Beyond the serotonin hypothesis: Mitochondria, inflammation and neurodegeneration in major depression and affective spectrum disorders von Gardner, Ann, Boles, Richard G.

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

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

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High degree of efficacy in the treatment of cyclic vomiting syndrome with combined co-enzyme Q10, L-carnitine and amitriptyline, a case series von Boles, Richard G

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

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North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition Consensus Statement on the Diagnosis and Management of Cyclic Vomiting Syndrome von Li, B UK, Lefevre, Frank, Chelimsky, Gisela G, Boles, Richard G, Nelson, Susanne P, Lewis, Donald W, Linder, Steven L, Issenman, Robert M, Rudolph, Colin D

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A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency von Arnold, Georgianne L., Van Hove, Johan, Freedenberg, Debra, Strauss, Arnold, Longo, Nicola, Burton, Barbara, Garganta, Cheryl, Ficicioglu, Can, Cederbaum, Stephen, Harding, Cary, Boles, Richard G., Matern, Dietrich, Chakraborty, Pranesh, Feigenbaum, Annette

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

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

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

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Treatment of cyclic vomiting syndrome with co-enzyme Q10 and amitriptyline, a retrospective study von Boles, Richard G, Lovett-Barr, Mary R, Preston, Amy, Li, B Uk, Adams, Kathleen

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State of the Art of Genetic Testing for Patients With Autism: A Practical Guide for Clinicians von Kreiman, Bracha L., Boles, Richard G.

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Maternal inheritance in recurrent early-onset depression von Bergemann, Eric R, Boles, Richard G

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Symptoms of somatization as a rapid screening tool for mitochondrial dysfunction in depression von Gardner, Ann, Boles, Richard G

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Mitochondrial DNA control region sequence variation in migraine headache and cyclic vomiting syndrome von Wang, Qingxue, Ito, Masamichi, Adams, Kathleen, Li, B U.K., Klopstock, Thomas, Maslim, Audrey, Higashimoto, Tomoyasu, Herzog, Juergen, Boles, Richard G.

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A genetic polymorphism that is associated with mitochondrial energy metabolism increases risk of fibromyalgia von van Tilburg, Miranda A.L., Parisien, Marc, Boles, Richard G., Drury, Gillian L., Smith-Voudouris, Julian, Verma, Vivek, Khoury, Samar, Chabot-Doré, Anne-Julie, Nackley, Andrea G., Smith, Shad B., Whitehead, William E., Zolnoun, Denniz A., Slade, Gary D., Tchivileva, Inna, Maixner, William, Diatchenko, Luda

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Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafne... von Schwartzentruber, Jeremy, Buhas, Daniela, Majewski, Jacek, Sasarman, Florin, Papillon-Cavanagh, Simon, Thiffaut, Isabelle, Sheldon, Katherine M., Massicotte, Christine, Patry, Lysanne, Simon, Mariella, Zare, Amir S., McKernan, Kevin J., Michaud, Jacques, Boles, Richard G., Deal, Cheri L., Desilets, Valerie, Shoubridge, Eric A., Samuels, Mark E.

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

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Hepatoblastoma in a patient with methylmalonic aciduria von Chan, Randall, Mascarenhas, Leo, Boles, Richard G, Kerkar, Nanda, Genyk, Yuri, Venkatramani, Rajkumar

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Mutation in the X-linked RAB40AL gene (Martin-Probst syndrome) with mental retardation, sensorineural hearing loss, and anomalies of the craniofacies and genitourinary tract: a sec... von Lee, James, Wong, Stacey, Boles, Richard G.

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