| Year |
Citation |
Score |
| 2023 |
Kavanaugh BC, Elacio J, Best CR, St Pierre DG, Pescosolido MF, Ouyang Q, Caruso P, Buch K, Biedermann J, Bradley RS, Liu JS, Jones RN, Morrow EM. Christianson Syndrome across the Lifespan: An International Longitudinal Study in Children, Adolescents, and Adults. Medrxiv : the Preprint Server For Health Sciences. PMID 37987014 DOI: 10.1101/2023.11.11.23298218 |
0.794 |
|
| 2023 |
Ma L, Kasula RK, Ouyang Q, Schmidt M, Morrow EM. GGA1 interacts with the endosomal Na+/H+ Exchanger NHE6 governing localization to the endosome compartment. Biorxiv : the Preprint Server For Biology. PMID 37986849 DOI: 10.1101/2023.11.08.565997 |
0.652 |
|
| 2023 |
Wu Q, Ma L, Joesch-Cohen L, Schmidt M, Gamsiz Uzun ED, Morrow EM. Targeting NHE6 gene expression identifies lysosome and neurodevelopmental mechanisms in a haploid in vitro cell model. Biology Open. PMID 37747131 DOI: 10.1242/bio.059778 |
0.377 |
|
| 2023 |
Pescosolido MF, Ouyang Q, Liu JS, Morrow EM. Live-Imaging Detection of Multivesicular Body-Plasma Membrane Fusion and Exosome Release in Cultured Primary Neurons. Methods in Molecular Biology (Clifton, N.J.). 2683: 213-220. PMID 37300778 DOI: 10.1007/978-1-0716-3287-1_17 |
0.759 |
|
| 2023 |
Ouyang Q, Schmidt M, Morrow EM. Dynamic Measurement of Endosome-Lysosome Fusion in Neurons Using High-Content Imaging. Methods in Molecular Biology (Clifton, N.J.). 2683: 201-212. PMID 37300777 DOI: 10.1007/978-1-0716-3287-1_16 |
0.624 |
|
| 2022 |
Fernandez MA, Bah F, Ma L, Lee Y, Schmidt M, Welch E, Morrow EM, Young-Pearse TL. Loss of endosomal exchanger NHE6 leads to pathological changes in tau in human neurons. Stem Cell Reports. 17: 2111-2126. PMID 36055242 DOI: 10.1016/j.stemcr.2022.08.001 |
0.671 |
|
| 2022 |
Baytas O, Kauer JA, Morrow EM. Loss of mitochondrial enzyme GPT2 causes early neurodegeneration in locus coeruleus. Neurobiology of Disease. 105831. PMID 35908744 DOI: 10.1016/j.nbd.2022.105831 |
0.79 |
|
| 2021 |
Lee Y, Miller MR, Fernandez MA, Berg EL, Prada AM, Ouyang Q, Schmidt M, Silverman JL, Young-Pearse TL, Morrow EM. Early lysosome defects precede neurodegeneration with amyloid-β and tau aggregation in NHE6-null rat brain. Brain : a Journal of Neurology. PMID 34928329 DOI: 10.1093/brain/awab467 |
0.756 |
|
| 2021 |
Kavanaugh BC, Gabert T, Jones RN, Sheinkopf SJ, Morrow EM. Parental age and autism severity in the Rhode Island Consortium for Autism Research and Treatment (RI-CART) study. Autism Research : Official Journal of the International Society For Autism Research. PMID 34866351 DOI: 10.1002/aur.2648 |
0.653 |
|
| 2021 |
Sipsock D, Tokadjian H, Righi G, Morrow EM, Sheinkopf SJ. Autism severity aggregates with family psychiatric history in a community-based autism sample. Autism Research : Official Journal of the International Society For Autism Research. PMID 34652072 DOI: 10.1002/aur.2625 |
0.586 |
|
| 2021 |
Pescosolido MF, Ouyang Q, Liu JS, Morrow EM. Loss of Christianson Syndrome Na+/H+ Exchanger 6 () Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 34526390 DOI: 10.1523/JNEUROSCI.1244-20.2021 |
0.801 |
|
| 2021 |
Baytas O, Davidson SM, DeBerardinis RJ, Morrow EM. Mitochondrial enzyme GPT2 regulates metabolic mechanisms required for neuron growth and motor function in vivo. Human Molecular Genetics. PMID 34519342 DOI: 10.1093/hmg/ddab269 |
0.783 |
|
| 2021 |
Ma L, Schmidt M, Morrow EM. Human iPSC lines from a Christianson syndrome patient with NHE6 W523X mutation, a biologically-related control, and CRISPR/Cas9 gene-corrected isogenic controls. Stem Cell Research. 54: 102435. PMID 34182254 DOI: 10.1016/j.scr.2021.102435 |
0.353 |
|
| 2021 |
Kavanaugh BC, Schremp CA, Jones RN, Best CR, Sheinkopf SJ, Morrow EM. Moderators of Age of Diagnosis in > 20,000 Females with Autism in Two Large US Studies. Journal of Autism and Developmental Disorders. PMID 33961180 DOI: 10.1007/s10803-021-05026-4 |
0.641 |
|
| 2021 |
Ma L, Prada AM, Schmidt M, Morrow EM. Generation of pathogenic TPP1 mutations in human stem cells as a model for neuronal ceroid lipofuscinosis type 2 disease. Stem Cell Research. 53: 102323. PMID 33845243 DOI: 10.1016/j.scr.2021.102323 |
0.341 |
|
| 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 |
0.786 |
|
| 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 |
0.811 |
|
| 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 |
0.789 |
|
| 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 |
0.797 |
|
| 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 |
0.692 |
|
| 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 |
0.788 |
|
| 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 |
0.786 |
|
| 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 |
0.8 |
|
| 2019 |
De Luca DM, Goldman M, Clarke E, Guerrero S, Sheinkopf S, Morrow E. ATTITUDES, PERSPECTIVES, AND PREVALENCE OF MOLECULAR GENETIC TESTING IN AUTISM SPECTRUM DISORDERS: BIG LESSONS FROM THE SMALLEST STATE European Neuropsychopharmacology. 29: S22. DOI: 10.1016/j.euroneuro.2019.07.045 |
0.35 |
|
| 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 |
0.756 |
|
| 2018 |
Pruett B, Pescosolido M, Best C, Bradley R, Marsland H, Morrow E. F46. Brain MRI Morphometry Changes Associated With Na+/H+ Exchanger 6 (NHE6) Mutations in Christianson Syndrome (CS) Biological Psychiatry. 83: S255. DOI: 10.1016/J.Biopsych.2018.02.659 |
0.78 |
|
| 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 |
0.784 |
|
| 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 |
0.618 |
|
| 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 |
0.572 |
|
| 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 |
0.788 |
|
| 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 |
0.753 |
|
| 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 |
0.578 |
|
| 2015 |
Morrow EM, Lizarraga SB, Ouyang Q. 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 26531385 DOI: 10.1016/j.ijdevneu.2015.04.063 |
0.764 |
|
| 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 |
0.615 |
|
| 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 |
0.797 |
|
| 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 |
0.807 |
|
| 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 |
0.824 |
|
| 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 |
0.779 |
|
| 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 |
0.802 |
|
| 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 |
0.776 |
|
| 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 |
0.793 |
|
| 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 |
0.813 |
|
| 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 |
0.796 |
|
| 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 |
0.79 |
|
| 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 |
0.797 |
|
| 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 |
0.788 |
|
| 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 |
0.654 |
|
| 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 |
0.791 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Morrow EM, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.787 |
|
| 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 |
0.772 |
|
| 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 |
0.824 |
|
| 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 |
0.797 |
|
| 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 |
0.77 |
|
| 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 |
0.785 |
|
| 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 |
0.807 |
|
| 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 |
0.77 |
|
| 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 |
0.798 |
|
| 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 |
0.782 |
|
| 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 |
0.654 |
|
| 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 |
0.785 |
|
| 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 |
0.619 |
|
| 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 |
0.801 |
|
| 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 |
0.715 |
|
| 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 |
0.494 |
|
| 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 |
0.629 |
|
| 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 |
0.557 |
|
| 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 |
0.807 |
|
| 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 |
0.606 |
|
| 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 |
0.642 |
|
| 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 |
0.672 |
|
| 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 DOI: 10.1016/S0896-6273(00)81171-X |
0.703 |
|
| 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 |
0.612 |
|
| 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 |
0.613 |
|
| 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 |
0.608 |
|
| 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 DOI: 10.1523/Jneurosci.18-10-03738.1998 |
0.596 |
|
| 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 DOI: 10.1016/S0092-8674(00)80439-0 |
0.601 |
|
| Show low-probability matches. |