6th Floor, Suite 600,
Room / Suite600
My research is focused on understanding and identifying genetic risk factors for complex diseases with a specific focus on diseases that disproportionately impact minorities and genetic factors related to women’s health and reproductive outcomes. To conduct these studies I utilize large clinical databases that link electronic health record (EHR) information to DNA and the Right from the Start cohort, a community-based prospective pregnancy cohort.
My current research projects include genetic studies of preterm birth, miscarriage, uterine fibroids, pelvic organ prolapse, and keloids. These studies include genome-wide association analyses, next-generation sequencing, evaluation of biomarkers, and phenome-wide association studies.