Priya Duggal

Priya Duggal

  • Director, Genetic Epidemiology Track

  • Departmental Affiliation(s):

    Epidemiology (Primary)
    Division: Genetic Epidemiology

    Contact Information

    615 N. Wolfe Street
    Room E6539
    Baltimore , Maryland   21205
    US        

    410-955-1213
    410-955-0863

    MD-GEM Training Program: http://www.hopkinsgenetics.org
    Genetic Epidemiology: http://www.hopkinsgenetics.org/genepi/
    Google Scholar: http://scholar.google.com/citations?user=5f316wwAAAAJ&hl=en

    Education

    PhD, Johns Hopkins Bloomberg School of Public Health, 2003
    MPH, Johns Hopkins Bloomberg School of Public Health, 1998

    Overview

    My primary research interest is on the host genetic susceptibility to infectious disease. Infectious diseases epitomize a complex disease because both genetic and environmental factors must play a role in susceptibility and progression of disease. The exposure to an environmental pathogen is critical to risk, but genes in the host can influence innate and adaptive immunity and thus the risk of disease and its severity. My goal is to identify the underlying mechanisms of infectious disease by identifying host genetic variants that alter or influence our immune response. My main research objectives are to decipher and understand host genes that control susceptibility and immunity to infection. I work with adult and pediatric populations within the United States and Internationally (Bangladesh, Brazil) to identify host genes associated with parasitic (E. histolytica, Cryptosporidium, Giardia) and viral (hepatitis C, human immunodeficiency virus, rotavirus) infections. I am especially interested in the role of malnutrition in diarrheal disease and the identification of ancestry specific mutations. I have worked to identify novel immune related genes that may explain the wide heterogeneity in both infection and disease susceptibility using both candidate gene and genome wide association methods. My work has led to the identification of loci for Leishmania related traits, Hepatitis C and Entamoeba histolytica.  I plan to expand the work I have done to date to include host genetic analysis of vaccine response, specifically focused on identifying genes that may contribute to vaccine failures for existing and experimental vaccines. I also am interested in ocular genetics. Working with the Beaver Dam Eye Study, I evaluate the genetics of glaucoma and glaucoma related traits. This includes candidate gene and exome analysis. Overall, my research is at the intersection of genes and environment. Outside of the applied studies I also work towards improving and evaluating genetic methodologies.

    Honors and Awards

    2002  NHGRI Directors Distinguished Service Award, NIH 2004  Fellows Award for Research Excellence, NIH 2005  NHGRI Intramural Research Award, NIH (1 of 3 awarded to an outstanding research fellow) 2012  Teaching Excellence, Johns Hopkins Bloomberg School of Public Health

    Research Interests

    epidemiology, genetics, infectious disease, intraocular pressure, glaucoma, diarrhea, malnutrition, HIV, snp, amebiasis, leishmaniasis, cholera

    Publications

    • Click here for a full list of my PubMed citations
    • Duggal P, Ibay G, Klein AP. Current gene discovery strategies for ocular conditions. In Press, IOVS
    • Jeronimo SMB,Duggal P, Ettinger NA, Nascimento ET, Monteiro GR, Cabrall AP, Pontes NN, Lacerda HG, Queiroz PV, Gomes CEM, Pearson RD, Blackwell JM, Beaty TH, Wilson ME. Genetic Predisposition to Self-Curing Infection with the Protozoan  Leishmania chagasi: A Genome Wide Scan. Journal of Infectious Disease,  2007;196:1261-1269 [PMID: 17955446, PMCID: PMC2330094]
    • Carmolli M, Duggal P, Haque R, Lindow J, Mondal D, Petri WA Jr, Mourningstat P, Larsson CJ, Sreenivasan M, Khan S, Kirkpatrick BD. Deficient serum mannose-binding lectin levels and MBL2 polymorphisms increase the risk of single and recurrent Cryptosporidium infections in young children. J Infect Dis, 2009, Nov; 200(10) 1540-7. [PMID: 19827946]
    • Duggal P#, Gillanders EM#, Holmes TN, Bailey-Wilson JE. Establishing an adjusted p-value threshold to control the family-wide type 1 error in genome wide association studies. BMC Genomics 2008, 9:516