A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3.
Research Articles
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.
Molecular cascades and cell-type specific signatures in ASD revealed by single cell genomics.
Phenotypically driven subgroups of ASD display distinct metabolomic profiles.
Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms.
Altered dendritic morphology in dorsolateral prefrontal cortex of nonhuman primates prenatally exposed to maternal immune activation.
Identifying phenotypic and physiological subgroups of preschoolers with autism spectrum disorder.
Accelerated longitudinal weight gain among infants with in utero COVID-19 exposure.
High-throughput functional analysis of autism genes in zebrafish identifies convergence in dopaminergic and neuroimmune pathways.
No differences in auditory steady-state responses in children with autism spectrum disorder and typically developing children.
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