Kavanaugh BC, Elacio J, Best CR, St Pierre DG, Pescosolido MF, Ouyang Q, Biedermann J, Bradley RS, Liu JS, Jones RN, Morrow EM.
"Christianson syndrome across the lifespan: genetic mutations and longitudinal study in children, adolescents, and adults." Journal of Medical Genetics, 2024.
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Morrow, Eric M.
"Early Human Postnatal Brain Development Through the Lens of Rare Genetic Disorders." Biological Psychiatry, vol. 90, no. 5, 2021, pp. 281-282.
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Lizarraga SB, Ma L, Maguire AM, van Dyck LI, Wu Q, Ouyang Q, Kavanaugh BC, Nagda D, Livi LL, Pescosolido MF, Schmidt M, Alabi S, Cowen MH, Brito-Vargas P, Hoffman-Kim D, Gamsiz Uzun ED, Schlessinger A, Jones RN, Morrow EM.
"Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies." Science Translational Medicine, vol. 13, no. 580, 2021.
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McCormick, Carolyn E. B., Kavanaugh, Brian C., Sipsock, Danielle, Righi, Giulia, Oberman, Lindsay M., Moreno De Luca, Daniel, Gamsiz Uzun, Ece D., Best, Carrie R., Jerskey, Beth A., Quinn, Joanne G., Jewel, Susan B., Wu, Pei‐Chi, McLean, Rebecca L., Levine, Todd P., Tokadjian, Hasmik, Perkins, Kayla A., Clarke, Elaine B., Dunn, Brittany, Gerber, Alan H., Tenenbaum, Elena J., Anders, Thomas F., Sheinkopf, Stephen J., Morrow, Eric M., None, None.
"Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study." Autism Research, vol. 13, no. 3, 2020, pp. 474-488.
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Moreno-De-Luca, Daniel, Kavanaugh, Brian C., Best, Carrie R., Sheinkopf, Stephen J., Phornphutkul, Chanika, Morrow, Eric M.
"Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample." JAMA Psychiatry, 2020.
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Warren EB, Morrow EM.
"Mitochondrial Function in 22q11 Deletion Syndrome." Neuron, vol. 102, no. 6, 2019, pp. 1089-1091.
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van Dyck LI, Morrow EM.
"Genetic control of postnatal human brain growth." Current opinion in neurology, vol. 30, no. 1, 2017, pp. 114-124.
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Ma L, Ouyang Q, Werthmann GC, Thompson HM, Morrow EM.
"Live-cell Microscopy and Fluorescence-based Measurement of Luminal pH in Intracellular Organelles." Frontiers in Cell and Developmental Biology, vol. 5, 2017, pp. 71.
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Ouyang, Qing, Nakayama, Tojo, Baytas, Ozan, Davidson, Shawn M., Yang, Chendong, Schmidt, Michael, Lizarraga, Sofia B., Mishra, Sasmita, EI-Quessny, Malak, Niaz, Saima, Gul Butt, Mirrat, Imran Murtaza, Syed, Javed, Afzal, Chaudhry, Haroon Rashid, Vaughan, Dylan J., Hill, R. Sean, Partlow, Jennifer N., Yoo, Seung-Yun, Lam, Anh-Thu N., Nasir, Ramzi, Al-Saffar, Muna, Barkovich, A. James, Schwede, Matthew, Nagpal, Shailender, Rajab, Anna, DeBerardinis, Ralph J., Housman, David E., Mochida, Ganeshwaran H., Morrow, Eric M.
"Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features." Proceedings of the National Academy of Sciences, vol. 113, no. 38, 2016, pp. E5598-E5607.
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Young-Pearse TL, Morrow EM.
"Modeling developmental neuropsychiatric disorders with iPSC technology: challenges and opportunities." Current opinion in neurobiology, vol. 36, 2015, pp. 66-73.
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Howe YJ, Yatchmink Y, Viscidi EW, Morrow EM.
"Ascertainment and gender in autism spectrum disorders." Journal of the American Academy of Child & Adolescent Psychiatry, vol. 53, no. 6, 2014, pp. 698-700.
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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.
"Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein." Journal of Medical Genetics, vol. 51, no. 9, 2014, pp. 587-9.
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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.
"Genetic and phenotypic diversity of NHE 6 mutations in Christianson syndrome." Annals of neurology, vol. 76, no. 4, 2014, pp. 581-593.
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Stein DM, Gerber A, Morrow EM.
"Inaugural Christianson Syndrome Association conference: families meeting for the first time." Journal of Neurodevelopmental Disorders, vol. 6, no. 1, 2014, pp. 13.
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Ouyang Q, Lizarraga SB, Schmidt M, Yang U, Gong J, Ellisor D, Kauer JA, Morrow EM.
"Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development." Neuron, vol. 80, no. 1, 2013, pp. 97-112.
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Viscidi EW, Triche EW, Pescosolido MF, McLean RL, Joseph RM, Spence SJ, Morrow EM.
"Clinical characteristics of children with autism spectrum disorder and co-occurring epilepsy." PLoS ONE, vol. 8, no. 7, 2013, pp. e67797.
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Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.
"Distribution of Disease-Associated Copy Number Variants Across Distinct Disorders of Cognitive Development." Journal of the American Academy of Child & Adolescent Psychiatry, vol. 52, no. 4, 2013, pp. 414-430.e14.
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Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M, Simons Simplex Collection Genetics Consortium, Triche EW, Geschwind DH, State MW, Istrail S, Cook EH Jr, Devlin B, Morrow EM.
"Intellectual disability is associated with increased runs of homozygosity in simplex autism." The American Journal of Human Genetics, vol. 93, no. 1, 2013, pp. 103-9.
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Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A.
"SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)." Molecular autism, vol. 4, no. 1, 2013, pp. 36.
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Morrow, Eric M.
"Genomic Copy Number Variation in Disorders of Cognitive Development." Journal of the American Academy of Child & Adolescent Psychiatry, vol. 49, no. 11, 2010, pp. 1091-1104.
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Walsh CA, Morrow EM, Rubenstein JL.
"Autism and brain development." Cell, vol. 135, no. 3, 2008, pp. 396-400.
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