Work Phone Number:
760 Westwood PlazaSuite 37-372ALos Angeles, CA 90024UNITED STATES
Dr. Wexler is an assistant professor in the Division of Geriatric Psychiatry at UCLA's David Geffen School of Medicine and the Semel Institute's Center for Neurobehavioral Genetics. Additionally, he is an attending psychiatrist in the UCLA Huntington's Disease Center of Excellence. Dr. Wexler received his MD/PhD from the Albert Einstein College of Medicine in 1998, prior to completing residency and fellowship training in the Department of Psychiatry and Behavioral Science at Stanford University, and subsequently, in neurobehavioral genetics at the UCLA School of Medicine. Dr. Wexler joined the UCLA faculty in 2006, where he engages in basic science research and continues to see patients in geriatric psychiatry and neurogenetics out patient clinics.
Dr. Wexler's research focuses on the role of Wnt signaling in adult neurogenesis. He is using human neural stem cells (NSCs) harvested from adult and fetal post-mortem brains as an in vitro model of neuronal regeneration and development. He is exploiting this system to obtain an improved understanding of how manipulating Wnt signals may explain the efficacy of accepted treatments for major mood disorders. Wnts are a diverse family of secreted ligands that are critical to fetal neural development, and continue to be widely expressed throughout the adult brain. The best-characterized ('canonial') Wnts signals inhibits GSK-3?, which in turn, stabilizes beta-catenin, an activator of LEF/TCF family transcription factors. He has shown that lithium, a common mood stabilizer, stimulates neurogenesis by targeting GSK-3b and beta-catenin, thereby mimicking the trophic effects of Wnt signaling. Currently, he is attempting to determine whether other mood stabilizers act similarly, possibly through convergent activation of LEF/TCF. In addition, he is generating new human NSC lines from diseased individuals, with the intent that these may be developed as tractable model systems for genomic and pheomic study of neuropsychiatric disease.
Fogel Brent L, Wexler Eric, Wahnich Amanda, Friedrich Tara, Vijayendran Chandran, Gao Fuying, Parikshak Neelroop, Konopka Genevieve, Geschwind Daniel H RBFOX1 regulates both splicing and transcriptional networks in human
Human molecular genetics
Wexler Eric M, Geschwind Daniel H DISC1: a schizophrenia gene with multiple personalities..
Wexler Eric M, Rosen Ezra, Lu Daning, Osborn Gregory E, Martin Elizabeth, Raybould Helen, Geschwind Daniel H Genome-wide analysis of a Wnt1-regulated transcriptional network
implicates neurodegenerative pathways..
Rosen Ezra Y, Wexler Eric M, Versano Revital, Coppola Giovanni, Gao Fuying, Winden Kellen D, Oldham Michael C, Martens Lauren Herl, Zhou Ping, Farese Robert V, Geschwind Daniel H Functional genomic analyses identify pathways dysregulated by
progranulin deficiency, implicating Wnt signaling..
Wexler Eric M, Paucer Andres, Kornblum Harley I, Palmer Theodore D, Plamer Theodore D, Geschwind Daniel H Endogenous Wnt signaling maintains neural progenitor cell potency..
Stem cells (Dayton, Ohio)
Wexler Eric M, Geschwind Daniel H Out FOXing Parkinson disease: where development meets
Coppola Giovanni, Choi Sang-Hyun, Santos Manuela M, Miranda Carlos J, Tentler Dmitri, Wexler Eric M, Pandolfo Massimo, Geschwind Daniel H Gene expression profiling in frataxin deficient mice: microarray
evidence for significant expression changes without detectable
Neurobiology of disease