Author

Raúl Jiménez Heredia

Ludwig Boltzmann Institute for Rare and Undiagnosed DiseasesORCID 0000-0002-1406-0608Unclaimed ORCID profile · follow to get notified of new preprints

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Molecular Biology· 1

Signature Assays, Organisms & Methods

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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

Molecular BiologybioRxivPreprintSep 6, 2022

Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome

Elizabeth A. Werren, Geneva R. LaForce, Anshika Srivastava…·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.

DOI 10.1101/2022.09.06.506502

humanmouse

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