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Wolfgang Schmidt

Medical University of Vienna

Austria

Research Interests

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Professors in Austria

Articles (14)

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2026

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2026

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2026

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2025

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2022

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2021

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2021

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2021

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2020

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2020

Collaborators (14)

Ashirwad Merve

Honorary Associate Professor

University College London

UNITED KINGDOM

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Gerhard Wiche

Universität Wien

AUSTRIA

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Berthold Pemp

Director Neuro-Ophthalmology Service

Medical University of Vienna

AUSTRIA

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Lilli Winter

Group leader

Medical University of Vienna

AUSTRIA

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Andy Sombke

Medical University of Vienna

AUSTRIA

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Anthony Robson

University College London

UNITED KINGDOM

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Andreas Wedrich

Head and Chair

Medical University of Graz

AUSTRIA

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Peter Kuess

Medical University of Vienna

AUSTRIA

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Natalia Stepien

Medical University of Vienna

AUSTRIA

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Klaus Holzmann

Principle Investigator at Institute of Cancer Research (ICR)

Medical University of Vienna

AUSTRIA

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Hermann Wolf

AUSTRIA

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Juergen Knoblich

Institute of Molecular Biotechnology

AUSTRIA

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Gregor Reiter

Medical University of Vienna

AUSTRIA

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Theresa Balber

Medical University of Vienna

AUSTRIA

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Wolfgang Schmidt

Research Interests

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Articles (14)

Impact of Inner Retinal Layer Thinning on Visual Function in OPA1 Autosomal Dominant Optic Atrophy and Associations With Age and Genetic Variant Class

Muscle biopsy to end a diagnostic odyssey in a genetically complex case of spinal muscular atrophy type 3: the importance of "old school" in the next-generation sequencing era

Frequent expression of aberrant chimeric Cdkn2a transcripts in mouse models of muscular dystrophy.

KMT2B-related disorders in Austria: clinical features and long-term outcome after deep brain stimulation.

Alternative lengthening of telomere-based immortalization renders H3G34R-mutant diffuse hemispheric glioma hypersensitive to PARP inhibitor combination regimens

Biallelic NSUN3 Variants Cause Diverse Phenotypic Spectrum Disease: From Isolated Optic Atrophy to Severe Early-Onset Mitochondrial Disorder

A recurrent missense variant in the PPIB gene encoding peptidylprolyl isomerase B underlies adult-onset autosomal dominant optic atrophy

Impaired Autophagic Flux in Skeletal Muscle of Plectin-Related Epidermolysis Bullosa Simplex With Muscular Dystrophy

A De Novo Missense NPTX1 Variant in an Individual with Infantile-Onset Cerebellar Ataxia.

Case Report: Meningoencephalitis With Thrombotic Occlusive Vasculopathy in a Young EBV-Naïve Boy Is Associated With a Novel <i>SH2D1A</i> Mutation.

The relation of etiology based on the 2017 ILAE classification to the effectiveness of the ketogenic diet in drug-resistant epilepsy in childhood.

Specific Cognitive Changes due to Hippocalcin Alterations? A Novel Familial Homozygous Hippocalcin Variant Associated with Inherited Dystonia and Altered Cognition.

Telomerase Reverse Transcriptase Promoter Mutations Identify a Genomically Defined and Highly Aggressive Human Pleural Mesothelioma Subgroup.

A novel de novo variant of GABRA1 causes increased sensitivity for GABA in vitro.

Collaborators (14)

Ashirwad Merve

Gerhard Wiche

Berthold Pemp

Lilli Winter

Andy Sombke

Anthony Robson

Andreas Wedrich

Peter Kuess

Natalia Stepien

Klaus Holzmann

Hermann Wolf

Juergen Knoblich

Gregor Reiter

Theresa Balber

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