Loss of Christianson Syndrome Na + /H + Exchanger 6 (NHE6) Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons von Pescosolido, Matthew F, Ouyang, Qing, Liu, Judy S, Morrow, Eric M

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Live-Imaging Detection of Multivesicular Body-Plasma Membrane Fusion and Exosome Release in Cultured Primary Neurons von Pescosolido, Matthew F., Ouyang, Qing, Liu, Judy S., Morrow, Eric M.

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Distribution of Disease-Associated Copy Number Variants Across Distinct Disorders of Cognitive Development von Pescosolido, Matthew F., B.A, Gamsiz, Ece D., Ph.D, Nagpal, Shailender, M.S, Morrow, Eric M., M.D., Ph.D

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Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy von Viscidi, Emma W, Triche, Elizabeth W, Pescosolido, Matthew F, McLean, Rebecca L, Joseph, Robert M, Spence, Sarah J, Morrow, Eric M

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Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders von Pescosolido, Matthew F., Yang, Unikora, Sabbagh, Mark, Morrow, Eric M.

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An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma von Minhas, Hassan M., Pescosolido, Matthew F., Schwede, Matthew, Piasecka, Justyna, Gaitanis, John, Tantravahi, Umadevi, Morrow, Eric M.

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Developmental Meta-Analysis of the Functional Neural Correlates of Autism Spectrum Disorders von Dickstein, Daniel P., M.D, Pescosolido, Matthew F., B.A, Reidy, Brooke L., B.A., B.S, Galvan, Thania, B.A, Kim, Kerri L., Ph.D, Seymour, Karen E., Ph.D, Laird, Angela R., Ph.D, Di Martino, Adriana, M.D, Barrett, Rowland P., Ph.D

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Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome von Pescosolido, Matthew F., Stein, David M., Schmidt, Michael, El Achkar, Christelle Moufawad, Sabbagh, Mark, Rogg, Jeffrey M., Tantravahi, Umadevi, McLean, Rebecca L., Liu, Judy S., Poduri, Annapurna, Morrow, Eric M.

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Emotional Face Identification in Youths With Primary Bipolar Disorder or Primary Attention-Deficit/Hyperactivity Disorder von Seymour, Karen E., Ph.D, Pescosolido, Matthew F., B.A, Reidy, Brooke L., B.A., B.S, Galvan, Thania, B.A, Kim, Kerri L., Ph.D, Young, Matthew, Ph.D, Dickstein, Daniel P., M.D

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Complex Neurological Phenotype in Female Carriers of NHE6 Mutations von Pescosolido, Matthew F., Kavanaugh, Brian C., Pochet, Nathalie, Schmidt, Michael, Jerskey, Beth A., Rogg, Jeffrey M., De Jager, Philip L., Young-Pearse, Tracy L., Liu, Judy S., Morrow, Eric M.

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Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms von Gamsiz, Ece D., Sciarra, Laura N., Maguire, Abbie M., Pescosolido, Matthew F., van Dyck, Laura I., Morrow, Eric M.

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Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein von Pescosolido, Matthew F, Schwede, Matthew, Johnson Harrison, Ashley, Schmidt, Michael, Gamsiz, Ece D, Chen, Wendy S, Donahue, John P, Shur, Natasha, Jerskey, Beth A, Phornphutkul, Chanika, Morrow, Eric M

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Family functioning Deficits in bipolar disorder and ADHD in youth von Young, Matthew E, Galvan, Thania, Reidy, Brooke L, Pescosolido, Matthew F, Kim, Kerri L, Seymour, Karen, Dickstein, Daniel P

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Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6 -Null Mouse Model of Christianson Syndrome von Xu, Meiyu, Ouyang, Qing, Gong, Jingyi, Pescosolido, Matthew F, Pruett, Brandon S, Mishra, Sasmita, Schmidt, Michael, Jones, Richard N, Gamsiz Uzun, Ece D, Lizarraga, Sofia B, Morrow, Eric M

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A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene von Sofos, Elvera, Pescosolido, Matthew F., Quintos, Jose B., Abuelo, Dianne, Gunn, Shelly, Hovanes, Karine, Morrow, Eric M., Shur, Natasha

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Genetic and phenotypic diversity of NHE 6 mutations in C hristianson syndrome von Pescosolido, Matthew F., Stein, David M., Schmidt, Michael, El Achkar, Christelle Moufawad, Sabbagh, Mark, Rogg, Jeffrey M., Tantravahi, Umadevi, McLean, Rebecca L., Liu, Judy S., Poduri, Annapurna, Morrow, Eric M.

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Clinical Characteristics of Children with Autism Spectrum Disorder and Co-Occurring Epilepsy von Viscidi, Emma W, Triche, Elizabeth W, Pescosolido, Matthew F, McLean, Rebecca L, Joseph, Robert M, Spence, Sarah J, Morrow, Eric M

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Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders: Autism and Related Developmental Disorders von PESCOSOLIDO, Matthew F, YANG, Unikora, SABBAGH, Mark, MORROW, Eric M

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Clinical Characteristics of Children with Autism Spectrum Disorder and Co-Occurring Epilepsy. e67797 von Viscidi, Emma W, Triche, Elizabeth W, Pescosolido, Matthew F, McLean, Rebecca L, Joseph, Robert M, Spence, Sarah J, Morrow, Eric M

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Guidelines to Establish an Equitable Mobile Health Ecosystem von Fortuna, Karen L., Kadakia, Arya, Cosco, Theodore D., Rotondi, Armando, Nicholson, Joanne, Mois, George, Myers, Amanda L., Hamilton, Jennifer, Brewer, LaPrincess C., Collins-Pisano, Caroline, Barr, Paul, Hudson, Matthew F., Joseph, Kalisa, Mullaly, Christa, Booth, Mark, Lebby, Stephanie, Walker, Robert

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