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
Exclusive: The 23 studies the FDA based its expanded leucovorin label on
The studies include 46 people, mostly toddlers, who have cerebral folate deficiency due to variants in a folate transporter.
Exclusive: The 23 studies the FDA based its expanded leucovorin label on
The studies include 46 people, mostly toddlers, who have cerebral folate deficiency due to variants in a folate transporter.
Autism researchers ‘pleasantly surprised’ by list of NIH data project grantees, despite initial concerns
An atypical funding mechanism, truncated application timeline and opaque review process had generated concern over the quality of projects that would be selected for the Autism Data Science Initiative.
Autism researchers ‘pleasantly surprised’ by list of NIH data project grantees, despite initial concerns
An atypical funding mechanism, truncated application timeline and opaque review process had generated concern over the quality of projects that would be selected for the Autism Data Science Initiative.
Exclusive: Who is Richard Frye, the neurologist who researches and advocates for leucovorin as an autism treatment?
Frye has led two placebo-controlled trials of the folate supplement in autistic people; the first was suspended by regulators, and the other has yet to be published.
Exclusive: Who is Richard Frye, the neurologist who researches and advocates for leucovorin as an autism treatment?
Frye has led two placebo-controlled trials of the folate supplement in autistic people; the first was suspended by regulators, and the other has yet to be published.