Author

Valerie B. DeLeon

University of FloridaORCID 0000-0001-5004-5977Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Hans Tomas BjornssoniD· 2 shared Aamir R. ZuberiiD· 1 shared Andrew BrinniD· 1 shared Ásbjörg Ósk SnorradóttiriD· 1 shared Cathleen M. LutziD· 1 shared Jill A. FahrneriD· 1 shared Juan OuyangiD· 1 shared Kasper D. HanseniD· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 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 papersGenetics

Hans Tomas BjornssonORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GeneticsbioRxivPreprintJul 19, 2024

In-utero rescue of neurological dysfunction in a mouse model of Wiedemann-Steiner syndrome

Tinna Reynisdottir, Kimberley Jade Anderson, Andrew Brinn…·Hans Tomas Bjornsson

This study demonstrates that in-utero restoration of KMT2A in a mouse model of WDSTS rescues neurological phenotypes, suggesting a therapeutic window during mid-gestation.

1 citation

mouseexperimental assay

𝕏 PostBluesky

GeneticsJCI InsightPeer-reviewedSep 26, 2019

Precocious Chondrocyte Differentiation Disrupts Skeletal Growth in Kabuki Syndrome Mice

Jill A. Fahrner, Wan-Ying Lin, Ryan C. Riddle…·Hans Tomas Bjornsson

This study identifies disrupted endochondral ossification in Kabuki syndrome mice due to precocious chondrocyte differentiation, linking KMT2D dysfunction to altered Shox2 expression and growth retardation.

41 citations

mousebulk RNA-seq

𝕏 PostBluesky