ASHG 2021
Recent articles
Community Newsletter: Twitter dispatches from the American Society of Human Genetics annual meeting
In this week’s Community Newsletter, we highlight online conversations about the conference’s technology foibles and scientific tours de force.
Community Newsletter: Twitter dispatches from the American Society of Human Genetics annual meeting
In this week’s Community Newsletter, we highlight online conversations about the conference’s technology foibles and scientific tours de force.
Subset of autism cases linked to mutations in noncoding genome
Autism involves mutations in noncoding portions of the genome in at least 3 percent of people with the condition. The mutations occur in regions that help regulate known autism-linked genes.
Subset of autism cases linked to mutations in noncoding genome
Autism involves mutations in noncoding portions of the genome in at least 3 percent of people with the condition. The mutations occur in regions that help regulate known autism-linked genes.
Autism-linked genetic variants increase, decrease intelligence
Common and rare variants in or near autism-associated genes can have opposite effects on cognition.
Autism-linked genetic variants increase, decrease intelligence
Common and rare variants in or near autism-associated genes can have opposite effects on cognition.
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.