Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia - Wikidata - wikimedia - TriplyDB

Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia

Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia

http://www.wikidata.org/entity/Q34290636

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An Updated Review on the Genetics of Primary Open Angle Glaucoma Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma Association of apolipoprotein E-219T>G promoter polymorphism with primary open angle glaucoma in Turkish population.The heritability of glaucoma-related traits corneal hysteresis, central corneal thickness, intraocular pressure, and choroidal blood flow pulsatility.A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma A common copy number variation (CNV) polymorphism in the CNTNAP4 gene: association with aging in females Role of the APOE ε2/ε3/ε4 polymorphism in the development of primary open-angle glaucoma: evidence from a comprehensive meta-analysis.Central corneal thickness correlates with oxygen levels in the human anterior chamber angle Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent.Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.Transcriptome networks in the mouse retina: An exon level BXD RI database A genome-wide association study of central corneal thickness in Latinos.Brittle cornea syndrome: recognition, molecular diagnosis and management Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States.Whole genome expression profiling of normal human fetal and adult ocular tissues.Rare variants in optic disc area gene CARD10 enriched in primary open-angle glaucoma.ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.The Ehlers-Danlos syndromes, rare types.Major review: Molecular genetics of primary open-angle glaucoma.Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.A Comparative Study of Central Corneal Epithelial, Stromal, and Total Thickness in Males With and Without Primary Open-Angle Glaucoma.On the Null Distribution of Bayes Factors in Linear Regression Brittle cornea syndrome: a case report and review of the literature Functional relevance for central cornea thickness-associated genetic variants by using integrative analyses

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Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia

http://www.wikidata.org/entity/Q34290636

description

2012 nî lūn-bûn

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2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2012 թվականի հուլիսին հրատարակված գիտական հոդված

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Investigative Ophthalmology & Visual Science

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Genome-wide analysis of centra ...... NEIGHBOR and GLAUGEN consortia

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Anthony Realini

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Ayse Bilge Ozel

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David S Friedman

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Donald J Zack

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Jae H Kang

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Janey L Wiggs

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P2860

Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

Caspr3 and caspr4, two novel members of the caspr family are expressed in the nervous system and interact with PDZ domains

Structural abnormalities of the cornea and lid resulting from collagen V mutations

Cloning of neurotrimin defines a new subfamily of differentially expressed neural cell adhesion molecules

Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome

PLINK: a tool set for whole-genome association and population-based linkage analyses

Principal components analysis corrects for stratification in genome-wide association studies

Primer3 on the WWW for general users and for biologist programmers

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

Correlation between intraocular pressure, central corneal thickness, stage of glaucoma, and demographic patient data: prospective analysis of biophysical parameters in tertiary glaucoma practice populations.

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4468-4474

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10.1167/IOVS.12-9784

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8

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53

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Joel S. Schuman

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