Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.
Research Articles
Diagnostic preferences include discussion of etiology for adults with cerebral palsy and their caregivers.
Altered structural brain connectivity involving the dorsal and ventral language pathways in 16p11.2 deletion syndrome.
Memo1-mediated tiling of radial glial cells facilitates cerebral cortical development.
Analysis of gait synchrony and balance in neurodevelopmental disorders using computer vision techniques.
Oxytocin normalizes altered circuit connectivity for social rescue of the Cntnap2 knockout mouse.
Two distinct types of nodes of Ranvier support auditory nerve function in the mouse cochlea.
Precise genome editing across kingdoms of life using retron-derived DNA.
SCEPTRE improves calibration and sensitivity in single-cell CRISPR screen analysis.
Excitatory/inhibitory imbalance in autism: The role of glutamate and GABA gene-sets in symptoms and cortical brain structure.
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