Author

Koenraad De Wispelaere

Icahn School of Medicine at Mount SinaiORCID 0000-0003-1946-3024Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Approach:experimental assay· 1 Assay:metabolomics· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Kathleen FresoniD· 2 shared Akira SawaguchiiD· 1 shared Ana Isabel Vega Pajares· 1 shared Andrea Katrinecz· 1 shared Andrea Sariego JamardoiD· 1 shared Andrew David MumfordiD· 1 shared Ángel CarracedoiD· 1 shared Anna Duat RodrígueziD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersCell Biology

Kathleen FresonORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintMay 22, 2025

Turbulence orchestrates actin-mitochondria dynamics to preserve GPIbα and support iPSC-derived platelet biogenesis

Emiri Nakamura, Yasuo Harada, Sou Nakamura…·Koji Eto

This study develops a turbulence-assisted system to enhance iPSC-platelet production by regulating actin dynamics and mitochondrial inheritance.

DOI 10.1101/2025.05.22.655481

humanproteomics

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Genetic & Genomic MedicineNature GeneticsPeer-reviewedApr 10, 2025

Mutations in the U2 snRNA gene RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy

Daniel Greene, Koenraad De Wispelaere, Jonathan Gill Lees…·Ernest Turro

The paper identifies recurrent mutations in the RNU2-2P gene, which encodes U2 snRNA, as a cause of a severe neurodevelopmental disorder with prominent epilepsy.

60 citationstop 1%

humanstatistical model

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