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Are there differences in the behavioural phenotypes of Autism Spectrum Disorder probands from simplex and multiplex families?Behavioural differences in children with Autism Spectrum Disorder from simplex and multiplex families
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Maternal vitamin D levels during pregnancy and offspring eating disorder risk in adolescenceThis is the first study to link low gestational vitamin D to increased eating disorder risk in female offspring of Caucasian mothers.
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Common variation contributes to the genetic architecture of social communication traitsSocial communication difficulties represent an autistic trait that is highly heritable and persistent during the course of development.
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A "bottom-up" approach to aetiological research in autism spectrum disordersAutism spectrum disorders (ASD) are currently diagnosed in the presence of impairments in social interaction and communication, and a restricted range of...
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Associations between Handedness and Cerebral Lateralisation for Language: A Comparison of Three Measures in ChildrenIt has been suggested that quantitative measures of differential hand skill or reaching preference may provide more valid measures than traditional...
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Do hypertensive diseases of pregnancy disrupt neurocognitive development in offspring?The current study sought to determine whether gestational hypertension and pre-eclampsia are associated with neurocognitive outcomes in middle childhood.
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Sex-specific associations between umbilical cord blood testosterone levels and language delay in early childhoodPreliminary evidence suggests that prenatal testosterone exposure may be associated with language delay. However, no study has examined a large sample of...
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Late-talking and risk for behavioral and emotional problems during childhood and adolescenceAlthough many toddlers with expressive vocabulary delay ("late talkers") present with age-appropriate language skills by the time they are of school age,...
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Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian populationWe have conducted an association study in a novel sample derived from the Australian population to further investigate the role of dyslexia candidate genes.