Eric H. Chang, PhD

Assistant Professor, Center for Psychiatric Neuroscience,
The Feinstein Institute for Medical Research

Head, Laboratory of Translational Neuroscience, Center for Psychiatric Neuroscience,
Zucker Hillside Hospital, Psychiatry Research

Phone: (516) 562-1466

About the Investigator

Dr. Chang leads the Laboratory of Translational Neuroscience and is an Assistant Professor at The Feinstein Institute for Medical Research. He is a neuroscientist interested in the pathophysiology underlying psychiatric disorders and in how brain connectivity becomes altered in the course of illness, or during its treatment.

Dr. Chang completed his graduate training at New York University’s Center for Neural Science with a focus on neurophysiology and animal behavior in the lab of Dr. Patricio T. Huerta. His doctoral work at NYU focused on electrophysiological and microstructural deficits in genetically modified (knock-in and knock-out) mouse models of Alzheimer’s disease. Following graduate school, Dr. Chang was a Goldsmith Research Fellow at the Burke Medical Research Institute, a research campus of Weill Cornell Medical College.

Currently, Dr. Chang is utilizing a broad range of modern neuroscience techniques that include state-of-the-art molecular/genetic manipulations, whole-brain tissue clearing, two-photon microscopy, and a battery of behavioral tasks to investigate the functional roles of identified schizophrenia risk genes. The overall aim of these approaches is to use the rodent brain as a model to better understand function, and dysfunction, of the human brain.

Research Focus

Schizophrenia is a highly heritable, disabling brain disorder that affects 1-2% of the world population and is the third leading cause of disability amongst people aged 15-44 in the U.S. Aside from some identified genetic risk factors, the underlying biology of the disorder is not well understood. In particular, what specifically goes wrong within the brain to cause the collection of negative, positive, and cognitive symptoms in schizophrenia is not clear. Thus, one aim of the Laboratory of Translational Neuroscience is to capitalize on recent advances in technology and understanding within the field of neuroscience, and apply them to challenges within psychiatry.

Through a combination of molecular biology and neuroscience techniques, the research group examines the impact of schizophrenia risk genes on a number of levels including mRNA expression in brain tissue, protein labeling and quantification, and whole-brain imaging of immunostained targets in mouse models. Innovative tissue clearing approaches are implemented to allow for brain-wide analyses of neural elements, such as axon-related proteins or specific neurotransmitter receptors. This technology, when coupled with laser microscopy, allows for three-dimensional mapping of mammalian neural circuits on multiple important biological scales.

The functional effect(s) of schizophrenia-related gene mutations in mice is examined using a collection of behavioral tasks, including novel object recognition, open-field, tail-suspension, elevated plus maze, social interaction, and the T-maze test. These assessments test for locomotion differences, anxiety, despair, novelty recognition, sociability, and working memory. Individuals with schizophrenia frequently have impairments in several of these behavioral and cognitive domains.

The ultimate objective in combining these genetic and neuroscientific approaches is to identify causal associations between genomic variation and the symptoms of schizophrenia. As research in the field progresses towards “biological psychiatry”, the hope is that novel therapies, drug targets, and biomarkers will emerge based on the biological processes underlying these disabling brain disorders.


Burke Medical Research Institute, Weill Cornell Medical College, White Plains, NY
Degree: Postdoctoral
Field of Study: Neurophysiology of Disease Models

New York University (NYU), New York, NY
Degree: PhD
Field of Study: Neural Science

University of California at Los Angeles (UCLA), Los Angeles, CA
Degree: BS
Field of Study: Neuroscience

Honors and Awards

2017 NARSAD Young Investigator grantee
2016 Helmsley Scholarship for Interdisciplinary Research
2015 ACNP Meeting Top Poster award
2014 ACNP Meeting Hot Topics selection
2012 Federation of Clinical Immunology Societies (FOCIS) Travel Award
2008 Goldsmith Foundation Research Fellowship
2005 Glenn Foundation, AFAR Scholarship for Research in the Biology of Aging
2004 Dean’s Student Travel Grant, NYU
1999 Departmental Honors in Neuroscience, UCLA
1999 Vice Provost’s Award for Undergraduate Research, UCLA

  1. Chang, E.H., Argyelan, M., Aggarwal, M., Chandon, T.S., Karlsgodt, K.H., Mori, S., Malhotra, A.K. (2017) The role of myelination in measures of white matter integrity: Combination of diffusion tensor imaging and two-photon microscopy of CLARITY intact brains. NeuroImage 147: 253-261. doi:10.1016/j.neuroimage.2016.11.068
  2. Chang, E.H., Argyelan, M., Aggarwal, M., Chandon, T.S., Karlsgodt, K.H., Mori, S., Malhotra, A.K. (2017) Diffusion tensor imaging measures of white matter compared to myelin basic protein immunofluorescence in tissue cleared intact brains. Data in Brief 10: 438-443. doi:10.1016/j.dib.2016.12.018
  3. Vingtdeux, V., Chang, E.H., Frattini, S.A., Zhao, H., Chandakkar, P., Adrien, L., Ohmoto, M., Matsumoto, I., Huerta, P.T., Marambaud, P. (2016) CALHM1 deficiency impairs cerebral neuron activity and memory flexibility in mice. Scientific Reports 6:24250. doi: 10.1038/srep24250.
  4. Chang, E.H., Kirtley, A., Chandon, T.S., Borger, P., Husain-Krautter, S., Vingtdeux, V., Malhotra, A.K. (2015) Postnatal neurodevelopmental expression and glutamate-dependent regulation of the ZNF804A rodent homologue. Schizophrenia Research doi:10.1016/j.schres.2015.06.023
  5. Chang, E.H., Volpe. B.T., Mackay, M., Aranow, C., Watson, P., Kowal, C., Storbeck, J., Mattis, P., Berlin, R., Chen, H., Mader, S., Huerta, T., Huerta P.T., Diamond, B. (2015) Selective impairment of spatial cognition caused by autoantibodies to the N-methyl-D-aspartate receptor. EBioMedicine doi:10.1016/j.ebiom.2015.05.027
  6. Chang, E.H., Frattini, S.A., Robbiati, S., Huerta P.T. (2013) Construction of microdrive arrays for chronic neuronal recordings in awake behaving mice. Journal of Visualized Experiments e50470, doi:10.3791/50470.
  7. Chang, E.H., Huerta P.T. (2012) Neurophysiological correlates of object recognition in the dorsal subiculum. Frontiers in Behavioral Neuroscience 6: 46. doi: 10.3389/fnbeh.2012.00046.
  8. Faust, T.W., Chang, E.H., Kowal, C.K., Berlin, R., Gazaryan, I.G., Bertini, E., Zhang, J., Sanchez-Guerrero, J., Fragoso-Loyo H., Volpe, B.T., Diamond, B., Huerta, P.T. (2010) Neurotoxic lupus antibodies alter brain function through two distinct mechanisms. Proceedings of the National Academy of Sciences USA 107(43): 18569-18574.
  9. Chang, E.H., Rigotti, A., Huerta, P.T. (2009) Age-related influence of the HDL receptor SR-BI on synaptic plasticity and cognition. Neurobiology of Aging 30(3): 407-19.
  10. Chang, E.H., Savage, M.J., Flood, D.G., Thomas, J.M., Levy, R.B., Mahadomrongkul, W., Shirao, R., Aoki, C. and Huerta, P.T. (2006) AMPA receptor downscaling at the onset of Alzheimer’s pathology in double knock-in mice. Proceedings of the National Academy of Sciences USA 103(9), 3410-3415.
  11. Chang, E.H., Kotak, .V.C., and Sanes, D.H. (2003). Long-term depression of synaptic inhibition is expressed postsynaptically in the developing auditory system. Journal of Neurophysiology 90: 1479-1488.

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