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Vandana Shashi is a Professor in the Department of Pediatrics at Duke University, specializing in Medical Genetics and Genomics. She is a significant figure in research focused on undiagnosed rare diseases, working as the principal investigator for the Duke site of the NIH Undiagnosed Diseases Network (UDN). Her role involves comprehensive clinical evaluations and genome sequencing to assist patients with undiagnosed illnesses. Shashi has a particular interest in the 22q11.2 deletion syndrome, which she studies in relation to learning disabilities and mental health risks. As co-chair of the UDN steering committee and an investigator with the International Brain Behavior Consortium, her work seeks to unravel the genetic underpinnings of serious mental illnesses, with a focus on schizophrenia, which affects a notable percentage of individuals with the condition. She has a rich educational background, holding MD and M.B.B.S. degrees from Kasturba Medical College, with further training in pediatric residency and medical genetics. Shashi has received multiple grants to promote early identification and comprehensive genomic medicine in children with rare diseases.
Duke University • Durham, NC
Leads research and teaches in Medical Genetics and Genomics.
Duke University • Durham, NC
Involved in teaching and clinical research.
Duke University • Durham, NC
Taught and conducted research in pediatrics.
Department of Biomedical Engineering (MS program)