Published in Invest Ophthalmol Vis Sci on September 17, 2013
The primary open-angle african american glaucoma genetics study: baseline demographics. Ophthalmology (2015) 0.96
Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. PLoS Genet (2014) 0.91
The genetics of POAG in black South Africans: a candidate gene association study. Sci Rep (2015) 0.88
A Population-based survey of the prevalence and types of glaucoma in Nigeria: results from the Nigeria National Blindness and Visual Impairment Survey. BMC Ophthalmol (2015) 0.85
Expression-associated polymorphisms of CAV1-CAV2 affect intraocular pressure and high-tension glaucoma risk. Mol Vis (2015) 0.81
DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2014) 0.80
Extracting Primary Open-Angle Glaucoma from Electronic Medical Records for Genetic Association Studies. PLoS One (2015) 0.79
Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. Sci Rep (2014) 0.78
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population. J Negat Results Biomed (2015) 0.78
Analysis of Genomic Regions Associated With Coronary Artery Disease Reveals Continent-Specific Single Nucleotide Polymorphisms in North African Populations. J Epidemiol (2016) 0.78
Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study. Invest Ophthalmol Vis Sci (2014) 0.77
Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study. Ophthalmology (2016) 0.75
Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort. J Negat Results Biomed (2016) 0.75
Ethnic specific association of the CAV1/CAV2 locus with primary open-angle glaucoma. Sci Rep (2016) 0.75
Exome Sequencing Identifies a Missense Variant in EFEMP1 Co-Segregating in a Family with Autosomal Dominant Primary Open-Angle Glaucoma. PLoS One (2015) 0.75
Caveolins and caveolae in ocular physiology and pathophysiology. Prog Retin Eye Res (2016) 0.75
CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma. Oncotarget (2017) 0.75
Major review: Molecular genetics of primary open-angle glaucoma. Exp Eye Res (2017) 0.75
PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet (2007) 209.92
The number of people with glaucoma worldwide in 2010 and 2020. Br J Ophthalmol (2006) 25.47
Causes and prevalence of visual impairment among adults in the United States. Arch Ophthalmol (2004) 13.78
Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix. Heredity (Edinb) (2005) 9.85
Racial variations in the prevalence of primary open-angle glaucoma. The Baltimore Eye Survey. JAMA (1991) 9.42
Identification of a gene that causes primary open angle glaucoma. Science (1997) 8.14
Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science (2002) 6.53
Prevalence of open-angle glaucoma among adults in the United States. Arch Ophthalmol (2004) 5.44
Prevalence of glaucoma. The Beaver Dam Eye Study. Ophthalmology (1992) 5.35
Primary open-angle glaucoma. N Engl J Med (2009) 4.89
An anatomy of normal and malignant gene expression. Proc Natl Acad Sci U S A (2002) 4.45
Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet (1997) 3.83
Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet (2005) 3.56
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Hum Mol Genet (1999) 3.24
Genetic analysis of RXR alpha developmental function: convergence of RXR and RAR signaling pathways in heart and eye morphogenesis. Cell (1994) 3.16
Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science (2011) 2.78
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet (2010) 2.75
Prevalence of glaucoma in a rural East African population. Invest Ophthalmol Vis Sci (2000) 2.50
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nat Genet (2011) 2.42
Blindness and visual impairment in an urban West African population: the Tema Eye Survey. Ophthalmology (2012) 2.24
Prevalence of glaucoma in an African population. Eye (Lond) (2004) 2.19
The genetics of primary open-angle glaucoma: a review. Exp Eye Res (2008) 2.14
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet (2012) 2.00
Candidate gene association analysis for a quantitative trait, using parent-offspring trios. Genet Epidemiol (2003) 1.88
A genome-wide association study of optic disc parameters. PLoS Genet (2010) 1.87
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA. Hum Mol Genet (2011) 1.77
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Hum Mol Genet (2011) 1.74
Primary open-angle glaucoma in blacks: a review. Surv Ophthalmol (2003) 1.70
A comparison of gene expression profiles produced by SAGE, long SAGE, and oligonucleotide chips. Genomics (2004) 1.65
Primary open-angle glaucoma genes. Eye (Lond) (2011) 1.60
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations. Invest Ophthalmol Vis Sci (2008) 1.51
Molecular genetics in glaucoma. Exp Eye Res (2011) 1.47
Glaucoma: genes, phenotypes, and new directions for therapy. J Clin Invest (2010) 1.39
Nine-year incidence of open-angle glaucoma in the Barbados Eye Studies. Ophthalmology (2007) 1.37
Survey of glaucoma in an eye clinic in Ghana, West Africa. J Glaucoma (2002) 1.26
A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma. Hum Mol Genet (2012) 1.24
Genetic variants associated with optic nerve vertical cup-to-disc ratio are risk factors for primary open angle glaucoma in a US Caucasian population. Invest Ophthalmol Vis Sci (2011) 1.23
CDKN2B polymorphism is associated with primary open-angle glaucoma (POAG) in the Afro-Caribbean population of Barbados, West Indies. PLoS One (2012) 1.16
Progression of visual field loss in untreated glaucoma patients and glaucoma suspects in St. Lucia, West Indies. Am J Ophthalmol (2002) 1.10
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice. Nat Genet (2011) 1.10
Epidemiology of glaucoma in sub-saharan Africa: prevalence, incidence and risk factors. Middle East Afr J Ophthalmol (2013) 1.10
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. PLoS One (2012) 1.10
Prevalence of glaucoma in an urban West African population: the Tema Eye Survey. JAMA Ophthalmol (2013) 1.05
Genome-wide association study of primary open angle glaucoma risk and quantitative traits. Mol Vis (2012) 1.01
Common variants on chromosome 9p21 are associated with normal tension glaucoma. PLoS One (2012) 0.98
Prevalence of myocilin mutations in adults with primary open-angle glaucoma in Ghana, West Africa. J Glaucoma (2002) 0.97
GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease. PLoS One (2011) 0.94
Clinical implications of old and new genes for open-angle glaucoma. Ophthalmology (2011) 0.88
Myocilin mutations in black South Africans with POAG. Mol Vis (2011) 0.88
Association between genetic variants associated with vertical cup-to-disc ratio and phenotypic features of primary open-angle glaucoma. Ophthalmology (2012) 0.88
Optineurin coding variants in Ghanaian patients with primary open-angle glaucoma. Mol Vis (2008) 0.88
Lack of association of SNP rs4236601 near CAV1 and CAV2 with POAG in a Saudi cohort. Mol Vis (2012) 0.87
Low prevalence of myocilin mutations in an African American population with primary open-angle glaucoma. Mol Vis (2012) 0.82
Complement factor H variant increases the risk of age-related macular degeneration. Science (2005) 17.95
Genome partitioning of genetic variation for complex traits using common SNPs. Nat Genet (2011) 8.57
Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science (2002) 6.53
Sugar-sweetened beverages and genetic risk of obesity. N Engl J Med (2012) 5.98
Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy. Nat Med (2002) 5.07
Three-year follow-up of the tube versus trabeculectomy study. Am J Ophthalmol (2009) 4.21
Cerebrospinal fluid pressure is decreased in primary open-angle glaucoma. Ophthalmology (2008) 4.09
Treatment outcomes in the Tube Versus Trabeculectomy (TVT) study after five years of follow-up. Am J Ophthalmol (2012) 3.93
Randomized controlled trial of patching vs acupuncture for anisometropic amblyopia in children aged 7 to 12 years. Arch Ophthalmol (2010) 3.92
Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet (2012) 3.68
Categorizing the stage of glaucoma from pre-diagnosis to end-stage disease. Am J Ophthalmol (2006) 3.66
Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1. Hum Mol Genet (2005) 3.56
PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease. Sci Transl Med (2010) 3.48
The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genet Epidemiol (2010) 3.48
The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited. Prog Retin Eye Res (2009) 3.40
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice. Nat Genet (2001) 3.30
Molecular markers of early Parkinson's disease based on gene expression in blood. Proc Natl Acad Sci U S A (2007) 3.03
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease. Am J Hum Genet (2004) 2.97
Surgical complications in the Tube Versus Trabeculectomy Study during the first year of follow-up. Am J Ophthalmol (2006) 2.94
Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration. Am J Hum Genet (2006) 2.89
A randomized trial of brimonidine versus timolol in preserving visual function: results from the Low-Pressure Glaucoma Treatment Study. Am J Ophthalmol (2011) 2.88
Postoperative complications in the Tube Versus Trabeculectomy (TVT) study during five years of follow-up. Am J Ophthalmol (2012) 2.82
Treatment outcomes in the tube versus trabeculectomy study after one year of follow-up. Am J Ophthalmol (2006) 2.73
Glaucomatous damage of the macula. Prog Retin Eye Res (2012) 2.70
The African Descent and Glaucoma Evaluation Study (ADAGES): design and baseline data. Arch Ophthalmol (2009) 2.59
Early rapid rise in intraocular pressure after intravitreal triamcinolone acetonide injection. Am J Ophthalmol (2004) 2.46
Macular ganglion cell-inner plexiform layer: automated detection and thickness reproducibility with spectral domain-optical coherence tomography in glaucoma. Invest Ophthalmol Vis Sci (2011) 2.46
Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease. Hepatology (2013) 2.42
Comparison of retinal nerve fiber layer measurements using time domain and spectral domain optical coherent tomography. Ophthalmology (2009) 2.41
Association between rates of binocular visual field loss and vision-related quality of life in patients with glaucoma. JAMA Ophthalmol (2013) 2.37
Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration. Hum Mol Genet (2005) 2.32
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells. Am J Hum Genet (2005) 2.20
Blood vessel contributions to retinal nerve fiber layer thickness profiles measured with optical coherence tomography. J Glaucoma (2008) 2.19
Measurement of local retinal ganglion cell layer thickness in patients with glaucoma using frequency-domain optical coherence tomography. Arch Ophthalmol (2009) 2.18
Choroidal thickness in unilateral advanced glaucoma. Invest Ophthalmol Vis Sci (2012) 2.17
SNPselector: a web tool for selecting SNPs for genetic association studies. Bioinformatics (2005) 2.14
Valsalva manoeuver, intra-ocular pressure, cerebrospinal fluid pressure, optic disc topography: Beijing intracranial and intra-ocular pressure study. Acta Ophthalmol (2013) 2.09
Differences in visual function and optic nerve structure between healthy eyes of blacks and whites. Arch Ophthalmol (2005) 2.09
Fried food consumption, genetic risk, and body mass index: gene-diet interaction analysis in three US cohort studies. BMJ (2014) 2.06
Discrimination between glaucomatous and nonglaucomatous eyes using quantitative imaging devices and subjective optic nerve head assessment. Invest Ophthalmol Vis Sci (2006) 2.05
The influence of peripheral iridotomy on the intraocular pressure course in patients with pigmentary glaucoma. J Glaucoma (2005) 2.05
Sturge-Weber Syndrome (Encephalotrigeminal Angiomatosis): Recent Advances and Future Challenges. Asia Pac J Ophthalmol (Phila) (2015) 2.04
Glaucoma diagnostic accuracy of ganglion cell-inner plexiform layer thickness: comparison with nerve fiber layer and optic nerve head. Ophthalmology (2012) 2.04
High failure rate associated with 180 degrees selective laser trabeculoplasty. J Glaucoma (2005) 2.03
Glaucoma Progression Analysis software compared with expert consensus opinion in the detection of visual field progression in glaucoma. Ophthalmology (2011) 2.01
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. Am J Hum Genet (2006) 2.00
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet (2012) 2.00
Enhanced depth imaging optical coherence tomography of deep optic nerve complex structures in glaucoma. Ophthalmology (2011) 1.98
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease. Hum Mol Genet (2003) 1.98
DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity. BMC Med Genet (2008) 1.95
African Descent and Glaucoma Evaluation Study (ADAGES): III. Ancestry differences in visual function in healthy eyes. Arch Ophthalmol (2010) 1.89
Initial arcuate defects within the central 10 degrees in glaucoma. Invest Ophthalmol Vis Sci (2011) 1.89
Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma. Mol Vis (2008) 1.87
Retinal ganglion cell layer thickness and local visual field sensitivity in glaucoma. Arch Ophthalmol (2011) 1.85
Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration. Hum Mol Genet (2007) 1.83
Optical coherence tomography of the retina and optic nerve - a review. Clin Experiment Ophthalmol (2009) 1.80
Ability of cirrus HD-OCT optic nerve head parameters to discriminate normal from glaucomatous eyes. Ophthalmology (2010) 1.79
Reproducibility of peripapillary retinal nerve fiber layer thickness and optic nerve head parameters measured with cirrus HD-OCT in glaucomatous eyes. Invest Ophthalmol Vis Sci (2010) 1.77
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in Caucasians from the USA. Hum Mol Genet (2011) 1.77
Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease. Gastroenterology (2013) 1.75
Topographic differences in the age-related changes in the retinal nerve fiber layer of normal eyes measured by Stratus optical coherence tomography. J Glaucoma (2011) 1.74
Optic disc morphology in open-angle glaucoma compared with anterior ischemic optic neuropathies. Invest Ophthalmol Vis Sci (2009) 1.71
Comparison of automated analysis of Cirrus HD OCT spectral-domain optical coherence tomography with stereo photographs of the optic disc. Ophthalmology (2011) 1.71
A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study. Am J Hum Genet (2004) 1.71
Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease. Am J Hum Genet (2004) 1.70
Agreement between gonioscopy and ultrasound biomicroscopy in detecting iridotrabecular apposition. Arch Ophthalmol (2007) 1.68
Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration. Hum Mol Genet (2007) 1.67
Combined fluocinolone acetonide intravitreal insertion and glaucoma drainage device placement for chronic uveitis and glaucoma. Am J Ophthalmol (2010) 1.66
Artifacts on the optic nerve head analysis of the optical coherence tomography in glaucomatous and nonglaucomatous eyes. J Glaucoma (2009) 1.65
Iridociliary apposition in plateau iris syndrome persists after cataract extraction. Am J Ophthalmol (2003) 1.65
Demographic and geographic features of exfoliation glaucoma in 2 United States-based prospective cohorts. Ophthalmology (2011) 1.64
Perceived barriers to care and attitudes about vision and eye care: focus groups with older African Americans and eye care providers. Invest Ophthalmol Vis Sci (2006) 1.64
A multicenter, retrospective pilot study of resource use and costs associated with severity of disease in glaucoma. Arch Ophthalmol (2006) 1.64
Intraocular pressure variation during weight lifting. Arch Ophthalmol (2006) 1.64
Assessing the need for posterior sclerotomy at the time of filtering surgery in patients with Sturge-Weber syndrome. Ophthalmology (2003) 1.63
Visual field and intraocular pressure asymmetry in the low-pressure glaucoma treatment study. Ophthalmology (2006) 1.60