Eric Morrow - Publications

Brown University, Providence, RI 

83 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 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, ... ... Morrow EM, et al. Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13. PMID 33568516 DOI: 10.1126/scitranslmed.aaw0682  1
2020 Schmitz-Abe K, Sanchez-Schmitz G, Doan RN, Hill RS, Chahrour MH, Mehta BK, Servattalab S, Ataman B, Lam AN, Morrow EM, Greenberg ME, Yu TW, Walsh CA, Markianos K. Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10: 14045. PMID 32820185 DOI: 10.1038/s41598-020-70656-0  1
2020 Moreno-De-Luca D, Kavanaugh BC, Best CR, Sheinkopf SJ, Phornphutkul C, Morrow EM. Clinical Genetic Testing in Autism Spectrum Disorder in a Large Community-Based Population Sample. Jama Psychiatry. PMID 32401282 DOI: 10.1001/jamapsychiatry.2020.0950  1
2020 McCormick CEB, Kavanaugh BC, Sipsock D, Righi G, Oberman LM, Moreno De Luca D, Gamsiz Uzun ED, Best CR, Jerskey BA, Quinn JG, Jewel SB, Wu PC, McLean RL, Levine TP, Tokadjian H, ... ... Morrow EM, et al. Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART Study. Autism Research : Official Journal of the International Society For Autism Research. PMID 31957984 DOI: 10.1002/aur.2261  1
2019 Ouyang Q, Joesch-Cohen L, Mishra S, Riaz HA, Schmidt M, Morrow EM. Functional Assessment of the Mouse Homologue of the Human Ala-9-Ser NHE6 Variant. Eneuro. PMID 31676550 DOI: 10.1523/ENEURO.0046-19.2019  1
2019 Ouyang Q, Kavanaugh BC, Joesch-Cohen L, Dubois B, Wu Q, Schmidt M, Baytas O, Pastore SF, Harripaul R, Mishra S, Hussain A, Kim KH, Holler-Managan YF, Ayub M, Mir A, ... ... Morrow EM, et al. GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics. PMID 31471722 DOI: 10.1007/s00439-019-02057-x  1
2019 Kavanaugh BC, Warren EB, Baytas O, Schmidt M, Merck D, Buch K, Liu JS, Phornphutkul C, Caruso P, Morrow EM. Longitudinal MRI findings in patient with SLC25A12 pathogenic variants inform disease progression and classification. American Journal of Medical Genetics. Part A. PMID 31403263 DOI: 10.1002/ajmg.a.61322  1
2019 Warren EB, Morrow EM. Mitochondrial Function in 22q11 Deletion Syndrome. Neuron. 102: 1089-1091. PMID 31220439 DOI: 10.1016/j.neuron.2019.05.052  0.32
2019 Pescosolido MF, Kavanaugh BC, Pochet N, Schmidt M, Jerskey BA, Rogg JM, De Jager PL, Young-Pearse TL, Liu JS, Morrow EM. Complex Neurological Phenotype in Female Carriers of Mutations. Molecular Neuropsychiatry. 5: 98-108. PMID 31192222 DOI: 10.1159/000496341  1
2018 Schwede M, Nagpal S, Gandal MJ, Parikshak NN, Mirnics K, Geschwind DH, Morrow EM. Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex. Journal of Neurodevelopmental Disorders. 10: 18. PMID 29859039 DOI: 10.1186/s11689-018-9237-x  1
2018 Baytaş O, Morrow EM. The Role of Mitochondrial Glutamate Metabolism in Cognitive Development and Disease. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 43: 229-230. PMID 29192671 DOI: 10.1038/npp.2017.202  0.76
2017 Xu M, Ouyang Q, Gong J, Pescosolido MF, Pruett BS, Mishra S, Schmidt M, Jones RN, Gamsiz Uzun ED, Lizarraga SB, Morrow EM. Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome. Eneuro. 4. PMID 29349289 DOI: 10.1523/ENEURO.0388-17.2017  1
2017 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. 5: 71. PMID 28871281 DOI: 10.3389/fcell.2017.00071  1
2017 Righi G, Benevides J, Mazefsky C, Siegel M, Sheinkopf SJ, Morrow EM. Predictors of Inpatient Psychiatric Hospitalization for Children and Adolescents with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 28536960 DOI: 10.1007/s10803-017-3154-9  1
2017 Wink LK, Pedapati EV, Adams R, Erickson CA, Pedersen KA, Morrow EM, Kaplan D, Siegel M. Characterization of Medication Use in a Multicenter Sample of Pediatric Inpatients with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 28516426 DOI: 10.1007/s10803-017-3153-x  1
2017 Gerber AH, McCormick CE, Levine TP, Morrow EM, Anders TF, Sheinkopf SJ. Brief Report: Factors Influencing Healthcare Satisfaction in Adults with Autism Spectrum Disorder. Journal of Autism and Developmental Disorders. PMID 28271179 DOI: 10.1007/s10803-017-3087-3  1
2016 van Dyck LI, Morrow EM. Genetic control of postnatal human brain growth. Current Opinion in Neurology. PMID 27898583 DOI: 10.1097/WCO.0000000000000405  1
2016 Ouyang Q, Nakayama T, Baytas O, Davidson SM, Yang C, Schmidt M, Lizarraga SB, Mishra S, Ei-Quessny M, Niaz S, Gul Butt M, Imran Murtaza S, Javed A, Chaudhry HR, Vaughan DJ, ... ... Morrow EM, et al. Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America. PMID 27601654 DOI: 10.1073/pnas.1609221113  1
2016 Yeo RA, Ryman SG, van den Heuvel MP, de Reus MA, Jung RE, Pommy J, Mayer AR, Ehrlich S, Schulz SC, Morrow EM, Manoach D, Ho BC, Sponheim SR, Calhoun VD. Graph Metrics of Structural Brain Networks in Individuals with Schizophrenia and Healthy Controls: Group Differences, Relationships with Intelligence, and Genetics. Journal of the International Neuropsychological Society : Jins. 22: 240-9. PMID 26888620 DOI: 10.1017/S1355617715000867  1
2015 Morrow EM, Lizarraga SB, Ouyang Q. REMOVED: Novel endosomal mechanisms in human axonal growth mediated by Christianson syndrome protein NHE6. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 20. PMID 29887063 DOI: 10.1016/j.ijdevneu.2015.04.063  1
2015 Brennand KJ, Marchetto MC, Benvenisty N, Brüstle O, Ebert A, Izpisua Belmonte JC, Kaykas A, Lancaster MA, Livesey FJ, McConnell MJ, McKay RD, Morrow EM, Muotri AR, Panchision DM, Rubin LL, et al. Creating Patient-Specific Neural Cells for the In Vitro Study of Brain Disorders. Stem Cell Reports. PMID 26610635 DOI: 10.1016/j.stemcr.2015.10.011  1
2015 Siegel M, Smith KA, Mazefsky C, Gabriels RL, Erickson C, Kaplan D, Morrow EM, Wink L, Santangelo SL. The autism inpatient collection: methods and preliminary sample description. Molecular Autism. 6: 61. PMID 26557975 DOI: 10.1186/s13229-015-0054-8  1
2015 Young-Pearse TL, Morrow EM. Modeling developmental neuropsychiatric disorders with iPSC technology: challenges and opportunities. Current Opinion in Neurobiology. 36: 66-73. PMID 26517284 DOI: 10.1016/j.conb.2015.10.006  1
2015 Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF, Klei L, Mandell JD, ... ... Morrow EM, et al. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233. PMID 26402605 DOI: 10.1016/j.neuron.2015.09.016  1
2015 Lizarraga SB, Morrow EM. Uncovering a Role for SK2 in Angelman Syndrome. Cell Reports. 12: 359-60. PMID 26200312 DOI: 10.1016/j.celrep.2015.07.009  1
2015 Gamsiz ED, Sciarra LN, Maguire AM, Pescosolido MF, van Dyck LI, Morrow EM. Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 12: 553-71. PMID 26105128 DOI: 10.1007/s13311-015-0363-9  1
2015 Howe YJ, O'Rourke JA, Yatchmink Y, Viscidi EW, Jones RN, Morrow EM. Female Autism Phenotypes Investigated at Different Levels of Language and Developmental Abilities. Journal of Autism and Developmental Disorders. PMID 26100851 DOI: 10.1007/s10803-015-2501-y  1
2015 Chaste P, Klei L, Sanders SJ, Hus V, Murtha MT, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Mane SM, Martin DM, ... Morrow EM, et al. A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Biological Psychiatry. 77: 775-84. PMID 25534755 DOI: 10.1016/j.biopsych.2014.09.017  1
2015 Morrow EM. MicroRNAs in copy number variants in schizophrenia: misregulation of genome-wide gene expression programs. Biological Psychiatry. 77: 93-4. PMID 25524307 DOI: 10.1016/j.biopsych.2014.11.006  1
2015 Morrow EM. Quantifying the effects of rare variants in pedigrees: how far does the apple fall from the tree? Jama Psychiatry. 72: 106-7. PMID 25493613 DOI: 10.1001/jamapsychiatry.2014.2442  1
2014 Stein DM, Gerber A, Morrow EM. Inaugural Christianson Syndrome Association conference: families meeting for the first time. Journal of Neurodevelopmental Disorders. 6: 13. PMID 25273398 DOI: 10.1186/1866-1955-6-13  1
2014 Harrison AJ, Zimak EH, Sheinkopf SJ, Manji KP, Morrow EM. Observation-centered approach to ASD assessment in Tanzania. Intellectual and Developmental Disabilities. 52: 330-47. PMID 25247726 DOI: 10.1352/1934-9556-52.5.330  1
2014 McLean RL, Johnson Harrison A, Zimak E, Joseph RM, Morrow EM. Executive function in probands with autism with average IQ and their unaffected first-degree relatives. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 1001-9. PMID 25151423 DOI: 10.1016/j.jaac.2014.05.019  1
2014 Pescosolido MF, Schwede M, Johnson Harrison A, Schmidt M, Gamsiz ED, Chen WS, Donahue JP, Shur N, Jerskey BA, Phornphutkul C, Morrow EM. Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. Journal of Medical Genetics. 51: 587-9. PMID 25057125 DOI: 10.1136/jmedgenet-2014-102444  1
2014 Pescosolido MF, Stein DM, Schmidt M, El Achkar CM, Sabbagh M, Rogg JM, Tantravahi U, McLean RL, Liu JS, Poduri A, Morrow EM. Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome. Annals of Neurology. 76: 581-93. PMID 25044251 DOI: 10.1002/ana.24225  1
2014 Howe YJ, Yatchmink Y, Viscidi EW, Morrow EM. Ascertainment and gender in autism spectrum disorders. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 698-700. PMID 24839890 DOI: 10.1016/j.jaac.2014.04.003  1
2014 Chaste P, Sanders SJ, Mohan KN, Klei L, Song Y, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, ... ... Morrow EM, et al. Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2. Autism Research : Official Journal of the International Society For Autism Research. 7: 355-62. PMID 24821083 DOI: 10.1002/aur.1378  1
2014 Gerber A, Morrow E, Sheinkopf SJ, Anders T. The Rhode Island Consortium for Autism Research and Treatment (RI-CART): a new statewide autism collaborative. Rhode Island Medical Journal (2013). 97: 31-4. PMID 24791265  1
2014 Yeo RA, Gangestad SW, Walton E, Ehrlich S, Pommy J, Turner JA, Liu J, Mayer AR, Schulz SC, Ho BC, Bustillo JR, Wassink TH, Sponheim SR, Morrow EM, Calhoun VD. Genetic influences on cognitive endophenotypes in schizophrenia. Schizophrenia Research. 156: 71-5. PMID 24768440 DOI: 10.1016/j.schres.2014.03.022  1
2014 Viscidi EW, Johnson AL, Spence SJ, Buka SL, Morrow EM, Triche EW. The association between epilepsy and autism symptoms and maladaptive behaviors in children with autism spectrum disorder. Autism : the International Journal of Research and Practice. 18: 996-1006. PMID 24165273 DOI: 10.1177/1362361313508027  1
2014 Schwede M, Garbett K, Mirnics K, Geschwind DH, Morrow EM. Genes for endosomal NHE6 and NHE9 are misregulated in autism brains. Molecular Psychiatry. 19: 277-9. PMID 23508127 DOI: 10.1038/mp.2013.28  1
2014 Aguiar D, Morrow E, Istrail S. Tractatus: An exact and subquadratic algorithm for inferring identical-by-descent multi-shared haplotype tracts Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8394: 1-17. DOI: 10.1007/978-3-319-05269-4_1  1
2014 Aguiar D, Morrow E, Istrail S. Tractatus: An exact and subquadratic algorithm for inferring identical-by-descent multi-shared haplotype tracts Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 8394: 1-17. DOI: 10.1007/978-3-319-05269-4-1  1
2013 Marano RM, Mercurio L, Kanter R, Doyle R, Abuelo D, Morrow EM, Shur N. Risk assessment models in genetics clinic for array comparative genomic hybridization: Clinical information can be used to predict the likelihood of an abnormal result in patients. Journal of Pediatric Genetics. 2: 25-31. PMID 27625836 DOI: 10.3233/PGE-13044  1
2013 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. 4: 36. PMID 24090431 DOI: 10.1186/2040-2392-4-36  1
2013 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. 80: 97-112. PMID 24035762 DOI: 10.1016/j.neuron.2013.07.043  1
2013 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. 8: e67797. PMID 23861807 DOI: 10.1371/journal.pone.0067797  1
2013 Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M, Triche EW, Geschwind DH, State MW, Istrail S, Cook EH, Devlin B, Morrow EM. Intellectual disability is associated with increased runs of homozygosity in simplex autism. American Journal of Human Genetics. 93: 103-9. PMID 23830515 DOI: 10.1016/j.ajhg.2013.06.004  1
2013 Chaste P, Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, ... ... Morrow EM, et al. Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biological Psychiatry. 74: 576-84. PMID 23746936 DOI: 10.1016/j.biopsych.2013.04.018  1
2013 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 and Adolescent Psychiatry. 52: 414-430.e14. PMID 23582872 DOI: 10.1016/j.jaac.2013.01.003  1
2013 Minhas HM, Pescosolido MF, Schwede M, Piasecka J, Gaitanis J, Tantravahi U, Morrow EM. An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma. American Journal of Medical Genetics. Part A. 161: 787-91. PMID 23495067 DOI: 10.1002/ajmg.a.35841  1
2013 Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, ... ... Morrow EM, et al. Using whole-exome sequencing to identify inherited causes of autism. Neuron. 77: 259-73. PMID 23352163 DOI: 10.1016/j.neuron.2012.11.002  1
2013 Yeo RA, Gangestad SW, Liu J, Ehrlich S, Thoma RJ, Pommy J, Mayer AR, Schulz SC, Wassink TH, Morrow EM, Bustillo JR, Sponheim SR, Ho BC, Calhoun VD. The impact of copy number deletions on general cognitive ability and ventricle size in patients with schizophrenia and healthy control subjects. Biological Psychiatry. 73: 540-5. PMID 23237311 DOI: 10.1016/j.biopsych.2012.10.013  1
2012 Pescosolido MF, Yang U, Sabbagh M, Morrow EM. Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders. Dialogues in Clinical Neuroscience. 14: 239-52. PMID 23226950  1
2012 Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin CL, ... ... Morrow EM, et al. Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism. 3: 9. PMID 23067556 DOI: 10.1186/2040-2392-3-9  1
2012 Aguiar D, Halldórsson BV, Morrow EM, Istrail S. DELISHUS: an efficient and exact algorithm for genome-wide detection of deletion polymorphism in autism. Bioinformatics (Oxford, England). 28: i154-62. PMID 22689755 DOI: 10.1093/bioinformatics/bts234  1
2012 Lizarraga SB, Coser KR, Sabbagh M, Morrow EM. Methods for study of neuronal morphogenesis: ex vivo RNAi electroporation in embryonic murine cerebral cortex. Journal of Visualized Experiments : Jove. e3621. PMID 22643694 DOI: 10.3791/3621  1
2012 Mefford HC, Rosenfeld JA, Shur N, Slavotinek AM, Cox VA, Hennekam RC, Firth HV, Willatt L, Wheeler P, Morrow EM, Cook J, Sullivan R, Oh A, McDonald MT, Zonana J, et al. Further clinical and molecular delineation of the 15q24 microdeletion syndrome. Journal of Medical Genetics. 49: 110-8. PMID 22180641 DOI: 10.1136/jmedgenet-2011-100499  1
2012 Sofos E, Pescosolido MF, Quintos JB, Abuelo D, Gunn S, Hovanes K, Morrow EM, Shur N. A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene. American Journal of Medical Genetics. Part A. 158: 50-8. PMID 22052655 DOI: 10.1002/ajmg.a.34290  1
2012 Gamsiz ED, Ouyang Q, Schmidt M, Nagpal S, Morrow EM. Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing. Genomics. 99: 44-51. PMID 22032952 DOI: 10.1016/j.ygeno.2011.09.003  1
2012 Morrow E, Mitrovica JX, Forte AM, Glišović P, Huybers P. An enigma in estimates of the Earth's dynamic ellipticity Geophysical Journal International. 191: 1129-1134. DOI: 10.1111/j.1365-246X.2012.05703.x  1
2011 Johnson HM, Gaitanis J, Morrow EM. Genetics in autism diagnosis: adding molecular subtypes to neurobehavioral diagnoses. Medicine and Health, Rhode Island. 94: 124-6. PMID 21710919  1
2011 Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, ... ... Morrow EM, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85. PMID 21658581 DOI: 10.1016/j.neuron.2011.05.002  1
2010 Morrow EM. Genomic copy number variation in disorders of cognitive development. Journal of the American Academy of Child and Adolescent Psychiatry. 49: 1091-104. PMID 20970697 DOI: 10.1016/j.jaac.2010.08.009  1
2010 Ching MS, Shen Y, Tan WH, Jeste SS, Morrow EM, Chen X, Mukaddes NM, Yoo SY, Hanson E, Hundley R, Austin C, Becker RE, Berry GT, Driscoll K, Engle EC, et al. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 937-47. PMID 20468056 DOI: 10.1002/ajmg.b.31063  1
2010 Ehrlich S, Morrow EM, Roffman JL, Wallace SR, Naylor M, Bockholt HJ, Lundquist A, Yendiki A, Ho BC, White T, Manoach DS, Clark VP, Calhoun VD, Gollub RL, Holt DJ. The COMT Val108/158Met polymorphism and medial temporal lobe volumetry in patients with schizophrenia and healthy adults. Neuroimage. 53: 992-1000. PMID 20026221 DOI: 10.1016/j.neuroimage.2009.12.046  1
2009 Weiss LA, Arking DE, Daly MJ, Chakravarti A, Brune CW, West K, O'Connor A, Hilton G, Tomlinson RL, West AB, Cook EH, Green T, Chang SC, Gabriel S, Gates C, ... ... Morrow EM, et al. A genome-wide linkage and association scan reveals novel loci for autism Nature. 461: 802-808. PMID 19812673 DOI: 10.1038/nature08490  1
2008 Walsh CA, Morrow EM, Rubenstein JL. Autism and brain development. Cell. 135: 396-400. PMID 18984148 DOI: 10.1016/j.cell.2008.10.015  1
2008 Morrow EM, Kane A, Goff DC, Walsh CA. Sequence analysis of P21-activated kinase 3 (PAK3) in chronic schizophrenia with cognitive impairment. Schizophrenia Research. 106: 265-7. PMID 18805672 DOI: 10.1016/j.schres.2008.08.021  1
2008 Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, et al. Identifying autism loci and genes by tracing recent shared ancestry. Science (New York, N.Y.). 321: 218-23. PMID 18621663 DOI: 10.1126/science.1157657  1
2008 Morrow EM, Chen CM, Cepko CL. Temporal order of bipolar cell genesis in the neural retina. Neural Development. 3: 2. PMID 18215319 DOI: 10.1186/1749-8104-3-2  1
2007 Levine JB, Morrow EM, Berdichevsky Y, Martin GE. BKca channel in autism and mental retardation. The American Journal of Psychiatry. 164: 977-8; author reply . PMID 17541064 DOI: 10.1176/appi.ajp.164.6.977-a  1
2006 Morrow EM, Lafayette JM, Bromfield EB, Fricchione G. Postictal psychosis: presymptomatic risk factors and the need for further investigation of genetics and pharmacotherapy. Annals of General Psychiatry. 5: 9. PMID 16859554 DOI: 10.1186/1744-859X-5-9  1
2006 Morrow EM, Smoller JW. The interface of genetics and clinical psychiatry. Introduction. Harvard Review of Psychiatry. 14: 45-6. PMID 16603471 DOI: 10.1080/10673220600655798  1
2005 Morrow EM, Furukawa T, Raviola E, Cepko CL. Synaptogenesis and outer segment formation are perturbed in the neural retina of Crx mutant mice. Bmc Neuroscience. 6: 5. PMID 15676071 DOI: 10.1186/1471-2202-6-5  1
2005 Morrow EM, Falk WE. Diagnosis and pharmacotherapy of anxiety in older patients Geriatrics and Aging. 8: 37-41.  1
2000 Cai L, Morrow EM, Cepko CL. Misexpression of basic helix-loop-helix genes in the murine cerebral cortex affects cell fate choices and neuronal survival. Development (Cambridge, England). 127: 3021-30. PMID 10862740  1
2000 Furukawa T, Mukherjee S, Bao ZZ, Morrow EM, Cepko CL. rax, Hes1, and notch1 promote the formation of Müller glia by postnatal retinal progenitor cells. Neuron. 26: 383-94. PMID 10839357  1
1999 Furukawa T, Morrow EM, Li T, Davis FC, Cepko CL. Retinopathy and attenuated circadian entrainment in Crx-deficient mice. Nature Genetics. 23: 466-70. PMID 10581037 DOI: 10.1038/70591  1
1999 Morrow EM, Furukawa T, Lee JE, Cepko CL. NeuroD regulates multiple functions in the developing neural retina in rodent. Development (Cambridge, England). 126: 23-36. PMID 9834183  1
1998 Morrow EM, Furukawa T, Cepko CL. Vertebrate photoreceptor cell development and disease. Trends in Cell Biology. 8: 353-8. PMID 9728396 DOI: 10.1016/S0962-8924(98)01341-5  1
1998 Morrow EM, Belliveau MJ, Cepko CL. Two phases of rod photoreceptor differentiation during rat retinal development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 3738-48. PMID 9570804  1
1997 Furukawa T, Morrow EM, Cepko CL. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell. 91: 531-41. PMID 9390562  1
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