Structural variation of the human genome sequence is the insertion, deletion, or rearrangement of stretches of DNA sequence sized from around 1,000 to millions of base pairs. Over the past few years, structural variation has been shown to be far more common in human genomes than previously thought. Very little is currently known about the effects…

Autism spectrum disorders (ASD) are pervasive neurodevelopmental disorders that affect an estimated 1 in 110 individuals. Although there is a strong genetic component associated with these disorders, this review focuses on the multifactorial nature of ASD and how different genome-wide (genomic) approaches contribute to our understanding of autism.…

Argues that motor and cognitive development may be fundamentally interrelated. Summarizes evidence of close co-activation of the neocerebellum and dorsolateral prefrontal cortex in functional neuroimaging, similarities in the cognitive sequelae of damage to dorsolateral prefrontal cortex and the neocerebellum, motor deficits in…