Jeroen van Reeuwijk

9PUBLICATIONS
89CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Infant and child healthProteomics and intermolecular interactions (excl. medical proteomics)
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Publications (9)

|Aug 18, 2026
Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

|Jun 19, 2025
Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Steven Laurie, Wouter Steyaert, Elke de Boer

|Jan 17, 2025
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Steven Laurie, Wouter Steyaert, Elke de Boer

|Sep 27, 2024
Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants.

Gaby Schobers, Maartje Pennings, Juliette de Vries

|May 14, 2024
Prevalence of comorbidities in individuals with neurodevelopmental disorders from the aggregated phenomics data of 51,227 pediatric individuals.

Alexander J M Dingemans, Sandra Jansen, Jeroen van Reeuwijk

|Aug 07, 2023
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework.

Alexander J M Dingemans, Max Hinne, Kim M G Truijen

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Frequent Collaborators

4 joint publications

Christian Gilissen

4 joint publications

Lisenka E L M Vissers

4 joint publications

Nicole de Leeuw

3 joint publications

Bert B A de Vries