Faculty > Stephen J. Haggarty    
       

Stephen J. Haggarty, Ph.D.

Stephen J. Haggarty, Ph.D.
Assistant Professor of Neurology
Harvard Medical School

Center for Human Genetic Research
Massachusetts General Hospital
Richard B. Simches Research Center
CPZN-5242
185 Cambridge St.
Boston, MA 02114

Phone: (617) 324-9633
Fax: (617) 643-3202
haggarty@chgr.mgh.harvard.edu
 
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Stephen J. Haggarty, Ph.D., is an Instructor of Neurology at Harvard Medical School and Assistant in Neuroscience at the Massachusetts General Hospital. He is also the director of the Chemical Neurobiology Laboratory (CNL) within the Stanley Center for Psychiatric Research at the Broad Institute. Dr. Haggarty graduated from The University of British Columbia, Vancouver in 1997 with a degree in Genetics and received his Ph.D. from Harvard University in 2003, for his work developing methodology for high-throughput chemical screening and the identification of small-molecule probes of the cell cycle and chromatin remodeling. Dr. Haggarty then joined the Broad Institute of Massachusetts Institute of Technology and Harvard University, as a research Fellow in the Chemical Biology Program and member of the Psychiatric Disease Initiative.

Dr. Haggarty’s current research interests focuses on using chemical approaches to understanding the molecular and genetic basis of neuropsychiatric and neurodegenerative disorders, including schizophrenia, bipolar disorder, and Huntington’s disease. The overall aims of his research group and the CNL are three-fold: 1) the development of novel cellular and biochemical assays for screening small molecules, RNAi, and cDNA libraries in order to identify probes targeting neuropsychiatric and neurodegenerative disease-relevant mechanisms and pathways; 2) the identification of targets and functional characterization of new molecular probes using the appropriate counter screens, proteomics and biochemical assays in neuronal cells and brain tissue models; and 3) through collaborators around the world, to characterize the function of candidate susceptibility genes and to test new mechanisms of action compounds in animal behavioral models involving the response to psychoactive drugs, memory, and disease-relevant mutations.