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Sanders, Stephan, Xin He, Jeremy Willsey, Gulhan Ercan-Sencicek, Kaitlin Samocha, Ercument Cicek, Michael Murtha, et al. 2015. “Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.”. Neuron 87 (6): 1215-33.

Yu, Timothy, Ganeshwaran Mochida, David Tischfield, Sema Sgaier, Laura Flores-Sarnat, Consolato Sergi, Meral Topçu, et al. 2010. “Mutations in WDR62, Encoding a Centrosome-Associated Protein, Cause Microcephaly With Simplified Gyri and Abnormal Cortical Architecture.”. Nat Genet 42 (11): 1015-20.

Clapham, Yu, Ganesh, Barry, Chan, Mei, Parrini, et al. 2012. “FLNA Genomic Rearrangements Cause Periventricular Nodular Heterotopia.”. Neurology 78 (4): 269-78.

Zhang, Xiaochang, Jiqiang Ling, Giulia Barcia, Lili Jing, Jiang Wu, Brenda Barry, Ganeshwaran Mochida, et al. 2014. “Mutations in QARS, Encoding Glutaminyl-TRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures.”. Am J Hum Genet 94 (4): 547-58.

Di Costanzo, Stefania, Anuradha Balasubramanian, Heather Pond, Anete Rozkalne, Chiara Pantaleoni, Simona Saredi, Vandana Gupta, et al. 2014. “POMK Mutations Disrupt Muscle Development Leading to a Spectrum of Neuromuscular Presentations.”. Hum Mol Genet 23 (21): 5781-92.

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.