Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

Author:

Khor Chiea Chuen12345,Miyake Masahiro67,Chen Li Jia8,Shi Yi9,Barathi Veluchamy A.2510,Qiao Fan4,Nakata Isao67,Yamashiro Kenji6,Zhou Xin4,Tam Pancy O.S.8,Cheng Ching-Yu245,Tai E Shyong114,Vithana Eranga N.25,Aung Tin25,Teo Yik-Ying1412,Wong Tien-Yin245,Moriyama Muka13,Ohno-Matsui Kyoko13,Mochizuki Manabu13,Matsuda Fumihiko7,Yong Rita Y.Y.14,Yap Eric P.H.14,Yang Zhenglin9,Pang Chi Pui8,Saw Seang-Mei24,Yoshimura Nagahisa6,

Affiliation:

1. Division of Human Genetics, Genome Institute of Singapore, Singapore, Singapore,

2. Department of Ophthalmology, Yong Loo Lin School of Medicine,

3. Department of Paediatrics, Yong Loo Lin School of Medicine,

4. Saw Swee Hock School of Public Health and

5. Singapore Eye Research Institute, Singapore, Singapore,

6. Department of Ophthalmology and Visual Sciences,

7. Center for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan,

8. Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China,

9. The Sichuan Provincial Key Laboratory for Human Disease Gene Study, the Institute of Laboratory Medicine, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu, Sichuan, China and

10. Duke-NUS Graduate Medical School, Singapore, Singapore

11. Department of Medicine, Yong Loo Lin School of Medicine,

12. Department of Statistics and Applied Probability, Faculty of Science, National University of Singapore, Singapore, Singapore,

13. Department of Ophthalmology and Visual Science, Tokyo Medical and Dental University, Tokyo, Japan,

14. Defence Medical and Environmental Research Institute, DSO National Laboratories, Singapore, Singapore,

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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