Published in Invest Ophthalmol Vis Sci on March 10, 2011
Quantitative mapping of collagen fiber orientation in non-glaucoma and glaucoma posterior human sclerae. Invest Ophthalmol Vis Sci (2012) 1.56
Comparison of Patient-Specific Computational Modeling Predictions and Clinical Outcomes of LASIK for Myopia. Invest Ophthalmol Vis Sci (2016) 0.76
A Large-Scale Computational Analysis of Corneal Structural Response and Ectasia Risk in Myopic Laser Refractive Surgery. Trans Am Ophthalmol Soc (2016) 0.75
An x-ray scattering study into the structural basis of corneal refractive function in an avian model. Biophys J (2013) 0.75
The structure and transparency of the cornea. J Physiol (1957) 4.58
Influence of corneal biomechanical properties on intraocular pressure measurement: quantitative analysis. J Cataract Refract Surg (2005) 3.69
The specific architecture of the anterior stroma accounts for maintenance of corneal curvature. Br J Ophthalmol (2001) 3.06
Morphogenesis of the collagenous stroma in the chick cornea. J Cell Biol (1971) 1.83
Fine structure of the developing avian cornea. Monogr Dev Biol (1969) 1.66
Three-dimensional modeling and computational analysis of the human cornea considering distributed collagen fibril orientations. J Biomech Eng (2008) 1.63
Assessment of corneal biomechanical properties and their variation with age. Curr Eye Res (2007) 1.61
Computational modeling of mechanical anisotropy in the cornea and sclera. J Cataract Refract Surg (2005) 1.46
Regional elastic performance of the human cornea. J Biomech (1996) 1.44
Full-field deformation of bovine cornea under constrained inflation conditions. Biomaterials (2008) 1.39
Lamellar orientation in human cornea in relation to mechanical properties. J Struct Biol (2005) 1.32
A comparison of biomechanical properties between human and porcine cornea. J Biomech (2001) 1.22
Application of structural analysis to the mechanical behaviour of the cornea. J R Soc Interface (2004) 1.18
Constitutive laws for biomechanical modeling of refractive surgery. J Biomech Eng (1996) 1.17
A nonlinear anisotropic viscoelastic model for the tensile behavior of the corneal stroma. J Biomech Eng (2008) 1.15
Effects of altered corneal stiffness on native and postoperative LASIK corneal biomechanical behavior: A whole-eye finite element analysis. J Refract Surg (2009) 1.13
Biomechanical properties of human and porcine corneas. Exp Eye Res (2008) 1.12
The architecture of the corneal stroma. Br J Ophthalmol (2001) 1.10
The effect of posture on intraocular pressure and pulsatile ocular blood flow in normal and glaucomatous eyes. Surv Ophthalmol (1994) 1.10
Morphogenesis of rabbit corneal stroma. Invest Ophthalmol Vis Sci (1983) 1.07
Collagen and mature elastic fibre organisation as a function of depth in the human cornea and limbus. J Struct Biol (2009) 1.06
Biomechanical characteristics of the ectatic cornea. J Cataract Refract Surg (2008) 1.05
Role of preconditioning and recovery time in repeated testing of aortic valve tissues: validation through quasilinear viscoelastic theory. Ann Biomed Eng (2000) 1.04
Interlamellar adhesive strength in human eyebank corneas. Invest Ophthalmol Vis Sci (1990) 1.00
Biomechanical analysis of the keratoconic cornea. J Mech Behav Biomed Mater (2008) 0.99
A model for the human cornea: constitutive formulation and numerical analysis. Biomech Model Mechanobiol (2006) 0.97
The distribution of strain in the human cornea. J Biomech (1997) 0.96
Modelling the elastic properties of the anterior eye and their contribution to maintenance of image quality: the role of the limbus. Eye (Lond) (2006) 0.94
Ultrastructural changes in the retinopathy, globe enlarged (rge) chick cornea. J Struct Biol (2009) 0.94
Clinical features of the retinopathy, globe enlarged (rge) chick phenotype. Vision Res (2003) 0.92
The mechanism of corneal accommodation in chicks. Vision Res (1994) 0.92
Mutation in the guanine nucleotide-binding protein beta-3 causes retinal degeneration and embryonic mortality in chickens. Invest Ophthalmol Vis Sci (2006) 0.89
Genetic, ophthalmic, morphometric and histopathological analysis of the Retinopathy Globe Enlarged (rge) chicken. Mol Vis (2003) 0.89
Collagen organization in the chicken cornea and structural alterations in the retinopathy, globe enlarged (rge) phenotype--an X-ray diffraction study. J Struct Biol (2007) 0.87
Mechanical anisotropy of porcine cornea and correlation with stromal microstructure. Exp Eye Res (2009) 0.87
Detection of corneal fibrosis by imaging second harmonic-generated signals in rabbit corneas treated with mitomycin C after excimer laser surface ablation. Invest Ophthalmol Vis Sci (2008) 0.85
Finite element simulation of arcuates for astigmatism correction. J Biomech (2008) 0.84
Impaired vision in chickens associated with retinal defects. Vet Rec (1987) 0.83
An inherited retinopathy in commercial breeding chickens. Avian Pathol (1988) 0.82
Architecture of the corneal stroma of the hen. Acta Anat (Basel) (1984) 0.81
Numerical study of the effect of corneal layered structure on ocular biomechanics. Curr Eye Res (2009) 0.81
Optically inspired biomechanical model of the human eyeball. J Biomed Opt (2008) 0.79
Effect of material properties of the eyeball coat on optical image stability. J Biomed Opt (2008) 0.78
The anisotropic material constitutive models for the human cornea. J Struct Biol (2006) 0.78
Measurement of intraocular pressure (IOP) in chickens using a rebound tonometer: quantitative evaluation of variance due to position inaccuracies. Exp Eye Res (2007) 0.77
Comparative rheology of cornea. Comp Biochem Physiol A Comp Physiol (1976) 0.76
Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial. Lancet (2005) 12.98
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus. Nat Genet (2006) 6.15
Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet (2009) 5.84
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. Nat Genet (2006) 5.26
A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms. Nature (2004) 5.24
Quantification of homozygosity in consanguineous individuals with autosomal recessive disease. Am J Hum Genet (2006) 3.52
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nat Genet (2009) 3.36
Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. Am J Hum Genet (2004) 2.70
Effect of complete epithelial debridement before riboflavin-ultraviolet-A corneal collagen crosslinking therapy. J Cataract Refract Surg (2008) 2.66
Null mutations in LTBP2 cause primary congenital glaucoma. Am J Hum Genet (2009) 2.35
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
X-ray scattering used to map the preferred collagen orientation in the human cornea and limbus. Structure (2004) 2.18
Breast-cancer screening with trained volunteers in a rural area of Sudan: a pilot study. Lancet Oncol (2013) 2.16
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis. Nat Genet (2007) 2.16
Elevated breast cancer mortality in women younger than age 40 years compared with older women is attributed to poorer survival in early-stage disease. J Am Coll Surg (2009) 2.14
Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions. BMC Biotechnol (2003) 2.05
Corneal thickness- and age-related biomechanical properties of the cornea measured with the ocular response analyzer. Invest Ophthalmol Vis Sci (2006) 1.97
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. Nat Genet (2012) 1.96
Development of a high density 600K SNP genotyping array for chicken. BMC Genomics (2013) 1.68
Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta. Am J Hum Genet (2009) 1.65
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. Am J Hum Genet (2009) 1.58
Quantitative mapping of collagen fiber orientation in non-glaucoma and glaucoma posterior human sclerae. Invest Ophthalmol Vis Sci (2012) 1.56
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism. Am J Hum Genet (2013) 1.53
Simultaneous mapping of epistatic QTL in chickens reveals clusters of QTL pairs with similar genetic effects on growth. Genet Res (2004) 1.52
Collagen fibrils appear more closely packed in the prepupillary cornea: optical and biomechanical implications. Invest Ophthalmol Vis Sci (2003) 1.38
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy. Am J Hum Genet (2010) 1.38
3D collagen orientation study of the human cornea using X-ray diffraction and femtosecond laser technology. Invest Ophthalmol Vis Sci (2009) 1.36
CFH, VEGF and HTRA1 promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration. Br J Ophthalmol (2011) 1.33
Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta. Am J Hum Genet (2013) 1.33
Lamellar orientation in human cornea in relation to mechanical properties. J Struct Biol (2005) 1.32
prp8 mutations that cause human retinitis pigmentosa lead to a U5 snRNP maturation defect in yeast. Nat Struct Mol Biol (2007) 1.32
Mapping collagen organization in the human cornea: left and right eyes are structurally distinct. Invest Ophthalmol Vis Sci (2006) 1.29
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. Am J Hum Genet (2012) 1.24
Effect of epithelial retention and removal on riboflavin absorption in porcine corneas. J Refract Surg (2009) 1.21
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy. Invest Ophthalmol Vis Sci (2009) 1.21
Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36. Eur J Hum Genet (2003) 1.21
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa. Eur J Hum Genet (2002) 1.20
Autosomal dominant optic atrophy: penetrance and expressivity in patients with OPA1 mutations. Am J Ophthalmol (2007) 1.19
Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy. Invest Ophthalmol Vis Sci (2004) 1.19
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice. Am J Hum Genet (2009) 1.16
Ectasia Detection by the Assessment of Corneal Biomechanics. Cornea (2016) 1.15
PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor. Exp Cell Res (2004) 1.15
ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature. Proc Natl Acad Sci U S A (2013) 1.08
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma. Am J Hum Genet (2011) 1.08
The effect of riboflavin/UVA collagen cross-linking therapy on the structure and hydrodynamic behaviour of the ungulate and rabbit corneal stroma. PLoS One (2013) 1.07
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR). Invest Ophthalmol Vis Sci (2012) 1.07
Collagen and mature elastic fibre organisation as a function of depth in the human cornea and limbus. J Struct Biol (2009) 1.06
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene. Invest Ophthalmol Vis Sci (2013) 1.06
Comparative study of fibrillar collagen arrangement in the corneas of primates and other mammals. Anat Rec (Hoboken) (2007) 1.04
Genotype-phenotype correlation for leber congenital amaurosis in Northern Pakistan. Arch Ophthalmol (2010) 1.04
Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma. Mol Vis (2010) 1.03
A study of corneal thickness, shape and collagen organisation in keratoconus using videokeratography and X-ray scattering techniques. Exp Eye Res (2006) 1.02
Characterization of age-related variation in corneal biomechanical properties. J R Soc Interface (2010) 1.02
Matrix morphogenesis in cornea is mediated by the modification of keratan sulfate by GlcNAc 6-O-sulfotransferase. Proc Natl Acad Sci U S A (2006) 1.02
Ultrastructural analysis of collagen fibrils and proteoglycans in keratoconus. Acta Ophthalmol (2008) 1.02
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta. Hum Mol Genet (2013) 1.01
Selective breeding for susceptibility to myopia reveals a gene-environment interaction. Invest Ophthalmol Vis Sci (2011) 1.00
Structural interactions between collagen and proteoglycans are elucidated by three-dimensional electron tomography of bovine cornea. Structure (2010) 1.00
Corneal biomechanical characteristics in patients with diabetes mellitus. J Cataract Refract Surg (2010) 0.97
Ultraviolet light transmission through the human corneal stroma is reduced in the periphery. Biophys J (2012) 0.97
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate. Eur J Hum Genet (2002) 0.97
Quantitative assessment of ultrastructure and light scatter in mouse corneal debridement wounds. Invest Ophthalmol Vis Sci (2012) 0.96
Detailed histopathologic characterization of the retinopathy, globe enlarged (rge) chick phenotype. Mol Vis (2005) 0.96
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration. Mol Vis (2008) 0.95
Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis. Mol Vis (2008) 0.94
Ultrastructural changes in the retinopathy, globe enlarged (rge) chick cornea. J Struct Biol (2009) 0.94
Organization of corneal collagen fibrils during the healing of trephined wounds in rabbits. Wound Repair Regen (2003) 0.94
Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degeneration. Invest Ophthalmol Vis Sci (2011) 0.94
Common determinants of body size and eye size in chickens from an advanced intercross line. Exp Eye Res (2009) 0.94
Light transmission in the human cornea as a function of position across the ocular surface: theoretical and experimental aspects. Biophys J (2008) 0.94
Riboflavin/UVA collagen cross-linking-induced changes in normal and keratoconus corneal stroma. PLoS One (2011) 0.93
Collagen ultrastructural changes during stromal wound healing in organ cultured bovine corneas. Exp Eye Res (2008) 0.92
Adhesion of laser in situ keratomileusis-like flaps in the cornea: Effects of crosslinking, stromal fibroblasts, and cytokine treatment. J Cataract Refract Surg (2011) 0.92
Analysis of Fcgamma receptor haplotypes in rheumatoid arthritis: FCGR3A remains a major susceptibility gene at this locus, with an additional contribution from FCGR3B. Arthritis Res Ther (2006) 0.91
The biomechanics of amnion rupture: an X-ray diffraction study. PLoS One (2007) 0.91
Age-related variations in the biomechanical properties of human sclera. J Mech Behav Biomed Mater (2012) 0.90
Replication of the recessive STBMS1 locus but with dominant inheritance. Invest Ophthalmol Vis Sci (2009) 0.90
Evaluation of transepithelial stromal riboflavin absorption with enhanced riboflavin solution using spectrophotometry. J Cataract Refract Surg (2012) 0.90