Maria Chahrour, Ph.D. Associate Professor School Medical School Department Eugene McDermott Center for Human Growth and Development | Center for Genetics of Host Defense | Neuroscience | Psychiatry Graduate Programs Genetics, Development and Disease, Neuroscience Biography Dr. Chahrour received her undergraduate degree in Biology from the American University of Beirut prior to attending the University of North Texas for a masters degree in Forensic Genetics. She obtained her Ph.D. in Molecular and Human Genetics from Baylor College of Medicine where she studied molecular mechanisms underlying Rett syndrome. She joined Harvard Medical school and Boston Children's Hospital as a postdoctoral fellow and later as an instructor in the Division of Genetics and Genomics, where she focused on identifying genetic causes of autism spectrum disorder. Dr. Chahrour joined the faculty at the Eugene McDermott Center for Human Growth and Development and the departments of Neuroscience and Psychiatry in 2015. Research Interest Autism spectrum disorder Chromatin remodeling Genetics of neurodevelopmental disorders Genomics and neurogenetics Ubiquitin proteasome pathway Publications Featured Publications The genetics of autism spectrum disorder in an East African familial cohort. Tuncay IO, DeVries D, Gogate A, Kaur K, Kumar A, Xing C, Goodspeed K, Seyoum-Tesfa L, Chahrour MH. Cell Genom 2023 3 7 Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. Tuncay IO, Parmalee NL, Khalil R, Kaur K, Kumar A, Jimale M, Howe JL, Goodspeed K, Evans P, Alzghoul L, Xing C, Scherer SW, Chahrour MH, NPJ Genom Med 2022 Feb 7 1 13 KDM5A mutations identified in autism spectrum disorder using forward genetics. El Hayek L, Tuncay IO, Nijem N, Russell J, Ludwig S, Kaur K, Li X, Anderton P, Tang M, Gerard A, Heinze A, Zacher P, Alsaif HS, Rad A, Hassanpour K, Abbaszadegan MR, Washington C, DuPont BR, Louie RJ, Couse M, Faden M, Rogers RC, Abou Jamra R, Elias ER, Maroofian R, Houlden H, Lehman A, Beutler B, Chahrour MH, Elife 2020 12 9 The ubiquitin ligase UBE3B, disrupted in intellectual disability and absent speech, regulates metabolic pathways by targeting BCKDK. Cheon S, Kaur K, Nijem N, Tuncay IO, Kumar P, Dean M, Juusola J, Guillen-Sacoto MJ, Bedoukian E, Ierardi-Curto L, Kaplan P, Schaefer GB, Mishra P, Chahrour MH Proc. Natl. Acad. Sci. U.S.A. 2019 Feb 116 9 3662-3667 Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy. Chahrour M, O'Roak BJ, Santini E, Samaco RC, Kleiman RJ, Manzini MC J. Neurosci. 2016 Nov 36 45 11402-11410 Using whole-exome sequencing to identify inherited causes of autism Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, LeClair E, Poduri A, Oner O, Al-Saad S, Al-Awadi SA, Bastaki L, Ben-Omran T, Teebi AS, Al-Gazali L, Eapen V, Stevens CR, Rappaport L, Gabriel SB, Markianos K, State MW, Greenberg ME, Taniguchi H, Braverman NE, Morrow EM, Walsh CA Neuron 2013 77 2 259-273 Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism Chahrour MH, Yu TW, Lim ET, Ataman B, Coulter ME, Hill RS, Stevens CR, Schubert CR; ARRA Autism Sequencing Collaboration, Greenberg ME, Gabriel SB, Walsh CA PLoS Genetics 2012 8 4 e1002635 MeCP2, a key contributor to neurological disease, activates and represses transcription Chahrour M, Jung SY, Shaw C, Zhou X, Wong ST, Qin J, Zoghbi HY Science 2008 320 5880 1224-1229 The story of Rett syndrome: from clinic to neurobiology Chahrour M, Zoghbi HY Neuron 2007 56 3 422-437 Genomic strategies to untangle the etiology of autism: A primer. Vashisth S, Chahrour MH. Autism Res 2023 16 1 31-39 Results 1-10 of 38 1 2 3 4 Next Last Books Featured Books Autism spectrum disorders. In Genomic and personalized medicine Yu TW, Coulter ME, Chahrour MH, Walsh CA (2012). Oxford, Academic Press Professional Associations/Affiliations American Academy of Forensic Sciences (2001-2004) American Society of Human Genetics (2004) Association of Forensic DNA Analysts and Administrators (2001-2003) International Rett Syndrome Foundation (2006-2009) International Society for Autism Research (2015) Sigma Xi, The Scientific Research Society (2004) Society for Neuroscience (2006)
