U.S. Department of Health and Human Services
Corinne Silva
 

 Contact Info

 
Tel: 301-451-7335
Email: silvacm@mail.nih.gov
 

 Select Experience

 
  • Assistant/Associate ProfessorDepartments of Medicine and Microbiology, University of Virginia2000-2009
  • Research Assistant ProfessorUniversity of Virginia1993-2000
  • Postdoctoral FellowshipUniversity of Virginia1989-1993
  • Ph.D.University of North Carolina, Chapel Hill1989

Corinne M. Silva, Ph.D.

Program Director, Division of Diabetes, Endocrinology, and Metabolic Diseases

Current Responsibilities & Activities

I administer two signaling research portfolios that together encompass over 100 grants.   One portfolio focuses on signaling and nutrient sensing by elucidating pathways that regulate cellular responses to insulin and other hormones/factors or that reveal the role of nutrient sensing signaling pathways in the development and/or progression of insulin resistance, type 2 diabetes, obesity, and metabolic disease.  Studies involve the identification of regulators, interacting partners, and substrates to elucidate modes of signal transmission, including circadian regulation, that impact physiological systems and result in metabolic dysfunction.  A second signaling related portfolio focuses on the nuclear hormone receptor superfamily, a unique class of proteins that regulate an array of molecular functions, such as homeostasis, reproduction, development, and metabolism. Research topics covered in this portfolio include signal transduction and regulation of gene expression, structure and function of the steroid hormones, receptor structure, interaction with cytoplasmic chaperones and ligands, nuclear translocation, and mediator proteins.

In addition, I oversee a smaller but growing portfolio of research grants that focuses on the role of the intrauterine environment in metabolic disease of the offspring.  These grants include both basic and translational studies that investigate the mechanisms by which the intrauterine environment alters metabolic responses in the offspring.  Research focuses on elucidating the signals that mediate these long-term effects including, but not limited to, intracellular signaling pathways, inflammatory cytokines, nutrient sensing pathways, and epigenetic imprinting.  The ultimate goal of this research is to identify molecular targets that could be used therapeutically to prevent metabolic disease.

In addition to overseeing these grant portfolios, I am the Project Scientist for the Nuclear Receptor Signaling Atlas Consortium that provides a web-accessible bioinformatics resource of current and emerging data on nuclear receptor structure, function, and role in disease.

​Research Programs

Endocrinology and Hormone Signaling
The Endocrinology and Hormone Signaling program supports basic and clinical research on neuroendocrinology, the HPA axis, bone metabolism, mechanisms of nuclear receptor signaling, and signaling pathways involved in nutrient sensing at target tissues

Metabolism, Energy Balance, and Obesity
This program supports research on metabolism, energy balance, and obesity

Obesity, Pregnancy, and the Intrauterine Environment
This program supports basic and clinical research to understand the effects of over-nutrition, obesity, and diabetes on pregnant women and the metabolic health of their offspring

Pathophysiology of Diabetes and Metabolic Disease
This program supports basic and clinical research that addresses the pathophysiology of metabolic diseases, including the etiology of type 1 diabetes and other autoimmune endocrine diseases

Current Committee Memberships

  • Obesity Research Working Group (NIDDK)Member
  • Large Grants Progress Review Committee (DEM)Chair
  • Endocrine Society Research Affairs Core CommitteeMember
  • Steering Committee, Nuclear Receptor Signaling AtlasMember