Author

Benjamin Röeben

German Center for Neurodegenerative DiseasesORCID 0000-0002-4905-8698Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Approach:Bayesian inference· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Isabel WursteriD· 2 shared Kathrin BrockmanniD· 2 shared Roswitha Kemmner· 2 shared Thomas GasseriD· 2 shared Wenhua Sun· 2 shared Alice BrauniD· 1 shared Claudia SchulteiD· 1 shared Fabian StreitiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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Focal author (center)Selected co-authorORCID co-authorUnlinked name

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2 shared papersGenetic & Genomic Medicine

Isabel WursterORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Lysosomal polygenic risk score in Parkinson's disease across populations.

Wenhua Sun, Kathrin Brockmann, Isabel Wurster, Roswitha Kemmner, Benjamin Röeben, Reda Skaiene, Stefanie Lerche, Claudia Schulte, Thomas Gasser, Manuela M. X. Tan, the Global Parkinson’s Genetic Program (GP2)

This study evaluates the performance of a lysosomal polygenic risk score (lyso-PRS) for Parkinson's disease risk across populations and its association with clinical outcomes in Europeans.

medRxiv · Sep 15, 2026 · PreprintGenetic & Genomic Medicine

Unraveling the Genetic Overlap Between Parkinson's Disease and Schizophrenia Through Genome-wide Association and Cell-Type Specific Transcriptomic Analysis

Wenhua Sun, Mohammad Dehestani, Alice Braun, Nasser Karmali, Isabel Wurster, Benjamin Röeben, Roswitha Kemmner, Kathrin Brockmann, Manu Sharma, Marina Mitjans, Fabian Streit, Thomas Gasser, Vikas Bansal

This study identifies shared genetic loci between Parkinson's disease and schizophrenia using GWAS and scRNA-seq, highlighting RAI1's role in mitochondrial dysfunction and non-motor symptoms.

medRxiv · Jun 16, 2026 · PreprintGenetic & Genomic Medicine