Tony Charman and Catherine Lord answer questions from Spectrum’s webinar on the Lancet Commission’s recommendations for autism research.

Konstantinos “Kostas” Zarbalis talks about the upside of unexpected experimental results, and why he eats just one meal per day.

The Rett Syndrome Global Registry is gathering data from people around the world with the rare condition to support clinical trials.

The current system to approve genetic and metabolic conditions for newborn screening can’t keep pace with research on new therapies. Don Bailey wants to bring it up to speed.

Excitatory and inhibitory neurons can derive from the same cellular source in the developing human brain, a new study suggests, overturning a 20-year-old hypothesis. Tomasz Nowakowski discusses the finding’s implications for autism research.

When pediatrician Kristin Sohl isn’t building programs to improve care for and research about autistic people, you can find her reading psychological thrillers or playing Pokémon Go.

The questionnaires used to screen for autism are far from perfect, and tweaking them may not be enough. Roald Øien wants researchers to find better solutions.

Insurance claims data are useful for autism research, but the field needs to standardize how they are mined, Shea says.

Andrew Whitehouse talks about his conservation efforts in the Australian Outback, what it’s like to be an identical twin and why he leaves work promptly at 5 p.m.

Audrey Brumback riffs about volunteering in Mexico, having a lab next door to her husband’s and why she sometimes cries at work.