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Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucomaCalpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degenerationThe Utility of Diaton Tonometer Measurements in Patients With Ocular Hypertension, Glaucoma, and Glaucoma Tube Shunts: A Preliminary Study for its Potential Use in Keratoprosthesis PatientsAge at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sampleA novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucoma.Vascular tone pathway polymorphisms in relation to primary open-angle glaucomaEvaluation of variants in the selectin genes in age-related macular degeneration.Myocilin glaucoma.Identification of a gene that causes primary open angle glaucoma.A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel LociMicroarray analysis of iris gene expression in mice with mutations influencing pigmentation.Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape.Complement component C5a activates ICAM-1 expression on human choroidal endothelial cellsDNA copy number variants of known glaucoma genes in relation to primary open-angle glaucomaHypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma.Copy number variations on chromosome 12q14 in patients with normal tension glaucomaCopy number variations of TBK1 in Australian patients with primary open-angle glaucoma.TBK1 gene duplication and normal-tension glaucoma.Copy number variations and primary open-angle glaucoma.Confirmation of TBK1 duplication in normal tension glaucomaStereo Photo Measured ONH Shape Predicts Development of POAG in Subjects With Ocular HypertensionSQSTM1 Mutations and Glaucoma.A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndromeStatistical tests for detecting rare variants using variance-stabilising transformations.Retinal ganglion cell death in glaucoma: mechanisms and neuroprotective strategies.Analysis of ASB10 variants in open angle glaucomaCircumferential iris transillumination defects in exfoliation syndrome.North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13.Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressure.Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.Genome-wide analysis of copy number variants in age-related macular degeneration.Familial cavitary optic disk anomalies: identification of a novel genetic locus.Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucoma.TBK1 and flanking genes in human retina.Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome.Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses.Automated segmentation of the optic disc from stereo color photographs using physiologically plausible features.Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss.Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.Primary open-angle glaucoma genes.
P50
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P50
description
hulumtues
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onderzoeker
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հետազոտող
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name
John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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John H. Fingert
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P1053
F-8787-2012
P106
P1153
6602136038
P21
P31
P3829
P496
0000-0002-0377-0479