Published in Invest Ophthalmol Vis Sci on January 25, 2012
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Screening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia. Biomed Res Int (2015) 0.78
Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis. Mol Syndromol (2017) 0.76
MicroRNA-184 Regulates Corneal Lymphangiogenesis. Invest Ophthalmol Vis Sci (2015) 0.76
Independent origin of c.57 C > T mutation in MIR184 associated with inherited corneal and lens abnormalities. Ophthalmic Genet (2014) 0.76
microRNAs and inherited retinal dystrophies. Proc Natl Acad Sci U S A (2015) 0.76
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Screening for MIR184 Mutations in Iranian Patients with Keratoconus. J Ophthalmic Vis Res (2016) 0.75
Genomic strategies to understand causes of keratoconus. Mol Genet Genomics (2016) 0.75
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MicroRNAs of the mammalian eye display distinct and overlapping tissue specificity. Mol Vis (2006) 2.68
Identification and functional characterization of microRNAs involved in the malignant progression of gliomas. Brain Pathol (2009) 2.67
Mutation altering the miR-184 seed region causes familial keratoconus with cataract. Am J Hum Genet (2011) 2.33
MicroRNA-184 antagonizes microRNA-205 to maintain SHIP2 levels in epithelia. Proc Natl Acad Sci U S A (2008) 2.25
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells. Am J Hum Genet (2005) 2.20
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. Am J Hum Genet (2009) 2.14
Identification and characterization of microRNAs expressed in the mouse eye. Invest Ophthalmol Vis Sci (2007) 2.05
Structural features of microRNA (miRNA) precursors and their relevance to miRNA biogenesis and small interfering RNA/short hairpin RNA design. J Biol Chem (2004) 2.01
MicroRNAs regulate ocular neovascularization. Mol Ther (2008) 1.89
MicroRNA-184 inhibits neuroblastoma cell survival through targeting the serine/threonine kinase AKT2. Mol Cancer (2010) 1.72
Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes. Invest Ophthalmol Vis Sci (2003) 1.65
Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1-q25.3. Am J Ophthalmol (2002) 1.56
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy. Invest Ophthalmol Vis Sci (2008) 1.52
Familial congenital cornea guttata with anterior polar cataracts. Am J Ophthalmol (1989) 1.50
MicroRNAs in early diabetic retinopathy in streptozotocin-induced diabetic rats. Invest Ophthalmol Vis Sci (2011) 1.39
Serial analysis of gene expression in the corneal endothelium of Fuchs' dystrophy. Invest Ophthalmol Vis Sci (2003) 1.36
Fine mapping of the keratoconus with cataract locus on chromosome 15q and candidate gene analysis. Mol Vis (2006) 1.13
Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis. Ophthalmology (2002) 1.00
Targeted deletion of Dicer disrupts lens morphogenesis, corneal epithelium stratification, and whole eye development. Dev Dyn (2009) 0.98
MiRNA expression in the eye. Mamm Genome (2008) 0.97
Major progress in Fuchs's corneal dystrophy. N Engl J Med (2010) 0.83
Cataract surgery in patients with Fuchs' corneal dystrophy: expanding recommendations for cataract surgery without simultaneous keratoplasty. Ophthalmology (2005) 4.35
Null mutations in LTBP2 cause primary congenital glaucoma. Am J Hum Genet (2009) 2.35
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p. Am J Hum Genet (2009) 2.14
Presoaking donor corneas reduces graft detachment rates in descemet stripping endothelial keratoplasty. Am J Ophthalmol (2008) 2.11
Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13pTel-13q12.13. Invest Ophthalmol Vis Sci (2006) 1.90
A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32. Invest Ophthalmol Vis Sci (2006) 1.81
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nat Genet (2008) 1.78
Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family. Mol Vis (2010) 1.75
Taking TASS to task. Ophthalmology (2012) 1.63
Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1-q25.3. Am J Ophthalmol (2002) 1.56
Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophy. Hum Mutat (2010) 1.54
Linkage of a mild late-onset phenotype of Fuchs corneal dystrophy to a novel locus at 5q33.1-q35.2. Invest Ophthalmol Vis Sci (2009) 1.52
Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy. Am J Hum Genet (2012) 1.49
Replication of the TCF4 intronic variant in late-onset Fuchs corneal dystrophy and evidence of independence from the FCD2 locus. Invest Ophthalmol Vis Sci (2011) 1.39
Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene. Hum Genet (2007) 1.36
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. PLoS One (2011) 1.30
A new locus for autosomal recessive congenital cataract identified in a Pakistani family. Mol Vis (2010) 1.30
Surgical management of anterior chamber epithelial cysts. Am J Ophthalmol (2003) 1.30
Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p. Mol Vis (2007) 1.27
Combined phacoemulsification, intraocular lens implantation, and vitrectomy for eyes with coexisting cataract and vitreoretinal pathology. Am J Ophthalmol (2003) 1.26
Mutations in FYCO1 cause autosomal-recessive congenital cataracts. Am J Hum Genet (2011) 1.26
Prevalence and severity of fuchs corneal dystrophy in Tangier Island. Am J Ophthalmol (2012) 1.19
Progression of Fuchs corneal dystrophy in a family linked to the FCD1 locus. Invest Ophthalmol Vis Sci (2009) 1.16
Immunohistochemistry and electron microscopy of early-onset fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation. Trans Am Ophthalmol Soc (2006) 1.12
Age-severity relationships in families linked to FCD2 with retroillumination photography. Invest Ophthalmol Vis Sci (2010) 1.09
Mutations in AGBL1 cause dominant late-onset Fuchs corneal dystrophy and alter protein-protein interaction with TCF4. Am J Hum Genet (2013) 1.08
A randomized trial of topical cyclosporin 0.05% in topical steroid-resistant atopic keratoconjunctivitis. Ophthalmology (2004) 1.05
Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes. Invest Ophthalmol Vis Sci (2011) 1.05
A morphologic study of Fuchs dystrophy and bullous keratopathy. Cornea (2005) 1.04
GNAT1 associated with autosomal recessive congenital stationary night blindness. Invest Ophthalmol Vis Sci (2012) 1.03
Treatment with voriconazole in 3 eyes with resistant Acanthamoeba keratitis. Am J Ophthalmol (2009) 1.02
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family. Br J Ophthalmol (2010) 1.00
Clinical and ultrastructural features of a novel hereditary anterior segment dysgenesis. Ophthalmology (2002) 1.00
Surgical approaches to the management of epithelial cysts. Trans Am Ophthalmol Soc (2002) 1.00
Fuchs' corneal dystrophy. Expert Rev Ophthalmol (2010) 0.97
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3. Hum Genet (2007) 0.97
A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa. Am J Hum Genet (2010) 0.95
Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa. Mol Vis (2011) 0.94
Spatial expression patterns of autophagy genes in the eye lens and induction of autophagy in lens cells. Mol Vis (2012) 0.94
The genetics of Fuchs' corneal dystrophy. Expert Rev Ophthalmol (2012) 0.93
Light-induced oxidative stress in choroidal endothelial cells in mice. Invest Ophthalmol Vis Sci (2005) 0.93
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1. Mol Vis (2010) 0.93
Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation. Mol Vis (2004) 0.92
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4. Hum Genet (2005) 0.91
Primary congenital glaucoma localizes to chromosome 14q24.2-24.3 in two consanguineous Pakistani families. Mol Vis (2008) 0.90
Secondary angle closure caused by air migrating behind the pupil in descemet stripping endothelial keratoplasty. Cornea (2009) 0.89
Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma. Mol Vis (2008) 0.89
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families. Br J Ophthalmol (2011) 0.89
Allele frequency distribution of 13 X-chromosomal STR loci in Pakistani population. Int J Legal Med (2008) 0.89
Documenting the corneal phenotype associated with the MIR184 c.57C>T mutation. Am J Hum Genet (2012) 0.88
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3. Hum Genet (2006) 0.88
Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p. Mol Vis (2010) 0.88
Cataract surgery in Fuchs corneal dystrophy. Curr Opin Ophthalmol (2010) 0.87
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q. Mol Vis (2010) 0.86
Retroillumination Photography Analysis Enhances Clinical Definition of Severe Fuchs Corneal Dystrophy. Cornea (2015) 0.86
CTG18.1 Expansion in TCF4 Increases Likelihood of Transplantation in Fuchs Corneal Dystrophy. Cornea (2017) 0.85
A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p. Am J Ophthalmol (2010) 0.85
Identification of paramyosin as a binding protein for calgranulin C in experimental helminthic keratitis. Invest Ophthalmol Vis Sci (2002) 0.84
A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene. Mol Vis (2005) 0.84
Ectopia lentis in a consanguineous pakistani family and a novel locus on chromosome 8q. Arch Ophthalmol (2010) 0.84
Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani families. Arch Ophthalmol (2011) 0.84
Haplotype analysis of two X-chromosome STR clusters in the Pakistani population. Int J Legal Med (2008) 0.81
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population. J Hum Genet (2012) 0.80
Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss. Hum Genet (2015) 0.78
Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy. Mol Vis (2013) 0.76
Automated Retroillumination Photography Analysis for Objective Assessment of Fuchs Corneal Dystrophy. Cornea (2017) 0.75
Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. PLoS One (2017) 0.75
Correction: Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts. PLoS One (2017) 0.75
Distinct Clinical Phenotype of Corneal Dystrophy Predicts the p.(Leu450Trp) Substitution in COL8A2. Cornea (2016) 0.75