KCTD13 a Driver of Neurodevelopmental Phenotypes Associated with the 16p11.2 CNV
Golzio, Willer et al., Nature
An international team led by investigators at Duke University shows that KCTD13 "is a major driver for the neurodevelopmental phenotypes associated with the 16p11.2 CNV [copy-number variant]," a finding that it says substantiates "the idea that one or a small number of transcripts within a CNV can underpin clinical phenotypes, and offer an efficient route to identifying dosage-sensitive loci."
Personalized Medicine and IT
We caught up with Sandy Aronson, executive director of IT of the Partners HealthCare Center for Personalized Genetic Medicine, during the Personalized Medicine Conference in Boston, MA. Aronson discussed IT challenges associated with the $1,000 genome, the GeneInsight Suite and GIGPAD software solutions developed by his lab to facilitate the use of genetic information in the clinic, and more.
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