Odd men out
Animal research hints that sex hormones may be responsible for the gender bias in autism. More research is needed in people to back this up, says a new review.
From parental age to infection during pregnancy, environmental elements can influence autism risk.
Animal research hints that sex hormones may be responsible for the gender bias in autism. More research is needed in people to back this up, says a new review.
No matter which of the numerous genetic and environmental risk factors has caused autism, the part of the system that is always affected is most likely to be found at the cognitive level, argues Uta Frith, a leader in the field of cognitive neuroscience.
Mice missing the autism candidate gene MET have connections in the cortex that are twice as strong as those in controls, according to a new study.
Identical twins can be genetically different, which could explain why they do not always share disorders such as schizophrenia or autism, according to a study published in March in PLoS One.
As awareness about autism has spread in California, lower-income families have become more likely to seek a diagnosis of autism, says a new study.
Early trauma alters both behavior and gene expression in three generations of mice, suggesting that epigenetic changes may contribute to ‘hidden heritability’ in neuropsychiatric disorders.
Children with autism and those who have fathers older than 31 both have lower-than-normal levels of proteins that regulate other genes, according to a study published in February in PLoS One.
Cultural stigma, lack of awareness about mental health and poor medical infrastructure have led to inaccurate diagnoses and artificially low autism prevalence in many countries around the world, epidemiologists say.
Clumsiness in children with autism may result from the same genetic mutations that contribute to the disorder, according to a study published in February in the Journal of Autism and Developmental Disorders.
Genetic syndromes associated with autism are increasingly being diagnosed in utero because of techniques that can identify subtle mutations in the genome. But the technology is ahead of the ethical debate on whether and how to inform parents about mutations with unknown effects.