Dup15q 2016
Recent articles
Registry for autism-linked syndrome spurs new research
Nine U.S. clinics are pooling their data to create a registry of people who have an extra copy of a region on chromosome 15 called 15q11-13, a genetic abnormality often found in people with autism.
Registry for autism-linked syndrome spurs new research
Nine U.S. clinics are pooling their data to create a registry of people who have an extra copy of a region on chromosome 15 called 15q11-13, a genetic abnormality often found in people with autism.
Motor troubles in Angelman may stem from nerve fiber anomaly
Unusually thin nerve fibers in the brain may underlie the motor difficulties seen in children with Angelman syndrome, an autism-related condition.
Motor troubles in Angelman may stem from nerve fiber anomaly
Unusually thin nerve fibers in the brain may underlie the motor difficulties seen in children with Angelman syndrome, an autism-related condition.
Explore more from The Transmitter
Open-access neuroscience comes to the classroom: Q&A with Liz Kirby
Neuroscience textbooks can be prohibitively expensive for some undergraduate students. A new open-access alternative seeks to change that.
Open-access neuroscience comes to the classroom: Q&A with Liz Kirby
Neuroscience textbooks can be prohibitively expensive for some undergraduate students. A new open-access alternative seeks to change that.
Solving intelligence requires new research and funding models
Our research ecosystem isn't built to deliver the breakthroughs needed to understand intelligence at scale. We need a dedicated research institution to take up the task.
Solving intelligence requires new research and funding models
Our research ecosystem isn't built to deliver the breakthroughs needed to understand intelligence at scale. We need a dedicated research institution to take up the task.
Impaired molecular ‘chaperone’ accompanies multiple brain changes, conditions
Rare genetic variants in a protein-folding complex contribute to a spectrum of phenotypes that encompass brain malformations, intellectual disability, autism and seizures, according to a new “hallmark” study.
Impaired molecular ‘chaperone’ accompanies multiple brain changes, conditions
Rare genetic variants in a protein-folding complex contribute to a spectrum of phenotypes that encompass brain malformations, intellectual disability, autism and seizures, according to a new “hallmark” study.