Departments & Organizations
Genetics: Cytogenetics Laboratory
Yale Combined Program in the Biological and Biomedical Sciences (BBS): Molecular Cell Biology, Genetics and Development: Genetics and Genomics; Human Disease
My laboratory focuses on the molecular characterization of human chromosome abnormalities. Molecular methods such as fluorescence in situ hybridization (FISH) mapping using YAC or BAC clones, microsatellite allelotyping, and sequencing analysis of SNP variants and gene mutations have been used. We are initiating high through-put chromosome-specific and genome-wide array-based analysis for mapping segmental deletions/duplication and sequencing rearrangement breakpoints. The goals of this laboratory are to identify disease-causing genes or genetic markers of diagnostic and prognostic values, and to dissect underlying molecular mechanisms.
Education & Training
|PhD||University of Alabama at Birmingham (1996)|
|Postdoc Fellow, Clinical Cytogenetics||Yale School of Medicine|
|Postdoc Fellow, Clinical Molecular Genetics||University of Alabama at Birmingham|