De‐Ann M. Pillers

Dystrophin expression in the human retina is required for normal function as defined by electroretinography

De‐Ann M. Pillers, Dennis E. Bulman, Richard G. Weleber et al. · Nature Genetics · 1993 · 161 citations

Ganglion Cell, Retina, Human Retina +11

Characterization of the Ocular Phenotype of Duchenne and Becker Muscular Dystrophy

Dayle Sigesmund, Richard G. Weleber, De‐Ann M. Pillers et al. · Ophthalmology · 1994 · 91 citations

Ocular Disease, Ocular Phenotype, Ophthalmology +6

Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm

Luke Boyd, Joseph S. Livingston, Michael G. Brown et al. · American Journal of Medical Genetics Part A · 2005 · 83 citations

Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations

De‐Ann M. Pillers, K.M. Fitzgerald, Nancy M. Duncan et al. · Human Genetics · 1999 · 73 citations

Duchenne/becker Muscular Dystrophy, Urology, Kinesiology +9

OA1 Mutations and Deletions in X-Linked Ocular Albinism

Rhonda E. Schnur, Mei Gao, Penelope A. Wick et al. · The American Journal of Human Genetics · 1998 · 64 citations · Full text