Author

Katharina Foreman

Radboud University Medical Center

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

Biology Disciplines

Click to filter author papers

Neuroscience· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Britt MossinkiD· 2 shared Dirk SchubertiD· 2 shared Jason M. Keller· 2 shared Katrin LindaiD· 2 shared Monica FregaiD· 2 shared Nael Nadif KasriiD· 2 shared Teun M. Klein GunnewiekiD· 2 shared Astrid R. Oudakker· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 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

Britt MossinkORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

NeuroscienceCell ReportsPeer-reviewedApr 1, 2020

Mitochondrial dysfunction impairs human neuronal development and reduces neuronal network activity and synchronicity

Teun M. Klein Gunnewiek, Eline van Hugte, Monica Frega…·Tamás Kozicz

This study shows that mitochondrial dysfunction in human neurons, caused by high heteroplasmy of the m.3243A>G variant, leads to impaired neural development, reduced synaptic connectivity, and decreased network activity.

90 citationstop 4%

humanbulk RNA-seq

𝕏 PostBluesky

NeuroscienceNature CommunicationsPeer-reviewedOct 30, 2019

Neuronal network dysfunction in a human model for Kleefstra syndrome mediated by enhanced NMDAR signaling

Monica Frega, Katrin Linda, Jason M. Keller…·Nael Nadif Kasri

This study shows that EHMT1 deficiency in human neurons leads to NMDAR hyperfunction, causing neuronal network dysfunction in Kleefstra syndrome, and demonstrates pharmacological rescue of these phenotypes.

137 citationstop 1%

humanbulk RNA-seq

𝕏 PostBluesky