Gijs W E Santen

13PUBLICATIONS
82CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Clinical neuropsychologyGene expression (incl. microarray and other genome-wide approaches)Quaternary environmentsInfant and child health
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Publications (13)

|Feb 28, 2026
Experiences of Dutch parents undergoing prenatal genomic testing for fetal structural anomalies: A prospective qualitative analysis.

Maayke A de Koning, Sarah Long, Holly E Evans

|Feb 10, 2026
"The Way We Do Things is Unsustainable"-Exploring Symptoms of Burnout Among Healthcare Professionals in Prenatal Genomics.

Maayke de Koning, Sarah Long, Marit de Vries

|Aug 21, 2025
Prenatal Variants of Uncertain Significance (VUS): to report or not to report?

Maayke A de Koning, Malgorzata I Srebniak, Esther J Oldekamp

|Mar 05, 2025
ARID2-related disorder: further delineation of the clinical phenotype of 27 novel individuals and description of an epigenetic signature.

Clara Houdayer, Kathleen Rooney, Liselot van der Laan

|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

Pleuntje J van der Sluijs

3 joint publications

Maayke de Koning

3 joint publications

Manon Suerink

2 joint publications

David A Koolen