- February 07, 2025
Valentina Greco Named to '50 Scientists that Inspire' List
- February 06, 2025
Rare Disease Celebration: Feb. 21
- October 01, 2024
Solving the mysteries of Parkinson’s disease
- August 09, 2024
Rebecca Starble and Danielle Miyagishima win 2024 Carolyn Slayman Prize in Genetics for exceptional research and service
- July 12, 2024
AI in Medicine Workshop Explores Cutting-Edge AI Applications in Drug Discovery
- July 09, 2024
Meet Maurizio Chioccioli and his research on lung injury repair
Department of Genetics
The information in genomes provides the instruction set for producing each living organism on the planet. While we have a growing understanding of the basic biochemical functions of many of the individual genes in genomes, understanding the complex processes by which this encoded information is read out to orchestrate production of incredibly diverse cell types and organ functions, and how different species use strikingly similar gene sets to nonetheless produce fantastically diverse organismal morphologies with distinct survival and reproductive strategies, comprise many of the deepest questions in all of science. Moreover, we recognize that inherited or acquired variation in DNA sequence and changes in epigenetic states contribute to the causation of virtually every disease that afflicts our species. Spectacular advances in genetic and genomic analysis now provide the tools to answer these fundamental questions.