Maria Chahrour, Ph.D.
Affiliations: | Harvard Medical School, Boston, MA, United States |
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"Maria Chahrour"Mean distance: 14.61 (cluster 11) | S | N | B | C | P |
Cross-listing: BCM Tree
Parents
Sign in to add mentor| Huda Y. Zoghbi | grad student | 2004-2009 | Baylor College of Medicine |
| Chris A. Walsh | post-doc | 2009-2014 | Harvard Medical School |
Children
Sign in to add trainee| 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 |
BETA: Related publications
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Publications
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| 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 |
| Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, et al. (2020) Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045 |