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De Rubeis, Silvia, Xin He, Arthur Goldberg, Christopher Poultney, Kaitlin Samocha, Erucment Cicek, Yan Kou, et al. 2014. “Synaptic, Transcriptional and Chromatin Genes Disrupted in Autism.”. Nature 515 (7526): 209-15.

Network and Pathway Analysis Subgroup of Psychiatric Genomics Consortium. 2015. “Psychiatric Genome-Wide Association Study Analyses Implicate Neuronal, Immune and Histone Pathways.”. Nat Neurosci 18 (2): 199-209.

Kodani, Andrew, Timothy Yu, Jeffrey Johnson, Divya Jayaraman, Tasha Johnson, Lihadh Al-Gazali, Lāszló Sztriha, et al. 2015. “Centriolar Satellites Assemble Centrosomal Microcephaly Proteins to Recruit CDK2 and Promote Centriole Duplication.”. Elife 4.

Manzini, Chiara, Dimira Tambunan, Sean Hill, Tim Yu, Thomas Maynard, Erin Heinzen, Kevin Shianna, et al. 2012. “Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations As a Cause of Walker-Warburg Syndrome.”. Am J Hum Genet 91 (3): 541-7.

Brownstein, Catherine, Alan Beggs, Nils Homer, Barry Merriman, Timothy Yu, Katherine Flannery, Elizabeth Dechene, et al. 2014. “An International Effort towards Developing Standards for Best Practices in Analysis, Interpretation and Reporting of Clinical Genome Sequencing Results in the CLARITY Challenge.”. Genome Biol 15 (3): R53.

Chaste, Pauline, Lambertus Klei, Stephan Sanders, Vanessa Hus, Michael Murtha, Jennifer Lowe, Jeremy Willsey, et al. 2015. “A Genome-Wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?”. Biol Psychiatry 77 (9): 775-84.

Maier, Robert, Gerhard Moser, Guo-Bo Chen, Stephan Ripke, Cross-Disorder Working Group of the Psychiatric Genomics Consortium, William Coryell, James Potash, et al. 2015. “Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder.”. Am J Hum Genet 96 (2): 283-94.

Chao, Yu, Fujisawa, Culotti, Gengyo-Ando, Mitani, Moulder, Barstead, Tessier-Lavigne, and Bargmann. 2001. “C. Elegans Slit Acts in Midline, Dorsal-Ventral, and Anterior-Posterior Guidance via the SAX-3/Robo Receptor.”. Neuron 32 (1): 25-38.

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.