W G Pearce
University of Calgary(CA)
Publications by Year
Research Areas
Retinal Development and Disorders, Connexins and lens biology, Intraocular Surgery and Lenses, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Photoreceptor and optogenetics research
Most-Cited Works
- → Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly(1998)326 cited
- Mutation of the PAX6 gene in patients with autosomal dominant keratitis.(1995)
- → Mutation in the RIEG1 Gene in Patients with Iridogoniodysgenesis Syndrome(1998)123 cited
- → Diagnostic and genetical aspects of tuberous sclerosis.(1968)108 cited
- → A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants(2001)102 cited
- → Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F(2000)98 cited
- → Congenital endothelial corneal dystrophy. Clinical, pathological, and genetic study.(1969)85 cited
- Unexpected stereoacuity following surgical correction of long-standing horizontal strabismus.(1993)
- → Autosomal Dominant Axenfeld-Rieger Anomaly Maps to 6p25(1997)59 cited
- → Doyne's honeycomb retinal degeneration. Clinical and genetic features.(1968)59 cited