Author

Sylvie Delcambre

University of LuxembourgORCID 0000-0003-1604-7199Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Organism:human· 3 Research Focus:differential expression· 2 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

Anne GrünewaldiD· 3 shared Ibrahim BoussaadiD· 2 shared Rejko KrügeriD· 2 shared Adrien J Ries· 1 shared Alex H. RajputiD· 1 shared Andrew A. HicksiD· 1 shared Anouk EweniD· 1 shared Anthony Edward LangiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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3 shared papersNeuroscience

Anne GrünewaldORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintSep 15, 2026

SNCA triplication shapes neuronal extracellular vesicle biology and promotes microglial activation in patient-derived iPSC-based models of Parkinson's disease

Ioanna Boumpoureka, Johanna Heider, Sylvie Delcambre…·Rejko Krüger

This study investigates how SNCA triplication affects neuronal extracellular vesicle biology and microglial activation in Parkinson's disease using iPSC-derived models.

DOI 10.64898/2026.09.09.750343

humanbulk RNA-seq

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NeurosciencebioRxivPreprintOct 31, 2024

DJ-1 mediates regulation of metabolism and immune response in Parkinsons disease astrocytes and Glioblastoma cells

Pauline Mencke, Jochen Ohnmacht, Félicia Jeannelle…·Ibrahim Boussaad

This study shows DJ-1 affects metabolism and immune response differently in Parkinson's disease and glioblastoma cells, with antioxidant treatment rescuing PD-related phenotypes.

DOI 10.1101/2024.10.31.621212

humanbulk RNA-seq

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Genetic & Genomic MedicineBrainPeer-reviewedDec 7, 2022

Mitochondrial DNA heteroplasmy distinguishes disease manifestation in PINK1- and PRKN-linked Parkinson's disease

Joanne Trinh, Andrew A. Hicks, Inke Regina König…·Anne Grünewald

The paper identifies mitochondrial DNA heteroplasmy as a marker distinguishing disease manifestation in PINK1/PRKN mutation carriers.

28 citations

humanDNA methylation

𝕏 PostBluesky