Whole exome/genome sequencing in cyclic vomiting syndrome reveals multiple candidate genes, suggesting a model of elevated intracellular cations and mitochondrial dysfunction by Omri Bar, Laurie Ebenau, Kellee Weiner, Mark Mintz, Richard G. Boles, Richard G. Boles

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Enraizamiento de internodios de Zea diploperennis Iltis, Doebley Guzman by G. Boles, M. Díaz Zorita, P. Gette, V. P. Vidales

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A Personalized Approach to Evaluating and Treating Autism Spectrum Disorder by Richard E Frye, Shannon Rose, Richard G. Boles, Daniel A. Rossignol

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Reanalysis of Trio Whole-Genome Sequencing Data Doubles the Yield in Autism Spectrum Disorder: De Novo Variants Present in Half by Omri Bar, Elizabeth Vahey, Mark Mintz, Richard E. Frye, Richard G. Boles

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Rare genetic variants in the endocannabinoid system genes CNR1 and DAGLA are associated with neurological phenotypes in humans. by Douglas R Smith, Christine M Stanley, Theodore Foss, Richard G Boles, Kevin McKernan

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Expanded genetic codes in next generation sequencing enable decontamination and mitochondrial enrichment. by Kevin J McKernan, Jessica Spangler, Lei Zhang, Vasisht Tadigotla, Stephen McLaughlin, Jason Warner, Amir Zare, Richard G Boles

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Synchrony 2022: The Role of Neuroinflammation in Behavioral Exacerbations in Autism Spectrum Disorder by Jennifer Frankovich, Heer Nanda, Elizabeth D. Mellins, Harumi Jyonouchi, Richard G. Boles, Stephen J. Walker, John Gaitanis, Richard E. Frye

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Synchrony 2022: Epilepsy and Seizures in Autism Spectrum Disorder Roundtable by Richard E. Frye, Heer Nanda, Samuel J. Pleasure, Manuel F. Casanova, Richard G. Boles, Jeffrey Lewine, John Gaitanis, James B. Adams

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The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism by Rena J. Vanzo, Aparna Prasad, Lauren Staunch, Charles H. Hensel, Moises A. Serrano, E. Robert Wassman, Alexander Kaplun, Temple Grandin, Richard G. Boles

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Molecular profiling of advanced malignancies guides first-line N-of-1 treatments in the I-PREDICT treatment-naïve study by Jason K. Sicklick, Shumei Kato, Ryosuke Okamura, Hitendra Patel, Mina Nikanjam, Paul T. Fanta, Michael E. Hahn, Pradip De, Casey Williams, Jessica Guido, Benjamin M. Solomon, Rana R. McKay, Amy Krie, Sarah G. Boles, Jeffrey S. Ross, J. Jack Lee, Brian Leyland-Jones, Scott M. Lippman, Razelle Kurzrock

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A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects. by Jinglan Zhang, Véronik Lachance, Adam Schaffner, Xianting Li, Anastasia Fedick, Lauren E Kaye, Jun Liao, Jill Rosenfeld, Naomi Yachelevich, Mary-Lynn Chu, Wendy G Mitchell, Richard G Boles, Ellen Moran, Mari Tokita, Elizabeth Gorman, Kaytee Bagley, Wei Zhang, Fan Xia, Magalie Leduc, Yaping Yang, Christine Eng, Lee-Jun Wong, Raphael Schiffmann, George A Diaz, Ruth Kornreich, Ryan Thummel, Melissa Wasserstein, Zhenyu Yue, Lisa Edelmann

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