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Neuron|January 7, 2021
Molecule-to-Circuit Disease Mechanisms of a Synaptic SNAREopathyRoman Praschberger, Julie Jacquemyn, Patrik VerstrekenBiomedicines|January 25, 2025
Disease-Associated Dopamine Receptor D2 Variants Exhibit Functional Consequences Depending on Different Heterotrimeric G-Protein Subunit CombinationsNele Niebrügge, Olga Trovato, Roman Praschberger, et al.Neuroscience|April 8, 2019
Mechanisms of Neurological Dysfunction in GOSR2 Progressive Myoclonus Epilepsy, a Golgi SNAREopathyJames E C Jepson, Roman Praschberger, Shyam S KrishnakumarCell Reports Methods|April 18, 2026
Light-inducible FLPase reconstitution enables temporal control of gene expression in Drosophila melanogasterRishi V Shridharan, Nils Schoovaerts, Patrik Verstreken, et al.Neuron|February 14, 2023
Neurodegeneration cell per cellSriram Balusu, Roman Praschberger, Elsa Lauwers, et al.NPJ Parkinson'S Disease|April 9, 2024
Elevated α-synuclein levels inhibit mitophagic fluxInge Kinnart, Liselot Manders, Thibaut Heyninck, et al.Movement Disorders Clinical Practice|October 27, 2018
Expanding the Phenotype and Genetic Defects Associated with the <i>GOSR2</i> GeneRoman Praschberger, Bettina Balint, Niccolo E Mencacci, et al.Neuron|March 22, 2023
Neuronal identity defines α-synuclein and tau toxicityRoman Praschberger, Sabine Kuenen, Nils Schoovaerts, et al.Biochimica Et Biophysica Acta|May 27, 2014
Impact of D181V and A69T on the function of ferroportin as an iron export pump and hepcidin receptorRoman Praschberger, Melanie Schranz, William J H Griffiths, et al.Cell Reports. Medicine|September 27, 2024
A candidate loss-of-function variant in SGIP1 causes synaptic dysfunction and recessive parkinsonismMarianna Decet, Patrick Scott, Sabine Kuenen, et al.Pageof 2