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Showing results for "autism"
The SNP-based heritability for ADHD symptom scores indicates a polygenic architecture, and genes involved in neurite outgrowth are possibly involved
Common variants at 2p12 show suggestive evidence for association with childhood aggression
Prenatal exposure to vitamin D is thought to be critical for optimal fetal neurodevelopment, yet vitamin D deficiency is apparent in a growing proportion of...
Twin studies indicate that dyscalculia (or mathematical disability) is caused partly by a genetic component, which is yet to be understood at the molecular...
It has been suggested that quantitative measures of differential hand skill or reaching preference may provide more valid measures than traditional...
To further explore the effect of disorder-associated genes on cognitive functions, we investigated whether they play a role in broader cognitive traits.
Clinical decision support systems (CDSS) are increasingly utilised within healthcare settings to enhance decision making. However, few studies have investigated their application in the context of clinical services for autistic people, with no research to date exploring the perspectives of the key stakeholders who are, or in the future may be, impacted by their use.
The Kids Research Institute Australia has two researchers and an innovative science engagement initiative as finalists in the 2017 Premier’s Science Awards.
The current data provide support for Bejerot et al.'s androgyny account since males and females with high levels of autistic-like traits generally showed...
We examined whether there were changes over time in the qualitative and quantitative phenotype of individuals who received the diagnosis of Autistic Disorder.