Balazs Varsanyi
Mária Str. 39
Budapest, BU 1085, Hungary
Budapest, BU 1085, Hungary
Last Updated: 09/26/2026
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Found 10 publications
Cystoid Macular Lesions in Inherited Retinal Diseases: Prevalence, Characteristics, and Genetic Associations in a Hungarian Cohort.
Journal: Genes
Published: August 20, 2025
Insights into eye genetics and recent advances in ocular gene therapy.
Journal: Molecular and cellular probes
Published: December 18, 2024
Variation in eye care professional distribution across Europe, a survey.
Journal: Eye (London, England)
Published: February 17, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 12, 2023
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.
Journal: Human mutation
Published: August 13, 2021
Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation.
Journal: Human mutation
Published: May 20, 2019
Ultrastructure of neurovascular changes in human diabetic retinopathy.
Journal: International journal of immunopathology and pharmacology
Published: December 19, 2017
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
Journal: PloS one
Published: September 09, 2015
Leber congenital amaurosis: first genotyped Hungarian patients and report of 2 novel mutations in the CRB1 and CEP290 genes.
Journal: European journal of ophthalmology
Published: June 03, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026