Marije Meuwissen

7PUBLICATIONS
83CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Central nervous systemCardiovascular medicine and haematology not elsewhere classifiedPaediatrics not elsewhere classifiedPhotonics, optoelectronics and optical communications
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Publications (7)

|Jan 28, 2026
A Systematic Review Illustrates the Expanding Clinical and Molecular Landscape of Helsmoortel-Van der Aa Syndrome.

Lusine Harutyunyan, Claudio P D'Incal, Anna C Jansen

|Oct 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC.

Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan

|Nov 28, 2020
Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication.

Saskia Koene, Cacha M P C D Peeters-Scholte, Jeroen Knijnenburg

|Aug 25, 2020
Sleep-disordered breathing and nocturnal hypoventilation in children with the MECP2 duplication syndrome: A case series and review of the literature.

Amber van Baelen, Louise Verhoustraeten, Sandra Kenis

|Jun 22, 2016
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome.

Marije E C Meuwissen, Rachel Schot, Sofija Buta

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Frequent Collaborators

3 joint publications

Anna Jansen

2 joint publications

R Frank Kooy

1 joint publications

Rachel Schot

1 joint publications

Sofija Buta