Author

Jan Baumgart

University Medical Center of the Johannes Gutenberg University MainzORCID 0000-0003-1996-4267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Neuroscience· 3

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Konstantin Radyushkin· 2 shared Verica VasićiD· 2 shared Alexey A. PonomarenkoiD· 1 shared Andrea HellwigiD· 1 shared Andreas BaueriD· 1 shared Andreas DaiberiD· 1 shared Andreas S. ReichertiD· 1 shared Andrew EscaygiD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

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

Curved chords = mutual co-authorship

2 shared papersNeuroscience

Konstantin Radyushkin

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

NeurosciencebioRxivPreprintApr 7, 2022

Less is more - loss of EGFL7 improves memory by upregulation of VEGF-D

Verica Vasić, Kathrin Barth, Frank Bicker…·Mirko H. H. Schmidt

This study shows that loss of EGFL7 enhances memory by increasing VEGF-D, which promotes adult neurogenesis and improves memory consolidation in mice.

1 citation

mousebulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintFeb 15, 2021

NECAB2 participates in an endosomal pathway of mitochondrial stress response at striatal synapses

Diones Bueno, Partha Narayan Dey, Teresa Schacht…·Axel Methner

This study identifies NECAB2's role in an endosomal pathway for mitochondrial stress response and repair in striatal synapses, linking its loss to synaptic loss and behavioral deficits.

DOI 10.1101/2021.02.15.431234

mouseexperimental assay

𝕏 PostBluesky

NeurosciencebioRxivPreprintMar 15, 2018

Mutant Plasticity Related Gene 1 (PRG1) acts as a potential modifier in SCN1A related epilepsy

Ellen Knierim, Johannes Vogt, Michael Kintscher…·Markus Schuelke

The paper identifies a PRG1 mutation that modifies SCN1A-related epilepsy in humans by exacerbating seizure susceptibility in a mouse model.

DOI 10.1101/282871

humanexperimental assay

𝕏 PostBluesky