Alberta Children's Hospital Research Institute (ACHRI)
Research facility
Location:
Calgary,
Canada (CA)
ROR: https://ror.org/00gmyvv50
ILAE-YES global webinar series: Integrating clinical and basic science in epilepsy research (2026)
Nome CG, Ravat P, Bartolomei F, de Curtis M, Di Sapia R, Galovic M, Gogou M, et al.
Journal article
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function (2025)
Asadollahi R, Ahmad A, Boonsawat P, Shahanoor Hinzen J, Lohse M, Bouazza-Arostegui B, Sun S, et al.
Journal article
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