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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.

Yu, Timothy, and Elizabeth Berry-Kravis. 2014. “Autism and Fragile X Syndrome.”. Semin Neurol 34 (3): 258-65.

Chahrour, Maria, Timothy Yu, Elaine Lim, Bulent Ataman, Michael Coulter, Sean Hill, Christine Stevens, et al. 2012. “Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism.”. PLoS Genet 8 (4): e1002635.

Klei, Lambertus, Stephan Sanders, Michael Murtha, Vanessa Hus, Jennifer Lowe, Jeremy Willsey, Daniel Moreno-De-Luca, et al. 2012. “Common Genetic Variants, Acting Additively, Are a Major Source of Risk for Autism.”. Mol Autism 3 (1): 9.

Brownstein, Catherine, Meghan Towne, Lovelace Luquette, David Harris, Nicholas Marinakis, Peter Meinecke, Kerstin Kutsche, et al. 2013. “Mutation of KCNJ8 in a Patient With Cantú Syndrome With Unique Vascular Abnormalities - Support for the Role of K(ATP) Channels in This Condition.”. Eur J Med Genet 56 (12): 678-82.

Gupta, Vandana, Gianina Ravenscroft, Ranad Shaheen, Emily Todd, Lindsay Swanson, Masaaki Shiina, Kazuhiro Ogata, et al. 2013. “Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination As an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy.”. Am J Hum Genet 93 (6): 1108-17.

Hu, Wen, Oz Pomp, Tawfeg Ben-Omran, Andrew Kodani, Katrin Henke, Ganeshwaran Mochida, Timothy Yu, et al. 2014. “Katanin P80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number.”. Neuron 84 (6): 1240-57.