14 research outputs found

    Rose diagrams of the frequency of points plotted along individual meridians for Goldmann and Octopus perimetry for children aged 5–6 years compared to 12–15 years.

    No full text
    <p>A larger area indicates a meridian with a larger number of plotted points. <i>*The empty sectors at 0° for Goldmann perimetry isopters III4e and I4e correspond to the ‘void’ area in the perimeter bowl</i>.</p

    Association of all hypermetropia and hypermetropia (low or moderate/high), by key socio-demographic factors.

    No full text
    <p>* No qualifications, State school examinations at 16 years of age (‘O’ levels), at 18 years (‘A’ levels) or University/other professional qualification</p><p><sup>+</sup>: Number of eyes;</p><p><sup>++</sup> model adjusted for eye laterality, gender, age (continuous), educational qualification, accommodation tenure, ethnicity and test centre.</p><p>Association of all hypermetropia and hypermetropia (low or moderate/high), by key socio-demographic factors.</p

    Distribution of refractive errors by key socio-demographic factors.

    No full text
    <p>* No qualifications, State school examinations at 16 years of age (‘O’ levels), at 18 years (‘A’ levels) or University/other professional qualification</p><p>Missing data: educational qualification: 1,466 (1.4%), accommodation tenure: 2,102 (2.0%), ethnicity: 779 (0.7%)</p><p>Distribution of refractive errors by key socio-demographic factors.</p

    Association of all myopia and myopia (low, moderate or high), by key socio-demographic factors.

    No full text
    <p>* No qualifications, State school examinations at 16 years of age (‘O’ levels), at 18 years (‘A’ levels) or University/other professional qualification</p><p><sup>+</sup>: Number of eyes;</p><p><sup>++</sup> model adjusted for eye laterality, gender, age (continuous), educational qualification, accommodation tenure, ethnicity and test centre.</p><p>Association of all myopia and myopia (low, moderate or high), by key socio-demographic factors.</p

    Results of the hyperopia analyses in the regions that were significantly associated with myopia age at onset by Kiefer <i>et al.</i>[18] showing meta-analysis association results for each chosen SNP.

    No full text
    <p>1. SNPs which are either genome-wide significant or meet our replication threshold are highlighted in bold text. Allele frequencies for these SNPs in each of our discovery populations can be found in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0107110#pone.0107110.s018" target="_blank">Table S8</a>.</p><p>2. For each SNP reported by Kiefer <i>et al. </i>, Replication P value is the P value of that SNP in our analysis. If that SNP was not genotyped or imputed in our data, it is indicated with N/A.</p><p>3. For regions where the most significant SNP in our analysis is not the original reported SNP, that SNP is reported as Best SNP.</p><p>4. Offset is the absolute distance in base pairs to the original SNP and the P value associated with Best SNP.</p><p>5. Z scores and direction of effect for all SNPs are in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0107110#pone.0107110.s012" target="_blank">Table S2</a>.</p><p>6. This column left blank where the original SNP is the most significant SNP in the region.</p><p>7. Nearest Gene(s) indicates the closest gene by physical position for these SNPs.</p><p>Results of the hyperopia analyses in the regions that were significantly associated with myopia age at onset by Kiefer <i>et al.</i><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0107110#pone.0107110-Kiefer1" target="_blank">[18]</a> showing meta-analysis association results for each chosen SNP.</p
    corecore