P. O. Tam

发表

HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration

C. Barnstable, S. Hartman, J. Hoh, 2006, Science.

Multiple gene polymorphisms in the complement factor h gene are associated with exudative age-related macular degeneration in chinese.

C. Pang, D. Lam, K. Chong, 2008, Investigative ophthalmology & visual science.

HTRA1 promoter polymorphism in wet age-related macular degeneration.

Chi Pui Pang, Josephine Hoh, C. Barnstable, 2007, Science.

A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy

S. Inoue, A. Laude, K. Nishida, 2016, Nature Genetics.

Novel myocilin mutation in a Chinese family with juvenile-onset open-angle glaucoma.

C. Pang, D. Lam, B. Fan, 2006, Archives of ophthalmology.

Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error

Peter K. Joshi, Milly S. Tedja, Claire L. Simpson, 2016, Nature Communications.

Gender specific association of a complement component 3 polymorphism with polypoidal choroidal vasculopathy

T. Lai, C. Pang, S. Chiang, 2014, Scientific Reports.

Association of C2 and CFB polymorphisms with anterior uveitis.

T. Lai, C. Pang, S. Chiang, 2012, Investigative Ophthalmology and Visual Science.

An αA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response

C. Pang, D. Lam, G. Yam, 2009, Molecular vision.

Tyrosinase gene (TYR) mutations in Chinese patients with oculocutaneous albinism type 1

T. Lai, K. Choy, T. Leung, 2010, Clinical & experimental ophthalmology.

Frequent loss of heterozygosity of chromosome 3 short arm detected by PCR-based microsatellite polymorphisms in cervical squamous cell carcinoma.

P. O. Tam, T. Cheung, Y. Wong, 1997, Cancer letters.

TGFbeta-induced factor: a candidate gene for high myopia.

Y. Leung, C. Pang, D. Lam, 2003, Investigative ophthalmology & visual science.

Genetic association of ANGPT2 with primary open-angle glaucoma

Poemen P. Chan, C. Pang, T. Ng, 2022, Eye and Vision.

Manganese superoxide dismutase and chemokine genes polymorphisms in chinese patients with anterior uveitis.

T. Lai, C. Pang, D. Lam, 2009, Investigative ophthalmology & visual science.

Diversified clinical presentations associated with a novel sal-like 4 gene mutation in a Chinese pedigree with Duane retraction syndrome

C. Pang, P. O. Tam, A. Young, 2013, Molecular vision.

A Novel Deletion Variant of Γ Γ Γ Γ Γd-crystallin Responsible for Congenital Nuclear Cataract

C. Pang, D. Lam, G. Yam, 2022 .

New loci and coding variants confer risk for age-related macular degeneration in East Asians

Feng Wen, Fang Lu, Peng Chen, 2015, Nature Communications.

A Cohesin Subunit Variant Identified from a Peripheral Sclerocornea Pedigree

C. Pang, V. Jhanji, P. O. Tam, 2019, Disease Markers.

Clinical investigation and genetic analysis of a peripheral sclerocornea pedigree

C. Pang, V. Jhanji, P. O. Tam, 2019 .

PAX6 Gene Associated with High Myopia: A Meta-analysis

C. Pang, P. O. Tam, L. J. Chen, 2014, Optometry and vision science : official publication of the American Academy of Optometry.

AC and AG dinucleotide repeats in the PAX6 P1 promoter are associated with high myopia

C. Pang, D. Lam, B. Fan, 2009, Molecular vision.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

H. Stefánsson, A. Sigurdsson, A. Jonasdottir, 2010, Nature Genetics.

Association of Apolipoprotein E Polymorphisms With Normal Tension Glaucoma in a Chinese Population

C. Pang, B. Fan, P. O. Tam, 2006, Journal of glaucoma.

Evaluation of NTF4 as a causative gene for primary open-angle glaucoma

X. Y. Liang, C. Pang, Ningli Wang, 2012, Molecular vision.

NOVEL AND HOMOZYGOUS BEST1 MUTATIONS IN CHINESE PATIENTS WITH BEST VITELLIFORM MACULAR DYSTROPHY

K. Choy, Haitao Li, P. Hou, 2010, Retina.

Association of coding and UTR variants in the known regions with wet age-related macular degeneration in Han Chinese population

F. Wen, Lulin Huang, Zhenglin Yang, 2018, Journal of Human Genetics.

Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma

C. Pang, D. Lam, P. O. Tam, 2010, Molecular vision.

Glaucoma Genes in East Asian Studies

P. O. Tam, C. Pang, S. Rong, 2018, Essentials in Ophthalmology.

Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese

R. Ritch, C. Pang, D. Lam, 2008, Molecular vision.

CFH 184G as a genetic risk marker for anterior uveitis in Chinese females

T. Lai, C. Pang, S. Chiang, 2011, Molecular vision.

Association of CFH and SERPING1 polymorphisms with anterior uveitis

T. Lai, C. Pang, S. Chiang, 2013, British Journal of Ophthalmology.

Evaluation of SPARC as a candidate gene of juvenile-onset primary open-angle glaucoma by mutation and copy number analyses

X. Y. Liang, R. Ritch, C. Pang, 2010, Molecular vision.

Molecular diagnostics of genetic eye diseases.

K. Choy, C. Pang, D. Lam, 2006, Clinical biochemistry.

PRPF4 mutations cause autosomal dominant retinitis pigmentosa.

D. Vollrath, Kanxing Zhao, C. Pang, 2014, Human molecular genetics.

Global Review and Meta-analysis of Diabetic Retinopathy Genetic Studies Highlight Gaps in the Pathogenesis between Various Populations

C. Pang, P. O. Tam, L. J. Chen, 2013 .

Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium

Claire L. Simpson, David M. Evans, C. Gieger, 2016, Scientific Reports.

SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma

C. Pang, B. Fan, Ningli Wang, 2012, Molecular vision.

Supporting Online Material for HTRA 1 Promoter Polymorphism in Wet Age-Related Macular Degeneration

C. Barnstable, S. Hartman, J. Hoh, 2006 .

Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population

Haixin Wang, Lulin Huang, Ling Zhong, 2018, Science China Life Sciences.

Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population

Haixin Wang, Lulin Huang, Ling Zhong, 2018, Science China Life Sciences.

Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma

T. Wong, X. Zuo, Xuejun Zhang, 2014, Nature Genetics.

Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis

Dean Y. Li, Xianjun Zhu, C. Mardin, 2019, Genetics in Medicine.

Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

S. R. Krishnadas, Chaw Chaw Khaing, Y. Teo, 2016, Nature Genetics.

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.

Dean Y. Li, Liangdan Sun, X. Zuo, 2011, American journal of human genetics.

Association of NR2E3 but not NRL mutations with retinitis pigmentosa in the Chinese population.

T. Lai, C. Pang, D. Lam, 2010, Investigative ophthalmology & visual science.

Differential pattern of RP1 mutations in retinitis pigmentosa

T. Lai, C. Pang, Ningli Wang, 2010, Molecular vision.

Compound heterozygosity of two novel truncation mutations in RP1 causing autosomal recessive retinitis pigmentosa.

T. Lai, C. Pang, D. Lam, 2010, Investigative ophthalmology & visual science.

The dual role of dexamethasone on anti-inflammation and outflow resistance demonstrated in cultured human trabecular meshwork cells.

Chi Pui Pang, Y. Leung, C. Pang, 2003, Molecular vision.

Associations of the C2-CFB-RDBP-SKIV2L locus with age-related macular degeneration and polypoidal choroidal vasculopathy.

Zhenglin Yang, Yi Shi, T. Lai, 2013, Ophthalmology.

Differentiation of exudative age-related macular degeneration and polypoidal choroidal vasculopathy in the ARMS2/HTRA1 locus.

X. Y. Liang, T. Lai, C. Pang, 2012, Investigative ophthalmology & visual science.

Association of complement factor H polymorphisms with exudative age-related macular degeneration.

Ke Liu, Li Jia Chen, Chi Pui Pang, 2006, Molecular vision.

SPP2 Mutations Cause Autosomal Dominant Retinitis Pigmentosa

Chen Zhao, D. Vollrath, Kanxing Zhao, 2015, Scientific Reports.

Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East Asians

Y. Teo, P. Mitchell, T. Wong, 2015, Nature Communications.

A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.

R. Ritch, C. Pang, D. Lam, 2006, Molecular vision.

A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5 q

R. Ritch, C. Pang, B. Fan, 2006 .

Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients

C. Leung, C. Pang, P. O. Tam, 2019, Disease markers.

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.

Liangdan Sun, X. Zuo, Xuejun Zhang, 2013, Human molecular genetics.

Evaluation of the association of C5 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy

T. Lai, C. Pang, M. Brelen, 2019, Eye and Vision.

Complement factor H and interleukin gene polymorphisms in patients with non-infectious intermediate and posterior uveitis

T. Lai, C. Pang, S. Chiang, 2012, Molecular vision.

SNPs and interaction analyses of myocilin, optineurin, and apolipoprotein E in primary open angle glaucoma patients.

C. Pang, D. Lam, B. Fan, 2005, Molecular vision.

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

Y. Teo, T. Wong, E. Tai, 2013, Human molecular genetics.

Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma

K. Nishida, C. Leung, A. Miki, 2016, Scientific Reports.

Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese

C. Pang, Ningli Wang, S. Chiang, 2009, Molecular vision.

SNP rs 1533428 at 2 p 16 . 3 as a marker for late-onset primary open-angle glaucoma

C. Pang, B. Fan, Ningli Wang, 2012 .

A Genome-wide Scan Maps a Novel Juvenile-Onset Primary Open-Angle Glaucoma Locus to 15 q

C. Leung, C. Pang, D. Lam, 2006 .

Absence of myocilin and optineurin mutations in a large Philippine family with juvenile onset primary open angle glaucoma.

R. Ritch, C. Pang, D. Lam, 2004, Molecular vision.

Polymorphisms in the Myocilin Promoter Unrelated to the Risk and Severity of Primary Open-Angle Glaucoma

Y. Leung, C. Pang, D. Lam, 2004, Journal of glaucoma.

HTRA1 promoter variant differentiates polypoidal choroidal vasculopathy from exudative age-related macular degeneration

X. Y. Liang, T. Lai, C. Pang, 2016, Scientific Reports.

Multi-Polymorphism Analysis Reveals Joint Effects in Males With Chronic Central Serous Chorioretinopathy

C. Pang, M. Brelen, T. Ng, 2023, Investigative ophthalmology & visual science.

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Jonathan H. Morgan, M. P. Concas, Adriana I. Iglesias, 2018, Nature Genetics.