Lubica Dudakova
Prague, PR 12808, Czech Republic
Last Updated: 09/26/2026
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Found 69 publications
Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.
Journal: Ophthalmology
Published: February 20, 2026
Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.
Journal: Ophthalmology
Published: February 20, 2026
Molecular characterization of CHST6 in Egyptian families with macular corneal dystrophy reveals recurrent and novel variants.
Journal: Ophthalmic genetics
Published: January 22, 2026
Targeted antisense oligonucleotide therapy rescues PRPF31 expression in retinitis pigmentosa caused by a splicing mutation.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: November 27, 2025
Decoding the Cornea-Glaucoma Association: Evidence From Mendelian Randomization.
Journal: Investigative ophthalmology & visual science
Published: July 08, 2025
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.
Journal: Nature genetics
Published: June 02, 2025
Rare variants in MIR184 are a novel genetic cause of Fuchs endothelial corneal dystrophy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 01, 2025
Loss-of-function variants in SAXO6, encoding a microtubule inner protein of photoreceptor cilia, cause a late-onset retinal dystrophy.
Journal: American journal of human genetics
Published: April 01, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity.
Journal: JAMA ophthalmology
Published: March 13, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.
Journal: medRxiv : the preprint server for health sciences
Published: January 20, 2025
Last Updated: 09/26/2026