New AAP Guidance: Exome and genome sequencing recommended as first-line tests. Learn more
The GeneDx Blog
A breakthrough in autism research: 230 new genes now associated with autism
How to talk to your child’s doctor about genetic testing
Introducing GeneDx Discover Snapshot for patient advocacy organizations
One courageous mom found the genetic cause behind her daughter’s cerebral palsy–and then found the silver lining
A rare disease diagnosis from the start: One family’s experience with genome-based newborn screening
Answers for Bodhi: After two years of searching, an exome test identified his rare condition
Like many children with a rare condition, Simon’s health problems were initially thought to be flukes
Rare Disease Month spotlight: The top five psychological benefits of a genetic diagnosis
What can a genetic diagnosis do for a child with epilepsy?
Are critically ill babies put on an unnecessary diagnostic odyssey because of conventional medical protocols? A new study says yes
Racial disparities in genetic testing: The problem may not be what you think
Just how much of a difference does it make to order exome sequencing first?
A genetic condition may be hiding behind epilepsy
A diagnosis even before symptoms begin: First results from the groundbreaking GUARDIAN study
One mom’s seven-year journey to find answers for her son’s illness
For Carlotta’s family, early intervention meant everything
Scientific showcase at ASHG 2024
