Complex genetics of complex traits: the case of primary open-angle glaucoma.
about
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in JapaneseA genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucomaCandidate gene study to investigate the genetic determinants of normal variation in central corneal thickness.A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel LociThe genetics of POAG in black South Africans: a candidate gene association study.Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma.The role of the Met98Lys optineurin variant in inherited optic nerve diseasesA novel de novo Myocilin variant in a patient with sporadic juvenile open angle glaucoma.Lack of association of SNP rs4236601 near CAV1 and CAV2 with POAG in a Saudi cohortEffects of polymorphisms in vitamin E-, vitamin C-, and glutathione peroxidase-related genes on serum biomarkers and associations with glaucoma.Differential Protein Expression Profiles in Glaucomatous Trabecular Meshwork: An Evaluation Study on a Small Primary Open Angle Glaucoma Population.Fine mapping of the GLC1K juvenile primary open-angle glaucoma locus and exclusion of candidate genes.Optineurin coding variants in Ghanaian patients with primary open-angle glaucomaLack of association between LOXL1 gene polymorphisms and primary open angle glaucoma in the Saudi Arabian populationInvestigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgroundsNull mutations in LTBP2 cause primary congenital glaucoma.Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese populationLifestyle, nutrition, and glaucomaA novel optineurin genetic mutation associated with open-angle glaucoma in a Chinese family.Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twins.Chromosome 9p21 primary open-angle glaucoma susceptibility locus: a review.OPA1 increases the risk of normal but not high tension glaucoma.MYOC mutations in black south african patients with primary open-angle glaucoma: genetic testing and cascade screening.DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma.Structure and Misfolding of the Flexible Tripartite Coiled-Coil Domain of Glaucoma-Associated Myocilin.Genetics of glaucoma.Australian and New Zealand Registry of Advanced Glaucoma: methodology and recruitment.Analysis of toll-like receptor rs4986790 polymorphism in Saudi patients with primary open angle glaucoma.The pathogenesis of the glaucomas: nature versus nurture
P2860
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P2860
Complex genetics of complex traits: the case of primary open-angle glaucoma.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@ast
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@en
type
label
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@ast
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@en
prefLabel
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@ast
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@en
P2860
P1476
Complex genetics of complex traits: the case of primary open-angle glaucoma.
@en
P2093
Alex W Hewitt
Jamie E Craig
P2860
P304
P356
10.1111/J.1442-9071.2006.01268.X
P577
2006-07-01T00:00:00Z