Alberta Children's Hospital Research Institute (ACHRI)
Research facility
Location:
Calgary,
Canada (CA)
ROR: https://ror.org/00gmyvv50
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway (2024)
Gong M, Li J, Qin Z, Machado Bressan Wilke MV, Liu Y, Li Q, Liu H, et al.
Journal article
BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations (2024)
Peron A, D’Arco F, Aldinger KA, Smith-Hicks C, Zweier C, Gradek GA, Bradbury K, et al.
Journal article
Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes. (2024)
Rinaldi B, Bayat A, Zachariassen LG, Sun JH, Ge YH, Zhao D, Bonde K, et al.
Journal article