Pavlina Skalicka

Prague, PR, Czech Republic

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 44 publications

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Journal: Ophthalmology

Published: February 20, 2026

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Genetic Prediction of Keratoplasty in Fuchs Endothelial Corneal Dystrophy.

Journal: Ophthalmology

Published: February 20, 2026

Rare variants in MIR184 are a novel genetic cause of Fuchs endothelial corneal dystrophy.

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

Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity.

Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity.

Journal: JAMA ophthalmology

Published: March 13, 2025

Genotype-Phenotype Correlations in Corneal Dystrophies: Advances in Molecular Genetics and Therapeutic Insights.

Genotype-Phenotype Correlations in Corneal Dystrophies: Advances in Molecular Genetics and Therapeutic Insights.

Journal: Clinical & experimental ophthalmology

Published: September 18, 2024

Tissue-specific TCF4 triplet repeat instability revealed by optical genome mapping.

Tissue-specific TCF4 triplet repeat instability revealed by optical genome mapping.

Journal: EBioMedicine

Published: May 08, 2024

Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.

Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.

Journal: PLoS genetics

Published: November 03, 2023

Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy.

Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy.

Journal: Human mutation

Published: October 17, 2023

Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1.

Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1.

Journal: American journal of ophthalmology

Published: July 02, 2023

Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy.

Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy.

Journal: Acta ophthalmologica

Published: August 15, 2022

Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant.

Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant.

Journal: Journal of clinical medicine

Published: July 28, 2022

Axenfeld-Rieger syndrome: more than meets the eye.

Axenfeld-Rieger syndrome: more than meets the eye.

Journal: Journal of medical genetics

Published: April 22, 2022

Showing 1-12 of 44

Last Updated: 09/26/2026