Wolfgang R. Berger

Zurich, ZH, Switzerland

Last Updated: 09/26/2026

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Found 89 publications

The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular Disease.

The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular Disease.

Journal: Clinical genetics

Published: June 26, 2025

Genetic Landscape of Congenital Cataracts in a Swiss Cohort: Addressing Diagnostic Oversights in Nance-Horan Syndrome.

Genetic Landscape of Congenital Cataracts in a Swiss Cohort: Addressing Diagnostic Oversights in Nance-Horan Syndrome.

Journal: Biomedicines

Published: May 31, 2025

Novel Genetic Variants and Clinical Profiles in Peters Anomaly Spectrum Disorders.

Novel Genetic Variants and Clinical Profiles in Peters Anomaly Spectrum Disorders.

Journal: International journal of molecular sciences

Published: April 19, 2025

SLC4A3-related short QT syndrome assessed in human induced pluripotent stem cell-derived cardiomyocytes: mechanisms of ventricular arrhythmia and sudden cardiac death.

SLC4A3-related short QT syndrome assessed in human induced pluripotent stem cell-derived cardiomyocytes: mechanisms of ventricular arrhythmia and sudden cardiac death.

Journal: European heart journal

Published: December 19, 2024

Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease.

Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: November 25, 2024

Retinal Dystrophy Associated with Homozygous Variants in NRL.

Retinal Dystrophy Associated with Homozygous Variants in NRL.

Journal: Genes

Published: November 15, 2024

Rescue of Aberrant Splicing Caused by a Novel Complex Deep-intronic ABCA4 Allele.

Rescue of Aberrant Splicing Caused by a Novel Complex Deep-intronic ABCA4 Allele.

Journal: Genes

Published: September 26, 2024

Autosomal Dominant RP1 c.2613dupA (p.Arg872Thrfs*2) Variant Retinitis Pigmentosa Shows Linear Loss of the Ellipsoid Zone over Time with Highly Variable Phenotype.

Autosomal Dominant RP1 c.2613dupA (p.Arg872Thrfs*2) Variant Retinitis Pigmentosa Shows Linear Loss of the Ellipsoid Zone over Time with Highly Variable Phenotype.

Journal: Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde

Published: September 12, 2024

Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes.

Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes.

Journal: International journal of molecular sciences

Published: August 08, 2024

Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development.

Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development.

Journal: Cells

Published: June 05, 2024

Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort.

Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient Cohort.

Journal: International journal of molecular sciences

Published: May 06, 2024

Macular Corneal Dystrophy - Molecular Genetics as the Key in Treatment-Refractory Keratopathy.

Macular Corneal Dystrophy - Molecular Genetics as the Key in Treatment-Refractory Keratopathy.

Journal: Klinische Monatsblatter fur Augenheilkunde

Published: April 23, 2024

Showing 1-12 of 89

Last Updated: 09/26/2026