Pages that link to "Q33969890"
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The following pages link to A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. (Q33969890):
Displaying 50 items.
- APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans (Q21144730) (← links)
- SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia (Q24298661) (← links)
- SLITRK6 mutations cause myopia and deafness in humans and mice (Q24337702) (← links)
- Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (Q24631992) (← links)
- RPE and Choroid Mechanisms Underlying Ocular Growth and Myopia (Q26796695) (← links)
- Challenges in elucidating the genetics of diabetic retinopathy (Q26998699) (← links)
- Advances in the genomics of common eye diseases (Q27008236) (← links)
- Genome-wide association studies of refractive error and myopia, lessons learned, and implications for the future (Q27687311) (← links)
- Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error (Q28300637) (← links)
- Epidemiology, genetics and treatments for myopia (Q28730195) (← links)
- Identification of a candidate gene for astigmatism (Q28943257) (← links)
- Genetic variants on chromosome 1q41 influence ocular axial length and high myopia (Q28943319) (← links)
- Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism (Q28943360) (← links)
- Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error (Q29417141) (← links)
- Automatic diagnosis of pathological myopia from heterogeneous biomedical data (Q30000795) (← links)
- Changes in protein profiles of guinea pig sclera during development of form deprivation myopia and recovery (Q30478305) (← links)
- Association study of 15q14 and 15q25 with high myopia in the Han Chinese population (Q33584906) (← links)
- Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients. (Q33682847) (← links)
- Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohorts (Q33698029) (← links)
- Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma (Q33838251) (← links)
- A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. (Q33969884) (← links)
- Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population (Q34189721) (← links)
- Genome-wide association studies: applications and insights gained in Ophthalmology (Q34200382) (← links)
- Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci (Q34214974) (← links)
- Genotype-phenotype analysis of SNPs associated with primary angle closure glaucoma (rs1015213, rs3753841 and rs11024102) and ocular biometry in the EPIC-Norfolk Eye Study (Q34333567) (← links)
- Exome sequencing reveals CCDC111 mutation associated with high myopia (Q34338729) (← links)
- Myopic anisometropia: ocular characteristics and aetiological considerations (Q34425331) (← links)
- Body stature growth trajectories during childhood and the development of myopia (Q34588936) (← links)
- Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia (Q34611207) (← links)
- Focusing in on the complex genetics of myopia (Q34672053) (← links)
- Nature and nurture: the complex genetics of myopia and refractive error (Q34679031) (← links)
- Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese (Q34700654) (← links)
- Evaluating the association between pathological myopia and SNPs in RASGRF1. ACTC1 and GJD2 genes at chromosome 15q14 and 15q25 in a Chinese population (Q34802573) (← links)
- Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium (Q34924529) (← links)
- Vitamin D Receptor (VDR) and Group-Specific Component (GC, Vitamin D–Binding Protein) Polymorphisms in Myopia (Q35027693) (← links)
- The Rotterdam Study: 2012 objectives and design update (Q35201574) (← links)
- High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2 (Q35204918) (← links)
- Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing (Q35221170) (← links)
- Linkage analysis of quantitative refraction and refractive errors in the Beaver Dam Eye Study (Q35221419) (← links)
- Current gene discovery strategies for ocular conditions (Q35247767) (← links)
- IGF-1 gene polymorphisms in Polish families with high-grade myopia (Q35255077) (← links)
- Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies (Q35629086) (← links)
- The FGF2 gene in a myopia animal model and human subjects (Q35794238) (← links)
- Prevalence of Myopia in France: A Cross-Sectional Analysis (Q35838725) (← links)
- Endophenotyping reveals differential phenotype-genotype correlations between myopia-associated polymorphisms and eye biometric parameters. (Q35883283) (← links)
- Assessment of exonic single nucleotide polymorphisms in the adenosine A2A receptor gene to high myopia susceptibility in Chinese subjects. (Q36050413) (← links)
- Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium (Q36162384) (← links)
- Correlation between polymorphisms in the MFN1 gene and myopia in Chinese population (Q36297008) (← links)
- The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables (Q36360724) (← links)
- Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia (Q36408718) (← links)