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Andrea L. Gropman, MD
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Center of Excellence, Departments, and Programs
The Center for Neuroscience and Behavioral Medicine
Neurology
Children’s Research Institute (CRI)
Center for Neuroscience Research
View CRI Profile for Andrea L. Gropman
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| Board Certifications |
American Board of Pediatrics
American Board of Medical Genetics
American Board of Psychiatry and Neurology
American Board of Psychiatry/Neurology-Child Neuro
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National Provider Identifier
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1407848005 |
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| Practice Locations |
Children's National Medical Center - Main Hospital
111 Michigan Avenue, NW
Washington, DC
Phone: 202-476-5000
 
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| Biography |
| mitochondrial disorders, neurogenetics, Smith Magenis syndrome, neurological evaluation of children with genetic conditions and metabolic disorders. |
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| Education |
| Type | School | Location | Degree | Field of Study | Years | | Undergraduate Education | Brandeis University | | Bachelor of Arts | BA | 1986 | | Medical School | University of Massachusetts Medical Center Medical School | Worcester, MA | Doctor of Medicine | | 1992 |
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| Training |
| Type | Institution | Location | Position | Specialty | Years | | Residency Program | Johns Hopkins University School of Medicine | Baltimore, MD | Resident | Pediatrics | 1992 - 1994 | | Residency Program | George Washington University | Washington, DC | Resident | Neurology | 1994 - 1995 | | Fellowship Program | Children's National Medical Center | Washington, DC | Fellow | Neurology | 1995 - 1997 | | Fellowship Program | National Institutes of Health | Bethesda, MD | Fellow | Medical Genetics | 1997 - 2000 |
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| National and International Recognition |
| Award | Institution | Event | Year | | Caring Star Award | Georgetown University | | 2006 | | 100 People to Watch | Washingtonian Magazine | | 1999 | | Outstanding Junior Member/Resident Award | Child Neurology Society | | 1998 | | Mark Platt Award | | | 1997 | | Janet M. Glasgow memorial achievement citation | American Medical Women’s Association | | 1992 | | | | | | | | | | | | | | | | | | | | |
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| Affiliations and Memberships |
| Title | Institution | Committee / Section | Years | | Member | American Academy of Pediatrics | | | | Member | American Academy of Neurology | | | | Member | American Society of Medical Genetics | | | | Member | American College of Medical Genetics | | | | Member | Child Neurology Society | | |
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| Publications |
Journal Article, Brewer, C., Brooks, B.P., Cannon III, R.O., Clauss, S., Collins, F., Domingo, D.L., Gahl, W.A., Gerber, L.H., Gordon, L.B., Graf, J., Gropman, A., Hart, T.C., Introne, W.J., Kim, J., Maria-Turner, M., (2008), The Comprehensive Phenotype of Hutchinson-Gilford Progeria Syndrome, The New England Journal of Medicine, 358, 6 , 592-604.
Journal Article, Bacino, C.A., Beaudet, A.L., Cheung, S.W., Chinault, A.C., Erickson, R., Gropman, A.L., Li, J., Lupski, J.R., Miller, D.T., Patel, A., Pursley, A., Sahoo, T., Scott, D.A., Seashore, M.R., Shaw, C.H., (2007), Microarray Based CGH Detects Chromosomal Mosaicism Not Revealed by Conventional Cytogenetics, American Journal of Medical Genetics.
Journal Article, Duncan, W.C. Jr, Elsea, S., Gropman, A.L., Smith, A.C. (2007), Developments in Smith-Magenis Syndrome, Current Opinions in Neurology, 20, 2 , 125-134.
Journal Article, Adams, D.R., Gropman, A.L. (2007), Atypical Patterns of Inheritance, Seminars in Pediatric Neurology, 14, 1 , 34-45.
Conference Presentation - Poster, Gropman, A. (2007), The New Horizon: Studying the Effects of UCDs on Brain Function, Poster session presented at the National Urea Cycle Disease Foundation, Washington, DC
Conference Presentation - Poster, Gropman, A. (2007), European Experience Conference, Poster session presented at the Neurological Implications of Urea Cycle Disorders at the Urea Cycle Disorders, Barcelona
Conference Presentation - Poster, Gropman, A. (2007), Ornithine Transcarbamylase Deficiency, an Inherited Cause of Hyperammonemia: Current Imaging Strategies, Poster session presented at the Huntington Medical Research Institute/California Institute of Technology-Section on Magnetic Resonance Spectroscopy, Pasadena, CA
Conference Presentation - Poster, Gropman, A. (2006), The Genetics of Fabry Disease, Implications for Female Carriers, Poster session presented at the Fabry Patient Advisory Panel, Crystal City, VA
Book Chapter, Gropman, A.L., Vanderver, A. (2005), Childhood Mitochondrial Disorders and Other Inborn Errors of Metabolism Presenting with White Matter Disease, In Gropman, A.L., Vanderver, A. , Bioimaging in Neurodegeneration, New York, NY, Humana Press, Inc.
Book Chapter, Gropman, A. & Muenke, M. (2005), Holoprosencephaly, In Gropman, A. & Muenke, M. , Management of Genetic Syndromes, 2nd Edition, 291-308, New York, NY, Wiley-Liss, Inc.
For a more comprehensive list of publications for Andrea Gropman, MD view the National Library of Medicine’s PubMed online database |
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