Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
Probabilistic record linkage of de-identified research datasets with discrepancies using diagnosis codes.
Auditory brainstem response in infants and children with autism spectrum disorder: A meta-analysis of wave V.
The shifting model in clinical diagnostics: how next-generation sequencing and families are altering the way rare diseases are discovered, studied, and treated.
