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Publications by Rando Allikmets
Genome-Wide Analyses Identify Common Variants Associated With Macular Telangiectasia Type 2
Nature Genetics
Genetics
Whole Exome Sequencing Identifies CRB1 Defect in an Unusual Maculopathy Phenotype
Ophthalmology
Ophthalmology
Structural and Genetic Assessment of theABCA4-Associated Optical Gap Phenotype
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
The External Limiting Membrane in Early-Onset Stargardt Disease
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Quantitative Fundus Autofluorescence and Optical Coherence Tomography inABCA4Carriers
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Quantitative Fundus Autofluorescence and Optical Coherence Tomography inPRPH2/RDS- AndABCA4-Associated Disease Exhibiting Phenotypic Overlap
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Author Response: Retinal Phenotypes in Patients Homozygous for the G1961E Mutation in theABCA4Gene
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Hyperautofluorescent Dots Are Characteristic in Ceramide Kinase Like-Associated Retinal Degeneration
Scientific Reports
Multidisciplinary
Correlation of Clinical and Genetic Findings in Hungarian Patients With Stargardt Disease
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Comprehensive Analysis of the Candidate GenesCCL2,CCR2, andTLR4in Age-Related Macular Degeneration
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
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