Zobrazeno 1 - 10
of 85
pro vyhledávání: '"O. S. Tam"'
Autor:
Ke Liu, Li Ma, Timothy Y. Y. Lai, Marten E. Brelen, Pancy O. S. Tam, Clement C. Tham, Chi Pui Pang, Li Jia Chen
Publikováno v:
Eye and Vision, Vol 6, Iss 1, Pp 1-7 (2019)
Abstract Background Neovascular age-related macular degeneration (AMD) and polypoidal choroidal vasculopathy (PCV) are sight-threatening maculopathies with both environmental and genetic risk factors. We have previously shown relative risks posed by
Externí odkaz:
https://doaj.org/article/ae43ac95f7c441b3ae6fd2ca561955ea
Autor:
Zhen Ji Chen, Danny S. C. Ng, Ling-Ping Cen, Tsz Kin Ng, Mary Ho, Marten E. Brelen, Tai-Ping Li, Shi Yao Lu, Pancy O. S. Tam, Alvin L. Young, Weiqi Chen, Jason C. Yam, Haoyu Chen, Clement C. Tham, Chi Pui Pang, Li Jia Chen
Publikováno v:
Investigative Opthalmology & Visual Science. 64:19
Autor:
Mingzhi Zhang, Shi Song Rong, Tsz Kin Ng, Kohji Nishida, Clement C Y Tham, Chukai Huang, Zhenggen Wu, Chi Pui Pang, Kenji Matsushita, Rumi Kawashima, Alvin L. Young, Janey L. Wiggs, Motokazu Tsujikawa, Li Jia Chen, Shi Yao Lu, Pancy O. S. Tam, Shinichi Usui, Christopher Kai-Shun Leung
Publikováno v:
Clinical & Experimental Ophthalmology. 48:658-665
Background The CAV1-CAV2 locus has been associated with primary open-angle glaucoma (POAG) and intraocular pressure. However, its association with normal-tension glaucoma (NTG) was inconclusive. Therefore, we evaluated this association in Chinese and
Autor:
Shi Yao Lu, Jason C. S. Yam, Fen Fen Li, Chi Pui Pang, Ka Wai Kam, Clement C Y Tham, Li Jia Chen, Shu Min Tang, Pancy O. S. Tam
Publikováno v:
British Journal of Ophthalmology. 104:1472-1476
ObjectiveTo investigate the associations of single-nucleotide polymorphisms (SNPs) in the ZC3H11B, ZFHX1B, VIPR2, SNTB1 and MIPEP genes with severities of myopia in Chinese populations.MethodsBased on previous myopia genome-wide association studies,
Autor:
Xue Chen, Shi Song Rong, Qihua Xu, Fang Yao Tang, Yuan Liu, Hong Gu, Pancy O S Tam, Li Jia Chen, Mårten E Brelén, Chi Pui Pang, Chen Zhao
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e108196 (2014)
Age-related macular degeneration (AMD) is a major cause of severe vision loss in elderly people. Diabetes mellitus is a common endocrine disorder with serious consequences, and diabetic retinopathy (DR) is the main ophthalmic complication. DR and AMD
Externí odkaz:
https://doaj.org/article/e0878bb9068e4777a7f8dc2303538fa9
Autor:
Shu Min Tang, Chi Pui Pang, Shi Yao Lu, Li Jia Chen, Clement C Y Tham, Pancy O. S. Tam, Alvin L. Young, Wilson W K Yip, Fen Fen Li, Jason C. S. Yam, Ka Wai Kam
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To evaluate the association between single-nucleotide polymorphisms (SNPs) in the ZC3H11B, RSPO1, C3orf26, GJD2, ZNRF3, and WNT7B genes and myopia endophenotypes in children. Methods Seven SNPs identified in previous genome-wide association s
Autor:
Vishal Jhanji, Shu Min Tang, Jason C. S. Yam, Shi Yao Lu, Clement C Y Tham, Pancy O. S. Tam, Chi Pui Pang, Li Jia Chen, Alvin L. Young, Ka Wai Kam, Tommy C Y Chan, Li Ma, Yu Meng Wang
Publikováno v:
British Journal of Ophthalmology. 102:1736-1741
ObjectiveTo investigate the associations between 16 single-nucleotide polymorphisms (SNPs) in 14 genetic loci and keratoconus in an independent Chinese cohort.MethodsThis cross-sectional, case-control association study included a Chinese cohort of 13
Autor:
Pancy O. S. Tam, Jason C. S. Yam, Shu Min Tang, Li Jia Chen, Shi Yao Lu, Chi Pui Pang, Ka Wai Kam, Li Ma, Yu Meng Wang, Alvin L. Young
Publikováno v:
British Journal of Ophthalmology. 102:570-574
AimsTo investigate the association of the paired box gene 6 (PAX6) with different severities of myopia.MethodsA total of four haplotype-tagging single-nucleotide polymorphisms (SNPs; rs2071754, rs3026354, rs3026390 and rs628224) and two previously re
Autor:
Chi Pui Pang, Ke Liu, Li Jia Chen, Marten E. Brelen, Li Ma, Timothy Y Y Lai, Pancy O. S. Tam, Clement C Y Tham
Publikováno v:
Eye and Vision, Vol 6, Iss 1, Pp 1-7 (2019)
BackgroundNeovascular age-related macular degeneration (AMD) and polypoidal choroidal vasculopathy (PCV) are sight-threatening maculopathies with both environmental and genetic risk factors. We have previously shown relative risks posed by genes of t
Autor:
Vishal Jhanji, Chi Pui Pang, Bi Ning Zhang, Li Jia Chen, Pancy O. S. Tam, Yu Liu, Tommy C Y Chan, Wai Kit Chu
Publikováno v:
Disease Markers
Disease Markers, Vol 2019 (2019)
Disease Markers, Vol 2019 (2019)
Background. Sclerocornea is a rare congenital disorder characterized with the opacification of the cornea. Here, we report a nonconsanguineous Chinese family with multiple peripheral sclerocornea patients spanning across three generations inherited i