After years of steady decline, the number of U.S. children without health insurance rose by 276,000 in 2017.

Adding motor and sensory data boosts the accuracy of Research Domain Criteria — a broad research framework adopted by the U.S. National Institute of Mental Health — for predicting autism.

Austria must train more autism specialists, expand its research funding and build more centers for autism diagnosis and treatment.

The network of researchers keeping tabs on autism prevalence in U.S. children plans to follow up with some of those children in adolescence.

A pioneering project is showing how, 17 years since the first draft of the human genome, our genes are giving up their secrets and bringing hope to parents around the world.

Telling coworkers you are autistic can bring acceptance, but it may also hinder advancement.

Too few doctors accept Medicaid, and foster families also face the challenge of coordinating treatment decisions between government welfare agencies and biological parents.

Responding to serious concerns about its policy defining certain kinds of research as ‘clinical trials,’ the U.S. National Institutes of Health has postponed enforcing parts of the policy until September 2019.

Papers in medical journals go through rigorous peer review and meticulous data analysis. Yet many of these articles are missing a key piece of information: the financial ties of the authors.

A newly formed group of leaders from the U.S. National Institutes of Health (NIH) is poised to generate funding opportunities for child health research, including autism science.