Author

Sonja de Munnik

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.

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Molecular Biology· 1

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

Frequent Co-Authors

Ahmet Oguzhan OzeniD· 1 shared Ana KroloiD· 1 shared Anju ShuklaiD· 1 shared Anshika SrivastavaiD· 1 shared Ashleigh E. SchafferiD· 1 shared Brandon A. BergeriD· 1 shared Christian D. Pfennig· 1 shared Christopher T. GordoniD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperMolecular Biology

Ahmet Oguzhan OzenORCID

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1 paper

Recent·Most cited

Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome

Elizabeth A. Werren, Geneva R. LaForce, Anshika Srivastava, Delia R. Perillo, Katherine Johnson, Safa Barış, Brandon A. Berger, Samantha L. Regan, Christian D. Pfennig, Sonja de Munnik, Rolph Pfundt, Malavika Hebbar, Raúl Jiménez Heredia, Elif Karakoç-Aydıner, Ahmet Oguzhan Ozen, , Ashleigh E. Schaffer

This study investigates mRNA processing defects in THOC6 intellectual disability syndrome by analyzing human and mouse models, revealing mRNA mis-splicing and novel TREX tetramer functions.

bioRxiv · Sep 6, 2022 · PreprintMolecular Biology