Simplex families
Recent articles
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
This month’s newsletter tackles null findings from an attempted replication of a “revolutionary” MRI approach and an analysis of family genetics.
Whole-genome trove ties new genes, variants to autism
A massive update to the MSSNG dataset gives qualified researchers ready access to explore autism’s genetic architecture on a cloud-based platform.
Whole-genome trove ties new genes, variants to autism
A massive update to the MSSNG dataset gives qualified researchers ready access to explore autism’s genetic architecture on a cloud-based platform.
X-chromosome variants help explain autism’s sex bias
The rare variants are also linked to ADHD and Tourette syndrome, two other conditions that disproportionately affect boys and men.
X-chromosome variants help explain autism’s sex bias
The rare variants are also linked to ADHD and Tourette syndrome, two other conditions that disproportionately affect boys and men.
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.
Analysis ups estimate of spontaneous mutations’ role in autism
Spontaneous genetic mutations contribute to autism in 30 to 39 percent of all people with the condition, and 52 to 67 percent of autistic children whose siblings do not also have the condition.
Analysis ups estimate of spontaneous mutations’ role in autism
Spontaneous genetic mutations contribute to autism in 30 to 39 percent of all people with the condition, and 52 to 67 percent of autistic children whose siblings do not also have the condition.
Ultra-rare variants point to new autism candidate genes
A large, whole-genome sequencing study of families yields insights into ultra-rare genetic variants that contribute to autism.
Ultra-rare variants point to new autism candidate genes
A large, whole-genome sequencing study of families yields insights into ultra-rare genetic variants that contribute to autism.
Analysis links 98 genes to neurodevelopmental conditions
Genetic sequences from nearly 53,000 people with autism, developmental delay or intellectual disability reveal strong ties to 98 genes.
Analysis links 98 genes to neurodevelopmental conditions
Genetic sequences from nearly 53,000 people with autism, developmental delay or intellectual disability reveal strong ties to 98 genes.
Decade of data dents idea of a ‘female protective effect’
Brothers and sisters of people with autism are both about two to three times more likely than the general population to have an autistic child themselves.
Decade of data dents idea of a ‘female protective effect’
Brothers and sisters of people with autism are both about two to three times more likely than the general population to have an autistic child themselves.
Fever eases behavioral problems in some children with autism
About 17 percent of children with autism are calmer and more communicative than usual when they have a fever.
Fever eases behavioral problems in some children with autism
About 17 percent of children with autism are calmer and more communicative than usual when they have a fever.
Sizeable fraction of autism risk traced to ‘mosaic’ mutations
Mutations that appear in only some of the body’s cells contribute to autism in about 4 percent of people with the condition.
Sizeable fraction of autism risk traced to ‘mosaic’ mutations
Mutations that appear in only some of the body’s cells contribute to autism in about 4 percent of people with the condition.
Explore more from The Transmitter
Cracking the code of the extracellular matrix
Despite evidence for a role in plasticity and other crucial functions, many neuroscientists still view these proteins as “brain goop.” The field needs technical advances and a shift in scientific thinking to move beyond this outdated perspective.
Cracking the code of the extracellular matrix
Despite evidence for a role in plasticity and other crucial functions, many neuroscientists still view these proteins as “brain goop.” The field needs technical advances and a shift in scientific thinking to move beyond this outdated perspective.
Huntington’s disease gene variants past a certain size poison select cells
The findings—providing “the next step in the whole pathway”—help explain the disease’s late onset and offer hope that it has an extended therapeutic window.
Huntington’s disease gene variants past a certain size poison select cells
The findings—providing “the next step in the whole pathway”—help explain the disease’s late onset and offer hope that it has an extended therapeutic window.
X marks the spot in search for autism variants
Genetic variants on the X chromosome, including those in the gene DDX53, contribute to autism’s gender imbalance, two new studies suggest.
X marks the spot in search for autism variants
Genetic variants on the X chromosome, including those in the gene DDX53, contribute to autism’s gender imbalance, two new studies suggest.