We are studying the chromodomain gene CHD7 in the inner ear and central nervous system. Specifically, we focus on genes predicted to influence neuronal differentiation and migration. 

CHD7 is mutated in CHARGE syndrome, a congenital anomaly condition affecting the brain, eyes, ears, heart, and craniofacial structures. We use genetic approaches in mice, mouse cells, and human cells to study how loss of CHD7 disrupts organ development. 

We also participate in collaborative studies to apply next-generation sequencing to better understand the genetic mechanisms of autism and other developmental disorders of the nervous system.  These studies have important implications for diagnosing and treating developmental disorders ranging from hearing loss and anosmia to autism and intellectual disability.

Please take a look at our Research, Publications & Lab Members. Please Contact Us if you would like to know more about our research!

Publications  

People   

BOOKWORM PROTOCOL

PLEASE JOIN YOUR 8th FLOOR MSRBIII

CO-WORKERS FOR BOOK CLUB

Meeting:

to be announced  

2-3 pm Taubman Library 6215



Future Titles:

A mix of “lab-related” fiction and non-fiction. Suggestions are welcomed.


Host:  Jennifer Skidmore camelot@umich.edu

Optional:

Reading the book &  Bring a snack to share