Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 copy number variations.
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Leveraging biobank-scale rare and common variant analyses to identify ASPHD1 as the main driver of reproductive traits in the 16p11.2 locus.
Oligogenic effects of 16p11.2 copy number variation on craniofacial development.
The human-specific BOLA2 duplication modifies iron homeostasis and anemia predisposition in chromosome 16p11.2 autism individuals.
Sensorimotor cortical oscillations during movement preparation in 16p11.2 deletion carriers.
Atypical neural variability in carriers of 16p11.2 copy number variants.
Psychiatric disorders in children with 16p11.2 deletion and duplication.
Human-specific NOTCH2NL genes affect notch signaling and cortical neurogenesis.
Quantifying the effects of 16p11.2 copy number variants on brain structure: A multisite genetic-first study.
Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human.
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