Heather Moore-Barton
St George's, University of London(GB)
Publications by Year
Research Areas
Genomics and Chromatin Dynamics, Genomic variations and chromosomal abnormalities, Glaucoma and retinal disorders, Ophthalmology and Visual Impairment Studies, Chromosomal and Genetic Variations
Most-Cited Works
- → Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome(2012)240 cited
- → SLITRK6 mutations cause myopia and deafness in humans and mice(2013)67 cited
- → Further delineation of the KAT6B molecular and phenotypic spectrum(2014)64 cited
- → Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic Paraplegia(2016)26 cited