PURPOSE: A classical twin study was performed to establish the relative importance of genes and environment in cortical cataract. METHODS: Five hundred six pairs of unselected female twin volunteers (226 monozygotic and 280 dizygotic) with a mean age of 62 years (range, 49-79 years) were examined. Cortical cataract was assessed using the slit-lamp-based Oxford Clinical Cataract Classification and Grading System (clinical grading) and the Wilmer Automated Grading System, which analyzed digital retroillumination images of subjects' lenses (digital grading). The worse eye categorized score for each individual was used in maximum likelihood path modeling of the correlations within twin pairs. These correlations were used to determine the underl...
PURPOSE: It has been suggested that ring-like patterns of macular pigment, as measured with dual wav...
Nuclear cataract is the most common type of age-related cataract and a leading cause ofblindness wor...
Childhood cataract affects 2.5–3.5 per 10,000 children in the UK, with a genetic mutation identified...
PURPOSE. A classical twin study was performed to establish the relative importance of genes and envi...
Cataract and age-related macular degeneration are important causes of blindness and visual impairmen...
PURPOSE: A classic twin study was performed to determine the heritability of central corneal thickne...
OBJECTIVE: Age-related macular degeneration (AMD) is the most common cause of blindness in industria...
PURPOSE: Several studies have reported higher levels of macular pigment (MP) in association with red...
Abstract We studied the scientific literature and disease guidelines in order to sum...
PURPOSE: A classical twin study was performed to examine the relative importance of genes and enviro...
PURPOSE: To determine the heritability of nuclear cataract progression and to explore prospectively ...
PURPOSE: To estimate heritability of parameters of human retinal electrophysiology and to explore wh...
PURPOSE: The relative importance of genetic factors in common vitreomacular interface (VMI) abnormal...
PURPOSE: To determine the heritability of nuclear cataract progression and to explore prospectively ...
PURPOSE: A classical twin study was performed to determine the heritability of central corneal thick...
PURPOSE: It has been suggested that ring-like patterns of macular pigment, as measured with dual wav...
Nuclear cataract is the most common type of age-related cataract and a leading cause ofblindness wor...
Childhood cataract affects 2.5–3.5 per 10,000 children in the UK, with a genetic mutation identified...
PURPOSE. A classical twin study was performed to establish the relative importance of genes and envi...
Cataract and age-related macular degeneration are important causes of blindness and visual impairmen...
PURPOSE: A classic twin study was performed to determine the heritability of central corneal thickne...
OBJECTIVE: Age-related macular degeneration (AMD) is the most common cause of blindness in industria...
PURPOSE: Several studies have reported higher levels of macular pigment (MP) in association with red...
Abstract We studied the scientific literature and disease guidelines in order to sum...
PURPOSE: A classical twin study was performed to examine the relative importance of genes and enviro...
PURPOSE: To determine the heritability of nuclear cataract progression and to explore prospectively ...
PURPOSE: To estimate heritability of parameters of human retinal electrophysiology and to explore wh...
PURPOSE: The relative importance of genetic factors in common vitreomacular interface (VMI) abnormal...
PURPOSE: To determine the heritability of nuclear cataract progression and to explore prospectively ...
PURPOSE: A classical twin study was performed to determine the heritability of central corneal thick...
PURPOSE: It has been suggested that ring-like patterns of macular pigment, as measured with dual wav...
Nuclear cataract is the most common type of age-related cataract and a leading cause ofblindness wor...
Childhood cataract affects 2.5–3.5 per 10,000 children in the UK, with a genetic mutation identified...