Baker, Laura A.
Gene-environment interplay in human behavior, including personality, cognitive and social development. Rich datasets from longitudinal twin study of risk factors for externalizing behavior problems available for analysis.
Chang, Karen T.
Associate Professor of Physiology and Neuroscience
Our lab is interested in understanding how neurons communicate with high fidelity to support complex brain functions. We aim to uncover the molecular and cellular mechanisms that enable precise synaptic signaling and to explore how disruptions in these processes contribute to neurodevelopmental and neurodegenerative disorders. Using Drosophila melanogaster as a genetically tractable model system, we integrate electrophysiology, molecular biology, confocal imaging, proteomics, and behavioral analysis to investigate synaptic function and plasticity.
Ching, Christopher
Assistant Professor Of Research Neurology
Dr. Ching’s research focuses on neuroimaging and genomic markers of psychiatric and neurodegenerative disorders. As a core organizing member of the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium, he designs and implements standardized processing and analysis techniques for large-scale neuroimaging studies. He leads the ENIGMA Bipolar Disorder Working Group, an effort pooling data and resources from around the world to improve our understanding of the biological processes driving bipolar disorder, and studies rare copy number variants like 22q11.2 Deletion Syndrome to understand how genetic mutations can lead to increased risk for developing psychiatric illness. He leads several large-scale transdiagnostic neuroimaging and genomic initiatives using machine learning to map common and distinct brain and clinical factors across mental illnesses.
Cohen, Pinchas
Distinguished Professor of Gerontology, Medicine and Biological Sciences
The Cohen lab studies mitochondrial microproteins. We take a systems biology approach to mitochondria, looking at mitochondrial ORFomics, mito-genomics, mitochondrial-epigenetics, mito-transcriptomics and mitochondrial-proteomics. Our discovery pipeline involves novel bioinformatic approaches to clone and advance disease-relevant mitochondrial-derived peptides. We utilize MiWAS (mitochondrial GWAS), MDPseq (mitochondrial RNAseq) and related tools, to identify new microproteins involved in diseases of aging. Over the last two decades we described multiple novel genes including humanin and its cytoprotective and neuroprotective roles; MOTS-c, which is an exercise-mimetic peptide in which a loss-of-function mutation predisposes to diabetes, that has been advanced to clinical trials in humans; SHLP2, which is involved in neurodegenerative diseases; SHMOOSE, a neuroprotective microprotein that harbors a mutation that predisposes to Alzheimer’s disease, and multiple other previously unrecognized microproteins. Our goal is to continue to develop diagnostic tools and therapeutic targets for health aging
Craft, Cheryl Mae
My well established vision research program encompasses my passion for discovery and deciphering rod and cone phototransduction mechanisms in health and disease using animal models for retinal degeneration. Throughout my academic career my research discoveries identified key genes in the pineal and retina, including arrestins to maintain normal high acuity vision. Currently, my personal goals include developing alternative therapeutic rescue treatment strategies with replacement gene therapy and in vitro stem cell technology. With Cobrinik and collaborators, we identified key developmental cone regulators controlling retinoblastoma genesis. I strongly believe in the importance of mentoring vision and clinician scientists and providing medical ethical training doctoral and medical students, and society.
Dickman, Dion
Associate Professor of Biological Sciences
Synaptic development, function, and plasticity in Drosophila.
