Author

Hidde H. Huidekoper

Erasmus MCORCID 0000-0003-1276-0931Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:gene regulatory network inference· 1 Assay:metabolomics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Martina WilkeiD· 2 shared Michiel BongaertsiD· 2 shared Walter G. de Valk· 2 shared Anneke J.A. KievitiD· 1 shared Esmee KasteleijniD· 1 shared Farah Sadeghi-Niaraki· 1 shared Frans W. Verheijen· 1 shared Geert GeeveniD· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Martina WilkeORCID

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2 papers

Recent·Most cited

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

Genetic & Genomic MedicineMolecular Genetics and MetabolismPeer-reviewedMay 25, 2022

Prioritizing disease-causing metabolic genes by integrating metabolomics with whole exome sequencing data

Michiel Bongaerts, Ramon Bonte, Serwet Demirdas…·George J. G. Ruijter

This paper introduces Reafect, a computational method that integrates metabolomics and whole exome sequencing to prioritize disease-causing genes in inborn errors of metabolism, showing improved accuracy in identifying causative variants.

12 citations

humanwhole-exome sequencing

𝕏 PostBluesky