Genetics of Keratoconus: Where Do We Stand?

Prevalence and Associated Factors of Keratoconus in Jerusalem: A Cross-sectional Study

(2016) Michel Millodot et al.   OPHTHALMIC EPIDEMIOLOGY

Segregation analysis suggests that keratoconus is a complex non-mendelian disease

(2014) Ágnes Kriszt et al.   ACTA OPHTHALMOLOGICA

Molecular Screening of Keratoconus Susceptibility Sequence Variants inVSX1, TGFBI, DOCK9, STK24, andIPO5Genes in Polish Patients and NovelTGFBIVariant Identification

(2014) Justyna A. Karolak et al.   OPHTHALMIC GENETICS

Impaired Corneal Biomechanical Properties and the Prevalence of Keratoconus in Mitral Valve Prolapse

(2014) Emine Kalkan Akcay et al.   Journal of Ophthalmology

Keratoconus in Costello Syndrome

(2013) Karen W. Gripp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Insights into keratoconus from a genetic perspective

(2013) Kathryn P Burdon et al.   Clinical and Experimental Optometry

An Association Between the Calpastatin (CAST) Gene and Keratoconus

(2013) Xiaohui Li et al.   CORNEA

Keratoplasty in Patients With Intellectual Disability

(2013) Barbara Koller et al.   CORNEA

The pathogenesis of keratoconus

(2013) A E Davidson et al.   EYE

Oxidative Stress in the Pathogenesis of Keratoconus and Fuchs Endothelial Corneal Dystrophy

(2013) Katarzyna Wojcik et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

(2013) Yi Lu et al.   NATURE GENETICS

Common Single Nucleotide Polymorphisms and Keratoconus in the Han Chinese Population

(2013) Yani Wang et al.   OPHTHALMIC GENETICS

Is Consanguinity a Risk Factor for Keratoconus?

(2013) Ariela Gordon-Shaag et al.   OPTOMETRY AND VISION SCIENCE

Keratoconus in 18 pairs of twins

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

Documenting the Corneal Phenotype Associated with the MIR184 c.57C>T Mutation

(2012) Benjamin W. Iliff et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Model animals for the study of oxidative stress from complex II

(2012) Takamasa Ishii et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Epidemiology of Keratoconus in an Iranian Population

(2012) Hossein Ziaei et al.   CORNEA

Changes in lysyl oxidase (LOX) distribution and its decreased activity in keratoconus corneas

(2012) Lubica Dudakova et al.   EXPERIMENTAL EYE RESEARCH

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

(2012) Tao Guan et al.   GENE

A New Case of Keratoconus Associated with Williams-Beuren Syndrome

(2012) Melissa Machado Viana et al.   OPHTHALMIC GENETICS

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

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

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

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

(2011) Marianne Rohrbach et al.   Orphanet Journal of Rare Diseases

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

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

(2010) Petra Liskova et al.   OPHTHALMIC GENETICS

Prevalence and Associations of Keratoconus in Rural Maharashtra in Central India: The Central India Eye and Medical Study

(2009) Jost B. Jonas et al.   AMERICAN JOURNAL OF OPHTHALMOLOGY

Collagen cross-linkage: a comprehensive review and directions for future research

(2009) P. T. Ashwin et al.   BRITISH JOURNAL OF 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

Deleterious Mutations in the Zinc-Finger 469 Gene Cause Brittle Cornea Syndrome

(2008) Almogit Abu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Keratoconus Clinical Findings According to Different Age and Gender Groups

(2008) Aylin Ertan et al.   CORNEA

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

VSX1 gene variants are associated with keratoconus in unrelated Korean patients

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

Genetic Mapping in Human Disease

(2008) D. Altshuler et al.   SCIENCE