1. Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract
- Author
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Yonova-Doing, E. (Ekaterina), Zhao, W. (Wanting), Igo Jr., R.P. (Robert), Wang, C. (Chunliang), Sundaresan, P. (Periasamy), Lee, K.E. (Kristine), Jun, G.R. (Gyungah R.), Alves, A.C. (Alexessander Couto), Chai, X. (Xiaoran), Chan, A.S.Y. (Anita S. Y.), Lee, M.C. (Mei Chin), Fong, A. (Allan), Tan, A.G. (Ava G.), Khor, C.C., Chew, E.Y. (Emily Y.), Hysi, P.G. (Pirro G.), Fan, Q. (Qiao), Chua, J. (Jacqueline), Chung, J. (Jaeyoon), Liao, J. (Jiemin), Colijn, J.M. (Johanna), Burdon, K.P. (Kathryn P.), Fritsche, L.G. (Lars), Swift, M.K. (Maria K.), Hilmy, M.H. (Maryam H.), Chee, M.L. (Miao Ling), Tedja, M. (Milly), Bonnemaijer, P.W.M. (Pieter), Gupta, P. (Preeti), Tan, Q.S. (Queenie S.), Li, Z. (Zheng), Vithana, E.N. (Eranga), Ravindran, R.D. (Ravilla D.), Chee, S.-P. (Soon-Phaik), Shi, Y. (Yuan), Liu, W. (Wenting), Su, X. (Xinyi), Sim, X. (Xueling), Shen, Y. (Yang), Wang, Y.X. (Ya Xing), Li, H. (Hengtong), Tham, Y.-C. (Yih-Chung), Teo, Y.Y. (Yik Ying), Aung, T. (Tin), Small, K.S. (Kerrin S.), Mitchell, P. (Paul), Jonas, J.B. (Jost B.), Wong, T.Y. (Tien Yin), Fletcher, A. (Astrid), Klaver, C.C.W. (Caroline), Klein, B.E.K. (Barbara E. K.), Wang, J.J. (Jie Jin), Iyengar, S.K. (Sudha K.), Hammond, C.J. (Christopher J.), Cheng, C.-Y. (Ching-Yu), Yonova-Doing, E. (Ekaterina), Zhao, W. (Wanting), Igo Jr., R.P. (Robert), Wang, C. (Chunliang), Sundaresan, P. (Periasamy), Lee, K.E. (Kristine), Jun, G.R. (Gyungah R.), Alves, A.C. (Alexessander Couto), Chai, X. (Xiaoran), Chan, A.S.Y. (Anita S. Y.), Lee, M.C. (Mei Chin), Fong, A. (Allan), Tan, A.G. (Ava G.), Khor, C.C., Chew, E.Y. (Emily Y.), Hysi, P.G. (Pirro G.), Fan, Q. (Qiao), Chua, J. (Jacqueline), Chung, J. (Jaeyoon), Liao, J. (Jiemin), Colijn, J.M. (Johanna), Burdon, K.P. (Kathryn P.), Fritsche, L.G. (Lars), Swift, M.K. (Maria K.), Hilmy, M.H. (Maryam H.), Chee, M.L. (Miao Ling), Tedja, M. (Milly), Bonnemaijer, P.W.M. (Pieter), Gupta, P. (Preeti), Tan, Q.S. (Queenie S.), Li, Z. (Zheng), Vithana, E.N. (Eranga), Ravindran, R.D. (Ravilla D.), Chee, S.-P. (Soon-Phaik), Shi, Y. (Yuan), Liu, W. (Wenting), Su, X. (Xinyi), Sim, X. (Xueling), Shen, Y. (Yang), Wang, Y.X. (Ya Xing), Li, H. (Hengtong), Tham, Y.-C. (Yih-Chung), Teo, Y.Y. (Yik Ying), Aung, T. (Tin), Small, K.S. (Kerrin S.), Mitchell, P. (Paul), Jonas, J.B. (Jost B.), Wong, T.Y. (Tien Yin), Fletcher, A. (Astrid), Klaver, C.C.W. (Caroline), Klein, B.E.K. (Barbara E. K.), Wang, J.J. (Jie Jin), Iyengar, S.K. (Sudha K.), Hammond, C.J. (Christopher J.), and Cheng, C.-Y. (Ching-Yu)
- Abstract
Nuclear cataract is the most common type of age-related cataract and a leading cause of blindness worldwide. Age-related nuclear cataract is heritable (h2 = 0.48), but little is known about specific genetic factors underlying this condition. Here we report findings from the largest to date multi-ethnic meta-analysis of genome-wide association studies (discovery cohort N = 14,151 and replication N = 5299) of the International Cataract Genetics Consortium. We confirmed the known genetic association of CRYAA (rs7278468, P = 2.8 × 10−16) with nuclear cataract and identified five new loci associated with this disease: SOX2-OT (rs9842371, P = 1.7 × 10
- Published
- 2020
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