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Maria Chahrour, Ph.D.

Affiliations: 
Harvard Medical School, Boston, MA, United States 
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"Maria Chahrour"
Mean distance: 14.61 (cluster 11)
 		SNBCP
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Parents

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Huda Y. Zoghbi grad student 2004-2009 Baylor College of Medicine
Chris A. Walsh post-doc 2009-2014 Harvard Medical School

Children

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Islam Oguz Tuncay grad student 2018- The University of Texas Southwestern Medical Center
Lauretta El Hayek grad student 2019- The University of Texas Southwestern Medical Center
Shayal Vashisth grad student 2020- The University of Texas Southwestern Medical Center

Collaborators

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BETA: Related publications

Publications

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Gogate A, Kaur K, Khalil R, et al. (2024) The genetic landscape of autism spectrum disorder in an ancestrally diverse cohort. Npj Genomic Medicine. 9: 62
Soueid J, Hamze Z, Bedran J, et al. (2023) A novel autism-associated UBLCP1 mutation impacts proteasome regulation/activity. Translational Psychiatry. 13: 404
El Hayek L, DeVries D, Gogate A, et al. (2023) Disruption of the autism gene and chromatin regulator KDM5A alters hippocampal cell identity. Science Advances. 9: eadi0074
Rios JJ, Li Y, Paria N, et al. (2023) RAB1A haploinsufficiency phenocopies the 2p14-p15 microdeletion and is associated with impaired neuronal differentiation. American Journal of Human Genetics
Kissel A, Gebreyohanns M, Chahrour MH. (2023) A Brief Survey of Medical Practitioner Knowledge and Attitudes Regarding Autism Spectrum Disorder in Bahir Dar, Ethiopia. African Journal of Health Sciences. 34: 364-373
Tuncay IO, DeVries D, Gogate A, et al. (2023) The genetics of autism spectrum disorder in an East African familial cohort. Cell Genomics. 3: 100322
Vashisth S, Chahrour MH. (2022) Genomic strategies to untangle the etiology of autism: A primer. Autism Research : Official Journal of the International Society For Autism Research
Tuncay IO, Parmalee NL, Khalil R, et al. (2022) Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. Npj Genomic Medicine. 7: 13
Vashisth S, Chahrour MH. (2021) Insights Into DDX3X Syndrome From a Novel Mouse Model With Construct and Face Validity. Biological Psychiatry. 90: 732-734
El Hayek L, Tuncay IO, Nijem N, et al. (2020) mutations identified in autism spectrum disorder using forward genetics. Elife. 9
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