Author

Yvette van Ierland

Erasmus MCORCID 0000-0003-1055-9855Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alexia BourgoisiD· 1 shared Allan Micheil InnesiD· 1 shared Angie Lichty· 1 shared Anneke J.A. KievitiD· 1 shared Antonio VitobelloiD· 1 shared Boris KereniD· 1 shared Brooke Rackel· 1 shared Chloé QuēliniD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexia BourgoisORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 20, 2025

Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizures.

Michelle Hua, Mohamad‐Reza Aghanoori, Melissa J MacPherson…·Guang Yang

The paper identifies CELF2 variants causing cytoplasmic mislocalization linked to neuronal hyperexcitability, learning deficits, and seizures.

3 citations

humanexperimental assay

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 5, 2022

RNA-sequencing improves diagnosis for neurodevelopmental disorders by identifying pathogenic non-coding variants and reinterpretation of coding variants

Jordy Dekker, Rachel Schot, Michiel Bongaerts…·Tjakko J. van Ham

This study uses RNA-seq to improve diagnosis of neurodevelopmental disorders by identifying non-coding variants and reinterpreting coding variants, increasing diagnostic yield by 12%.

3 citations

humanbulk RNA-seq

𝕏 PostBluesky