Laser technique pins source of brain waves linked to autism
Researchers have for the first time identified the type of neurons that produce gamma rhythms, the high-frequency brain waves that are thought to go awry in autism and schizophrenia.
Researchers have for the first time identified the type of neurons that produce gamma rhythms, the high-frequency brain waves that are thought to go awry in autism and schizophrenia.
Applying an emerging technique that combines genetic data and brain scans, researchers have identified two new genes involved in schizophrenia. The method, called ‘imaging genetics’, holds promise for linking genes to brain function in complex psychiatric disorders, including autism.
Newly discovered clusters of proteins in the brains of mice might help researchers understand how connections between neurons go awry in disorders such as mental retardation and autism.
Deleting the gene associated with Rett syndrome from the amygdala region of mouse brains triggers anxiety and problems with learning and memory, according to research published today in the Journal of Neuroscience.
A single gene variant is found more often in people who have both autism and gastrointestinal problems than in healthy controls, and could help explain the mysterious link between autism and the gut, according to a study published in the March issue of Pediatrics.
MeCP2, the gene that causes the autism-related Rett syndrome, is expressed not just in neurons but in glia ― cells that support neurons and help process information ― in the brain, according to a study published online in the March issue of Nature Neuroscience.
The saliva of roughly two-thirds of people on the autism spectrum contains abnormal chemical variations in small proteins, called peptides, according to a study published in the December issue of the Journal of Proteome Research.
The risks of taking sodium valproate or VPA ― a commonly used antiepileptic drug ― during pregnancy may far outweigh the benefits, researchers are cautioning.
A specific deletion on chromosome 15 occurs in one percent of people with a common form of epilepsy, establishing the mutation as the most common risk factor for the disorder, according to research published online 11 January in Nature Genetics.
The absence of a protein involved in a prominent cancer pathway leads to repetitive behaviors and learning deficits in mice, creating a viable model for autism research, according to a study published last week in Neuron.