Keratoconus in 18 pairs of twins

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

A twin approach to unraveling epigenetics

(2011) Jordana T. Bell et al.   TRENDS IN GENETICS

Evidence for Keratoconus Susceptibility Locus on Chromosome 14

(2010) Petra Liskova   ARCHIVES OF OPHTHALMOLOGY

Intrastromal corneal ring segments to correct low myopia in eyes with irregular or abnormal topography including forme fruste keratoconus: 4-year follow-up

(2010) José L. Güell et al.   JOURNAL OF CATARACT AND REFRACTIVE SURGERY

Non-identical monozygotic twins, intermediate twin types, zygosity testing, and the non-random nature of monozygotic twinning: A review

(2009) Geoffrey Machin   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Prevalence of Orbscan II corneal abnormalities in relatives of patients with keratoconus

(2009) Timothy M Steele et al.   CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

Longitudinal analysis of corneal topography in suspected keratoconus

(2008) M Shirayama-Suzuki et al.   BRITISH 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