Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
O'Roak, Brian J, Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J, Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P +8 more·2011·Nature Genetics
DOI 10.1038/ng.835
Cited by (114)
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- Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathwaysCappi, C, Brentani, H, Lima, L, Sanders, S J, Zai, G, Diniz, B J, Reis, V N S, Hounie, A G, Conceição do Rosário, M, Mariani, D et al. · 2016 · Translational Psychiatry
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- Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplicationon behalf of the Simons VIP consortium, Green Snyder, LeeAnne, D’Angelo, Debra, Chen, Qixuan, Bernier, Raphael, Goin-Kochel, Robin P., Wallace, Arianne Stevens, Gerdts, Jennifer, Kanne, Stephen, Berry, Leandra et al. · 2016 · Journal of Autism and Developmental Disorders
- Increased female autosomal burden of rare copy number variants in human populations and in autism familiesDesachy, G, Croen, L A, Torres, A R, Kharrazi, M, Delorenze, G N, Windham, G C, Yoshida, C K, Weiss, L A · 2015 · Molecular Psychiatry
- Current perspectives in autism spectrum disorder: from genes to therapyChahrour, Maria, O'Roak, Brian J., Santini, Emanuela, Samaco, Rodney C., Kleiman, Robin J., Manzini, M. Chiara · 2016 · The Journal of Neuroscience
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- Severity of ASD symptoms and their correlation with the presence of copy number variations and exposure to first trimester ultrasoundWebb, Sara Jane, Garrison, Michelle M., Bernier, Raphael, McClintic, Abbi M., King, Bryan H., Mourad, Pierre D. · 2017 · Autism Research
- Stem cells and modeling of autism spectrum disordersFreitas, Beatriz C.G., Trujillo, Cleber A., Carromeu, Cassiano, Yusupova, Marianna, Herai, Roberto H., Muotri, Alysson R. · 2014 · Experimental Neurology
- Migraine genetics: current findings and future lines of researchPersico, A. M., Verdecchia, M., Pinzone, V., Guidetti, V. · 2015 · neurogenetics
- Erratum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutationsO'Roak, Brian J, Deriziotis, Pelagia, Lee, Choli, Vives, Laura, Schwartz, Jerrod J, Girirajan, Santhosh, Karakoc, Emre, MacKenzie, Alexandra P, Ng, Sarah B, Baker, Carl et al. · 2012 · Nature Genetics
- CYFIP1 Dosages Exhibit Divergent Behavioral Impact via Diametric Regulation of NMDA Receptor Complex Translation in Mouse Models of Psychiatric DisordersKim, Nam-Shik, Ringeling, Francisca Rojas, Zhou, Ying, Nguyen, Ha Nam, Temme, Stephanie J., Lin, Yu-Ting, Eacker, Stephen, Dawson, Valina L., Dawson, Ted M., Xiao, Bo et al. · 2022 · Biological Psychiatry