Jacqueline Harris, MD

Jacqueline Harris, MD's picture
Director, Tuberous Sclerosis Clinic

Kennedy Krieger Institute
707 N. Broadway, 5001
Baltimore, MD 21205
Phone: (443) 923-2746
Email: Weissman@kennedykrieger.org

Dr. Jacqueline Harris is the director of the Tuberous Sclerosis Clinic at Kennedy Krieger Institute and an assistant professor in neurology at Johns Hopkins Hospital.

Biographical Sketch: 

Dr. Harris received her BA with Honors in English Language and Literature and Neurobiology from The University of Chicago. She earned an MD from Cleveland Clinic Lerner College of Medicine of Case Western Reserve University and an MS in Clinical Research Scholars Program from Case Western Reserve University.

She completed a residency in pediatrics at the Children's Medical Center at UT Southwestern.

Dr. Harris was chief resident in the Neurodevelopmental Disabilities Program at Johns Hopkins Hospital through 2016. She is currently the director of the Tuberous Sclerosis and Related Disorders Clinic at Kennedy Krieger Institute, an attending in the Rehabilitation Unite and Neurology and Neurogenetics Clinic, and a Neurology/Medical consultant to the Neurobehavioral Unit at Kennedy Krieger Institute.

Research Summary: 

Dr. Harris is interested in genetic and epigenetic causes of neurdevelopmental disorders - particularly intellectual disability - and how specific genetic and epigenetic changes lead to specific neuroanatomic, neurophysiologic and cognitive phenotypes. She is also interested in developing specific cognitive profiles in genetic syndromes as potential outcome measures for trails and to help localize deficits. Most of her research is currently centered around Kabuki syndrome.

Research Publications:

Bjornsson HT, Benjamin JS, Zhang L, Weissman J, Gerber EE, Chen YC, Vaurio RG, Potter MC, Hansen KD, Dietz HC (2014). Histone deacetylase inhibition rescues structural and functional brain deficits in a mouse model of Kabuki syndrome. Sci Transl Med. 6(256), 256ra135. Abstract
Weissman JR, Kelley RI, Bauman ML, Cohen BH, Murray KF, Mitchell RL, Kern RL, Natowicz MR (2008). Mitochondrial disease in autism spectrum disorder patients: a cohort analysis. PLoS One. 3(11), e3815. Abstract

Other Publications:

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