Associated Papers
Chronic Catatonia in an Individual With a De Novo Missense SHANK1 Variant.
Dahlberg PM et al.
American Journal of Medical Genetics. Part A, 2025
A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling.
Qin Y et al.
Molecular Psychiatry, 2022
Multiple Rare Risk Coding Variants in Postsynaptic Density-Related Genes Associated With Schizophrenia Susceptibility.
Hu TM et al.
Frontiers in Genetics, 2020
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