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> Research Assistant Oi Sin Pancy TAM
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Ms TAM Oi Sin Pancy
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CUHK Research Outputs
1 of 3
Association of WNT7B and RSPO1 with Axial Length in School Children
(
2020
)
Genetic associations of myopia severities and endophenotypes in children
(
2020
)
A Cohesin Subunit Variant Identified from a Peripheral Sclerocornea Pedigree
(
2019
)
Evaluation of the association of C5 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy
(
2019
)
ABCG1 as a new susceptibility gene for neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in Chinese and Japanese
(
2016
)
A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy
(
2016
)
Association of ABCG1 With Neovascular Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy in Chinese and Japanese
(
2016
)
Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium
(
2016
)
Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma
(
2016
)
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma
(
2016
)
HTRA1 promoter variant differentiates polypoidal choroidal vasculopathy from exudative age-related macular degeneration
(
2016
)
Identification of PFG as a New Gene for Neovascular Age-related Macular Degeneration
(
2016
)
Identification of PGF as a New Gene for Neovascular Age-Related Macular Degeneration in a Chinese Population
(
2016
)
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error
(
2016
)
Protective effects of a HTRA1 insertion-deletion variant against age-related macular degeneration
(
2016
)
ABCG1 as a new susceptibility gene for age-related macular degeneration and polypoidal choroidal vsculopathy
(
2015
)
Association of the PAX6 Gene with High and Extreme Myopia
(
2015
)
Association of the vascular endothelial growth factor genes with age-related macular degeneration and polypoidal choroidal vasculopathy
(
2015
)
Ethnic differences in the association of SERPING1 with age-related macular degeneration and polypoidal choroidal vasculopathy
(
2015
)
New loci and coding variants confer risk for age-related macular degeneration in East Asians
(
2015
)
New loci and coding variants confer risk for age-related macular degeneration in East Asians
(
2015
)
SPP2 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
(
2015
)
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma
(
2014
)
Diabetes mellitus and risk of age-related macular degeneration: A systematic review and meta-analysis
(
2014
)
Differential Associations of Genes in the Complement Pathway with Neovascular Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy
(
2014
)
FPR1 interacts with CFH, HTRA1 and smoking in exudative age-related macular degeneration and polypoidal choroidal vasculopathy
(
2014
)
Gender specific association of a complement component 3 polymorphism with polypoidal choroidal vasculopathy
(
2014
)
Genes in the High-Density Lipoprotein Metabolic Pathway in Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy
(
2014
)
PAX6 Gene Associated with High Myopia: A Meta-analysis
(
2014
)
PRPF4 mutations cause autosomal dominant retinitis pigmentosa
(
2014
)
Whole Exome Sequencing Reveals Genetic Predisposition in a Large Family with Retinitis Pigmentosa
(
2014
)
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population
(
2013
)
Association of C3 with Neovascular Age-Related Macular Degeneration And Ploypoidal Choroidal Vasculopathy
(
2013
)
Association of CFH and SERPING1 polymorphisms with anterior uveitis
(
2013
)
Associations of C3 with Neovascular Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy
(
2013
)
Associations of the C2-CFB-RDBP-SKIV2L Locus with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy
(
2013
)
Contribution of SNRNP200 sequence variations to retinitis pigmentosa
(
2013
)
Diversified clinical presentations associated with a novel Sal-like 4 gene mutation in a Chinese pedigree with Duane retraction syndrome
(
2013
)
Genetic Risk Factors for Primary Glaucoma: a Systematic Review and Critical Assessment
(
2013
)
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
(
2013
)
Global Review And Meta-analysis of Diabetic Retinopathy Genetic Studies Highlight Gaps in The Pathogenesis between Various Populations
(
2013
)
Revisit The Association of CAV1/CAV2 with Primary Open-Angle Glaucoma
(
2013
)
Association of C2 and CFB Polymorphisms with Anterior Uveitis
(
2012
)
Association of C2 And CFB Polymorphisms with Anterior Uveitis
(
2012
)
Association of C2 and CFB polymorphisms with anterior uveitis
(
2012
)
Association of C2 and CFB Polymorphisms with Anterior Uveitis
(
2012
)
Association of the C2-CFB-RDBP-SKIV2L Locus with Age-Related Macular Degeneration
(
2012
)
Assoications of the C2-CFB-RDBP-SKIV2L Locus with Age-Related Macular Degeneration
(
2012
)
Complement factor H and interleukin gene polymorphisms in patients with non-infectious intermediate and posterior uveitis
(
2012
)
Diabetic Retinopathy Genetic Variants in Inflammatory & Oxidative Stress Pathways: Meta-analyses of 9 Candidate Genes
(
2012
)
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Last updated on 2019-16-08 at 07:19
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