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20篇 您的检索式：作者名="VITHANA EN"

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	题名	作者	年代	出处	被引量
1	Association analysis of CFH,C2,BF,and HTRA1 gene polymorphisms in Chinese patients With polypoidal choroidal vasculopathy显示文摘	Lee KY Vithana EN Mathur R	2008	Invest Ophthatmol Vis Sc2008，49，：	1
2	Association of LOXL1 gene polymorph isms with pseudoexfoliation in the Japanese 显示文摘	Ozaki M Lee KY Vithana EN	2008	Invest Ophthalmol Vis Sci2008，49，9：	1
3	Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma显示文摘	Vithana EN Khor CC Qiao C	2012	Nat Genet2012，44，10：	1
4	Collagen-related genes influence the glaucoma risk factor,central corneal thickness显示文摘	VITHANA EN AUNG T KHOR CC	2011	Hum Mol Genet2011，20，4：	1
5	Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma显示文摘	CHEN Y LIN Y VITHANA EN	2014	Nat Genet2014，46，10：	1
6	Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3,and further identify CARD10 as a novel locus influencing optic disc area显示文摘	KHOR CC RAMDAS WD VITHANA EN	2011	Hum Mol Genet2011，20，9：	1
7	Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese显示文摘	Ozaki M Lee KY Vithana EN		0，，09：	1
8	Segregation of a PRKCG mutation in two RP11 families显示文摘	Vithana EN Inglehearn CF	1998	Am J Hum Genet1998，62，5：	1
9	Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma显示文摘	Vithana EN Khor CC Qiao C	2012	Nat Genet2012，44，10：	1
10	A large deletion in the adRP gene PRPF31:evidence that haploinsufficiency is the cause of disease显示文摘	Abu-Safieh L Vithana EN Mantel I	2006	Mol Vis2006，12，：	1
11	A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophy显示文摘	Lakshminarayanan R Vithana EN Chai SM	2011	Br J Ophthalmol2011，95，10：	1
12	Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration:Same or different disease 显示文摘	Laude A Cackett PD Vithana EN Yeo IY Wong D Koh AH	2010	Prog Retin Eye Res2010，29，1：	1
13	A large deletion in the adRP gene PRPF31:evidence that haploinsufficiency is the cause of disease 显示文摘	Abu-Safieh L Vithana EN Mantel 1	2006	Molecular vision2006，12，：	1
14	Analysis of con- juncfival fibroblasts from a proband with Schnyder corneal dystrophy 显示文摘	Mehta JS Vithana EN Venkataraman D	2008	Mol Vis2008，14，：	1
15	Polypoidal choroidal vasculopathy and neovascular age-related macular de-generation: same or different disease显示文摘	LAUDE A CACKETT PD VITHANA EN	2010	Progress in Retinal and Eye Research2010，29，1：	1
16	Disease mechanism for retinitis pigmentosa (RP11 ) caused by mutations in the splicing factor gene PRPF31 显示文摘	Deery EC Vithana EN Newbold RJ	2002	Hum Mol Genet2002，11，：	1
17	Disease mechanism for retinitis pigmentosa ( RP11 ) caused by mutations in the splicing factor gene PRPF31 显示文摘	Derry EC Vithana EN Newbold R J	2002	Hum Mol Genet2002，11，25：	1
18	Surgical management and genetic analysis of a Chinese family with the S171P nmtation in the UBIAD1 gene, the gene for schnyder corneal dystrophy显示文摘	MEHTA JS VITHANA EN VENKATARAMAN D	2009	British Journal of Ophthalmology2009，93，7：	1
19	Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population显示文摘	Vithana EN Nongpiur ME Venkataraman D	2010	Mol Vis2010，16，：	1
20	Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration:same or different disease?显示文摘	Laude A Cackett PD Vithana EN	2010	Prog Retin Eye Res2010，29，：	1

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