Bernd Wissinger

Elfriede Aulhorn Str. 7
Tuebingen, BW 72076, Germany

Last Updated: 09/26/2026

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Found 146 publications

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

Journal: Research square

Published: July 17, 2026

The AP5B1 p.(Leu785Pro) variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

The AP5B1 p.(Leu785Pro) variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

Journal: HGG advances

Published: June 23, 2026

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations.

Journal: HGG advances

Published: June 23, 2026

Identification of Brimonidine as a Novel Substrate of Organic Cation Transporters OCT2 and MATE1 Expressed in Human Eye.

Identification of Brimonidine as a Novel Substrate of Organic Cation Transporters OCT2 and MATE1 Expressed in Human Eye.

Journal: Investigative ophthalmology & visual science

Published: April 02, 2026

Clinical manifestations of dual-gene variants in retinitis pigmentosa.

Clinical manifestations of dual-gene variants in retinitis pigmentosa.

Journal: Acta ophthalmologica

Published: February 21, 2026

Flavoprotein Fluorescence Imaging in Stargardt Disease: Linking Metabolic Stress to Structural Damage.

Flavoprotein Fluorescence Imaging in Stargardt Disease: Linking Metabolic Stress to Structural Damage.

Journal: Investigative ophthalmology & visual science

Published: August 06, 2025

Investigating the Immunogenic Potential of Variations in Host Cell Protein Levels in Clinical-Grade AAV8 Products.

Investigating the Immunogenic Potential of Variations in Host Cell Protein Levels in Clinical-Grade AAV8 Products.

Journal: Investigative ophthalmology & visual science

Published: June 11, 2025

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics

Published: June 02, 2025

Clinical manifestations of dual-gene variants involving ABCA4 in retinal dystrophies.

Clinical manifestations of dual-gene variants involving ABCA4 in retinal dystrophies.

Journal: BMC ophthalmology

Published: January 21, 2025

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

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

Natural History of Autosomal Recessive IMPG2-Associated Retinal Dystrophy.

Natural History of Autosomal Recessive IMPG2-Associated Retinal Dystrophy.

Journal: American journal of ophthalmology

Published: January 03, 2025

Safety and vision outcomes of subretinal gene supplementation therapy in PDE6A-associated retinitis pigmentosa: a non-randomised controlled trial.

Safety and vision outcomes of subretinal gene supplementation therapy in PDE6A-associated retinitis pigmentosa: a non-randomised controlled trial.

Journal: The British journal of ophthalmology

Published: September 11, 2024

Showing 1-12 of 146

Last Updated: 09/26/2026