Pleuntje J van der Sluijs

6PUBLICATIONS
62CO-AUTHORS
Quaternary environmentsGene expression (incl. microarray and other genome-wide approaches)Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Publications (6)

|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

|Dec 31, 2024
Clonazepam repurposing in ARID1B patients through conventional RCT and N-of-1 trials: an experimental strategy for orphan disease development.

Pleuntje J van der Sluijs, Koshar Safai Pour, Cécile L Berends

|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

|Jul 27, 2023
Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders.

Alfredo M Valencia, Akshay Sankar, Pleuntje J van der Sluijs

|Aug 27, 2021
A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria.

Pleuntje J van der Sluijs, Mariëlle Alders, Alexander J M Dingemans

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Frequent Collaborators

4 joint publications

Gijs W E Santen

2 joint publications

Anita Rauch

2 joint publications

R Frank Kooy

2 joint publications

David A Koolen