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Chaste, Pauline, Stephan Sanders, Kommu Mohan, Lambertus Klei, Youeun Song, Michael Murtha, Vanessa Hus, et al. 2014. “Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2.”. Autism Res 7 (3): 355-62.

Yu, Timothy, Maria Chahrour, Michael Coulter, Sarn Jiralerspong, Kazuko Okamura-Ikeda, Bulent Ataman, Klaus Schmitz-Abe, et al. 2013. “Using Whole-Exome Sequencing to Identify Inherited Causes of Autism.”. Neuron 77 (2): 259-73.

Cross-Disorder Group of the Psychiatric Genomics Consortium, Hong Lee, Stephan Ripke, Benjamin Neale, Stephen Faraone, Shaun Purcell, Roy Perlis, et al. 2013. “Genetic Relationship Between Five Psychiatric Disorders Estimated from Genome-Wide SNPs.”. Nat Genet 45 (9): 984-94.

Jamuar, Saumya, Anh-Thu Lam, Martin Kircher, Alissa D’Gama, Jian Wang, Brenda Barry, Xiaochang Zhang, et al. 2014. “Somatic Mutations in Cerebral Cortical Malformations.”. N Engl J Med 371 (8): 733-43.

Gitai, Zemer, Timothy Yu, Erik Lundquist, Marc Tessier-Lavigne, and Cornelia Bargmann. 2003. “The Netrin Receptor UNC-40/DCC Stimulates Axon Attraction and Outgrowth through Enabled And, in Parallel, Rac and UNC-115/AbLIM.”. Neuron 37 (1): 53-65.

Chang, Chieh, Timothy Yu, Cornelia Bargmann, and Marc Tessier-Lavigne. 2004. “Inhibition of Netrin-Mediated Axon Attraction by a Receptor Protein Tyrosine Phosphatase.”. Science 305 (5680): 103-6.

Sanders, Stephan, Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael Murtha, Daniel Moreno-De-Luca, Su Chu, et al. 2011. “Multiple Recurrent de Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated With Autism.”. Neuron 70 (5): 863-85.

Chaste, Pauline, Lambertus Klei, Stephan Sanders, Michael Murtha, Vanessa Hus, Jennifer Lowe, Jeremy Willsey, et al. 2013. “Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait.”. Biol Psychiatry 74 (8): 576-84.

Mitsuhashi, Satomi, Steven Boyden, Elicia Estrella, Takako Jones, Fedik Rahimov, Timothy Yu, Basil Darras, et al. 2013. “Exome Sequencing Identifies a Novel SMCHD1 Mutation in Facioscapulohumeral Muscular Dystrophy 2.”. Neuromuscul Disord 23 (12): 975-80.

Reiff, Rachel, Bassam Ali, Byron Baron, Timothy Yu, Salma Ben-Salem, Michael Coulter, Christian Schubert, et al. 2014. “METTL23, a Transcriptional Partner of GABPA, Is Essential for Human Cognition.”. Hum Mol Genet 23 (13): 3456-66.