Marije E C Meuwissen (Marije E Meuwissen, Marije Meuwissen)

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Obstructive Sleep Apnea

Top Venues

American journal of medical genetics. Part A

The Journal of experimental medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Liene Thys, Diane Beysen, Anna C Jansen, Katrien Janssens, Marije E C Meuwissen
Confirmation of gray matter heterotopia as part of the DDX23 phenotypic spectrum. American journal of medical genetics. Part A 191 (9) (2023)
Saskia Koene, Cacha M P C D Peeters-Scholte, Jeroen Knijnenburg, Linda S de Vries, Phebe N Adama van Scheltema, Marije E C Meuwissen, Sylke J Steggerda, Gijs W E Santen
Intracerebral hemorrhage in a neonate with an intragenic COL4A2 duplication. American journal of medical genetics. Part A 185 (2) (2020)
Amber van Baelen, Louise Verhoustraeten, Sandra Kenis, Marije E C Meuwissen, An Boudewyns, Kim van Hoorenbeeck, Stijn Verhulst
Sleep-disordered breathing and nocturnal hypoventilation in children with the MECP2 duplication syndrome: A case series and review of the literature. American journal of medical genetics. Part A 182 (10) (2020)
Julie Voet, Berten Ceulemans, R Frank Kooy, Marije E C Meuwissen
PUM1 haploinsufficiency is associated with syndromic neurodevelopmental delay and epilepsy. American journal of medical genetics. Part A 182 (3) (2019)
Marije E C Meuwissen, Rachel Schot, Sofija Buta, Grétel Oudesluijs, Sigrid Tinschert, Scott D Speer, Zhi Li, Leontine M van Unen, Daphne Heijsman, Tobias Goldmann, Maarten H Lequin, Johan M Kros, Wendy Stam, Mark Hermann, Rob Willemsen, Rutger W W Brouwer, Wilfred F J Van IJcken, Marta Martín-Fernández, Irenaeus F M de Coo, Jeroen Dudink, Femke A T de Vries, Aida Bertoli Avella, Marco Prinz, Yanick J Crow, Frans W Verheijen, Sandra Pellegrini, Dusan Bogunovic, Grazia M S Mancini
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome. The Journal of experimental medicine 213 (7) (2016)