ASHG 2020
Recent articles
Analysis combining variants, conditions uncovers hundreds of neurodevelopmental genes
The first genetic analysis of multiple types of variants from people with autism or other neurodevelopmental conditions reveals hundreds of genes that may be linked to neurodevelopment.
Analysis combining variants, conditions uncovers hundreds of neurodevelopmental genes
The first genetic analysis of multiple types of variants from people with autism or other neurodevelopmental conditions reveals hundreds of genes that may be linked to neurodevelopment.
Reactions from ASHG 2020
Get the inside scoop from the 2020 American Society of Human Genetics annual meeting.
Reactions from ASHG 2020
Get the inside scoop from the 2020 American Society of Human Genetics annual meeting.
First analysis of African autism cohort reveals millions of new variants
Genome sequences from a research cohort of autistic African children and their families have revealed more than 4 million novel variants, some of which occur in genes not previously linked to the condition.
First analysis of African autism cohort reveals millions of new variants
Genome sequences from a research cohort of autistic African children and their families have revealed more than 4 million novel variants, some of which occur in genes not previously linked to the condition.
Parental age plays small role in large mutations tied to autism
Most of the large, spontaneous genetic mutations tied to autism are passed down from fathers. But, unlike with smaller mutations, a parent's age is unlikely to up the rate at which they occur.
Parental age plays small role in large mutations tied to autism
Most of the large, spontaneous genetic mutations tied to autism are passed down from fathers. But, unlike with smaller mutations, a parent's age is unlikely to up the rate at which they occur.
Explore more from The Transmitter
Molecular changes after MECP2 loss may drive Rett syndrome traits
Knocking out the gene in adult mice triggered up- and down-regulated expression of myriad genes weeks before there were changes in neuronal function.
Molecular changes after MECP2 loss may drive Rett syndrome traits
Knocking out the gene in adult mice triggered up- and down-regulated expression of myriad genes weeks before there were changes in neuronal function.
Learning scientific rigor: Q&A with Konrad Kording and Hao Ye
The developers of a new open-access curriculum to teach rigor discuss confirmation bias and other common errors in scientific thinking, plus ways to avoid these missteps.
Learning scientific rigor: Q&A with Konrad Kording and Hao Ye
The developers of a new open-access curriculum to teach rigor discuss confirmation bias and other common errors in scientific thinking, plus ways to avoid these missteps.
This paper changed my life: Stephanie Palmer on the ties between human speech and birdsong—and her ‘informal life coach’
A groundbreaking review by Allison Doupe, who was Palmer’s mentor, and Patricia Kuhl helped shape the field’s understanding of the neural and evolutionary dynamics of speech.
This paper changed my life: Stephanie Palmer on the ties between human speech and birdsong—and her ‘informal life coach’
A groundbreaking review by Allison Doupe, who was Palmer’s mentor, and Patricia Kuhl helped shape the field’s understanding of the neural and evolutionary dynamics of speech.