Variants in Non-Coding DNA Contribute to Inherited Autism Risk
Personalized Medicine Initiatives Offer Hope to Acutely Ill Children at Nicklaus Children’s Hospital
MIAMI – April 17, 2018 – Nicklaus Children’s Hospital, in collaboration with Rady Children’s Institute for Genomic Medicine and Sanford Health, has launched two genomic medicine research protocols to more effectively diagnose and treat children with unexplained illnesses. The three participating entities have a shared commitment to clinical innovation and research collaboration that enhance patient […]
Nicklaus Children’s to Implement Rady WGS to Diagnose Sick Kids
KFSHRC seminar’s stress on impact of Precision Medicine
Clinical Trial in Record Time
Rady Team Demos Improved Outcomes, Cost Savings of Rapid Whole Genome Sequencing in NICU
NEW YORK (GenomeWeb) – Researchers at the Rady Children’s Institute for Genomic Medicine have demonstrated that their rapid whole-genome sequencing diagnostic test for infants with unknown but suspected genetic disorders who are in the neonatal intensive care can save babies’ lives and be cost-effective.
Faster, Faster!
Doctors Could Help Sick Babies With Rapid Genetic Tests
In August 2016, Amy Jaeger and Robert Supple became the parents of a daughter they named Rylee. Instead of spending their first months with their baby in blissful exhaustion, the new parents were faced with panic — their baby was shaking and spasming, and they didn’t know why. They took Rylee to a number of […]
Fast genome tests are diagnosing some of the sickest babies in time to save them
Rylee Supple seemed like a perfectly healthy baby when she was born in August 2016. But after a few months, her parents, Amy Jaeger and Robert Supple, realized something wasn’t right: instead of making normal baby movements, like kicking and grasping, Rylee’s body would shake and spasm.