Maria Chahrour, Ph.D.

Affiliations: 
Harvard Medical School, Boston, MA, United States 
Google:
"Maria Chahrour"
Mean distance: 14.61 (cluster 11)
 
SNBCP
Cross-listing: BCM Tree

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Publications

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Khalil R, Kenny C, Hill RS, et al. (2018) PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics
Chahrour M, Kleiman RJ, Manzini MC. (2017) Translating genetic and preclinical findings into autism therapies. Dialogues in Clinical Neuroscience. 19: 335-343
Lu HC, Tan Q, Rousseaux MW, et al. (2017) Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nature Genetics
Chahrour M, O'Roak BJ, Santini E, et al. (2016) Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 11402-11410
Ataman B, Boulting GL, Harmin DA, et al. (2016) Evolution of Osteocrin as an activity-regulated factor in the primate brain. Nature. 539: 242-247
De Rubeis S, He X, Goldberg AP, et al. (2014) Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15
Hu WF, Chahrour MH, Walsh CA. (2014) The diverse genetic landscape of neurodevelopmental disorders. Annual Review of Genomics and Human Genetics. 15: 195-213
Heckman LD, Chahrour MH, Zoghbi HY. (2014) Rett-causing mutations reveal two domains critical for MeCP2 function and for toxicity in MECP2 duplication syndrome mice. Elife. 3
Kim S, Chahrour M, Ben-Shachar S, et al. (2013) Ube3a/E6AP is involved in a subset of MeCP2 functions. Biochemical and Biophysical Research Communications. 437: 67-73
Yu TW, Chahrour MH, Coulter ME, et al. (2013) Using whole-exome sequencing to identify inherited causes of autism. Neuron. 77: 259-73
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