Frederick T. Collison
Lighthouse Guild(US)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, Glaucoma and retinal disorders, Visual perception and processing mechanisms, Photoreceptor and optogenetics research
Most-Cited Works
- → Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degeneration(2017)190 cited
- → Analysis of the ABCA4 genomic locus in Stargardt disease(2014)132 cited
- → Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia(2016)109 cited
- → Genotype-Dependent Variability in Residual Cone Structure in Achromatopsia: Toward Developing Metrics for Assessing Cone Health(2014)78 cited
- → Extremely hypomorphic and severe deep intronic variants in the ABCA4 locus result in varying Stargardt disease phenotypes(2018)73 cited
- → Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT)(2015)68 cited
- → REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA(2017)60 cited
- → Genetic and Clinical Analysis of ABCA 4 ‐Associated Disease in African American Patients(2014)51 cited
- → Correlating Photoreceptor Mosaic Structure to Clinical Findings in Stargardt Disease(2016)43 cited
- → Genotypic spectrum and phenotype correlations of ABCA4-associated disease in patients of south Asian descent(2017)40 cited