Liselot van der Laan
13PUBLICATIONS
112CO-AUTHORS
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Publications (13)
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|Jan 08, 2026
DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects.Gregor Dombrowsky, Liselot van der Laan, Ananília Silva
|Nov 25, 2025
Identification of an episignature for the MEF2C-associated syndrome.Ananília Silva, Sadegheh Haghshenas, Liselot van der Laan
|Oct 01, 2025
DNA methylation episignature for Smith-Magenis and Potocki-Lupski syndromes: a mirror perspective.Liselot van der Laan, Karim Karimi, Kathleen Rooney
|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
|Jun 17, 2024
Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype.Camilla Sarli, Liselot van der Laan, Jack Reilly
|Apr 11, 2024
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options.Niels Vos, Lotte Kleinendorst, Liselot van der Laan
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Frequent Collaborators
7 joint publications
Kathleen Rooney
7 joint publications
Bekim Sadikovic
5 joint publications
Matthew L Tedder
5 joint publications
Marcel Mannens
4 joint publications
Jennifer Kerkhof
3 joint publications
Antonio Vitobello
3 joint publications
Alfredo Brusco
3 joint publications
Mieke M van Haelst
3 joint publications
Peter Henneman
2 joint publications
Peter Lauffer
