SNPs
Null and Noteworthy: Modified MRI; father findings
This month’s newsletter tackles null findings from an attempted replication of a “revolutionary” MRI approach and an analysis of family genetics.
Null and Noteworthy: Modified MRI; father findings
Genome scan spots common variant differences between autism and ADHD
Common variants in five regions of the genome may determine whether someone has one condition versus the other.
Genome scan spots common variant differences between autism and ADHD
New resource maps gene expression, regulation in neuron subtypes
The catalog could help researchers understand the effects of autism-linked DNA variants that fall outside genes.
New resource maps gene expression, regulation in neuron subtypes
Information loss may weaken autism genetic scores
Even the best data practices and technology drop key variants in attempts to predict autism likelihood.
Information loss may weaken autism genetic scores
New resource tracks genetic variations in Han Chinese populations
An online database called NyuWa catalogs genetic variations among nearly 3,000 individuals and provides a comprehensive reference genome for the Han people.
New resource tracks genetic variations in Han Chinese populations
X chromosome exerts extra influence on brain development
The X chromosome holds stronger-than-expected genetic sway over the structure of several brain regions. The genes that may underlie this oversized influence have ties to autism.
X chromosome exerts extra influence on brain development
Patchwork mutations present a new frontier for autism research
Mosaic mutations, which affect only some of the body’s cells, play a small but meaningful role in autism. Though they are difficult to study, researchers are working to master their complexity.
Patchwork mutations present a new frontier for autism research
Disrupted cell skeletons may explain brain wiring changes in autism-linked condition
Neuronal axons ignore guidance cues after a mutation in the gene TSC2 disrupts signaling through RhoA, a protein regulated by many autism-linked genes.
Disrupted cell skeletons may explain brain wiring changes in autism-linked condition
Genetic variants in protein target sites may contribute to autism
Mutations that disrupt binding sites in RNA molecules may play a role in autism and a variety of psychiatric conditions, according to a new study.
Genetic variants in protein target sites may contribute to autism
Scan of genomes for inherited variants lays bare new autism candidate
Lowered expression of a gene called DDHD2 may increase a person's likelihood of having autism, according to a new analysis.
Scan of genomes for inherited variants lays bare new autism candidate
Explore more from The Transmitter
Some minimally verbal autistic people show signs of written-language familiarity, study suggests
But researchers not involved in the work worry the findings could be used to support discredited facilitated-communication techniques.
Some minimally verbal autistic people show signs of written-language familiarity, study suggests
But researchers not involved in the work worry the findings could be used to support discredited facilitated-communication techniques.
Cocaine, morphine commandeer neurons normally activated by food, water in mice
Confirming a long-held hypothesis, repeated exposure to the drugs alters neurons in the nucleus accumbens, the brain’s reward center, and curbs an animal’s urge for sustenance.
Cocaine, morphine commandeer neurons normally activated by food, water in mice
Confirming a long-held hypothesis, repeated exposure to the drugs alters neurons in the nucleus accumbens, the brain’s reward center, and curbs an animal’s urge for sustenance.
X chromosome inactivation; motor difficulties in 16p11.2 duplication and deletion; oligodendroglia
Here is a roundup of autism-related news and research spotted around the web for the week of 6 May.
X chromosome inactivation; motor difficulties in 16p11.2 duplication and deletion; oligodendroglia
Here is a roundup of autism-related news and research spotted around the web for the week of 6 May.