Michael J. Denton

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

Sumin Gu, Debra A. Thompson, C.R. Srikumari et al. · Nature Genetics · 1997 · 662 citations

Ocular Disease, Retina, Mendelian Disorder +7

Mutation of the gene encoding cellular retinaldehyde–binding protein in autosomal recessive retinitis pigmentosa

Marion A. Maw, Breandán N. Kennedy, Allison Knight et al. · Nature Genetics · 1997 · 329 citations

Ocular Disease, Retina, Photoreceptor Cell +5

Durability of the balloon-expandable covered versus bare-metal stents in the Covered versus Balloon Expandable Stent Trial (COBEST) for the treatment of aortoiliac occlusive disease

Bibombe P. Mwipatayi, Surabhi Sharma, Ali Daneshmand et al. · Journal of Vascular Surgery · 2016 · 237 citations · Full text

Endovascular Technique, Cardiovascular Disease, Aortoiliac Occlusive Disease +7

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa

Lori S. Sullivan, John R. Heckenlively, Sara J. Bowne et al. · Nature Genetics · 1999 · 174 citations · Full text

Retina, Ophthalmology, Genetic Disorder +4

Autosomal dominant ‘sector’ retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin

Holger Kranich, Sigrid Bartkowski, Michael J. Denton et al. · Human Molecular Genetics · 1993 · 86 citations

Ocular Disease, Genetics, Genetic Epidemiology +24