The GeneDx Blog
Two brave parents said yes to genome-based newborn screening—and found answers right away when their newborn started having seizures.
Like many children with a rare condition, Simon’s health problems were initially thought to be flukes
Answers for Bodhi: After two years of searching, an exome test identified his rare condition
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
