Published in Exp Eye Res on August 18, 2011
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Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry. Invest Ophthalmol Vis Sci (2013) 1.10
Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia. Invest Ophthalmol Vis Sci (2012) 1.06
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M98K-OPTN induces transferrin receptor degradation and RAB12-mediated autophagic death in retinal ganglion cells. Autophagy (2013) 0.96
GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease. PLoS One (2011) 0.94
Gene expression profile in human trabecular meshwork from patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2013) 0.93
Genome-wide association study identifies a novel canine glaucoma locus. PLoS One (2013) 0.91
Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. PLoS Genet (2014) 0.91
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CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States. Am J Ophthalmol (2012) 0.83
TBK1 and flanking genes in human retina. Ophthalmic Genet (2013) 0.82
Low prevalence of myocilin mutations in an African American population with primary open-angle glaucoma. Mol Vis (2012) 0.82
Association study in a South Indian population supports rs1015213 as a risk factor for primary angle closure. Invest Ophthalmol Vis Sci (2013) 0.81
DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2014) 0.80
Copy number variation at chromosome 5q21.2 is associated with intraocular pressure. Invest Ophthalmol Vis Sci (2013) 0.78
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucoma. Mol Vis (2012) 0.78
Single nucleotide polymorphism of MYOC affected the severity of primary open angle glaucoma. Int J Ophthalmol (2013) 0.78
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Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population. PLoS One (2013) 0.78
MTHFR C677T predisposes to POAG but not to PACG in a North Indian population: a case control study. PLoS One (2014) 0.77
Establishment of inducible wild type and mutant myocilin-GFP-expressing RGC5 cell lines. PLoS One (2012) 0.77
Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil. PLoS One (2015) 0.76
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
Development of an Experimental Drug Eluting Suprachoroidal Microstent as Glaucoma Drainage Device. Transl Vis Sci Technol (2015) 0.75
Associations of vitamin D deficiency and vitamin D receptor (Cdx-2, Fok I, Bsm I and Taq I) polymorphisms with the risk of primary open-angle glaucoma. BMC Ophthalmol (2016) 0.75
YBR/EiJ mice: a new model of glaucoma caused by genes on chromosomes 4 and 17. Dis Model Mech (2016) 0.75
Association of Common Variants in eNOS Gene with Primary Open Angle Glaucoma: A Meta-Analysis. J Ophthalmol (2016) 0.75
An updated meta-analysis: apolipoprotein E genotypes and risk of primary open-angle glaucoma. Mol Vis (2014) 0.75
LOXL1-associated candidate epithelial pathomechanisms in exfoliation glaucoma. J Glaucoma (2014) 0.75
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CDKN2B gene rs1063192 polymorphism decreases the risk of glaucoma. Oncotarget (2017) 0.75
Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma. PLoS One (2015) 0.75
Whole exome sequencing identifies multiple diagnoses in congenital glaucoma with systemic anomalies. Clin Genet (2016) 0.75
A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations. Front Cardiovasc Med (2017) 0.75
Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma. Hum Genet (2017) 0.75
Association of Toll-like receptor 4 single-nucleotide polymorphisms Asp299Gly and Thr399Ile with the risk of primary open angle glaucoma. Graefes Arch Clin Exp Ophthalmol (2017) 0.75
Major review: Molecular genetics of primary open-angle glaucoma. Exp Eye Res (2017) 0.75
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet (2009) 12.19
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Identification of a gene that causes primary open angle glaucoma. Science (1997) 8.14
Genome-wide association study identifies five new breast cancer susceptibility loci. Nat Genet (2010) 7.62
Genome-wide association study identifies five susceptibility loci for glioma. Nat Genet (2009) 7.62
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Science (2007) 7.55
Genome structural variation discovery and genotyping. Nat Rev Genet (2011) 7.34
Adult-onset primary open-angle glaucoma caused by mutations in optineurin. Science (2002) 6.53
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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Nat Genet (2010) 5.72
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Mutations of optineurin in amyotrophic lateral sclerosis. Nature (2010) 4.54
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A (2010) 4.30
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
Exome sequencing: the sweet spot before whole genomes. Hum Mol Genet (2010) 3.50
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). Proc Natl Acad Sci U S A (2010) 3.33
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice. Nat Genet (2001) 3.30
Massively parallel sequencing and rare disease. Hum Mol Genet (2010) 3.28
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Hum Mol Genet (1999) 3.24
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Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31. Nat Genet (1993) 3.12
Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis. J Cell Biol (2005) 3.07
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nat Genet (2010) 2.75
A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36. Arch Ophthalmol (1997) 2.64
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Nat Genet (2011) 2.42
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. Proc Natl Acad Sci U S A (2004) 2.41
Modification of ocular defects in mouse developmental glaucoma models by tyrosinase. Science (2003) 2.41
Null mutations in LTBP2 cause primary congenital glaucoma. Am J Hum Genet (2009) 2.35
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Enhanced binding of TBK1 by an optineurin mutant that causes a familial form of primary open angle glaucoma. FEBS Lett (2008) 2.17
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Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. Am J Hum Genet (2002) 2.13
A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region. Hum Mol Genet (1996) 2.06
Optineurin negatively regulates TNFalpha- induced NF-kappaB activation by competing with NEMO for ubiquitinated RIP. Curr Biol (2007) 1.98
Gene mapping for primary open angle glaucoma. Clin Biochem (2005) 1.98
Cellular pharmacology and molecular biology of the trabecular meshwork inducible glucocorticoid response gene product. Ophthalmologica (1997) 1.98
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. Hum Mol Genet (2011) 1.98
Tissue-specific regulation of retinal and pituitary precursor cell proliferation. Science (2002) 1.88
A genome-wide association study of optic disc parameters. PLoS Genet (2010) 1.87
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Pigment dispersion syndrome and pigmentary glaucoma--a major review. Clin Experiment Ophthalmol (2008) 1.81
Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein. Proc Natl Acad Sci U S A (2005) 1.80
Targeted Disruption of the Myocilin Gene (Myoc) Suggests that Human Glaucoma-Causing Mutations Are Gain of Function. Mol Cell Biol (2001) 1.75
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Hum Mol Genet (2011) 1.74
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma. Hum Mol Genet (2009) 1.74
Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma. Am J Hum Genet (2009) 1.71
Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC). Invest Ophthalmol Vis Sci (2004) 1.69
Role of CYP1B1 in glaucoma. Annu Rev Pharmacol Toxicol (2008) 1.69
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Exfoliation syndrome-the most common identifiable cause of open-angle glaucoma. J Glaucoma (1994) 1.64
Common genetic variants associated with open-angle glaucoma. Hum Mol Genet (2011) 1.58
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. Nat Genet (2010) 1.58
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. Nat Genet (2010) 1.57
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genet (2010) 1.55
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Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Hum Mol Genet (2010) 1.53
Collagen-related genes influence the glaucoma risk factor, central corneal thickness. Hum Mol Genet (2010) 1.52
Genetic context determines susceptibility to intraocular pressure elevation in a mouse pigmentary glaucoma. BMC Biol (2006) 1.52
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
Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2006) 1.51
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations. Invest Ophthalmol Vis Sci (2008) 1.51
Anterior segment development relevant to glaucoma. Int J Dev Biol (2004) 1.50
Latent TGF-beta-binding protein 2 binds to DANCE/fibulin-5 and regulates elastic fiber assembly. EMBO J (2007) 1.48
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Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. Mol Vis (2010) 1.45
Transgenic mice expressing the Tyr437His mutant of human myocilin protein develop glaucoma. Invest Ophthalmol Vis Sci (2008) 1.44
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. Hum Mol Genet (2010) 1.41
Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11. Am J Hum Genet (1998) 1.40
By altering ocular immune privilege, bone marrow-derived cells pathogenically contribute to DBA/2J pigmentary glaucoma. J Exp Med (2003) 1.39
Optineurin increases cell survival and translocates to the nucleus in a Rab8-dependent manner upon an apoptotic stimulus. J Biol Chem (2006) 1.39
Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patients. Am J Pathol (2008) 1.38
Myocilin allele-specific glaucoma phenotype database. Hum Mutat (2008) 1.35
Expression of mutated mouse myocilin induces open-angle glaucoma in transgenic mice. J Neurosci (2006) 1.32
Molecular pathology of pseudoexfoliation syndrome/glaucoma--new insights from LOXL1 gene associations. Exp Eye Res (2008) 1.30
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
Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. Ophthalmology (2010) 1.28
Genome-wide scan of exfoliation syndrome. Invest Ophthalmol Vis Sci (2007) 1.26
Glaucoma-associated myocilin: a better understanding but much more to learn. Exp Eye Res (2008) 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
Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene. Invest Ophthalmol Vis Sci (2005) 1.22
Krabbe disease: genetic aspects and progress toward therapy. Mol Genet Metab (2000) 1.22
Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation. Proc Natl Acad Sci U S A (2009) 1.20
Combined loss of INK4a and caveolin-1 synergistically enhances cell proliferation and oncogene-induced tumorigenesis: role of INK4a/CAV-1 in mammary epithelial cell hyperplasia. J Biol Chem (2004) 1.18
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Exfoliation (pseudoexfoliation) syndrome: toward a new understanding. Proceedings of the First International Think Tank. Acta Ophthalmol Scand (2001) 1.15
Ethnicity-based subgroup meta-analysis of the association of LOXL1 polymorphisms with glaucoma. Mol Vis (2010) 1.15
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. Eur J Hum Genet (2010) 1.14
Overexpression of optineurin E50K disrupts Rab8 interaction and leads to a progressive retinal degeneration in mice. Hum Mol Genet (2010) 1.13
Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucoma. Invest Ophthalmol Vis Sci (1998) 1.12
Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort. Mol Vis (2011) 1.11
Mutant myocilin nonsecretion in vivo is not sufficient to cause glaucoma. Mol Cell Biol (2006) 1.11
Latent transforming growth factor-beta-binding protein 2 is an adhesion protein for melanoma cells. J Biol Chem (2003) 1.10
Cerebrospinal fluid pressure is decreased in primary open-angle glaucoma. Ophthalmology (2008) 4.09
Early rapid rise in intraocular pressure after intravitreal triamcinolone acetonide injection. Am J Ophthalmol (2004) 2.46
High failure rate associated with 180 degrees selective laser trabeculoplasty. J Glaucoma (2005) 2.03
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genet (2012) 2.00
Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma. Mol Vis (2008) 1.87
Health literacy and adherence to glaucoma therapy. Am J Ophthalmol (2006) 1.57
Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2006) 1.51
Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations. Invest Ophthalmol Vis Sci (2008) 1.51
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nat Genet (2013) 1.49
Clinical comparison of the Proview eye pressure monitor with the Goldmann applanation tonometer and the Tonopen. Arch Ophthalmol (2004) 1.48
Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population. Mol Vis (2010) 1.45
Intracranial pressure in primary open angle glaucoma, normal tension glaucoma, and ocular hypertension: a case-control study. Invest Ophthalmol Vis Sci (2008) 1.40
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. PLoS One (2011) 1.30
Survey of glaucoma in an eye clinic in Ghana, West Africa. J Glaucoma (2002) 1.26
Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma. Arch Ophthalmol (2003) 1.15
Characterization and prevalence of PITX2 microdeletions and mutations in Axenfeld-Rieger malformations. Invest Ophthalmol Vis Sci (2004) 1.12
Body mass index has a linear relationship with cerebrospinal fluid pressure. Invest Ophthalmol Vis Sci (2012) 1.11
Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry. Invest Ophthalmol Vis Sci (2013) 1.10
Analysis of LOXL1 polymorphisms in a Saudi Arabian population with pseudoexfoliation glaucoma. Mol Vis (2010) 1.09
Intracranial pressure and glaucoma. Curr Opin Ophthalmol (2010) 1.08
No evidence of association of heterozygous NTF4 mutations in patients with primary open-angle glaucoma. Am J Hum Genet (2010) 1.08
Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation. Mol Vis (2011) 1.07
Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia. Invest Ophthalmol Vis Sci (2012) 1.06
Confirmation of TBK1 duplication in normal tension glaucoma. Exp Eye Res (2012) 1.06
Aqueous humor in primary open-angle glaucoma contains an increased level of CD44S. Invest Ophthalmol Vis Sci (2002) 1.05
Novel software strategy for glaucoma diagnosis: asymmetry analysis of retinal thickness. Arch Ophthalmol (2011) 1.00
Ankyrin-B syndrome: enhanced cardiac function balanced by risk of cardiac death and premature senescence. PLoS One (2007) 1.00
No association between OPA1 polymorphisms and primary open-angle glaucoma in three different populations. Mol Vis (2007) 0.98
Genome-wide association study and meta-analysis of intraocular pressure. Hum Genet (2013) 0.98
The Genetics of Keratoconus: A Review. Reprod Syst Sex Disord (2012) 0.96
Cerebrospinal fluid pressure decreases with older age. PLoS One (2012) 0.95
GALC deletions increase the risk of primary open-angle glaucoma: the role of Mendelian variants in complex disease. PLoS One (2011) 0.94
Dorsomedial/Perifornical hypothalamic stimulation increases intraocular pressure, intracranial pressure, and the translaminar pressure gradient. Invest Ophthalmol Vis Sci (2012) 0.94
Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Hum Genet (2014) 0.93
The influence of health literacy level on an educational intervention to improve glaucoma medication adherence. Patient Educ Couns (2011) 0.93
Gene expression profile in human trabecular meshwork from patients with primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2013) 0.93
Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States. Mol Vis (2013) 0.90
Serial analysis of gene expression (SAGE) in normal human trabecular meshwork. Mol Vis (2011) 0.90
Surgical management of hypotony owing to overfiltration in eyes receiving glaucoma drainage devices. J Glaucoma (2009) 0.89
Correlation among retinal thickness, optic disc, and visual field in glaucoma patients and suspects: a pilot study. J Glaucoma (2003) 0.88
Patient and family attitudes about an eye donation registry for research. Curr Eye Res (2013) 0.88
Genome-wide linkage scan for primary open angle glaucoma: influences of ancestry and age at diagnosis. PLoS One (2011) 0.88
Optineurin coding variants in Ghanaian patients with primary open-angle glaucoma. Mol Vis (2008) 0.88
Myocilin mutations in black South Africans with POAG. Mol Vis (2011) 0.88
Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds. Mol Vis (2007) 0.88
Hypophosphorylation of aqueous humor sCD44 and primary open-angle glaucoma. Invest Ophthalmol Vis Sci (2005) 0.87
Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene. Mol Vis (2006) 0.86
Aqueous humor sCD44 concentration and visual field loss in primary open-angle glaucoma. J Glaucoma (2007) 0.86
AQP1 and SLC4A10 as candidate genes for primary open-angle glaucoma. Mol Vis (2010) 0.85
Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG. J Hum Genet (2010) 0.85
The dawn of genetic testing for glaucoma. Curr Opin Ophthalmol (2004) 0.84
Association between chromosome 2p16.3 variants and glaucoma in populations of African descent. Proc Natl Acad Sci U S A (2010) 0.84
A genome-wide association study of central corneal thickness in Latinos. Invest Ophthalmol Vis Sci (2013) 0.84
Lack of association between LOXL1 gene polymorphisms and primary open angle glaucoma in the Saudi Arabian population. Ophthalmic Genet (2011) 0.83
Pigment epithelium-derived factor decreases outflow facility. Invest Ophthalmol Vis Sci (2013) 0.83
CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States. Am J Ophthalmol (2012) 0.83
The role of cerebrospinal fluid pressure in glaucoma and other ophthalmic diseases: A review. Saudi J Ophthalmol (2013) 0.83
Low prevalence of myocilin mutations in an African American population with primary open-angle glaucoma. Mol Vis (2012) 0.82
Expanded polytetrafluoroethylene membrane alters tissue response to implanted Ahmed glaucoma valve. Curr Eye Res (2009) 0.80
Mitochondrial genetic background in Ghanaian patients with primary open-angle glaucoma. Mol Vis (2012) 0.80
Review: The role of LOXL1 in exfoliation syndrome/glaucoma. Saudi J Ophthalmol (2011) 0.80
Systemic diseases associated with exfoliation syndrome. Int Ophthalmol Clin (2014) 0.79
Cerebrospinal fluid pressure and glaucomatous optic disc cupping. Graefes Arch Clin Exp Ophthalmol (2009) 0.79
Cerebrospinal fluid pressure may play a role in reversal of cupping after glaucoma surgery. Am J Ophthalmol (2009) 0.78
Glaucoma patients' trust in the physician. J Ophthalmol (2009) 0.78
Body mass, spinal fluid, and glaucoma. Ophthalmology (2011) 0.78
Mathematical Modeling of Outflow Facility Increase With Trabecular Meshwork Bypass and Schlemm Canal Dilation. J Glaucoma (2016) 0.78
Glaucoma in Ghana, West Africa: clinical features and the role of mutations in Myocilin. Ophthalmol Clin North Am (2003) 0.78
The role of lysyl oxidase-like 1 DNA copy number variants in exfoliation glaucoma. Mol Vis (2012) 0.78
Evaluation of the beta2-adrenergic receptor gene as a candidate glaucoma gene in 2 ancestral populations. Arch Ophthalmol (2007) 0.77
Increasing intraocular pressure as treatment for papilledema. Exp Eye Res (2013) 0.77
Clinical experience with a novel glaucoma drainage implant. J Glaucoma (2014) 0.76
Genetics of exfoliation syndrome and glaucoma. Int Ophthalmol Clin (2014) 0.76
A prospective study of early intraocular pressure changes after a single intravitreal triamcinolone injection. J Glaucoma (2008) 0.76
In vitro fluid dynamics of the Ahmed glaucoma valve modified with expanded polytetrafluoroethylene. Curr Eye Res (2011) 0.75
Disc swelling and space flight. Ophthalmology (2012) 0.75
Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause (2016) 0.75
Using the arteriolar Pressure Attenuation Index to predict ocular hypertension progression to open-angle glaucoma. Arch Ophthalmol (2003) 0.75
Stromal duplication of the iris. JAMA Ophthalmol (2013) 0.75
A newer technique for glaucoma tube trimming. Arch Ophthalmol (2003) 0.75
Clinical course and origin of epithelium in cases of epithelial downgrowth after Descemet stripping automated endothelial keratoplasty. Cornea (2014) 0.75
Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nat Genet (2015) 0.75
DYNAMIC CHANGES OF THE ANTERIOR CHAMBER ANGLE PRODUCED BY INTRAVITREAL ANTI-VASCULAR GROWTH FACTOR INJECTIONS. Retina (2016) 0.75
Simultaneous bilateral angle closure glaucoma in a patient with giant cell arteritis. J Glaucoma (2010) 0.75
Developments in Ocular Genetics: Annual Review. Asia Pac J Ophthalmol (Phila) (2015) 0.75