메뉴 건너뛰기




Volumn 14, Issue 3, 2012, Pages 239-252

Lighting a path: Genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders

Author keywords

Autism; Brain development; Regulation of gene expression; Rell signaling; Reuronal cell adhesion molecule; Rynaptic transmission

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR; FRAGILE X MENTAL RETARDATION PROTEIN; HISTONE METHYLTRANSFERASE; INITIATION FACTOR 4E; NERVE CELL ADHESION MOLECULE; NEUREXIN; NEUROLIGIN; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; POSTSYNAPTIC RECEPTOR;

EID: 84875792913     PISSN: 12948322     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (25)

References (119)
  • 1
    • 34147168331 scopus 로고    scopus 로고
    • The lifetime distribution of the incremental societal costs of autism
    • Ganz ML. The lifetime distribution of the incremental societal costs of autism. Arch Pediatr Adolesc Med. 2007;161:343-349.
    • (2007) Arch Pediatr Adolesc Med. , vol.161 , pp. 343-349
    • Ganz, M.L.1
  • 2
    • 84859394070 scopus 로고    scopus 로고
    • Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network
    • 14 sites, United States, 2008. MMWR Surveill Summ
    • Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2008. MMWR Surveill Summ. 2012;61:1-19.
    • (2012) , vol.61 , pp. 1-19
  • 3
    • 69549095841 scopus 로고    scopus 로고
    • Patterns of growth in adaptive social abilities among children with autism spectrum disorders
    • Anderson DK, Oti RS, Lord C, Welch K. Patterns of growth in adaptive social abilities among children with autism spectrum disorders. J Abnorm Child Psychol. 2009;37:1019-1034.
    • (2009) J Abnorm Child Psychol. , vol.37 , pp. 1019-1034
    • Anderson, D.K.1    Oti, R.S.2    Lord, C.3    Welch, K.4
  • 4
    • 82255192290 scopus 로고    scopus 로고
    • The conundrums of understanding genetic risks for autism spectrum disorders
    • State MW, Levitt P. The conundrums of understanding genetic risks for autism spectrum disorders. Nat Neurosci. 2011;14:1499-1506.
    • (2011) Nat Neurosci. , vol.14 , pp. 1499-1506
    • State, M.W.1    Levitt, P.2
  • 7
    • 70349173328 scopus 로고    scopus 로고
    • Genetics and biology of microcephaly and lissencephaly
    • Mochida GH. Genetics and biology of microcephaly and lissencephaly. Semin Pediatr Neurol. 2009;16:120-126.
    • (2009) Semin Pediatr Neurol. , vol.16 , pp. 120-126
    • Mochida, G.H.1
  • 9
    • 0034255316 scopus 로고    scopus 로고
    • Neuronal migration disorders:from genetic diseases to developmental mechanisms
    • Gleeson JG, Walsh CA. Neuronal migration disorders:from genetic diseases to developmental mechanisms. Trends Neurosci. 2000;23:352-359.
    • (2000) Trends Neurosci. , vol.23 , pp. 352-359
    • Gleeson, J.G.1    Walsh, C.A.2
  • 10
    • 79960937678 scopus 로고    scopus 로고
    • The ciliopathies in neuronal development:a clinical approach to investigation of Joubert syndrome and Joubert syndromerelated disorders
    • Sattar S, Gleeson JG. The ciliopathies in neuronal development:a clinical approach to investigation of Joubert syndrome and Joubert syndromerelated disorders. Dev Med Child Neurol. 2011;53:793-798.
    • (2011) Dev Med Child Neurol. , vol.53 , pp. 793-798
    • Sattar, S.1    Gleeson, J.G.2
  • 11
    • 84875763931 scopus 로고    scopus 로고
    • Targeted treatment trials for tuberous sclerosis and autism:no longer a dream
    • In press
    • Sahin M. Targeted treatment trials for tuberous sclerosis and autism:no longer a dream. Curr Opin Neurobiol. In press.
    • Curr Opin Neurobiol
    • Sahin, M.1
  • 13
    • 79953846144 scopus 로고    scopus 로고
    • Connectivity and the corpus callosum in autism spectrum conditions:insights from comparison of autism and callosal agenesis
    • Booth R, Wallace GL, Happe F. Connectivity and the corpus callosum in autism spectrum conditions:insights from comparison of autism and callosal agenesis. Prog Brain Res. 2011;189:303-317.
    • (2011) Prog Brain Res. , vol.189 , pp. 303-317
    • Booth, R.1    Wallace, G.L.2    Happe, F.3
  • 14
    • 0021337105 scopus 로고
    • Synapse elimination and plasticity in developing human cerebral cortex
    • Huttenlocher PR. Synapse elimination and plasticity in developing human cerebral cortex. Am J Ment Defic. 1984;88:488-496.
    • (1984) Am J Ment Defic. , vol.88 , pp. 488-496
    • Huttenlocher, P.R.1
  • 15
    • 0020262681 scopus 로고
    • Synaptogenesis in human visual cortex - evidence for synapse elimination during normal development
    • Huttenlocher PR, de Courten C, Garey LJ, Van der Loos H. Synaptogenesis in human visual cortex - evidence for synapse elimination during normal development. Neurosci Lett. 1982;33:247-252.
    • (1982) Neurosci Lett. , vol.33 , pp. 247-252
    • Huttenlocher, P.R.1    de Courten, C.2    Garey, L.J.3    Van der Loos, H.4
  • 16
    • 79551594543 scopus 로고    scopus 로고
    • Toward fulfilling the promise of molecular medicine in fragile X syndrome
    • Krueger DD, Bear MF. Toward fulfilling the promise of molecular medicine in fragile X syndrome. Annu Rev Med. 2011;62:411-429.
    • (2011) Annu Rev Med. , vol.62 , pp. 411-429
    • Krueger, D.D.1    Bear, M.F.2
  • 17
    • 82455212924 scopus 로고    scopus 로고
    • Cognition and lobar morphology in full mutation boys with fragile X syndrome
    • Meguid NA, Fahim C, Sami R, et al. Cognition and lobar morphology in full mutation boys with fragile X syndrome. Brain Cogn. 2012;78:74-84.
    • (2012) Brain Cogn. , vol.78 , pp. 74-84
    • Meguid, N.A.1    Fahim, C.2    Sami, R.3
  • 18
    • 0034639298 scopus 로고    scopus 로고
    • Head circumference is an independent clinical finding associated with autism
    • Miles JH, Hadden LL, Takahashi TN, Hillman RE. Head circumference is an independent clinical finding associated with autism. Am J Med Genet. 2000;95:339-350.
    • (2000) Am J Med Genet. , vol.95 , pp. 339-350
    • Miles, J.H.1    Hadden, L.L.2    Takahashi, T.N.3    Hillman, R.E.4
  • 19
    • 50849130596 scopus 로고    scopus 로고
    • Mapping early brain development in autism
    • Courchesne E, Pierce K, Schumann CM, et al. Mapping early brain development in autism. Neuron. 2007;56:399-413.
    • (2007) Neuron. , vol.56 , pp. 399-413
    • Courchesne, E.1    Pierce, K.2    Schumann, C.M.3
  • 20
    • 20244367771 scopus 로고    scopus 로고
    • Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations
    • Butler MG, Dasouki MJ, Zhou XP, et al. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations. J Med Genet. 2005;42:318-321.
    • (2005) J Med Genet. , vol.42 , pp. 318-321
    • Butler, M.G.1    Dasouki, M.J.2    Zhou, X.P.3
  • 21
    • 73149102059 scopus 로고    scopus 로고
    • Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network
    • United States, 2006.
    • Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006. MMWR Surveill Summ. 2009;58:1-20.
    • (2009) MMWR Surveill Summ. , vol.58 , pp. 1-20
  • 22
    • 65349122404 scopus 로고    scopus 로고
    • Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome:evidence for disruption of neuronal networks
    • Belichenko PV, Wright EE, Belichenko NP, et al. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome:evidence for disruption of neuronal networks. J Comp Neurol. 2009;514:240-258.
    • (2009) J Comp Neurol. , vol.514 , pp. 240-258
    • Belichenko, P.V.1    Wright, E.E.2    Belichenko, N.P.3
  • 23
    • 67649921127 scopus 로고    scopus 로고
    • The genetic landscape of intellectual disability arising from chromosome X
    • Gecz J, Shoubridge C, Corbett M. The genetic landscape of intellectual disability arising from chromosome X. Trends Genet. 2009;25:308-316.
    • (2009) Trends Genet. , vol.25 , pp. 308-316
    • Gecz, J.1    Shoubridge, C.2    Corbett, M.3
  • 24
    • 84855513774 scopus 로고    scopus 로고
    • Dendritic spine abnormalities in mental retardation
    • von Bohlen Und Halbach O. Dendritic spine abnormalities in mental retardation. Cell Tissue Res. 2010;342:317-323.
    • (2010) Cell Tissue Res. , vol.342 , pp. 317-323
    • von Bohlen Und Halbach, O.1
  • 25
    • 67651010456 scopus 로고    scopus 로고
    • Genetic advances in autism: heterogeneity and convergence on shared pathways
    • Bill BR, Geschwind DH. Genetic advances in autism: heterogeneity and convergence on shared pathways. Curr Opin Genet Dev. 2009;19:271-278.
    • (2009) Curr Opin Genet Dev. , vol.19 , pp. 271-278
    • Bill, B.R.1    Geschwind, D.H.2
  • 26
    • 84860780495 scopus 로고    scopus 로고
    • De novo mutations revealed by whole-exome sequencing are strongly associated with autism
    • Sanders SJ, Murtha MT, Gupta AR, et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 2012;485:237-241.
    • (2012) Nature. , vol.485 , pp. 237-241
    • Sanders, S.J.1    Murtha, M.T.2    Gupta, A.R.3
  • 27
    • 84860712363 scopus 로고    scopus 로고
    • Patterns and rates of exonic de novo mutations in autism spectrum disorders
    • Neale BM, Kou Y, Liu L, et al. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 2012;485:242-245.
    • (2012) Nature. , vol.485 , pp. 242-245
    • Neale, B.M.1    Kou, Y.2    Liu, L.3
  • 28
    • 84860741138 scopus 로고    scopus 로고
    • Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
    • O'Roak BJ, Vives L, Girirajan S, et al. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature. 2012;485:246-250.
    • (2012) Nature. , vol.485 , pp. 246-250
    • O'Roak, B.J.1    Vives, L.2    Girirajan, S.3
  • 29
    • 79957589237 scopus 로고    scopus 로고
    • Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
    • O'Roak BJ, Deriziotis P, Lee C, et al. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet. 2011;43:585-589.
    • (2011) Nat Genet. , vol.43 , pp. 585-589
    • O'Roak, B.J.1    Deriziotis, P.2    Lee, C.3
  • 30
    • 84860297457 scopus 로고    scopus 로고
    • De novo gene disruptions in children on the autistic spectrum
    • Iossifov I, Ronemus M, Levy D, et al. De novo gene disruptions in children on the autistic spectrum. Neuron. 2012;74:285-299.
    • (2012) Neuron. , vol.74 , pp. 285-299
    • Iossifov, I.1    Ronemus, M.2    Levy, D.3
  • 31
    • 0242300612 scopus 로고    scopus 로고
    • DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
    • Martinowich K, Hattori D, Wu H, et al. DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science. 2003;302:890-893.
    • (2003) Science. , vol.302 , pp. 890-893
    • Martinowich, K.1    Hattori, D.2    Wu, H.3
  • 32
    • 2942731425 scopus 로고    scopus 로고
    • CBP histone acetyltransferase activity is a critical component of memory consolidation
    • Korzus E, Rosenfeld MG, Mayford M. CBP histone acetyltransferase activity is a critical component of memory consolidation. Neuron. 2004;42:961-972.
    • (2004) Neuron. , vol.42 , pp. 961-972
    • Korzus, E.1    Rosenfeld, M.G.2    Mayford, M.3
  • 33
    • 0037111980 scopus 로고    scopus 로고
    • Integration of long-termmemory- related synaptic plasticity involves bidirectional regulation of gene expression and chromatin structure
    • Guan Z, Giustetto M, Lomvardas S, et al. Integration of long-termmemory- related synaptic plasticity involves bidirectional regulation of gene expression and chromatin structure. Cell. 2002;111:483-493.
    • (2002) Cell. , vol.111 , pp. 483-493
    • Guan, Z.1    Giustetto, M.2    Lomvardas, S.3
  • 34
    • 79959262465 scopus 로고    scopus 로고
    • Transcriptomic analysis of autistic brain reveals convergent molecular pathology
    • Voineagu I, Wang X, Johnston P, et al. Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature. 2011;474:380-384.
    • (2011) Nature. , vol.474 , pp. 380-384
    • Voineagu, I.1    Wang, X.2    Johnston, P.3
  • 35
    • 34748887795 scopus 로고    scopus 로고
    • Regulation of dendritic development by neuron-specific chromatin remodeling complexes
    • Wu JI, Lessard J, Olave IA, et al. Regulation of dendritic development by neuron-specific chromatin remodeling complexes. Neuron. 2007;56:94- 108.
    • (2007) Neuron. , vol.56 , pp. 94-108
    • Wu, J.I.1    Lessard, J.2    Olave, I.A.3
  • 36
    • 80053592226 scopus 로고    scopus 로고
    • Intrinsic epigenetic factors cooperate with the steroid hormone ecdysone to govern dendrite pruning in Drosophila
    • Kirilly D, Wong JJ, Lim EK, et al. Intrinsic epigenetic factors cooperate with the steroid hormone ecdysone to govern dendrite pruning in Drosophila. Neuron. 2011;72:86-100.
    • (2011) Neuron. , vol.72 , pp. 86-100
    • Kirilly, D.1    Wong, J.J.2    Lim, E.K.3
  • 37
    • 0342437491 scopus 로고    scopus 로고
    • MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
    • Nan X, Campoy FJ, Bird A. MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. Cell. 1997;88:471-481.
    • (1997) Cell. , vol.88 , pp. 471-481
    • Nan, X.1    Campoy, F.J.2    Bird, A.3
  • 38
    • 67249150482 scopus 로고    scopus 로고
    • Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus
    • Ben-Shachar S, Chahrour M, Thaller C, Shaw CA, Zoghbi HY. Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus. Hum Mol Genet. 2009;18:2431-2442.
    • (2009) Hum Mol Genet. , vol.18 , pp. 2431-2442
    • Ben-Shachar, S.1    Chahrour, M.2    Thaller, C.3    Shaw, C.A.4    Zoghbi, H.Y.5
  • 39
    • 76849094693 scopus 로고    scopus 로고
    • Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state
    • Skene PJ, Illingworth RS, Webb S, et al. Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state. Mol Cell. 2010;37:457-468.
    • (2010) Mol Cell. , vol.37 , pp. 457-468
    • Skene, P.J.1    Illingworth, R.S.2    Webb, S.3
  • 40
    • 80053579176 scopus 로고    scopus 로고
    • Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function
    • Cohen S, Gabel HW, Hemberg M, et al. Genome-wide activity-dependent MeCP2 phosphorylation regulates nervous system development and function. Neuron. 2011;72:72-85.
    • (2011) Neuron. , vol.72 , pp. 72-85
    • Cohen, S.1    Gabel, H.W.2    Hemberg, M.3
  • 41
    • 77954658446 scopus 로고    scopus 로고
    • Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
    • Cukier HN, Rabionet R, Konidari I, et al. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. Neurogenetics. 2010;11:291-303.
    • (2010) Neurogenetics. , vol.11 , pp. 291-303
    • Cukier, H.N.1    Rabionet, R.2    Konidari, I.3
  • 42
    • 80053931230 scopus 로고    scopus 로고
    • Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.
    • Talkowski ME, Mullegama SV, Rosenfeld JA, et al. Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. Am J Hum Genet. 2011;89:551-563.
    • (2011) Am J Hum Genet. , vol.89 , pp. 551-563
    • Talkowski, M.E.1    Mullegama, S.V.2    Rosenfeld, J.A.3
  • 43
    • 84860347597 scopus 로고    scopus 로고
    • Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries
    • Talkowski ME, Rosenfeld JA, Blumenthal I, et al. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 2012;149:525-537.
    • (2012) Cell. , vol.149 , pp. 525-537
    • Talkowski, M.E.1    Rosenfeld, J.A.2    Blumenthal, I.3
  • 44
    • 70350719241 scopus 로고    scopus 로고
    • Autism spectrum conditions in individuals with Mobius sequence, CHARGE syndrome and oculo-auriculovertebral spectrum:diagnostic aspects
    • Johansson M, Gillberg C, Rastam M. Autism spectrum conditions in individuals with Mobius sequence, CHARGE syndrome and oculo-auriculovertebral spectrum:diagnostic aspects. Res Dev Disabil. 2010;31:9-24.
    • (2010) Res Dev Disabil. , vol.31 , pp. 9-24
    • Johansson, M.1    Gillberg, C.2    Rastam, M.3
  • 45
    • 20244368362 scopus 로고    scopus 로고
    • Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome
    • Kleefstra T, Smidt M, Banning MJ, et al. Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome. J Med Genet. 2005;42:299-306.
    • (2005) J Med Genet. , vol.42 , pp. 299-306
    • Kleefstra, T.1    Smidt, M.2    Banning, M.J.3
  • 46
    • 77958500315 scopus 로고    scopus 로고
    • Genomic copy number variation in disorders of cognitive development
    • Morrow EM. Genomic copy number variation in disorders of cognitive development. J Am Acad Child Adolesc Psychiatry. 2010;49:1091-1104.
    • (2010) J Am Acad Child Adolesc Psychiatry. , vol.49 , pp. 1091-1104
    • Morrow, E.M.1
  • 47
    • 80053106248 scopus 로고    scopus 로고
    • Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
    • Mikhail FM, Lose EJ, Robin NH, et al. Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders. Am J Med Genet A. 2011;155A:2386-2396.
    • (2011) Am J Med Genet A. , vol.155 A , pp. 2386-2396
    • Mikhail, F.M.1    Lose, E.J.2    Robin, N.H.3
  • 48
    • 35148885611 scopus 로고    scopus 로고
    • Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism
    • Martin CL, Duvall JA, Ilkin Y, et al. Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism. Am J Med Genet B Neuropsychiatr Genet. 2007;144B:869-876.
    • (2007) Am J Med Genet B Neuropsychiatr Genet. , vol.144 B , pp. 869-876
    • Martin, C.L.1    Duvall, J.A.2    Ilkin, Y.3
  • 49
    • 34547668506 scopus 로고    scopus 로고
    • Adhesion molecules in the nervous system: structural insights into function and diversity
    • Shapiro L, Love J, Colman DR. Adhesion molecules in the nervous system: structural insights into function and diversity. Annu Rev Neurosci. 2007;30:451-474.
    • (2007) Annu Rev Neurosci. , vol.30 , pp. 451-474
    • Shapiro, L.1    Love, J.2    Colman, D.R.3
  • 50
    • 54949144402 scopus 로고    scopus 로고
    • The autistic neuron:troubled translation?
    • Kelleher RJ, 3rd, Bear MF. The autistic neuron:troubled translation? Cell. 2008;135:401-406.
    • (2008) Cell , vol.135 , pp. 401-406
    • Kelleher, R.J.1    Bear, M.F.2
  • 51
    • 79960779323 scopus 로고    scopus 로고
    • FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism
    • Darnell JC, Van Driesche SJ, Zhang C, et al. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism. Cell. 2011;146:247-261.
    • (2011) Cell. , vol.146 , pp. 247-261
    • Darnell, J.C.1    Van Driesche, S.J.2    Zhang, C.3
  • 52
    • 0037188502 scopus 로고    scopus 로고
    • Altered synaptic plasticity in a mouse model of fragile X mental retardation
    • U S A.
    • Huber KM, Gallagher SM, Warren ST, Bear MF. Altered synaptic plasticity in a mouse model of fragile X mental retardation. Proc Natl Acad Sci U S A. 2002;99:7746-7750.
    • (2002) Proc Natl Acad Sci , vol.99 , pp. 7746-7750
    • Huber, K.M.1    Gallagher, S.M.2    Warren, S.T.3    Bear, M.F.4
  • 53
    • 70450208984 scopus 로고    scopus 로고
    • Deregulation of EIF4E:a novel mechanism for autism
    • Neves-Pereira M, Muller B, Massie D, et al. Deregulation of EIF4E:a novel mechanism for autism. J Med Genet. 2009;46:759-765.
    • (2009) J Med Genet. , vol.46 , pp. 759-765
    • Neves-Pereira, M.1    Muller, B.2    Massie, D.3
  • 54
    • 84860668936 scopus 로고    scopus 로고
    • Harnessing the power of the endosome to regulate neural development
    • Yap CC, Winckler B. Harnessing the power of the endosome to regulate neural development. Neuron. 2012;74:440-451.
    • (2012) Neuron. , vol.74 , pp. 440-451
    • Yap, C.C.1    Winckler, B.2
  • 58
    • 0038238370 scopus 로고    scopus 로고
    • The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism
    • Castermans D, Wilquet V, Parthoens E, et al. The neurobeachin gene is disrupted by a translocation in a patient with idiopathic autism. J Med Genet. 2003;40:352-356.
    • (2003) J Med Genet. , vol.40 , pp. 352-356
    • Castermans, D.1    Wilquet, V.2    Parthoens, E.3
  • 59
    • 76249116225 scopus 로고    scopus 로고
    • Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly
    • Giannandrea M, Bianchi V, Mignogna ML, et al. Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly. Am J Hum Genet. 2010;86:185-195.
    • (2010) Am J Hum Genet. , vol.86 , pp. 185-195
    • Giannandrea, M.1    Bianchi, V.2    Mignogna, M.L.3
  • 60
    • 45149113695 scopus 로고    scopus 로고
    • A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder
    • Roohi J, Tegay DH, Pomeroy JC, et al. A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet. 2008;147B:411-417.
    • (2008) Am J Med Genet B Neuropsychiatr Genet. , vol.147 B , pp. 411-417
    • Roohi, J.1    Tegay, D.H.2    Pomeroy, J.C.3
  • 61
    • 33845396840 scopus 로고    scopus 로고
    • Plasticity-induced growth of dendritic spines by exocytic trafficking from recycling endosomes
    • Park M, Salgado JM, Ostroff L, et al. Plasticity-induced growth of dendritic spines by exocytic trafficking from recycling endosomes. Neuron. 2006;52:817-830.
    • (2006) Neuron. , vol.52 , pp. 817-830
    • Park, M.1    Salgado, J.M.2    Ostroff, L.3
  • 62
    • 70350417360 scopus 로고    scopus 로고
    • Axonal targeting of Caspr2 in hippocampal neurons via selective somatodendritic endocytosis
    • Bel C, Oguievetskaia K, Pitaval C, Goutebroze L, Faivre-Sarrailh C. Axonal targeting of Caspr2 in hippocampal neurons via selective somatodendritic endocytosis. J Cell Sci. 2009;122:3403-3413.
    • (2009) J Cell Sci. , vol.122 , pp. 3403-3413
    • Bel, C.1    Oguievetskaia, K.2    Pitaval, C.3    Goutebroze, L.4    Faivre-Sarrailh, C.5
  • 63
    • 58949088309 scopus 로고    scopus 로고
    • Contact in the genetics of autism and schizophrenia
    • Burbach JP, van der Zwaag B. Contact in the genetics of autism and schizophrenia. Trends Neurosci. 2009;32:69-72.
    • (2009) Trends Neurosci. , vol.32 , pp. 69-72
    • Burbach, J.P.1    van der Zwaag, B.2
  • 64
    • 81755183108 scopus 로고    scopus 로고
    • Relative burden of large CNVs on a range of neurodevelopmental phenotypes
    • Girirajan S, Brkanac Z, Coe BP, et al. Relative burden of large CNVs on a range of neurodevelopmental phenotypes. PLoS Genet. 2011;7:e1002334.
    • (2011) PLoS Genet. , vol.7
    • Girirajan, S.1    Brkanac, Z.2    Coe, B.P.3
  • 65
    • 78751500005 scopus 로고    scopus 로고
    • Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism
    • Chapleau CA, Larimore JL, Theibert A, Pozzo-Miller L. Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism. J Neurodev Disord. 2009;1:185-196.
    • (2009) J Neurodev Disord. , vol.1 , pp. 185-196
    • Chapleau, C.A.1    Larimore, J.L.2    Theibert, A.3    Pozzo-Miller, L.4
  • 66
    • 67349182343 scopus 로고    scopus 로고
    • Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
    • Glessner JT, Wang K, Cai G, et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 2009;459:569-573.
    • (2009) Nature. , vol.459 , pp. 569-573
    • Glessner, J.T.1    Wang, K.2    Cai, G.3
  • 67
    • 0034703133 scopus 로고    scopus 로고
    • Biochemistry. Ubiquitination - more than two to tango
    • Joazeiro CA, Hunter T. Biochemistry. Ubiquitination - more than two to tango. Science. 2000;289:2061-2062.
    • (2000) Science. , vol.289 , pp. 2061-2062
    • Joazeiro, C.A.1    Hunter, T.2
  • 68
    • 0037179795 scopus 로고    scopus 로고
    • New roles for ubiquitin in the assembly and function of neuronal circuits
    • Murphey RK, Godenschwege TA. New roles for ubiquitin in the assembly and function of neuronal circuits. Neuron. 2002;36:5-8.
    • (2002) Neuron. , vol.36 , pp. 5-8
    • Murphey, R.K.1    Godenschwege, T.A.2
  • 69
    • 80053626726 scopus 로고    scopus 로고
    • Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice
    • Smith SE, Zhou YD, Zhang G, Jin Z, Stoppel DC, Anderson MP. Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice. Sci Transl Med. 2011;3:103ra97.
    • (2011) Sci Transl Med. , vol.3
    • Smith, S.E.1    Zhou, Y.D.2    Zhang, G.3    Jin, Z.4    Stoppel, D.C.5    Anderson, M.P.6
  • 70
    • 79957560791 scopus 로고    scopus 로고
    • Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes
    • Mabb AM, Judson MC, Zylka MJ, Philpot BD. Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes. Trends Neurosci. 2011;34:293-303.
    • (2011) Trends Neurosci. , vol.34 , pp. 293-303
    • Mabb, A.M.1    Judson, M.C.2    Zylka, M.J.3    Philpot, B.D.4
  • 71
    • 33748645750 scopus 로고    scopus 로고
    • UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel Xlinked mental retardation syndrome
    • Nascimento RM, Otto PA, de Brouwer AP, Vianna-Morgante AM. UBE2A, which encodes a ubiquitin-conjugating enzyme, is mutated in a novel Xlinked mental retardation syndrome. Am J Hum Genet. 2006;79:549-555.
    • (2006) Am J Hum Genet. , vol.79 , pp. 549-555
    • Nascimento, R.M.1    Otto, P.A.2    de Brouwer, A.P.3    Vianna-Morgante, A.M.4
  • 72
    • 33645233648 scopus 로고    scopus 로고
    • Reelin glycoprotein in autism and schizophrenia
    • Fatemi SH. Reelin glycoprotein in autism and schizophrenia. Int Rev Neurobiol. 2005;71:179-187.
    • (2005) Int Rev Neurobiol. , vol.71 , pp. 179-187
    • Fatemi, S.H.1
  • 73
    • 0344197741 scopus 로고    scopus 로고
    • Regulation of protein tyrosine kinase signaling by substrate degradation during brain development
    • Arnaud L, Ballif BA, Cooper JA. Regulation of protein tyrosine kinase signaling by substrate degradation during brain development. Mol Cell Biol. 2003;23:9293-9302.
    • (2003) Mol Cell Biol. , vol.23 , pp. 9293-9302
    • Arnaud, L.1    Ballif, B.A.2    Cooper, J.A.3
  • 74
    • 32344440647 scopus 로고    scopus 로고
    • Synapse formation and plasticity:recent insights from the perspective of the ubiquitin proteasome system
    • Patrick GN. Synapse formation and plasticity:recent insights from the perspective of the ubiquitin proteasome system. Curr Opin Neurobiol. 2006;16:90-94.
    • (2006) Curr Opin Neurobiol. , vol.16 , pp. 90-94
    • Patrick, G.N.1
  • 75
    • 0035924590 scopus 로고    scopus 로고
    • Chemotropic responses of retinal growth cones mediated by rapid local protein synthesis and degradation
    • Campbell DS, Holt CE. Chemotropic responses of retinal growth cones mediated by rapid local protein synthesis and degradation. Neuron. 2001;32:1013-1026.
    • (2001) Neuron. , vol.32 , pp. 1013-1026
    • Campbell, D.S.1    Holt, C.E.2
  • 76
    • 0037162692 scopus 로고    scopus 로고
    • Comm sorts robo to control axon guidance at the Drosophila midline
    • Keleman K, Rajagopalan S, Cleppien D, et al. Comm sorts robo to control axon guidance at the Drosophila midline. Cell. 2002;110:415-427.
    • (2002) Cell. , vol.110 , pp. 415-427
    • Keleman, K.1    Rajagopalan, S.2    Cleppien, D.3
  • 77
    • 77950899212 scopus 로고    scopus 로고
    • Connecting genes to brain in the autism spectrum disorders
    • Abrahams BS, Geschwind DH. Connecting genes to brain in the autism spectrum disorders. Arch Neurol. 2010;67:395-399.
    • (2010) Arch Neurol. , vol.67 , pp. 395-399
    • Abrahams, B.S.1    Geschwind, D.H.2
  • 78
    • 67650750977 scopus 로고    scopus 로고
    • A synaptic trek to autism
    • Bourgeron T. A synaptic trek to autism. Curr Opin Neurobiol. 2009;19:231- 234.
    • (2009) Curr Opin Neurobiol. , vol.19 , pp. 231-234
    • Bourgeron, T.1
  • 80
    • 79957456437 scopus 로고    scopus 로고
    • SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function
    • Fassio A, Patry L, Congia S, et al. SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function. Hum Mol Genet. 2011;20:2297-307.
    • (2011) Hum Mol Genet. , vol.20 , pp. 2297-307
    • Fassio, A.1    Patry, L.2    Congia, S.3
  • 81
    • 0032516032 scopus 로고    scopus 로고
    • A third member of the synapsin gene family
    • U S A.
    • Kao HT, Porton B, Czernik AJ, et al. A third member of the synapsin gene family. Proc Natl Acad Sci U S A. 1998;95:4667-4672.
    • (1998) Proc Natl Acad Sci , vol.95 , pp. 4667-4672
    • Kao, H.T.1    Porton, B.2    Czernik, A.J.3
  • 82
    • 0036617908 scopus 로고    scopus 로고
    • Regulation of neurotransmitter release by synapsin III
    • Feng J, Chi P, Blanpied TA, et al. Regulation of neurotransmitter release by synapsin III. J Neurosci. 2002;22:4372-4380.
    • (2002) J Neurosci. , vol.22 , pp. 4372-4380
    • Feng, J.1    Chi, P.2    Blanpied, T.A.3
  • 83
    • 0033615054 scopus 로고    scopus 로고
    • Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles
    • Augustin I, Rosenmund C, Sudhof TC, Brose N. Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles. Nature. 1999;400:457- 461.
    • (1999) Nature. , vol.400 , pp. 457-461
    • Augustin, I.1    Rosenmund, C.2    Sudhof, T.C.3    Brose, N.4
  • 84
    • 79953326969 scopus 로고    scopus 로고
    • The autism candidate gene Neurobeachin encodes a scaffolding protein implicated in membrane trafficking and signaling
    • Volders K, Nuytens K, Creemers JW. The autism candidate gene Neurobeachin encodes a scaffolding protein implicated in membrane trafficking and signaling. Curr Mol Med. 2011;11:204-217.
    • (2011) Curr Mol Med. , vol.11 , pp. 204-217
    • Volders, K.1    Nuytens, K.2    Creemers, J.W.3
  • 85
    • 13444259647 scopus 로고    scopus 로고
    • Regulation of cap-dependent translation by eIF4E inhibitory proteins
    • Richter JD, Sonenberg N. Regulation of cap-dependent translation by eIF4E inhibitory proteins. Nature. 2005;433:477-480.
    • (2005) Nature. , vol.433 , pp. 477-480
    • Richter, J.D.1    Sonenberg, N.2
  • 87
    • 51949094890 scopus 로고    scopus 로고
    • Tuberous sclerosis complex proteins control axon formation
    • Choi YJ, Di Nardo A, Kramvis I, et al. Tuberous sclerosis complex proteins control axon formation. Genes Dev. 2008;22:2485-2495.
    • (2008) Genes Dev. , vol.22 , pp. 2485-2495
    • Choi, Y.J.1    Di Nardo, A.2    Kramvis, I.3
  • 88
    • 79959289977 scopus 로고    scopus 로고
    • Loss of Tsc1 in vivo impairs hippocampal mGluR-LTD and increases excitatory synaptic function
    • Bateup HS, Takasaki KT, Saulnier JL, Denefrio CL, Sabatini BL. Loss of Tsc1 in vivo impairs hippocampal mGluR-LTD and increases excitatory synaptic function. J Neurosci. 2011;31:8862-889.
    • (2011) J Neurosci. , vol.31 , pp. 8862-889
    • Bateup, H.S.1    Takasaki, K.T.2    Saulnier, J.L.3    Denefrio, C.L.4    Sabatini, B.L.5
  • 90
    • 84860446920 scopus 로고    scopus 로고
    • High-throughput sequencing of mGluR signaling pathway genes reveals enrichment of rare variants in autism
    • Kelleher RJ, Geigenmuller U, Hovhannisyan H, et al. High-throughput sequencing of mGluR signaling pathway genes reveals enrichment of rare variants in autism. PLoS One. 2012;7:e35003.
    • (2012) PLoS One. , vol.7
    • Kelleher, R.J.1    Geigenmuller, U.2    Hovhannisyan, H.3
  • 91
    • 80053984176 scopus 로고    scopus 로고
    • A comprehensive functional analysis of PTEN mutations:implications in tumor- and autism-related syndromes
    • Rodriguez-Escudero I, Oliver MD, Andres-Pons A, Molina M, Cid VJ, Pulido R. A comprehensive functional analysis of PTEN mutations:implications in tumor- and autism-related syndromes. Hum Mol Genet. 2011;20:4132-4142.
    • (2011) Hum Mol Genet. , vol.20 , pp. 4132-4142
    • Rodriguez-Escudero, I.1    Oliver, M.D.2    Andres-Pons, A.3    Molina, M.4    Cid, V.J.5    Pulido, R.6
  • 92
    • 84860162767 scopus 로고    scopus 로고
    • Pten deletion in adult hippocampal neural stem/progenitor cells causes cellular abnormalities and alters neurogenesis
    • Amiri A, Cho W, Zhou J, et al. Pten deletion in adult hippocampal neural stem/progenitor cells causes cellular abnormalities and alters neurogenesis. J Neurosci. 2012;32:5880-5890.
    • (2012) J Neurosci. , vol.32 , pp. 5880-5890
    • Amiri, A.1    Cho, W.2    Zhou, J.3
  • 93
    • 33646142995 scopus 로고    scopus 로고
    • Pten regulates neuronal arborization and social interaction in mice
    • Kwon CH, Luikart BW, Powell CM, et al. Pten regulates neuronal arborization and social interaction in mice. Neuron. 2006;50:377-388.
    • (2006) Neuron. , vol.50 , pp. 377-388
    • Kwon, C.H.1    Luikart, B.W.2    Powell, C.M.3
  • 94
    • 38849126088 scopus 로고    scopus 로고
    • Recurrent 16p11.2 microdeletions in autism.
    • Kumar RA, KaraMohamed S, Sudi J, et al. Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet. 2008;17:628-638.
    • (2008) Hum Mol Genet. , vol.17 , pp. 628-638
    • Kumar, R.A.1    KaraMohamed, S.2    Sudi, J.3
  • 95
    • 39049163023 scopus 로고    scopus 로고
    • Association between microdeletion and microduplication at 16p11.2 and autism.
    • Weiss LA, Shen Y, Korn JM, et al. Association between microdeletion and microduplication at 16p11.2 and autism. N Engl J Med. 2008;358:667- 675.
    • (2008) N Engl J Med. , vol.358 , pp. 667-675
    • Weiss, L.A.1    Shen, Y.2    Korn, J.M.3
  • 96
    • 79959941657 scopus 로고    scopus 로고
    • Association of upregulated Ras/Raf/ERK1/2 signaling with autism
    • Zou H, Yu Y, Sheikh AM, et al. Association of upregulated Ras/Raf/ERK1/2 signaling with autism. Genes Brain Behav. 2011;10:615-624.
    • (2011) Genes Brain Behav. , vol.10 , pp. 615-624
    • Zou, H.1    Yu, Y.2    Sheikh, A.M.3
  • 97
    • 84875789751 scopus 로고    scopus 로고
    • Up-regulation of Ras/Raf/ERK1/2 signaling impairs cultured neuronal cell migration, neurogenesis, synapse formation, and dendritic spine development Brain Struct Funct
    • In press.
    • Yang K, Cao F, Sheikh AM, et al. Up-regulation of Ras/Raf/ERK1/2 signaling impairs cultured neuronal cell migration, neurogenesis, synapse formation, and dendritic spine development. Brain Struct Funct. In press.
    • Yang, K.1    Cao, F.2    Sheikh, A.M.3
  • 98
    • 84875765729 scopus 로고    scopus 로고
    • Dyrk1A influences neuronal morphogenesis through regulation of cytoskeletal dynamics in mammalian cortical neurons
    • In press
    • Martinez de Lagran M, Benavides-Piccione R, Ballesteros-Yanez I, et al. Dyrk1A influences neuronal morphogenesis through regulation of cytoskeletal dynamics in mammalian cortical neurons. Cereb Cortex. In press.
    • Cereb Cortex.
    • Martinez de Lagran, M.1    Benavides-Piccione, R.2    Ballesteros-Yanez, I.3
  • 99
    • 77952827032 scopus 로고    scopus 로고
    • Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
    • Berkel S, Marshall CR, Weiss B, et al. Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nat Genet. 2010;42:489-491.
    • (2010) Nat Genet. , vol.42 , pp. 489-491
    • Berkel, S.1    Marshall, C.R.2    Weiss, B.3
  • 100
    • 33845889998 scopus 로고    scopus 로고
    • Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
    • Durand CM, Betancur C, Boeckers TM, et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet. 2007;39:25-27.
    • (2007) Nat Genet. , vol.39 , pp. 25-27
    • Durand, C.M.1    Betancur, C.2    Boeckers, T.M.3
  • 101
    • 84860739976 scopus 로고    scopus 로고
    • SHANK1 deletions in males with autism spectrum disorder
    • Sato D, Lionel AC, Leblond CS, et al. SHANK1 deletions in males with autism spectrum disorder. Am J Hum Genet. 2012;90:879-887.
    • (2012) Am J Hum Genet. , vol.90 , pp. 879-887
    • Sato, D.1    Lionel, A.C.2    Leblond, C.S.3
  • 102
    • 70349610083 scopus 로고    scopus 로고
    • Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection
    • Sykes NH, Toma C, Wilson N, et al. Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. Eur J Hum Genet. 2009;17:1347-1353.
    • (2009) Eur J Hum Genet. , vol.17 , pp. 1347-1353
    • Sykes, N.H.1    Toma, C.2    Wilson, N.3
  • 103
    • 33750431676 scopus 로고    scopus 로고
    • Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.
    • Bonaglia MC, Giorda R, Mani E, et al. Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome. J Med Genet. 2006;43:822-828.
    • (2006) J Med Genet. , vol.43 , pp. 822-828
    • Bonaglia, M.C.1    Giorda, R.2    Mani, E.3
  • 104
    • 79551596834 scopus 로고    scopus 로고
    • Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation
    • Grabrucker AM, Knight MJ, Proepper C, et al. Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation. EMBO J. 2011;30:569-581.
    • (2011) EMBO J. , vol.30 , pp. 569-581
    • Grabrucker, A.M.1    Knight, M.J.2    Proepper, C.3
  • 105
    • 79955672523 scopus 로고    scopus 로고
    • Neurexin-neuroligin transsynaptic interaction mediates learning-related synaptic remodeling and long-term facilitation in aplysia
    • Choi YB, Li HL, Kassabov SR, et al. Neurexin-neuroligin transsynaptic interaction mediates learning-related synaptic remodeling and long-term facilitation in aplysia. Neuron. 2011;70:468-481.
    • (2011) Neuron. , vol.70 , pp. 468-481
    • Choi, Y.B.1    Li, H.L.2    Kassabov, S.R.3
  • 106
    • 40749089626 scopus 로고    scopus 로고
    • Structural variation of chromosomes in autism spectrum disorder
    • Marshall CR, Noor A, Vincent JB, et al. Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet. 2008;82:477-488.
    • (2008) Am J Hum Genet. , vol.82 , pp. 477-488
    • Marshall, C.R.1    Noor, A.2    Vincent, J.B.3
  • 107
    • 38749140677 scopus 로고    scopus 로고
    • Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
    • Alarcon M, Abrahams BS, Stone JL, et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet. 2008;82:150-159.
    • (2008) Am J Hum Genet. , vol.82 , pp. 150-159
    • Alarcon, M.1    Abrahams, B.S.2    Stone, J.L.3
  • 108
    • 0037656313 scopus 로고    scopus 로고
    • Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
    • Jamain S, Quach H, Betancur C, et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet. 2003;34:27-29.
    • (2003) Nat Genet. , vol.34 , pp. 27-29
    • Jamain, S.1    Quach, H.2    Betancur, C.3
  • 109
    • 58849092285 scopus 로고    scopus 로고
    • Membrane fusion:grappling with SNARE and SM proteins
    • Sudhof TC, Rothman JE. Membrane fusion:grappling with SNARE and SM proteins. Science. 2009;323:474-477.
    • (2009) Science. , vol.323 , pp. 474-477
    • Sudhof, T.C.1    Rothman, J.E.2
  • 110
    • 33748531328 scopus 로고    scopus 로고
    • Neuroligins determine synapse maturation and function
    • Varoqueaux F, Aramuni G, Rawson RL, et al. Neuroligins determine synapse maturation and function. Neuron. 2006;51:741-754.
    • (2006) Neuron. , vol.51 , pp. 741-754
    • Varoqueaux, F.1    Aramuni, G.2    Rawson, R.L.3
  • 111
    • 42649125261 scopus 로고    scopus 로고
    • Familial deletion within NLGN4 associated with autism and Tourette syndrome
    • Lawson-Yuen A, Saldivar JS, Sommer S, Picker J. Familial deletion within NLGN4 associated with autism and Tourette syndrome. Eur J Hum Genet. 2008;16:614-618.
    • (2008) Eur J Hum Genet. , vol.16 , pp. 614-618
    • Lawson-Yuen, A.1    Saldivar, J.S.2    Sommer, S.3    Picker, J.4
  • 112
    • 38749096303 scopus 로고    scopus 로고
    • A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
    • Arking DE, Cutler DJ, Brune CW, et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet. 2008;82:160-164.
    • (2008) Am J Hum Genet. , vol.82 , pp. 160-164
    • Arking, D.E.1    Cutler, D.J.2    Brune, C.W.3
  • 114
    • 58149347147 scopus 로고    scopus 로고
    • Epigenetics in the nervous system
    • Jiang Y, Langley B, Lubin FD, et al. Epigenetics in the nervous system. J Neurosci. 2008;28:11753-11759.
    • (2008) J Neurosci. , vol.28 , pp. 11753-11759
    • Jiang, Y.1    Langley, B.2    Lubin, F.D.3
  • 115
    • 84863247768 scopus 로고    scopus 로고
    • Epigenetic signatures of autism:trimethylated H3K4 landscapes in prefrontal neurons
    • Shulha HP, Cheung I, Whittle C, et al. Epigenetic signatures of autism:trimethylated H3K4 landscapes in prefrontal neurons. Arch Gen Psychiatry. 2012;69:314-324.
    • (2012) Arch Gen Psychiatry. , vol.69 , pp. 314-324
    • Shulha, H.P.1    Cheung, I.2    Whittle, C.3
  • 116
    • 34548849750 scopus 로고    scopus 로고
    • Patterns of growth in verbal abilities among children with autism spectrum disorder
    • Anderson DK, Lord C, Risi S, et al. Patterns of growth in verbal abilities among children with autism spectrum disorder. J Consult Clin Psychol. 2007;75:594-604.
    • (2007) J Consult Clin Psychol. , vol.75 , pp. 594-604
    • Anderson, D.K.1    Lord, C.2    Risi, S.3
  • 117
    • 38349127623 scopus 로고    scopus 로고
    • Development of the human cerebral cortex: Boulder Committee revisited
    • Bystron I, Blakemore C, Rakic P. Development of the human cerebral cortex: Boulder Committee revisited. Nat Rev Neurosci. 2008;9:110-122.
    • (2008) Nat Rev Neurosci. , vol.9 , pp. 110-122
    • Bystron, I.1    Blakemore, C.2    Rakic, P.3
  • 118


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.