Ingrid van de Laar
11PUBLICATIONS
178CO-AUTHORS
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Publications (11)
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|Dec 19, 2025
DE NOVO VARIANTS IN THE POLY(RC)-BINDING PROTEIN GENE PCBP1 CAUSE A NEURODEVELOPMENTAL DISORDER.Wallid Deb, Thomas Besnard, Florence Desprez
|Sep 10, 2024
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina
|Apr 16, 2024
Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients.Serwet Demirdas, Lisa M van den Bersselaar, Rosan Lechner
|Oct 17, 2022
High-yield identification of pathogenic NF1 variants by skin fibroblast transcriptome screening after apparently normal diagnostic DNA testing.Hannie C W Douben, Mark Nellist, Leontine van Unen
|Sep 30, 2022
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification.Marijke H van der Meulen, Johanna C Herkert, Susanna L den Boer
|Feb 15, 2022
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome.Aidin Foroutan, Sadegheh Haghshenas, Pratibha Bhai
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Frequent Collaborators
3 joint publications
Judith Verhagen
2 joint publications
Peter J van Tintelen
2 joint publications
Annette F Baas
2 joint publications
Antonio Vitobello
1 joint publications
Peter Bauer
1 joint publications
Aida M Bertoli-Avella
1 joint publications
Santhosh Girirajan
1 joint publications
Daphné Lehalle
1 joint publications
Caroline Nava
1 joint publications
Elsa Leitão
