Associated Papers
Genetics of Keratoconus: A Comprehensive Review.
Barcelo-Canton RH et al.
Genes, 2025
The association between VSX1 exon3 gene variants and keratoconus in Malaysian patients.
Deva JP et al.
Indian Journal of Ophthalmology, 2023
A very early diagnosis of Alstrӧm syndrome by next generation sequencing.
Gatticchi L et al.
Bmc Medical Genetics, 2020
Genetic associations for keratoconus: a systematic review and meta-analysis.
Rong SS et al.
Scientific Reports, 2017
Novel visual system homeobox 1 gene mutations in Turkish patients with keratoconus.
Bardak H et al.
Genetics and Molecular Research : Gmr, 2016
Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.
Karolak JA et al.
Ophthalmic Genetics, 2016
Two novel missense substitutions in the VSX1 gene: clinical and genetic analysis of families with Keratoconus from India.
Shetty R et al.
Bmc Medical Genetics, 2015
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus.
Verma A et al.
Bmc Research Notes, 2013
Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method.
Dehkordi FA et al.
Acta Cytologica, 2013
VSX1 gene and keratoconus: genetic analysis in Korean patients.
Jeoung JW et al.
Cornea, 2012
The Genetics of Keratoconus: A Review.
Wheeler J et al.
Reproductive System & Sexual Disorders : Current Research, 2012
Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus.
Saee-Rad S et al.
Molecular Vision, 2011
Mutational screening of VSX1 in keratoconus patients from the European population.
Dash DP et al.
Eye (london, England), 2010
Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus.
Stabuc-Silih M et al.
Cornea, 2010
Genetics and clinical characteristics of keratoconus.
Stabuc-Silih M et al.
Acta Dermatovenerologica Alpina, Pannonica, Et Adriatica, 2010
VSX1 gene variants are associated with keratoconus in unrelated Korean patients.
Mok JW et al.
Journal of Human Genetics, 2008
Molecular analysis of the VSX1 gene in familial keratoconus.
Liskova P et al.
Molecular Vision, 2007
VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the South of Iran.
Nejabat M et al.
Journal of Ophthalmic & Vision Research, 0