CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders

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European journal of human genetics - ISSN 1018-4813-34:8 (2026) p. 1070-1080
Auteur(s)
    Matthias De Wachter, Mathijs van der Lei, Amber Decleve, Kevin De Man, Ellen Elinck, An-Sofie Schoonjans, Evan Gouy, Louis Januel, Pauline Monin, Audrey Labalme, Amelle Shillington, Himanshu Goel, Juliet P. Taylor, Katherine Neas, David A. Koolen, Francois Lecoquierre, Alice Goldenberg, Theresa Brunet, Melanie Brugger, Minjie Luo, Magdalena Krygier, Maria Mazurkiewicz-Beldzinska, Manon Degoutin, Claire Beneteau, Cyril Goizet, David D. Weaver, Emily G. Farrow, Angela Lee, Randi N. Gadea, Berten Ceulemans, Peter A.M. de Witte, Danielle Copmans, Anna Jansen, Frank Kooy

An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice

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EBioMedicine - ISSN 2352-3964-128 (2026) p.
Auteur(s)

Next-generation mouse phenotyping identifies inhibitory network deficits and establishes a platform for preclinical drug screening in Fragile X Syndrome

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Antwerp, University of Antwerp, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Department of Biomedical Sciences, 2026,346 p.

From discovery to innovative translational approaches in 80 years of fragile X syndrome research

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Biomedicines - ISSN 2227-9059-13:4 (2025) p. 1-27

Cognitive deficits in human ApoE4 knock-in mice : a systematic review and meta-analysis

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Behavioural brain research - ISSN 0166-4328-471 (2024) p. 1-27
Auteur(s)
    Marieke J.G. van Heuvelen, Mathijs van der Lei, Pien M. Alferink, Peter Roemers, Eddy A. van der Zee