Mariëlle Alders

7PUBLICATIONS
96CO-AUTHORS
Developmental genetics (incl. sex determination)Gene and molecular therapyEpigenetics (incl. genome methylation and epigenomics)Anthropological geneticsPredictive and prognostic markers
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Publications (7)

|May 12, 2026
Distinct sub-clusters of developmental disorder-associated variants in the switch II region of RAC1.

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

Liselot van der Laan, Karim Karimi, Kathleen Rooney

|Aug 06, 2024
Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement.

Christy W LaFlamme, Cassandra Rastin, Soham Sengupta

|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

|Oct 24, 2023
Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature.

Christy W LaFlamme, Cassandra Rastin, Soham Sengupta

|Mar 02, 2022
Prenatal NeuN+ neurons of Down syndrome display aberrant integrative DNA methylation and gene expression profiles.

Peter Henneman, Adri N Mul, Andrew Yf Li Yim

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Frequent Collaborators

3 joint publications

David Genevieve

2 joint publications

Sophia B Gibson

2 joint publications

Kristen L Park

2 joint publications

Emily V Walker