This summer will mark ten years since scientists sequenced the human genome. What have we gained from knowing those 3 billion base pairs?
Spectrum: Autism Research News
Rare or common, inherited or spontaneous, mutations form the core of autism risk.
Young mouse models of fragile X syndrome show a significant lag in the development of synapses, the connections between neurons, according to a study published in Neuron. The findings suggest that a similar mistiming may be responsible for the sensory problems — such as hypersensitivity to touch and sound — sometimes seen in people with fragile X syndrome.
With an openness to collaboration and a healthy dose of daring, Evan Eichler has turned his offbeat interest in repeat DNA sequences into a new understanding of how genomes evolve, expediting the search for genes disrupted in autism.
The ability to recognize faces and interpret facial expressions is programmed partly by genes and inherited separately from other traits, according to three independent studies published this year.
Researchers have found a higher density of several types of interneurons — nerve cells that connect sensory and motor neurons in the brain— in postmortem brain tissue from individuals with autism, compared with healthy controls. The findings appear in the February issue of Acta Neurologica Scandinavica.
Several genetic and animal studies in the past year have found intriguing ties between autism and DISC1, one of the oldest candidate genes for psychiatric disorders.
When thinking about themselves, adults with autism have lower activity in two specific brain regions than do healthy controls, according to an imaging study published in the February issue of Brain.
Researchers are using dogs as models of psychiatric and behavioral conditions, including obsessive-compulsive disorder and autism.