Associated Papers
Impact of Genetic Variants Associated with Neurodevelopmental Disorders on the WAVE Regulatory Complex.
Xie S et al.
Journal of Chemical Information and Modeling, 2025
Recent advances in CYFIP2-associated neurodevelopmental disorders: From human genetics to molecular mechanisms and mouse models.
Ma R et al.
Brain & Development, 2025
Molecular basis of the CYFIP2 and NCKAP1 autism-linked variants in the WAVE regulatory complex.
Xie S et al.
Protein Science : a Publication of the Protein Society, 2025
Common characteristics of variants linked to autism spectrum disorder in the WAVE regulatory complex.
Xie S et al.
Frontiers in Computational Neuroscience, 2025
41312356 (PubMed )
Supplement: Data_Sheet_1.docx
A novel variant in CYFIP2 in a girl with severe disabilities and bilateral perisylvian polymicrogyria.
Salokivi T et al.
American Journal of Medical Genetics. Part A, 2024
New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics.
Begemann A et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures.
Zweier M et al.
European Journal of Human Genetics : Ejhg, 2019
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