Jennifer Gladys Mulle, MHS, PhD
Department of Human Genetics, Emory University School of Medicine
Genetic and Molecular Epidemiology Certificate Program
Office: Whitehead Biomedical Research Building 305M
Additional Contact Information
My research program is focused on understanding the phenotypic spectrum, natural history, and molecular mechanism of two rare genomic syndromes, 3q29 deletion syndrome and 3q29 duplication syndrome.
The 3q29 deletion is associated with neurodevelopmental and psychiatric phenotypes, including intellectual disability, anxiety disorder, autism spectrum disorder, and an astonishing 40-fold increased risk for schizophrenia.
The 3q29 duplication is associated with a 14-fold increased risk for seizures, as well as increased risk for autism spectrum disorders.
The Emory 3q29 Project (http://genome.emory.edu/3q29/) unites a large, collaborative, interdisciplinary team toward the common goal of understanding these disorders. We examine human subjects and use animal models and cell-based systems, all to identify biological consequences due to altered dosage of 3q29 interval genes.
Areas of Specialization
- 3q29 Deletion Syndrome
- 3q29 Duplication Syndrome
- Psychiatric Genetics
- Rare Genetic Variation and Disease Association
- Postdoctoral Fellow, Emory University, 2011
- PhD, Human Genetics, Johns Hopkins School of Medicine, 2005
- MHS, Genetic Epidemiology, Johns Hopkins School of Public Health, 2001
- BA, Johns Hopkins University, 1993
American Society of Human Genetics
Society of Biological Psychiatry