By studying genetic data from people born with congenital heart disease or autism, researchers have uncovered almost two dozen genes […]
Researchers have identified a form of autism that is caused by the presence of an excessive number of synapses in […]
Researchers have identified ultra-rare, likely gene-disruptive variants unique to autism families, revealing 28 novel candidate risk genes. The genetics of […]
A recent study has revealed underlying genetic mechanisms behind some of the shared cognitive impairments in both autism spectrum disorder […]
Using machine learning, researchers have identified several patterns of maternal autoantibodies highly associated with the diagnosis and severity of autism. […]
Biomarkers in human sperm have been found to indicate a propensity to autism spectrum disorder in the fathers’ offspring. Autism […]
Autism spectrum disorder (ASD) affects one in 54 children in the US and is associated with a heritability between 50-90%. […]
With the upcoming FIFA World Cup being hosted in Qatar, our latest World of Genomics takes us to the Persian […]
Dr Dianne Newbury is a Senior Lecturer and Researcher at Oxford Brookes University, UK. Dianne’s research focusses on speech and […]
Stephen Scherer is a Canadian scientist who founded Canada’s first human genome centre, the Centre for Applied Genomics (TCAG) at […]
