Human cerebral organoids reveal early spatiotemporal dynamics and pharmacological responses of UBE3A.
Research Articles
Chd8 haploinsufficiency impairs early brain development and protein homeostasis later in life.
Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
A genetics-first approach to dissecting the heterogeneity of autism: Phenotypic comparison of autism risk copy number variants.
Estimating genetic nurture with summary statistics of multi-generational genome-wide association studies.
FMRP sustains presynaptic function via control of activity-dependent bulk endocytosis.
Eliciting language samples for analysis (ELSA): A new protocol for assessing expressive language and communication in autism.
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
The organization and developmental establishment of cortical interneuron presynaptic circuits.
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
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