Roman Praschberger

Leuven, VLG 3000, Belgium

Last Updated: 09/26/2026

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Found 13 publications

Parkinson's disease-associated PINK1 loss disrupts ensheathing glia and causes dopaminergic neuron synapse loss.

Parkinson's disease-associated PINK1 loss disrupts ensheathing glia and causes dopaminergic neuron synapse loss.

Journal: eLife
Published: August 13, 2026

Light-inducible FLPase reconstitution enables temporal control of gene expression in Drosophila melanogaster.

Light-inducible FLPase reconstitution enables temporal control of gene expression in Drosophila melanogaster.

Journal: Cell reports methods
Published: September 08, 2025

Disease-Associated Dopamine Receptor D2 Variants Exhibit Functional Consequences Depending on Different Heterotrimeric G-Protein Subunit Combinations.

Disease-Associated Dopamine Receptor D2 Variants Exhibit Functional Consequences Depending on Different Heterotrimeric G-Protein Subunit Combinations.

Journal: Biomedicines
Published: December 05, 2024

Behavioral screening defines the molecular Parkinsonism-related subgroups in Drosophila.

Behavioral screening defines the molecular Parkinsonism-related subgroups in Drosophila.

Journal: Nature communications
Published: July 17, 2024

A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonism.

A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonism.

Journal: Cell reports. Medicine
Published: March 14, 2024

Elevated α-synuclein levels inhibit mitophagic flux.

Elevated α-synuclein levels inhibit mitophagic flux.

Journal: NPJ Parkinson's disease
Published: September 14, 2023

Neurodegeneration cell per cell.

Neurodegeneration cell per cell.

Journal: Neuron
Published: September 08, 2022

Neuronal identity defines α-synuclein and tau toxicity.

Neuronal identity defines α-synuclein and tau toxicity.

Journal: Neuron
Published: June 24, 2022

Molecule-to-Circuit Disease Mechanisms of a Synaptic SNAREopathy.

Molecule-to-Circuit Disease Mechanisms of a Synaptic SNAREopathy.

Journal: Neuron
Published: January 07, 2021

Mechanisms of Neurological Dysfunction in GOSR2 Progressive Myoclonus Epilepsy, a Golgi SNAREopathy.

Mechanisms of Neurological Dysfunction in GOSR2 Progressive Myoclonus Epilepsy, a Golgi SNAREopathy.

Journal: Neuroscience
Published: July 31, 2018

Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity.

Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity.

Journal: Cell reports
Published: June 05, 2017

Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene.

Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene.

Journal: Movement disorders clinical practice
Published: February 12, 2015
Showing 1-12 of 13

Last Updated: 09/26/2026