Teri Manolio, MD, PhD

Teri A Manolio, MD, PhD

Name: Teri A Manolio, MD, PhD

USU Department of Primary Appointment: 
Medicine
Title: 
Professor of Medicine
Faculty Rank: 
Full Professor
Location: 
Walter Reed National Military Medical Center, Bethesda, MD

Research Interests:
Incorporating genomic findings into clinical care
Genome-wide association studies of complex diseases, ethnic differences in disease risk

Office Phone: 
(301) 402-2915

Education

1973-1976 University of Maryland at College Park, Bachelor of Science in Biochemistry
1976-1980 University of Maryland at Baltimore, Doctor of Medicine
1985-1987 The Johns Hopkins University School of Hygiene and Public Health, Master of Health Sciences in Epidemiology
1998-2001 The Johns Hopkins University School of Hygiene and Public Health, Doctor of Philosophy, Human Genetics/Genetic Epidemiology

Representative publications, projects, and/or deployments

  • 1980-1983 Boston City Hospital, Straight Medical Intern and Resident
  • 1983-1984 District of Columbia General Hospital, Chief Medical Resident, Georgetown Service
  • 1984-1987 The Johns Hopkins Medical Institutions, Fellow, Division of Internal Medicine
  • 1987-1994 Medical Officer, Clinical and Genetic Epidemiology Branch, National Heart, Lung, and Blood Institute
  • 1994-2005 Director, Epidemiology and Biometry Program, National Heart, Lung, and Blood Institute
  • 2005-2007 Senior Advisor to the Director, NHGRI, for Population Genomics, National Human Genome Research Institute
  • 2007-2012 Director, Office of Population Genomics, National Human Genome Research Institute
  • 2012- Director, Division of Genomic Medicine, National Human Genome Research Institute
  • 1990- Fellow, American Heart Association, Council on Epidemiology
  • 2003- Fellow, American College of Physicians

Bibliography

  • Manolio TA, Collins FS. Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, Rotimi CN, Slatkin M, Valle D, Whittemore AS, Boehnke M, Clark A, Eichler EE, Gibson G, Haines JL, Mackay TFC, McCarroll SA, Visscher PM. Finding the missing heritability of complex diseases. Nature 2009; 461:747-53.
  • Manolio TA, Brooks LD, Collins FS. A HapMap harvest of insights into the genetics of common disease. Journal of Clinical Investigation 2008; 118:1590-1625.
  • Chanock SJ, Manolio T, Boehnke M, Boerwinkle E, Hunter DJ, Thomas G, Hirschhorn JN, Abecasis G, Altshuler D, Bailey-Wilson JE, Brooks LD, Cardon LR, Daly M, Donnelly P, Fraumeni JF Jr, Freimer NB, Gerhard DS, Gunter C, Guttmacher AE, Guyer MS, Harris EL, Hoh J, Hoover R, Kong CA, Merikangas KR, Morton CC, Palmer LJ, Phimister EG, Rice JP, Roberts J, Rotimi C, Tucker MA, Vogan KJ, Wacholder S, Wijsman EM, Winn DM, Collins FS. NCI-NHGRI Working Group on Replication in Association Studies. Replicating genoty
  • Manolio TA. Genome-wide association studies and disease risk assessment. New England Journal of Medicine 2010; 363:166-76.
  • . Manolio TA, Chisholm RL, Ozenberger B, Roden DM, Williams MS, Wilson R, Bick D, Bottinger EP, Brilliant MH, Eng C, Frazer KA, Korf B, Ledbetter DH, Lupski JR, Marsh C, Mrazek D, Murray MF, O’Donnell PH, Rader D, Relling MV, Shuldiner AR, Valle D, Weinshilboum R, Green ED, Ginsburg GS. Implementing genomic medicine in the clinic: The future is here. Genetics in Medicine 2013; 15:258-67.
  • Manolio TA. Bringing genome-wide association findings into clinical use. Nature Reviews Genetics 2013; 14:549-58.
  • Manolio TA, Murray MF, for the Inter-Society Coordinating Committee on Practitioner Education in Genomics.. The growing role of professional societies in educating clinicians in genomics. Genetics in Medicine 2014; 16:571-72.
  • MacArthur DG, Manolio TA, Dimmock DP, Rehm HL, Shendure J, Abecasis GR, Adams DR, Altman RB, Antonarakis SE, Ashley EA, Barrett JC, Biesecker LG, Conrad DF, Cooper GM, Cox NJ, Daly MJ, Gerstein MB, Goldstein DB, Hirschhorn JN, Leal SM, Pennacchio LA, Stamatoyannopoulos JA, Sunyaev SR, Valle D, Voight BF, Winckler W, Gunter C. Guidelines for investigating causality of sequence variants in human disease. Nature. 2014; 508:469-76.
  • . Manolio TA, Abramowicz M, Al-Mulla F, Anderson W, Balling R, Berger AC, Bleyl S, Chakravarti A, Chantratita W, Chisholm RL, Dissanayake VHW, Dunn M, Dzau VJ, Han B-G, Hubbard T, Kolbe A, Korf B, Kubo M, Lasko P, Leego E, Mahasirimongkol S, Majumdar PP, Matthijs G, McLeod HL, Metspalu A, Meulien P, Miyano S, Naparstek Y, O’Rourke PP, Patrinos GP, Rehm HL, Relling MV, Rennert G, Rodriguez LL, Roden DM, Shuldiner AR, Sinha S, Tan P, Ulfendahl M, Ward R, Williams MS, Wong JEL, Green ED, Ginsburg GS. Global
  • Manolio TA, Fowler DM, Starita LM, Haendel MA, MacArthur DG, Biesecker LG, Worthey E, Chisholm RL, Green ED, Jacob HJ, McLeod HL, Roden D, Rodriguez LL, Williams MS, Cooper GM, Cox NJ, Herman GE, Kingsmore S, Lo C, Lutz C, MacRae CA, Nussbaum RL, Ordovas JM, Ramos EM, Robinson PN, Rubinstein WS, Seidman C, Stranger BE, Wang H, Westerfield M, Bult C. Bedside back to bench: Building bridges between basic and clinical genomic research. Cell 2017; 169:6-12.