Author

Tom S. Koemans

Radboud University Medical CenterORCID 0000-0001-9162-2267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Alessandro VitrioloiD· 1 shared Catherine B. MillariD· 1 shared Celeste Franconi· 1 shared Connie T.R.M. Schrander-Stumpel· 1 shared Daniele CapocefaloiD· 1 shared Davide CastaldiiD· 1 shared Erika TenderiniiD· 1 shared Gabriella Maria SqueoiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

1 shared paperGenetics

Alessandro VitrioloORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

GeneticsbioRxivPreprintApr 22, 2021

KMT2D haploinsufficiency in Kabuki Syndrome disrupts neuronal function through transcriptional and chromatin rewiring independent of H3K4-monomethylation

Michele Gabriele, Alessandro Vitriolo, Sara Cuvertino…·Giuseppe Testa

This study investigates how KMT2D mutations in Kabuki Syndrome disrupt neuronal function through chromatin and transcriptional changes, independent of H3K4me1.

10 citations

humanbulk RNA-seq

𝕏 PostBluesky