Liselot van der Laan

14PUBLICATIONS
118CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyQuaternary environmentsAnthropological genetics
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Publications (14)

|Sep 25, 2026
Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age-Dependent Clinical Trajectory.

|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

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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