Linkage Mapping of Thiel–Behnke Corneal Dystrophy (CDB2) to Chromosome 10q23–q24

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

Life Sciences, Genetics, Genomics +16

Kerato-epithelin mutations in four 5q31-linked corneal dystrophies

Francis L. Munier, Elena Korvatska, Assia Djemaï et al. · Nature Genetics · 1997 · 610 citations

Medicine, Genetics, Ophthalmology +14

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set–recoding and fuzzy inheritance

Jeffrey R. O’Connell, Daniel E. Weeks · Nature Genetics · 1995 · 504 citations

Life Sciences, Bioinformatics, Genetics +12

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Alan D. Irvine, Laura D. Corden, Ole Swensson et al. · Nature Genetics · 1997 · 257 citations

Medicine, Genetics, Molecular Genetics +15

Linkage of congenital hereditary endothelial dystrophy to chromosome 20

Naoki Toma, Neil D. Ebenezer, Chris F. Inglehearn et al. · Human Molecular Genetics · 1995 · 135 citations

Life Sciences, Genetics, Molecular Genetics +9