Author
Centre Hospitalier de LuxembourgORCID 0000-0002-7721-3317Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
5 papers
Recent·Most cited
Z. Landoulsi, Ashwin Ashok Kumar Sreelatha, Kuznetsov N.…·Rachel J. Saunders-Pullman
This study conducts a genome-wide association study of copy number variations in Parkinson's disease, identifying a significant PRKN deletion but limited replication in an independent dataset.
Lara Mariah Lange, Zih‐Hua Fang, Laurel A. Screven…·the Global Parkinson's Genetics Program (GP2)
The paper assesses the frequency of dystonia-linked pathogenic variants in Parkinson's disease patients and finds they are present in 0.57% of cases, with GCH1 being the most common gene affected.
Ahmed Abdelmonem Hemedan, Marek Ostaszewski, Armin Rauschenberger…·Venkata Satagopam
This study uses Boolean modeling on PD cohorts to show sex-specific miRNA dysregulation affects mitochondrial biogenesis, mitophagy, and autophagy in Parkinson's disease.
Sinthuja Pachchek, Zied Landoulsi, Lukas Pavelka…·Rejko Krüger
The paper uses long-read sequencing to accurately identify GBA variants as a major genetic risk factor for Parkinson's disease in a Luxembourg cohort.
Peter A. Barbuti, Bruno F. R. Santos, Paul M. A. Antony…·Rejko Krüger
This study shows that the A30P alpha-synuclein mutation in Parkinson's disease neurons reduces branching and function, with mitochondrial dysfunction and susceptibility to Rotenone.