Found: 17
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Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafish.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02185-z
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- Article
Post-GWAS screening of candidate genes for refractive error in mutant zebrafish models.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-28944-y
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- Article
Post-GWAS screening of candidate genes for refractive error in mutant zebrafish models.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-28944-y
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- Article
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.
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- Nature Genetics, 2014, v. 46, n. 10, p. 1126, doi. 10.1038/ng.3087
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- Article
Interaction between lifestyle and genetic susceptibility in myopia: the Generation R study.
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- European Journal of Epidemiology, 2019, v. 34, n. 8, p. 777, doi. 10.1007/s10654-019-00512-7
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- Article
Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.
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- Human Genetics, 2018, v. 137, n. 10, p. 847, doi. 10.1007/s00439-018-1943-7
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- Article
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-07819-1
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- Article
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.
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- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0634-9
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- Article
A combined linkage, microarray and exome analysis suggests <italic>MAP3K11</italic> as a candidate gene for left ventricular hypertrophy.
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- BMC Medical Genomics, 2018, v. 11, p. 1, doi. 10.1186/s12920-018-0339-9
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- Article
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
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- Human Molecular Genetics, 2017, v. 26, n. 2, p. 438, doi. 10.1093/hmg/ddw399
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- Article
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness.
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- Human Molecular Genetics, 2015, v. 24, n. 17, p. 5060, doi. 10.1093/hmg/ddv211
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- Article
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure.
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- Human Molecular Genetics, 2015, v. 24, n. 9, p. 2689, doi. 10.1093/hmg/ddv027
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- Article
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve degeneration at old age.
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- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1320, doi. 10.1093/hmg/ddt522
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- Publication type:
- Article
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03646-6
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- Article
Haplotype reference consortium panel: Practical implications of imputations with large reference panels.
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- Human Mutation, 2017, v. 38, n. 8, p. 1025, doi. 10.1002/humu.23247
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- Article
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
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- Genetic Epidemiology, 2015, v. 39, n. 3, p. 207, doi. 10.1002/gepi.21886
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- Article
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-022-04323-7
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- Article