaluate MYOC (myocilin) gene expression at the RNA level in normal intact human eyes and optic nerve using in situ hybridization. Methods: Normal human eyes and optic nerves...
12.
Simm R, Fingert J, Craig J, McNaught A, Mackey D
Ophthalmic Genet
. 1999 Dec;
20(3):205-7.
PMID: 10610189
No abstract available.
13.
Mellott M, Brown Jr J, Fingert J, Taylor C, Keech R, Sheffield V, et al.
Arch Ophthalmol
. 1999 Dec;
117(12):1630-3.
PMID: 10604668
Objectives: To identify a congenital nystagmus locus on the X chromosome and to characterize the phenotype of a 4-generation family affected with congenital nystagmus and color deficiency. Methods: Sixty-five patients...
14.
Fingert J, Heon E, Liebmann J, Yamamoto T, Craig J, Rait J, et al.
Hum Mol Genet
. 1999 Apr;
8(5):899-905.
PMID: 10196380
A glaucoma locus, GLC1A, was identified previously on chromosome 1q. A gene within this locus (encoding the protein myocilin) subsequently was shown to harbor mutations in 2-4% of primary open...
15.
Kennan A, Mansergh F, Fingert J, Clark T, Ayuso C, Kenna P, et al.
J Med Genet
. 1998 Dec;
35(11):957-60.
PMID: 9832047
Glaucoma describes a clinically and genetically heterogeneous group of diseases that result in optic neuropathy and progressive loss of visual fields. A gene for juvenile onset primary open angle glaucoma...
16.
Fingert J, Ying L, Swiderski R, Nystuen A, Arbour N, Alward W, et al.
Genome Res
. 1998 Jun;
8(4):377-84.
PMID: 9548973
The GLC1A gene (which encodes the protein myocilin) has been associated with the development of primary open angle glaucoma. Bacterial artificial chromosomes containing the human GLC1A gene and its mouse...
17.
Alward W, Fingert J, Coote M, Johnson A, Lerner S, Junqua D, et al.
N Engl J Med
. 1998 Apr;
338(15):1022-7.
PMID: 9535666
Background: A substantial proportion of cases of glaucoma have a genetic basis. Mutations causing glaucoma have been identified in the chromosome 1 open-angle glaucoma gene (GLC1A), which encodes a 57-kd...
18.
Lam B, Fingert J, Shutt B, Singleton E, Merin L, Brown H, et al.
Ophthalmic Genet
. 1998 Feb;
18(4):175-84.
PMID: 9457748
Thirty-one members of a family affected with X-linked ocular albinism (OA1) were studied to characterize the clinical phenotype and identify the disease-causing mutation. The family members were examined with ophthalmoscopy,...
19.
Stone E, Fingert J, Alward W, Nguyen T, Polansky J, Sunden S, et al.
Science
. 1997 Jan;
275(5300):668-70.
PMID: 9005853
Glaucoma is a major cause of blindness and is characterized by progressive degeneration of the optic nerve and is usually associated with elevated intraocular pressure. Analyses of sequence tagged site...
20.
Brown Jr J, Fingert J, Taylor C, Lake M, Sheffield V, Stone E
Arch Ophthalmol
. 1997 Jan;
115(1):95-9.
PMID: 9006432
Objectives: To refine the dominant optic atrophy locus, OPA1, on chromosome 3q and to characterize the phenotype of a 6-generation family pedigree affected with this disease. Methods: Fifty-six family members...