An international collaborative family-based whole-genome linkage scan for high-grade myopia
about
Exome sequencing identifies ZNF644 mutations in high myopiaAPLP2 Regulates Refractive Error and Myopia Development in Mice and HumansEpidemiology, genetics and treatments for myopiaA genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore ChineseGenetic association of insulin-like growth factor-1 polymorphisms with high-grade myopia in an international family cohortAssociation of high myopia with crystallin beta A4 (CRYBA4) gene polymorphisms in the linkage-identified MYP6 locus.Nature and nurture: the complex genetics of myopia and refractive error.Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in ChineseVitamin D receptor (VDR) and group-specific component (GC, vitamin D-binding protein) polymorphisms in myopia.Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family.An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.Genetic factors for choroidal neovascularization associated with high myopia.Evaluation of MMP2 as a candidate gene for high myopia.Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.Association mapping of the high-grade myopia MYP3 locus reveals novel candidates UHRF1BP1L, PTPRR, and PPFIA2.Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort.An evidence-based update on myopia and interventions to retard its progression.Molecular genetics of human myopia: an update.Myopia genetics: a review of current research and emerging trends.Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.Quality of DNA extracted from mouthwashesFine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36.AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia.COL1A1 and COL2A1 genes and myopia susceptibility: evidence of association and suggestive linkage to the COL2A1 locus.The association between IGF-1 polymorphisms and high myopia.Isotope-coded protein label based quantitative proteomic analysis reveals significant up-regulation of apolipoprotein A1 and ovotransferrin in the myopic chick vitreous.Identification of novel suggestive loci for high-grade myopia in Polish familiesInsight into the molecular genetics of myopia.Myopia in Chinese families shows linkage to 10q26.13.Genetic variations in the dopamine system and facial expression recognition in healthy chinese college students.Common variants in chromosome 4q25 are associated with myopia in Chinese adults.Exome sequencing study of 20 patients with high myopiaUpdate on the epidemiology and genetics of myopic refractive errorMissense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity
P2860
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P2860
An international collaborative family-based whole-genome linkage scan for high-grade myopia
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
An international collaborative ...... age scan for high-grade myopia
@en
type
label
An international collaborative ...... age scan for high-grade myopia
@en
prefLabel
An international collaborative ...... age scan for high-grade myopia
@en
P2093
P2860
P50
P356
P1476
An international collaborative ...... age scan for high-grade myopia
@en
P2093
Anuradha Bulusu
Diana Abbott
Francois Malecaze
Michael J Owen
Patrick Calvas
Ravikanth Metlapally
Rosalind C Creer
Sandrine Paget
Terri L Young
P2860
P304
P356
10.1167/IOVS.08-2781
P407
P577
2009-03-25T00:00:00Z