Ang, M., Flanagan, J.L., Wong, C.W., Muller, A., Davis, A., Keys, D., Resnikoff, S., Jong, M., Wong, T.Y.,Sankaridurg, P., 2020. Review:myopia control strategies recommendations from the 2018 WHO/IAPB/BHVI meeting on myopia. Br. J. Ophthalmol..
|
Ashraf, T., Collinson, M.N., Fairhurst, J., Wang, R., Wilson, L.C.,Foulds, N., 2015. Two further patients with the 1q24 deletion syndrome expand the phenotype:a possible role for the miR199-214 cluster in the skeletal features of the condition. Am. J. Med. Genet. A 167A, 3153-3160.
|
Azar, D.T., Chang, J.H.,Han, K.Y., 2012. Wound healing after keratorefractive surgery:review of biological and optical considerations. Cornea 31 Suppl. 1, S9-S19.
|
Bai, Y., Liang, S., Yu, W., Zhao, M., Huang, L., Zhao, M.,Li, X., 2014. Semaphorin 3A blocks the formation of pathologic choroidal neovascularization induced by transforming growth factor beta. Mol. Vis. 20, 1258-1270.
|
Bruse, S., Moreau, M., Bromberg, Y., Jang, J.H., Wang, N., Ha, H., Picchi, M., Lin, Y., Langley, R.J., Qualls, C., et al., 2016. Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility. Hum. Genom. 10, 1.
|
Cheng, C.Y., Yamashiro, K., Chen, L.J., Ahn, J., Huang, L., Huang, L., Cheung, C.M., Miyake, M., Cackett, P.D., Yeo, I.Y., et al., 2015. New loci and coding variants confer risk for age-related macular degeneration in East Asians. Nat. Commun. 6, 6063.
|
Consortium, G., 2015a. The Genotype-Tissue Expression (GTEx) pilot analysis:multitissue gene regulation in humans. Science 348, 648-660.
|
Consortium, G.P., 2015b. A global reference for human genetic variation. Nature 526, 68.
|
Davies, G., Lam, M., Harris, S.E., Trampush, J.W., Luciano, M., Hill, W.D., Hagenaars, S.P., Ritchie, S.J., Marioni, R.E., Fawns-Ritchie, C., et al., 2018. Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nat. Commun. 9, 2098.
|
Fan, Q., Guo, X., Tideman, J.W., Williams, K.M., Yazar, S., Hosseini, S.M., Howe, L.D., Pourcain, B.S., Evans, D.M., Timpson, N.J., et al., 2016. Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia:the CREAM Consortium. Sci. Rep. 6, 25853.
|
Fricke, T.R., Jong, M., Naidoo, K.S., Sankaridurg, P., Naduvilath, T.J., Ho, S.M., Wong, T.Y.,Resnikoff, S., 2018. Global prevalence of visual impairment associated with myopic macular degeneration and temporal trends from 2000 through 2050:systematic review, meta-analysis and modelling. Br. J. Ophthalmol. 102, 855-862.
|
Ghorbani Mojarrad, N., Plotnikov, D., Williams, C., Guggenheim, J.A., Eye, U.K.B.,Vision, C., 2019. Association between polygenic risk score and risk of myopia. JAMA Ophthalmol.
|
Gregson, C.L., Newell, F., Leo, P.J., Clark, G.R., Paternoster, L., Marshall, M., Forgetta, V., Morris, J.A., Ge, B., Bao, X., et al., 2018. Genome-wide association study of extreme high bone mass:contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Bone 114, 62-71.
|
Guo, X., Xiao, O., Chen, Y., Wu, H., Chen, L., Morgan, I.G.,He, M., 2017. Three-dimensional eye shape, myopic maculopathy, and visual acuity:the Zhongshan ophthalmic center-brien holden vision Institute high myopia cohort study. Ophthalmology 124, 679-687.
|
Gupta, A., Khandalavala, B., Bansal, R.K., Jain, I.S.,Grewal, S.P., 1990. Atrophy of myelinated nerve fibers in pituitary adenoma. J. Clin. Neuroophthalmol. 10, 100-102.
|
Hasanzadehkiabi, M. 2016. Genome-wide Association Study to Identify Single Nucleotide Polymorphisms Associated with Diabetic Nephropathy and Estimated Glomerular Filtration Rate in FIND Study Memorial University of Newfoundland.
|
Hill, W.D., Marioni, R.E., Maghzian, O., Ritchie, S.J., Hagenaars, S.P., McIntosh, A.M., Gale, C.R., Davies, G.,Deary, I.J., 2019. A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. Mol. Psychiatr. 24, 169-181.
|
Ho, R.W., Huang, H.M.,Ho, J.T., 2015. The influence of pituitary adenoma size on vision and visual outcomes after trans-sphenoidal adenectomy:a report of 78 cases. J. Kor. Neurosurg. Soc. 57, 23-31.
|
Holden, B.A., Fricke, T.R., Wilson, D.A., Jong, M., Naidoo, K.S., Sankaridurg, P., Wong, T.Y., Naduvilath, T.J.,Resnikoff, S., 2016. Global prevalence of myopia and high myopia and temporal trends from 2000 through 2050. Ophthalmology 123, 1036-1042.
|
Hysi, P.G., Choquet, H., Khawaja, A.P., Wojciechowski, R., Tedja, M.S., Yin, J., Simcoe, M.J., Patasova, K., Mahroo, O.A., Thai, K.K., et al., 2020. Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. Nat. Genet. 52, 401-407.
|
Inoue, J., Ueda, Y., Bando, T., Mito, T., Noji, S.,Ohuchi, H., 2013. The expression of LIM-homeobox genes, Lhx1 and Lhx5, in the forebrain is essential for neural retina differentiation. Dev. Growth Differ. 55, 668-675.
|
Jiang, Y., Friedman, D.S., He, M., Huang, S., Kong, X.,Foster, P.J., 2010. Design and methodology of a randomized controlled trial of laser iridotomy for the prevention of angle closure in southern China:the Zhongshan angle Closure Prevention trial. Ophthalmic Epidemiol.. 17, 321-332.
|
Kandel, H., Khadka, J., Goggin, M.,Pesudovs, K., 2017. Impact of refractive error on quality of life:a qualitative study. Clin. Exp. Ophthalmol. 45, 677-688.
|
Kang, R., Zhang, Y., Huang, Q., Meng, J., Ding, R., Chang, Y., Xiong, L.,Guo, Z., 2019. EnhancerDB:a Resource of Transcriptional Regulation in the Context of Enhancers. Database (Oxford) 2019.
|
Kober, P., Boresowicz, J., Rusetska, N., Maksymowicz, M., Paziewska, A., Dabrowska, M., Kunicki, J., Bonicki, W., Ostrowski, J., Siedlecki, J.A., et al., 2019. The role of aberrant DNA methylation in misregulation of gene expression in gonadotroph nonfunctioning pituitary tumors. Cancers (Basel) 11, 1650.
|
Lee, J.J., Wedow, R., Okbay, A., Kong, E., Maghzian, O., Zacher, M., Nguyen-Viet, T.A., Bowers, P., Sidorenko, J., Karlsson Linner, R., et al., 2018. Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nat. Genet. 50, 1112-1121.
|
Levkovitch-Verbin, H., Dardik, R., Vander, S., Nisgav, Y., Kalev-Landoy, M.,Melamed, S., 2006. Experimental glaucoma and optic nerve transection induce simultaneous upregulation of proapoptotic and prosurvival genes. Invest. Ophthalmol. Vis. Sci. 47, 2491-2497.
|
Liao, X., Tan, Q.Q.,Lan, C.J., 2019. Myopia genetics in genome-wide association and post-genome-wide association study era. Int. J. Ophthalmol. 12, 1487-1492.
|
Lu, Y., Quan, C., Chen, H., Bo, X.,Zhang, C., 2017. 3DSNP:a database for linking human noncoding SNPs to their three-dimensional interacting genes. Nucleic Acids Res.. 45, D643-D649.
|
Ma, M., Zhang, Z., Du, E., Zheng, W., Gu, Q., Xu, X.,Ke, B., 2014. Wnt signaling in form deprivation myopia of the mice retina. PloS One 9, e91086.
|
Majithia, S., Tham, Y.C., Chee, M.L., Nusinovici, S., Teo, C.L., Chee, M.L., Thakur, S., Soh, Z.D., Kumari, N., Lamoureux, E., et al., 2021. Cohort profile:the Singapore epidemiology of eye diseases study (SEED). Int. J. Epidemiol. 50, 41-52.
|
Marmamula, S.,Barrenkala, N.R., 2019. Myopia:an emerging public health challenge in South Asia. Community Eye Health 32, S1-S2.
|
Meguro, A., Yamane, T., Takeuchi, M., Miyake, M., Fan, Q., Zhao, W., Wang, I.J., Mizuki, Y., Yamada, N., Nomura, N., et al., 2020. Genome-wide association study in Asians identifies novel loci for high myopia and highlights a nervous system role in its pathogenesis. Ophthalmology.
|
Morgan, I.G., Ohno-Matsui, K.,Saw, S.M., 2012. Myopia. Lancet 379, 1739-1748.
|
Mountjoy, E., Davies, N.M., Plotnikov, D., Smith, G.D., Rodriguez, S., Williams, C.E., Guggenheim, J.A.,Atan, D., 2018. Education and myopia:assessing the direction of causality by mendelian randomisation. BMJ. 361, k2022.
|
Okbay, A., Beauchamp, J.P., Fontana, M.A., Lee, J.J., Pers, T.H., Rietveld, C.A., Turley, P., Chen, G.B., Emilsson, V., Meddens, S.F., et al., 2016. Genome-wide association study identifies 74 loci associated with educational attainment. Nature 533, 539-542.
|
Ong, S.Y., Ikram, M.K., Haaland, B.A., Cheng, C.Y., Saw, S.M., Wong, T.Y.,Cheung, C.Y., 2013. Myopia and cognitive dysfunction:the Singapore Malay eye study. Invest. Ophthalmol. Vis. Sci. 54, 799-803.
|
Peng, G.,Westerfield, M., 2006. Lhx5 promotes forebrain development and activates transcription of secreted Wnt antagonists. Development 133, 3191-3200.
|
Prud'homme, G.J.,Glinka, Y., 2012. Neuropilins are multifunctional coreceptors involved in tumor initiation, growth, metastasis and immunity. Oncotarget 3, 921-939.
|
Ramamurthy, D., Lin Chua, S.Y.,Saw, S.M., 2015. A review of environmental risk factors for myopia during early life, childhood and adolescence. Clin. Exp. Optom. 98, 497-506.
|
Sewer, A., Paul, N., Landgraf, P., Aravin, A., Pfeffer, S., Brownstein, M.J., Tuschl, T., van Nimwegen, E.,Zavolan, M., 2005. Identification of clustered microRNAs using an ab initio prediction method. BMC Bioinf. 6, 267.
|
Shah, R.L., Guggenheim, J.A., Eye, U.K.B.,Vision, C., 2018. Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Hum. Genet. 137, 881-896.
|
Tedja, M.S., Haarman, A.E.G., Meester-Smoor, M.A., Kaprio, J., Mackey, D.A., Guggenheim, J.A., Hammond, C.J., Verhoeven, V.J.M., Klaver, C.C.W.,Consortium, C., 2019. IMI-myopia genetics report. Invest. Ophthalmol. Vis. Sci. 60, M89-M105.
|
Thea Bjoernland, A.B., Einar Ryeng, Ulrik Wisloeff, Mette Langaas, 2017. Improving Power of Genetic Association Studies by Extreme Phenotype Sampling:a Review and Some New Results. arXivorg.
|
Thienpont, B., Dimitriadou, E., Theodoropoulos, K., Breckpot, J., Fryssira, H., Kitsiou-Tzeli, S., Tzoufi, M., Vermeesch, J.R., Syrrou, M.,Devriendt, K., 2009. Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1. Eur. J. Med. Genet. 52, 393-397.
|
Van Wyk, J.J.,Grumbach, M.M., 1960. Syndrome of precocious menstruation and galactorrhea in juvenile hypothyroidism:an example of hormonal overlap in pituitary feedback. J. Pediatr. 57, 416-435.
|
Wei, C.C., Kung, Y.J., Chen, C.S., Chang, C.Y., Lin, C.J., Tien, P.T., Chang, H.Y., Chen, H.J., Huang, Y.S., Lin, H.J., et al., 2018. Allergic conjunctivitis-induced retinal inflammation promotes myopia progression. EBioMedicine 28, 274-286.
|
Wolffsohn, J.S., Calossi, A., Cho, P., Gifford, K., Jones, L., Jones, D., Guthrie, S., Li, M., Lipener, C., Logan, N.S., et al., 2020. Global trends in myopia management attitudes and strategies in clinical practice-2019 Update. Contact Lens Anterior Eye 43, 9-17.
|
Yang, J., Jiang, H., Yeh, C.T., Yu, J., Jeddeloh, J.A., Nettleton, D.,Schnable, P.S., 2015. Extreme-phenotype genome-wide association study (XP-GWAS):a method for identifying trait-associated variants by sequencing pools of individuals selected from a diversity panel. Plant J.. 84, 587-596.
|
Zhao, F., Zhang, D., Zhou, Q., Zhao, F., He, M., Yang, Z., Su, Y., Zhai, Y., Yan, J., Zhang, G., et al., 2020. Scleral HIF-1alpha is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis. EBioMedicine 57, 102878.
|
Zhao, Y.G., Zhao, H., Miao, L., Wang, L., Sun, F.,Zhang, H., 2012. The p53-induced gene Ei24 is an essential component of the basal autophagy pathway. J. Biol. Chem. 287, 42053-42063.
|
Zheng, Y., Cheng, C.Y., Lamoureux, E.L., Chiang, P.P., Rahman Anuar, A., Wang, J.J., Mitchell, P., Saw, S.M.,Wong, T.Y., 2013a. How much eye care services do Asian populations need? Projection from the Singapore Epidemiology of Eye Disease (SEED) study. Invest. Ophthalmol. Vis. Sci. 54, 2171-2177.
|
Zheng, Y., Ding, X., Chen, Y.,He, M., 2013b. The Guangzhou twin project:an update. Twin Res. Hum. Genet. 16, 73-78.
|