Associated Papers
Genetic Architecture of Myopia and Its Implications for Risk Stratification and Prognosis.
Seo Y et al.
Diagnostics (basel, Switzerland), 2026
Clinical and Molecular Landscape of GLRA2 in X-Linked Early-Onset High Myopia.
Li X et al.
Investigative Ophthalmology & Visual Science, 2025
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism.
Wang Y et al.
Investigative Ophthalmology & Visual Science, 2023
Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA.
Haer-Wigman L et al.
Npj Genomic Medicine, 2022
An association-adjusted consensus deleterious scheme to classify homozygous Mis-sense mutations for personal genome interpretation.
Preeprem T et al.
Biodata Mining, 2013
24365473 (PubMed )
Supplement: 1756-0381-6-24-S2.xlsx › Additional_Table_9
Signatures of selection and gene conversion associated with human color vision variation.
Verrelli BC et al.
American Journal of Human Genetics, 2004
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