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Andrea L. Saperstein Gropman, MD

The Center for Neuroscience and Behavioral Medicine

Departments
Neurology
Neurodevelopmental Pediatrics and Neurogenetics
Genetics and Metabolism

Programs
Movement Disorders Program
Division Chief, Neurogenetics Program


Children’s Research Institute (CRI)
Center for Neuroscience Research
View CRI Profile for Andrea L. Gropman
Specialties: Genetic Disorders
Board CertificationsAmerican Board of Pediatrics
American Brd of Med Genetics/Clin Biochemical Gen
American Board of Psychiatry/Neurology-Child Neuro
American Board of Med. Genetics/Clinical Genetics
American Board of Ped/Neurodevelop. Disabilities
National Provider Identifier1407848005
E-Mail
Service LocationsChildren's National Medical Center - Sheikh Zayed Campus for Advanced Children's Medicine
111 Michigan Avenue, NW
Washington, DC 20010
Map | Driving Directions
Phone: 202-476-5000

Children's Outpatient Center in Annapolis
888 Bestgate Road
Suite 320
Annapolis, MD 21401
Map | Driving Directions

Phone: 410-266-6582
Fax: 410-266-0943
Center Manager: Sheilah Pape
Biography

Dr. Gropman specializes in neurogenetics, with a focus on mitochondrial disorders and Smith Magenis syndrome.
Education
TypeSchoolLocationDegreeField of StudyYears
Undergraduate Education Brandeis University Bachelor of Arts Biology 1986
Medical School University of Massachusetts Medical Center Medical School Worcester, MADoctor of Medicine 1992

Training
TypeInstitutionLocationPositionSpecialtyYears
Residency Program Johns Hopkins University School of Medicine Baltimore, MDResident Pediatrics 1992 - 1994
Internship Program Johns Hopkins Hospital Baltimore, MDInternship Pediatrics 1993 - 1994
Residency Program George Washington University Washington, DCResident Neurology 1994 - 1995
Fellowship Program Children's National Medical Center Washington, DCFellow Neurology 1995 - 1997
Fellowship Program National Institutes of Health Bethesda, MDFellow Medical Genetics 1997 - 2000
National & International Recognitions
AwardInstitutionEventYear
Top DoctorsNorthern Virginia Magazine2013
Caring Star AwardGeorgetown University2006
100 People to WatchWashingtonian Magazine1999
Outstanding Junior Member/Resident AwardChild Neurology Society1998
Mark Platt Award1997
Janet M. Glasgow memorial achievement citationAmerican Medical Women’s Association1992

Affiliations and Memberships
TitleInstitutionCommittee / SectionYears
MemberAmerican Academy of Pediatrics
MemberAmerican Academy of Neurology
MemberAmerican Society of Medical Genetics
MemberAmerican College of Medical Genetics
MemberChild Neurology Society
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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