Associated Papers
Prevalence of risk alleles in the lysyl oxidase-like 1 gene in pseudoexfoliation glaucoma patients in India.
Vallabh NA et al.
Indian Journal of Ophthalmology, 2022
LOXL1 gene analysis in Turkish patients with exfoliation glaucoma.
Yilmaz SG et al.
International Ophthalmology, 2016
Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study.
Anastasopoulos E et al.
Investigative Ophthalmology & Visual Science, 2014
Evaluation of lysyl oxidase-like 1 gene polymorphisms in pseudoexfoliation syndrome in a Korean population.
Park DY et al.
Molecular Vision, 2013
Development of novel LOXL1 genotyping method and evaluation of LOXL1, APOE and MTHFR polymorphisms in exfoliation syndrome/glaucoma in a Greek population.
Chiras D et al.
Molecular Vision, 2013
Association of lysyl oxidase-like 1 gene common sequence variants in Greek patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.
Metaxaki I et al.
Molecular Vision, 2013
Analysis of LOXL1 single nucleotide polymorphisms in Polish population with pseudoexfoliation syndrome.
Malukiewicz G et al.
Acta Ophthalmologica, 2011
Analysis of LOXL1 polymorphisms in a Saudi Arabian population with pseudoexfoliation glaucoma.
Abu-Amero KK et al.
Molecular Vision, 2010
LOXL1 genetic polymorphisms are associated with exfoliation glaucoma in the Japanese population.
Mori K et al.
Molecular Vision, 2008
LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States.
Fingert JH et al.
American Journal of Ophthalmology, 2007
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