Clinical conundrum; double data; mission control
Some say a focus on basic neuroscience is crushing clinical research, a gene database gets a big upgrade, and Autism Speaks revises its goals.
Some say a focus on basic neuroscience is crushing clinical research, a gene database gets a big upgrade, and Autism Speaks revises its goals.
It’s been 50 years since the first description of Rett syndrome, a hodgepodge of supplements sickens a boy with autism, and gender stereotypes make it hard to spot girls on the spectrum.
The presidential candidates sound off on science, dogs may hold clues about social behavior in people, and gender matters when it comes to reference letters for postdocs.
A group of savvy parents jump-started autism research in California, but they also set the research agenda.
Non-white adults with autism may feel forgotten, names on papers may bias peer reviewers, and eLife will begin charging publication fees.
Some parents are starting ‘N-of-1’ studies for autism, but their efforts don’t always get taken seriously.
Mark Zuckerberg and Priscilla Chan pledge $3 billion to treat disease, new rules require researchers to share clinical trial results, and neuroscientists unite for big brain projects.
A university must pay the U.S. government $9.5 billion for false claims on federal grants, a mother explains her decision to donate her son’s brain to science, and investigators struggle to enroll families in autism research.
Hillary Clinton releases an expansive mental health care agenda; researchers call for autism research in sub-Saharan Africa; and a scientist alleges gender bias at the National Institutes of Health.