Insights into keratoconus from a genetic perspective

Keratoconus in 18 pairs of twins

(2012) Stephen J. Tuft et al.   ACTA OPHTHALMOLOGICA

Review

(2012) Yee Onn Kok et al.   CORNEA

Corneal collagen cross-linking

(2012) Kunal Suri et al.   CURRENT OPINION IN OPHTHALMOLOGY

The point mutation and polymorphism in keratoconus candidate gene TGFBI in Chinese population

(2012) Tao Guan et al.   GENE

Mutation Altering the miR-184 Seed Region Causes Familial Keratoconus with Cataract

(2011) Anne E. Hughes et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Posterior Polymorphous Dystrophy Associated With Nonkeratoconic Steep Corneal Curvatures

(2011) Irving M Raber et al.   CORNEA

A Prospective Study of Filaggrin Null Mutations in Keratoconus Patients with or without Atopic Disorders

(2011) C. Droitcourt et al.   DERMATOLOGY

Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus

(2011) Marta Czugala et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

(2011) Xiaohui Li et al.   HUMAN MOLECULAR GENETICS

Computerized corneal tomography and associated features in a large New Zealand keratoconic population

(2011) Charlotte A. Jordan et al.   JOURNAL OF CATARACT AND REFRACTIVE SURGERY

Evidence for Keratoconus Susceptibility Locus on Chromosome 14

(2010) Petra Liskova   ARCHIVES OF OPHTHALMOLOGY

Unusual Presentation of Presumed Posterior Polymorphous Dystrophy Associated With Iris Heterochromia, Band Keratopathy, and Keratoconus

(2010) Helene Y Lam et al.   CORNEA

Absence of Pathogenic Mutations in VSX1 and SOD1 Genes in Patients With Keratoconus

(2010) Mirna Štabuc-Šilih et al.   CORNEA

Collagen-related genes influence the glaucoma risk factor, central corneal thickness

(2010) Eranga N. Vithana et al.   HUMAN MOLECULAR GENETICS

New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8

(2010) Veronique Vitart et al.   HUMAN MOLECULAR GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in theZEB1gene

(2010) Petra Liskova et al.   OPHTHALMIC GENETICS

Keratoconus associated with Williams–Beuren syndrome: First case reports

(2010) Loic Pinsard et al.   OPHTHALMIC GENETICS

Common Genetic Variants near the Brittle Cornea Syndrome Locus ZNF469 Influence the Blinding Disease Risk Factor Central Corneal Thickness

(2010) Yi Lu et al.   PLoS Genetics

2008 Sir Norman McAlister Gregg Lecture: 150 years of practical observations on the conical cornea - what have we learned?

(2009) Charles NJ McGhee   CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

Three VSX1 Gene Mutations, L159M, R166W, and H244R, Are Not Associated With Keratoconus

(2009) Yongming G Tang et al.   CORNEA

Keratoconus Associated With Other Corneal Dystrophies

(2009) Federico A Cremona et al.   CORNEA

Mutational screening of VSX1 in keratoconus patients from the European population

(2009) D P Dash et al.   EYE

Role of the Hepatocyte Growth Factor Gene in Refractive Error

(2009) Sundar Veerappan et al.   OPHTHALMOLOGY

The Value of Keratometry and Central Corneal Thickness Measurements in the Clinical Diagnosis of Marfan Syndrome

(2008) Martin Heur et al.   AMERICAN JOURNAL OF OPHTHALMOLOGY

Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci

(2008) Kathryn P. Burdon et al.   HUMAN GENETICS

Confocal microscopy identification of keratoconus associated with posterior polymorphous corneal dystrophy

(2008) Cosimo Mazzotta et al.   JOURNAL OF CATARACT AND REFRACTIVE SURGERY

VSX1 gene variants are associated with keratoconus in unrelated Korean patients

(2008) Jee-Won Mok et al.   JOURNAL OF HUMAN GENETICS

The D144E Substitution in theVSX1Gene: A Non-pathogenic Variant or a Disease Causing Mutation?

(2008) Pras Eran et al.   OPHTHALMIC GENETICS