A genome-wide association study of optic disc parameters. - Wikidata - wikimedia - TriplyDB

A genome-wide association study of optic disc parameters.

A genome-wide association study of optic disc parameters.

http://www.wikidata.org/entity/Q33604802

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Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia Novel Insights into the Role of Long Noncoding RNA in Ocular Diseases An Updated Review on the Genetics of Primary Open Angle Glaucoma Advances in the genomics of common eye diseases Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region Epidemiology, genetics and treatments for myopia Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma.Association of SIX1/SIX6 locus polymorphisms with regional circumpapillary retinal nerve fibre layer thickness: The Nagahama study.Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.Identification and characterization of variants and a novel 4 bp deletion in the regulatory region of SIX6, a risk factor for primary open-angle glaucoma.GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease Copy number variation at chromosome 5q21.2 is associated with intraocular pressure.Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia Genome-wide association studies: applications and insights gained in Ophthalmology.Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.Common genetic determinants of intraocular pressure and primary open-angle glaucoma.Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies.Common variants on chromosome 9p21 are associated with normal tension glaucoma.Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness.Association of open-angle glaucoma loci with incident glaucoma in the Blue Mountains Eye Study DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma Associations with retinal nerve fiber layer measures in the EPIC-Norfolk Eye Study Common and rare genetic risk factors for glaucoma.Laser scanning tomography in the EPIC-Norfolk Eye Study: principal components and associations.Genetic variants associated with optic nerve vertical cup-to-disc ratio are risk factors for primary open angle glaucoma in a US Caucasian population.Corneal biomechanical properties and glaucoma-related quantitative traits in the EPIC-Norfolk Eye Study.The genetics of POAG in black South Africans: a candidate gene association study.The Rotterdam Study: 2012 objectives and design update.Genetic association of SNPs near ATOH7, CARD10, CDKN2B, CDC7 and SIX1/SIX6 with the endophenotypes of primary open angle glaucoma in Indian population.Current gene discovery strategies for ocular conditions Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects.A common variant near TGFBR3 is associated with primary open angle glaucoma.Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

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A genome-wide association study of optic disc parameters.

http://www.wikidata.org/entity/Q33604802

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2010年の論文

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2010年論文

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2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

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name

A genome-wide association study of optic disc parameters.

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A genome-wide association study of optic disc parameters.

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type

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A genome-wide association study of optic disc parameters.

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A genome-wide association study of optic disc parameters.

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prefLabel

A genome-wide association study of optic disc parameters.

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A genome-wide association study of optic disc parameters.

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A genome-wide association study of optic disc parameters.

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Aaron Isaacs

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Arthur A B Bergen

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Ben A Oostra

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Caroline C W Klaver

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Hans G Lemij

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Johannes R Vingerling

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Leonieke M E van Koolwijk

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M Kamran Ikram

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Nomdo M Jansonius

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Paulus T V M de Jong

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P2860

Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

Transcriptional activation of the SALL1 by the human SIX1 homeodomain during kidney development

Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development

A SALL1 mutation causes a branchio-oto-renal syndrome-like phenotype

Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.

Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

GDF11 controls the timing of progenitor cell competence in developing retina

Math5 is required for retinal ganglion cell and optic nerve formation

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Fernando Rivadeneira

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2010-06-10T00:00:00Z

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