Author

Jeannette Hübener‐Schmid

University of TübingenORCID 0000-0002-4973-0923Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Bart P.C. van de WarrenburgiD· 2 shared Héctor García‐MorenoiD· 2 shared Jennifer FaberiD· 2 shared Jon InfanteiD· 2 shared Luís Pereira de AlmeidaiD· 2 shared Mafalda RaposoiD· 2 shared Magda M. SantanaiD· 2 shared Manuela Caroline Ferreira LimaiD· 2 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersNeuroscience

Bart P.C. van de WarrenburgORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintJan 4, 2024

Small non-coding RNA content in plasma-derived extracellular vesicles distinguish ataxic SCA3 mutation carriers from pre-ataxic and control subjects

Magda M. Santana, Patrick Silva, Maria M Pinto…·Luís Pereira de Almeida

DOI 10.1101/2024.01.04.574044

humanbulk RNA-seq

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GeneticsbioRxivPreprintApr 22, 2023

Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease

Mafalda Raposo, Jeannette Hübener‐Schmid, Rebecca Tagett…·Manuela Caroline Ferreira Lima

The paper identifies and compares the abundance of ATXN3 splice variants in blood and cerebellum of SCA3/MJD patients and controls, finding tissue-specific expression patterns of full-length ataxin-3 isoforms.

1 citation

humanbulk RNA-seq

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NeurosciencebioRxivPreprintFeb 28, 2020

A novel Ataxin-3 knock-in mouse model mimics the human SCA3 disease phenotype including neuropathological, behavioral, and transcriptional abnormalities

Eva Haas, Rana Dilara Incebacak Eltemur, Thomas Hentrich…·Jeannette Hübener‐Schmid

This paper describes a novel Ataxin-3 knock-in mouse model that replicates key neuropathological, behavioral, and transcriptional features of human SCA3 disease.

5 citations

mousebulk RNA-seq

𝕏 PostBluesky