Published in Invest Ophthalmol Vis Sci on April 30, 2008
Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese population. Proc Natl Acad Sci U S A (2009) 1.51
Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. Mol Vis (2010) 1.45
LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract. Mol Vis (2008) 1.42
Glaucoma: genes, phenotypes, and new directions for therapy. J Clin Invest (2010) 1.39
Evaluation of LOXL1 polymorphisms in exfoliation syndrome in a Chinese population. Mol Vis (2009) 1.28
Pseudoexfoliation syndrome, a systemic disorder with ocular manifestations. Hum Genomics (2012) 1.22
Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese. Mol Vis (2009) 1.19
Genetics of pseudoexfoliation syndrome. Curr Opin Ophthalmol (2009) 1.19
Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma. Mol Vis (2010) 1.15
LOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population. Invest Ophthalmol Vis Sci (2011) 1.09
Whole genome association studies in complex diseases: where do we stand? Dialogues Clin Neurosci (2010) 1.06
Genetics and genomics of pseudoexfoliation syndrome/glaucoma. Middle East Afr J Ophthalmol (2011) 1.02
Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese. Mol Vis (2008) 0.98
Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma. Mol Vis (2008) 0.96
Tumor necrosis factor alpha-308 gene polymorphism and pseudoexfoliation glaucoma. Mol Vis (2008) 0.93
LOXL1 expression in lens capsule tissue specimens from individuals with pseudoexfoliation syndrome and glaucoma. Mol Vis (2010) 0.93
Genetic analysis of the clusterin gene in pseudoexfoliation syndrome. Mol Vis (2008) 0.92
Disruption of the blood-aqueous barrier and lens abnormalities in mice lacking lysyl oxidase-like 1 (LOXL1). Invest Ophthalmol Vis Sci (2014) 0.92
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma. Mol Vis (2008) 0.90
Different WDR36 mutation pattern in Chinese patients with primary open-angle glaucoma. Mol Vis (2009) 0.90
Evaluation of LOXL1 polymorphisms in exfoliation syndrome in the Uygur population. Mol Vis (2011) 0.89
Haplotype analysis of the ARMS2/HTRA1 region in Japanese patients with typical neovascular age-related macular degeneration or polypoidal choroidal vasculopathy. Jpn J Ophthalmol (2010) 0.87
Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma. Mol Vis (2009) 0.87
Association of lysyl oxidase-like 1 gene polymorphisms with exfoliation syndrome in Koreans. Mol Vis (2011) 0.87
Evaluation of lysyl oxidase-like 1 gene polymorphisms in pseudoexfoliation syndrome in a Korean population. Mol Vis (2013) 0.84
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nat Genet (2015) 0.84
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma. BMC Ophthalmol (2014) 0.83
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. Sci Rep (2014) 0.82
Retracted The association of LOXL1 polymorphisms with exfoliation syndrome/glaucoma: Meta-analysis. Int J Ophthalmol (2015) 0.82
Association of lysyl oxidase-like 1 gene common sequence variants in Greek patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Mol Vis (2013) 0.82
Review: The role of LOXL1 in exfoliation syndrome/glaucoma. Saudi J Ophthalmol (2011) 0.80
Evaluation of CNTNAP2 gene polymorphisms for exfoliation syndrome in Japanese. Mol Vis (2012) 0.77
Consideration for gene-environment interactions as novel determinants of exfoliation syndrome. Int Ophthalmol Clin (2014) 0.76
Circumferential iris transillumination defects in exfoliation syndrome. J Glaucoma (2013) 0.76
Genetics of exfoliation syndrome and glaucoma. Int Ophthalmol Clin (2014) 0.76
Animal models of exfoliation syndrome, now and future. J Glaucoma (2014) 0.76
Association between polymorphisms in lysyl oxidase-like 1 and susceptibility to pseudoexfoliation syndrome and pseudoexfoliation glaucoma. PLoS One (2014) 0.75
Lysyl oxidase-like 1 polymorphisms in a southwestern Greek cataract population with pseudoexfoliation syndrome. Clin Ophthalmol (2016) 0.75
LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients. BMC Med Genet (2015) 0.75
Analysis of LOXL1 gene variants in Japanese patients with branch retinal vein occlusion. Mol Vis (2011) 0.75
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nat Genet (2017) 0.75
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. N Engl J Med (2007) 12.24
A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer. Nat Med (2012) 4.90
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat Genet (2011) 4.50
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet (2014) 4.13
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat Genet (2011) 4.04
Seven new loci associated with age-related macular degeneration. Nat Genet (2013) 3.81
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet (2011) 3.46
Meta-analysis identifies common variants associated with body mass index in east Asians. Nat Genet (2012) 2.70
Cataract progression after prophylactic laser peripheral iridotomy: potential implications for the prevention of glaucoma blindness. Ophthalmology (2005) 2.53
A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. PLoS Genet (2009) 2.45
SLC4A11 mutations in Fuchs endothelial corneal dystrophy. Hum Mol Genet (2007) 2.41
Detection of primary angle closure using anterior segment optical coherence tomography in Asian eyes. Ophthalmology (2006) 2.39
Association tests using kernel-based measures of multi-locus genotype similarity between individuals. Genet Epidemiol (2010) 2.39
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet (2013) 2.36
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa. Hum Mol Genet (2002) 2.34
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2). Nat Genet (2006) 2.20
Comparison of gonioscopy and anterior segment ocular coherence tomography in detecting angle closure in different quadrants of the anterior chamber angle. Ophthalmology (2007) 2.17
Prevalence and risk factors for diabetic retinopathy: the Singapore Malay Eye Study. Ophthalmology (2008) 2.11
Glaucoma management in patients with osteo-odonto-keratoprosthesis (OOKP): the Singapore OOKP Study. J Glaucoma (2009) 2.08
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nat Genet (2012) 2.05
FTO variants are associated with obesity in the Chinese and Malay populations in Singapore. Diabetes (2008) 2.05
Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. Hum Mol Genet (2005) 2.04
Social franchising of TB care through private GPs in Myanmar: an assessment of treatment results, access, equity and financial protection. Health Policy Plan (2007) 2.03
An outbreak of Fusarium keratitis associated with contact lens wear in Singapore. JAMA (2006) 1.98
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging Behav (2014) 1.90
Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration: same or different disease? Prog Retin Eye Res (2009) 1.81
Rationale and methodology for a population-based study of eye diseases in Malay people: The Singapore Malay eye study (SiMES). Ophthalmic Epidemiol (2007) 1.68
Methodology of the Singapore Indian Chinese Cohort (SICC) eye study: quantifying ethnic variations in the epidemiology of eye diseases in Asians. Ophthalmic Epidemiol (2009) 1.64
Imaging of trabeculectomy blebs using anterior segment optical coherence tomography. Ophthalmology (2006) 1.64
The singapore 5-Fluorouracil trabeculectomy study: effects on intraocular pressure control and disease progression at 3 years. Ophthalmology (2009) 1.63
Distribution and determinants of ocular biometric parameters in an Asian population: the Singapore Malay eye study. Invest Ophthalmol Vis Sci (2009) 1.62
Anterior segment optical coherence tomography parameters in subtypes of primary angle closure. Invest Ophthalmol Vis Sci (2013) 1.57
Postoperative complications after glaucoma surgery for primary angle-closure glaucoma vs primary open-angle glaucoma. Arch Ophthalmol (2011) 1.55
Deep whole-genome sequencing of 100 southeast Asian Malays. Am J Hum Genet (2013) 1.55
Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy. Hum Mutat (2010) 1.54
Lens vault, thickness, and position in Chinese subjects with angle closure. Ophthalmology (2010) 1.54
A combined analysis of genome-wide association studies in breast cancer. Breast Cancer Res Treat (2010) 1.54
Changes in the optic disc after acute primary angle closure. Ophthalmology (2006) 1.54
Cataract surgery after trabeculectomy: the effect on trabeculectomy function. Arch Ophthalmol (2011) 1.54
Assessment of the scleral spur in anterior segment optical coherence tomography images. Arch Ophthalmol (2008) 1.54
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy. Invest Ophthalmol Vis Sci (2008) 1.52
Collagen-related genes influence the glaucoma risk factor, central corneal thickness. Hum Mol Genet (2010) 1.52
Comparison of slitlamp optical coherence tomography and scanning peripheral anterior chamber depth analyzer to evaluate angle closure in Asian eyes. Arch Ophthalmol (2009) 1.51
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat Genet (2013) 1.49
Comparison of the scanning peripheral anterior chamber depth analyzer and the modified van Herick grading system in the assessment of angle closure. Ophthalmology (2006) 1.48
Use of optical coherence tomography to assess variations in macular retinal thickness in myopia. Invest Ophthalmol Vis Sci (2005) 1.48
Reproducibility of anterior chamber angle measurements obtained with anterior segment optical coherence tomography. Invest Ophthalmol Vis Sci (2007) 1.46
Polymorphisms identified through genome-wide association studies and their associations with type 2 diabetes in Chinese, Malays, and Asian-Indians in Singapore. J Clin Endocrinol Metab (2009) 1.46
Peripheral artery disease and glaucoma: the singapore malay eye study. Arch Ophthalmol (2009) 1.42
Peripapillary retinal nerve fiber layer thickness variations with myopia. Ophthalmology (2006) 1.42
A tale of two systems: health reform in China and the United States. Ophthalmology (2010) 1.41
The safety and efficacy of brinzolamide 1%/timolol 0.5% fixed combination versus dorzolamide 2%/timolol 0.5% in patients with open-angle glaucoma or ocular hypertension. J Glaucoma (2009) 1.41
Angle closure glaucoma: a mechanistic review. Curr Opin Ophthalmol (2011) 1.41
Visual impairment, causes of vision loss, and falls: the singapore malay eye study. Invest Ophthalmol Vis Sci (2008) 1.39
A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of disease. Mol Vis (2006) 1.38
Determinants of angle closure in older Singaporeans. Arch Ophthalmol (2008) 1.37
High-definition optical coherence tomography imaging of the iridocorneal angle of the eye. Arch Ophthalmol (2009) 1.36
Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies. Hum Mol Genet (2013) 1.34
Prevalence and risk factors for refractive errors in the Singapore Malay Eye Survey. Ophthalmology (2008) 1.33
Novel association of smaller anterior chamber width with angle closure in Singaporeans. Ophthalmology (2010) 1.31
Comparison of central corneal thickness measurements by visante anterior segment optical coherence tomography with ultrasound pachymetry. Am J Ophthalmol (2007) 1.31
Quantitative iris parameters and association with narrow angles. Ophthalmology (2009) 1.29
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. Hum Mol Genet (2011) 1.29
Determinants of quantitative optic nerve measurements using spectral domain optical coherence tomography in a population-based sample of non-glaucomatous subjects. Invest Ophthalmol Vis Sci (2011) 1.29
A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region. Hum Mol Genet (2011) 1.28
Optic disk ovality as an index of tilt and its relationship to myopia and perimetry. Am J Ophthalmol (2005) 1.27
Prevalence and causes of visual impairment and blindness in an urban Indian population: the Singapore Indian Eye Study. Ophthalmology (2011) 1.27
Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations. Invest Ophthalmol Vis Sci (2005) 1.27
Evidence of retinal vascular narrowing in glaucomatous eyes in an Asian population. Invest Ophthalmol Vis Sci (2008) 1.27
Diabetes, metabolic abnormalities, and glaucoma. Arch Ophthalmol (2009) 1.27
Determinants of ganglion cell-inner plexiform layer thickness measured by high-definition optical coherence tomography. Invest Ophthalmol Vis Sci (2012) 1.26
Association analysis of CFH, C2, BF, and HTRA1 gene polymorphisms in Chinese patients with polypoidal choroidal vasculopathy. Invest Ophthalmol Vis Sci (2008) 1.25
Equity and the Sun Quality Health Private Provider Social Franchise: comparative analysis of patient survey data and a nationally representative TB prevalence survey. Int J Equity Health (2013) 1.24
Prevalence of plateau iris in primary angle closure suspects an ultrasound biomicroscopy study. Ophthalmology (2007) 1.22
Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Invest Ophthalmol Vis Sci (2011) 1.22
The relationship of intraocular pressure with age, systolic blood pressure, and central corneal thickness in an asian population. Invest Ophthalmol Vis Sci (2009) 1.21
Superpixel classification based optic disc and optic cup segmentation for glaucoma screening. IEEE Trans Med Imaging (2013) 1.20
Prevalence and risk factors for refractive errors in Indians: the Singapore Indian Eye Study (SINDI). Invest Ophthalmol Vis Sci (2011) 1.20
Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese. Mol Vis (2009) 1.19
Diagnostic accuracy of the Heidelberg Retina Tomograph for glaucoma a population-based assessment. Ophthalmology (2010) 1.19
Multi-variant pathway association analysis reveals the importance of genetic determinants of estrogen metabolism in breast and endometrial cancer susceptibility. PLoS Genet (2010) 1.19
Refractive error, axial dimensions, and primary open-angle glaucoma: the Singapore Malay Eye Study. Arch Ophthalmol (2010) 1.19
Changes in angle configuration after phacoemulsification measured by anterior segment optical coherence tomography. J Glaucoma (2008) 1.18
The heritability and sibling risk of angle closure in Asians. Ophthalmology (2010) 1.17