Automated Prioritization of Sick Newborns for Rapid Whole Genome Sequencing Expedites Diagnosis
Eight Years of Improving Outcomes through Rapid Precision Medicine™ – What’s Next?
Leveraging Genomic Sequencing in Ambulatory Care to End the Diagnostic Odyssey and Enable Gene Discovery
Advances in Precision Medicine in Pediatric Liver Disease
Genomic Mosaicism and Precision Therapeutics in Pediatric Brain Disease
AI, Genomes, Electronic Health Records and the NICU
Dark Matter, Meth and the Truly Gross: The seedy underbelly of genomics
The Broad Phenotypic Spectrum of Autism Is Attributable to a Genetic Spectrum of Rare and Common Variants
2022: A Pivotal Year for Screening, Diagnosis, and Treatment of Childhood Genetic Diseases
n-Lorem: A Novel Non-Profit Solution for Treatment of Nano-Rare Patients
