Marcel Mannens

8PUBLICATIONS
66CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyDevelopmental genetics (incl. sex determination)Immunogenetics (incl. genetic immunology)Global Indigenous studies health and wellbeing
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Publications (8)

|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

|Oct 01, 2025
DNA methylation episignature for Smith-Magenis and Potocki-Lupski syndromes: a mirror perspective.

Liselot van der Laan, Karim Karimi, Kathleen Rooney

|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

|Sep 28, 2023
Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature.

Liselot van der Laan, Kathleen Rooney, Sadegheh Haghshenas

|May 30, 2023
DNA methylation episignatures are sensitive and specific biomarkers for detection of patients with KAT6A/KAT6B variants.

Niels Vos, Jack Reilly, Mariet W Elting

|Dec 20, 2022
DNA methylation episignatures: insight into copy number variation.

Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster

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Frequent Collaborators

5 joint publications

Liselot van der Laan

4 joint publications

Peter Henneman

4 joint publications

Bekim Sadikovic

3 joint publications

Kathleen Rooney