C.F. Inglehearn

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

John A. Wells, John J. Wroblewski, Jeffrey Keen et al. · Nature Genetics · 1993 · 438 citations

Medicine, Genetics, Molecular Genetics +12

Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site

T J Keen, C.F. Inglehearn, Douglas H. Lester et al. · Genomics · 1991 · 169 citations

Medicine, Genetics, Ophthalmology +14

A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.

C.F. Inglehearn, R. Bashir, Douglas H. Lester et al. · PubMed · 1991 · 139 citations · Full text

Medicine, Genetics, Molecular Genetics +12

Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6

Ilham Ratbi, Kim D. Falkenberg, Manou Sommen et al. · The American Journal of Human Genetics · 2015 · 128 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

Kevin Gregory-Evans, Alan Fryer, C.F. Inglehearn et al. · Nature Genetics · 1994 · 121 citations

Life Sciences, Genetics, Molecular Genetics +17