Author

Stefanie Bröer

German Center for Neurodegenerative Diseases

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:imaging· 1 Assay:long-read sequencing· 1

Frequent Co-Authors

Alexandra G. BeilinaiD· 1 shared Amanda Courtright-LimiD· 1 shared Amber Logemann· 1 shared Anastasia IllarionovaiD· 1 shared Andrew SingletoniD· 1 shared Bessie Meechoovet· 1 shared Brooke E. HjelmiD· 1 shared Caroline B. PantazisiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Alexandra G. BeilinaORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

The Foundational data initiative for Parkinsons disease (FOUNDIN-PD): enabling efficient translation from genetic maps to mechanism

Elisângela Bressan, Xylena Reed, Vikas Bansal, Elizabeth D. Hutchins, Melanie M. Cobb, Michelle G. Webb, Eric B. Alsop, Francis P. Grenn, Anastasia Illarionova, Natalia Savytska, Ivo Violich, Stefanie Bröer, Noémia Fernandes, Ramiyapriya Sivakumar, Alexandra G. Beilina, , Cornelis Blauwendraat

The paper presents a multi-layered molecular dataset from iPSC-derived dopaminergic neurons to model Parkinson's disease genetic risk and provides a data browser for accessing these resources.

Cell Genomics · Feb 6, 2023Peer-reviewedGenomics