Elise Héon
University of Toronto(CA)Hospital for Sick Children(CA)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Glaucoma and retinal disorders, Photoreceptor and optogenetics research, RNA regulation and disease
Most-Cited Works
- → Mutation Analysis of Patients with Hermansky-Pudlak Syndrome: A Frameshift Hot Spot in the HPS Gene and Apparent Locus Heterogeneity(1998)161 cited
- → Visual Function and Central Retinal Structure in Choroideremia(2016)74 cited
- → Mutational Spectrum of theZEB1Gene in Corneal Dystrophies Supports a Genotype–Phenotype Correlation(2013)73 cited
- → Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness(2016)60 cited
- → Phenotypic Characteristics Including In Vivo Cone Photoreceptor Mosaic inKCNV2-Related “Cone Dystrophy with Supernormal Rod Electroretinogram”(2012)47 cited
- → Biallelic Mutations inCRB1Underlie Autosomal Recessive Familial Foveal Retinoschisis(2016)44 cited
- → OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium(2014)44 cited
- → Sleep and daytime sleepiness in retinitis pigmentosa patients(2001)42 cited
- → THE CHARACTERIZATION OF RETINAL PHENOTYPE IN A FAMILY WITH C1QTNF5-RELATED LATE-ONSET RETINAL DEGENERATION(2012)35 cited
- A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.(2011)