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Publications by Valentina Cipriani
Unique Non-Coding Variants Upstream of PRDM13 Are Associated With a Spectrum of Developmental Retinal Dystrophies Including Progressive Bifocal Chorioretinal Atrophy
Human Mutation
Genetics
Ophthalmic Statistics Note 7: Multiple Hypothesis Testing—to Adjust or Not to Adjust
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Related publications
Non-Coding and Loss-Of-Function Coding Variants in TET2 Are Associated With Multiple Neurodegenerative Diseases
A Novel Mutation in TTC8 Is Associated With Progressive Retinal Atrophy in the Golden Retriever
Canine Genetics and Epidemiology
PAX6 Non‐coding Regions Variants Leading to Aniridia Spectrum
Acta Ophthalmologica
Medicine
Ophthalmology
Non-Coding RNAs in Muscle Dystrophies
International Journal of Molecular Sciences
Organic Chemistry
Molecular Biology
Theoretical Chemistry
Inorganic Chemistry
Computer Science Applications
Spectroscopy
Medicine
Catalysis
Physical
Severe Chorioretinal Atrophy in Boucher-Neuhauser Syndrome
Canadian Journal of Ophthalmology
Medicine
Ophthalmology
Microcornea-Myopic Chorioretinal Atrophy-Telecanthus Syndrome
Origin of JC Polyomavirus Variants Associated With Progressive Multifocal Leukoencephalopathy.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Psy85 - Economic Burden Associated With Rpe65 Gene Related Inherited Retinal Dystrophies: A Systematic Literature Review
Value in Health
Medicine
Health Policy
Public Health
Occupational Health
Environmental
The Phenotypic Variability of Retinal Dystrophies Associated With Mutations in CRX, With Report of a Novel Macular Dystrophy Phenotype
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
