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Volumn 4, Issue 9, 2014, Pages

Modulation of interhemispheric functional coordination in electroconvulsive therapy for depression

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANGULAR GYRUS; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; COORDINATION; DEPRESSION; EDUCATIONAL STATUS; ELECTROCONVULSIVE THERAPY; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HAMILTON DEPRESSION RATING SCALE; HUMAN; INTERHEMISPHERIC FUNCTIONAL COORDINATION; MALE; MIDDLE FRONTAL GYRUS; RIGHT HEMISPHERE; SUPERIOR FRONTAL GYRUS; BRAIN; BRAIN MAPPING; DEPRESSIVE DISORDER; IMAGE PROCESSING; MIDDLE AGED; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PROCEDURES; STATISTICS AND NUMERICAL DATA;

EID: 84927798274     PISSN: None     EISSN: 21583188     Source Type: Journal    
DOI: 10.1038/tp.2014.101     Document Type: Article
Times cited : (47)

References (92)
  • 1
    • 84859394070 scopus 로고    scopus 로고
    • Prevalence of autism spectrum disorders-Autism and developmental disabilities monitoring network, 14 sites, united states 2008
    • Baio J. Prevalence of autism spectrum disorders-Autism and developmental disabilities monitoring network, 14 Sites, United States, 2008. Centers Dis Control Prev MMWR Surveill Summ 2012; 61: 1-19.
    • (2012) Centers Dis Control Prev MMWR Surveill Summ , vol.61 , pp. 1-19
    • Baio, J.1
  • 3
    • 67650732715 scopus 로고    scopus 로고
    • Advances in autism
    • Geschwind DH. Advances in autism. Annu Rev Med 2009; 60: 367-380.
    • (2009) Annu Rev Med , vol.60 , pp. 367-380
    • Geschwind, D.H.1
  • 4
    • 77954657070 scopus 로고    scopus 로고
    • Functional impact of global rare copy number variation in autism spectrum disorders
    • Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010; 466: 368-372.
    • (2010) Nature , vol.466 , pp. 368-372
    • Pinto, D.1    Pagnamenta, A.T.2    Klei, L.3    Anney, R.4    Merico, D.5    Regan, R.6
  • 5
    • 34147145963 scopus 로고    scopus 로고
    • Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation
    • Kalscheuer VM, FitzPatrick D, Tommerup N, Bugge M, Niebuhr E, Neumann LM et al. Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation. Hum Genet 2007; 121: 501-509.
    • (2007) Hum Genet , vol.121 , pp. 501-509
    • Kalscheuer, V.M.1    Fitzpatrick, D.2    Tommerup, N.3    Bugge, M.4    Niebuhr, E.5    Neumann, L.M.6
  • 6
    • 38749099110 scopus 로고    scopus 로고
    • Molecular cytogenetic analysis and resequencing of contactin associated protein-Like 2 in autism spectrum disorders
    • Bakkaloglu B, Roak BJO, Louvi A, Gupta AR, Abelson JF, Morgan TM et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-Like 2 in autism spectrum disorders. Am J Hum Genet 2008; 82: 165-173.
    • (2008) Am J Hum Genet , vol.82 , pp. 165-173
    • Bakkaloglu, B.1    Roak, B.J.O.2    Louvi, A.3    Gupta, A.R.4    Abelson, J.F.5    Morgan, T.M.6
  • 7
    • 77955301410 scopus 로고    scopus 로고
    • A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism
    • Huang X-L, Zou YS, Maher T a, Newton S, Milunsky JM. A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism. Am J Med Genet A 2010; 152A: 2112-2114.
    • (2010) Am J Med Genet A. , vol.152 A , pp. 2112-2114
    • Huang, X.-L.1    Zou, Y.S.2    Maher, T.A.3    Newton, S.4    Milunsky, J.M.5
  • 8
    • 67349182343 scopus 로고    scopus 로고
    • Autism genomewide copy number variation reveals ubiquitin and neuronal genes
    • Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S et al. Autism genomewide 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    Korvatska, O.4    Kim, C.E.5    Wood, S.6
  • 9
    • 80052233376 scopus 로고    scopus 로고
    • Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression
    • Ben-David E, Granot-Hershkovitz E, Monderer-Rothkoff G, Lerer E, Levi S, Yaari M et al. Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression. Hum Mol Genet 2011; 20: 3632-3641.
    • (2011) Hum Mol Genet , vol.20 , pp. 3632-3641
    • Ben-David, E.1    Granot-Hershkovitz, E.2    Monderer-Rothkoff, G.3    Lerer, E.4    Levi, S.5    Yaari, M.6
  • 10
    • 81755183108 scopus 로고    scopus 로고
    • Relative burden of large CNVs on a range of neurodevelopmental phenotypes
    • Girirajan S, Brkanac Z, Coe BP, Baker C, Vives L, Vu TH et al. Relative burden of large CNVs on a range of neurodevelopmental phenotypes. PLoS Genet 2011; 7: e1002334.
    • (2011) PLoS Genet , vol.7 , pp. e1002334
    • Girirajan, S.1    Brkanac, Z.2    Coe, B.P.3    Baker, C.4    Vives, L.5    Vu, T.H.6
  • 11
    • 84860347597 scopus 로고    scopus 로고
    • Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries
    • Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A 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    Pillalamarri, V.4    Chiang, C.5    Heilbut, A.6
  • 12
    • 84874113937 scopus 로고    scopus 로고
    • Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders
    • Nagamani SCS, Erez A, Ben-Zeev B, Frydman M, Winter S, Zeller R et al. Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders. Eur J Hum Genet 2013; 21: 1-4.
    • (2013) Eur J Hum Genet , vol.21 , pp. 1-4
    • Nagamani, S.C.S.1    Erez, A.2    Ben-Zeev, B.3    Frydman, M.4    Winter, S.5    Zeller, R.6
  • 13
    • 84873732078 scopus 로고    scopus 로고
    • Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus
    • Beunders G, Voorhoeve E, Golzio C, Pardo LM, Rosenfeld J a, Talkowski ME et al. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. Am J Hum Genet 2013; 92: 210-220.
    • (2013) Am J Hum Genet , vol.92 , pp. 210-220
    • Beunders, G.1    Voorhoeve, E.2    Golzio, C.3    Pardo, L.M.4    Rosenfeld, J.A.5    Talkowski, M.E.6
  • 15
    • 65449139457 scopus 로고    scopus 로고
    • Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder
    • Cusco I, Medrano A, Gener B. Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder. Hum Mol Genet 2009; 18: 1795-1804.
    • (2009) Hum Mol Genet , vol.18 , pp. 1795-1804
    • Cusco, I.1    Medrano, A.2    Gener, B.3
  • 16
    • 84876337451 scopus 로고    scopus 로고
    • Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders
    • Tropeano M, Ahn JW, Dobson RJB, Breen G, Rucker J, Dixit A et al. Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders. PLoS ONE 2013; 8: e61365.
    • (2013) PLoS ONE , vol.8 , pp. e61365
    • Tropeano, M.1    Ahn, J.W.2    Dobson, R.J.B.3    Breen, G.4    Rucker, J.5    Dixit, A.6
  • 17
    • 84907314413 scopus 로고    scopus 로고
    • De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review
    • Jolley A, Corbett M, McGregor L, Waters W, Brown S, Nicholl J et al. De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: a case report and literature review. Am J Med Genet A 2013; 2: 1-5.
    • (2013) Am J Med Genet A , vol.2 , pp. 1-5
    • Jolley, A.1    Corbett, M.2    McGregor, L.3    Waters, W.4    Brown, S.5    Nicholl, J.6
  • 18
    • 77956628767 scopus 로고    scopus 로고
    • Genomewide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
    • Mefford HC, Muhle H, Ostertag P, von Spiczak S, Buysse K, Baker C et al. Genomewide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet 2010; 6: e1000962.
    • (2010) PLoS Genet , vol.6 , pp. e1000962
    • Mefford, H.C.1    Muhle, H.2    Ostertag, P.3    Von Spiczak, S.4    Buysse, K.5    Baker, C.6
  • 19
    • 67650924855 scopus 로고    scopus 로고
    • Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept
    • Hamshere ML, Green EK, Jones IR, Jones L, Moskvina V, Kirov G et al. Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. Br J Psychiatry 2009; 195: 23-29.
    • (2009) Br J Psychiatry , vol.195 , pp. 23-29
    • Hamshere, M.L.1    Green, E.K.2    Jones, I.R.3    Jones, L.4    Moskvina, V.5    Kirov, G.6
  • 21
    • 84872876216 scopus 로고    scopus 로고
    • A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder
    • Lee H, Woo H, Greenwood T. A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder. J Affect Disord 2012; 145: 200-207.
    • (2012) J Affect Disord , vol.145 , pp. 200-207
    • Lee, H.1    Woo, H.2    Greenwood, T.3
  • 22
    • 77952887857 scopus 로고    scopus 로고
    • Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
    • Elia J, Gai X, Xie HM, Perin JC, Geiger E, Glessner JT et al. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol Psychiatry 2010; 15: 637-646.
    • (2010) Mol Psychiatry , vol.15 , pp. 637-646
    • Elia, J.1    Gai, X.2    Xie, H.M.3    Perin, J.C.4    Geiger, E.5    Glessner, J.T.6
  • 23
    • 79952312897 scopus 로고    scopus 로고
    • Whole genome association scan for genetic polymorphisms influencing information processing speed
    • Luciano M, Hansell N, Lahti J. Whole genome association scan for genetic polymorphisms influencing information processing speed. Biol Psychol 2011; 86: 193-202.
    • (2011) Biol Psychol , vol.86 , pp. 193-202
    • Luciano, M.1    Hansell, N.2    Lahti, J.3
  • 24
    • 84874251894 scopus 로고    scopus 로고
    • Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene
    • Chojnicka I, Gajos K, Strawa K, Broda G, Fudalej S, Fudalej M et al. Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene. PLoS ONE 2013; 8: e57199.
    • (2013) PLoS ONE , vol.8 , pp. e57199
    • Chojnicka, I.1    Gajos, K.2    Strawa, K.3    Broda, G.4    Fudalej, S.5    Fudalej, M.6
  • 25
    • 79955569025 scopus 로고    scopus 로고
    • Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
    • Schumann G, Coin LJ, Lourdusamy A, Charoen P, Berger KH, Stacey D et al. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Proc Natl Acad Sci USA 2011; 108: 7119-7124.
    • (2011) Proc Natl Acad Sci USA , vol.108 , pp. 7119-7124
    • Schumann, G.1    Coin, L.J.2    Lourdusamy, A.3    Charoen, P.4    Berger, K.H.5    Stacey, D.6
  • 27
    • 33750737061 scopus 로고    scopus 로고
    • Accelerated evolution of conserved noncoding sequences in humans
    • Prabhakar S, Noonan JP, Paabo S, Rubin EM. Accelerated evolution of conserved noncoding sequences in humans. Science 2006; 314: 786.
    • (2006) Science , vol.314 , pp. 786
    • Prabhakar, S.1    Noonan, J.P.2    Paabo, S.3    Rubin, E.M.4
  • 29
    • 73749086083 scopus 로고    scopus 로고
    • Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology
    • Bedogni F, Hodge RD, Nelson BR, Frederick E a, Shiba N, Daza Ra et al. Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology. Gene Exp Patterns 2010; 10: 9-15.
    • (2010) Gene Exp Patterns , vol.10 , pp. 9-15
    • Bedogni, F.1    Hodge, R.D.2    Nelson, B.R.3    Frederick, E.A.4    Shiba, N.5    Daza, R.A.6
  • 30
    • 84873506311 scopus 로고    scopus 로고
    • Function and regulation of AUTS2, a gene implicated in autism and human evolution
    • Oksenberg N, Stevison L, Wall JD, Ahituv N. Function and regulation of AUTS2, a gene implicated in autism and human evolution. PLoS Genet 2013; 9: e1003221.
    • (2013) PLoS Genet , vol.9 , pp. e1003221
    • Oksenberg, N.1    Stevison, L.2    Wall, J.D.3    Ahituv, N.4
  • 31
    • 0036993811 scopus 로고    scopus 로고
    • Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins
    • Sultana R, Yu C-E, Yu J, Munson J, Chen D, Hua W et al. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics 2002; 80: 129-134.
    • (2002) Genomics , vol.80 , pp. 129-134
    • Sultana, R.1    Yu, C.-E.2    Yu, J.3    Munson, J.4    Chen, D.5    Hua, W.6
  • 32
    • 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, Karakoc E, Krumm N, Coe BP 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    Karakoc, E.4    Krumm, N.5    Coe, B.P.6
  • 36
    • 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 C a, 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
  • 37
    • 40349085928 scopus 로고    scopus 로고
    • Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-Targeted mice
    • Young EJ, Lipina T, Tam E, Mandel a, Clapcote SJ, Bechard a R et al. Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-Targeted mice. Genes Brain Behav 2008; 7: 224-234.
    • (2008) Genes Brain Behav , vol.7 , pp. 224-234
    • Young, E.J.1    Lipina, T.2    Tam, E.3    Mandel, A.4    Clapcote, S.J.5    Becharda, R.6
  • 38
    • 80052328281 scopus 로고    scopus 로고
    • Global analysis of gene expression in the developing brain of Gtf2ird1 knockout mice
    • O'Leary J, Osborne LR. Global analysis of gene expression in the developing brain of Gtf2ird1 knockout mice. PLoS ONE 2011; 6: e23868.
    • (2011) PLoS ONE , vol.6 , pp. e23868
    • O'leary, J.1    Osborne, L.R.2
  • 40
    • 84884416967 scopus 로고    scopus 로고
    • The role of AUTS2 in neurodevelopment and human evolution
    • Oksenberg N, Ahituv N. The role of AUTS2 in neurodevelopment and human evolution. Trends Genet 2013; 29: 1-9.
    • (2013) Trends Genet , vol.29 , pp. 1-9
    • Oksenberg, N.1    Ahituv, N.2
  • 41
    • 84892684890 scopus 로고    scopus 로고
    • Tay bridge is a negative regulator of egfr signalling and interacts with erk and mkp3 in the drosophila melanogaster wing
    • Molnar C, de Celis JF. Tay Bridge is a negative regulator of EGFR signalling and interacts with Erk and Mkp3 in the Drosophila melanogaster wing. PLoS Genet 2013; 9: e1003982.
    • (2013) PLoS Genet , vol.9 , pp. e1003982
    • Molnar, C.1    De Celis, J.F.2
  • 42
    • 53849138043 scopus 로고    scopus 로고
    • Interaction between Reelin and Notch signaling regulates neuronal migration in the cerebral cortex
    • Hashimoto-Torii K, Torii M, Sarkisian MR, Bartley CM, Shen J, Radtke F et al. Interaction between Reelin and Notch signaling regulates neuronal migration in the cerebral cortex. Neuron 2008; 60: 273-284.
    • (2008) Neuron , vol.60 , pp. 273-284
    • Hashimoto-Torii, K.1    Torii, M.2    Sarkisian, M.R.3    Bartley, C.M.4    Shen, J.5    Radtke, F.6
  • 43
    • 11144354900 scopus 로고    scopus 로고
    • Transcriptional modification by a CASK-interacting nucleosome assembly protein
    • Wang G-S, Hong C-J, Yen T-Y, Huang H-Y, Ou Y, Huang T-N et al. Transcriptional modification by a CASK-interacting nucleosome assembly protein. Neuron 2004; 42: 113-128.
    • (2004) Neuron , vol.42 , pp. 113-128
    • Wang, G.-S.1    Hong, C.-J.2    Yen, T.-Y.3    Huang, H.-Y.4    Ou, Y.5    Huang, T.-N.6
  • 44
    • 34247125714 scopus 로고    scopus 로고
    • Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model
    • William D a, Saitta B, Gibson JD, Traas J, Markov V, Gonzalez DM et al. Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model. Dev Biol 2007; 305: 172-186.
    • (2007) Dev Biol , vol.305 , pp. 172-186
    • William, D.A.1    Saitta, B.2    Gibson, J.D.3    Traas, J.4    Markov, V.5    Gonzalez, D.M.6
  • 45
    • 33845444174 scopus 로고    scopus 로고
    • A complex oscillating network of signaling genes underlies the mouse segmentation clock
    • Dequeant M-L, Glynn E, Gaudenz K, Wahl M, Chen J, Mushegian A et al. A complex oscillating network of signaling genes underlies the mouse segmentation clock. Science 2006; 314: 1595-1598.
    • (2006) Science , vol.314 , pp. 1595-1598
    • Dequeant, M.-L.1    Glynn, E.2    Gaudenz, K.3    Wahl, M.4    Chen, J.5    Mushegian, A.6
  • 46
    • 84863011309 scopus 로고    scopus 로고
    • PCGF homologs CBX proteins, and RYBP define functionally distinct PRC1 family complexes
    • Gao Z, Zhang J, Bonasio R, Strino F, Sawai A, Parisi F et al. PCGF homologs, CBX proteins, and RYBP define functionally distinct PRC1 family complexes. Mol Cell 2012; 45: 344-356.
    • (2012) Mol Cell , vol.45 , pp. 344-356
    • Gao, Z.1    Zhang, J.2    Bonasio, R.3    Strino, F.4    Sawai, A.5    Parisi, F.6
  • 47
    • 84880251662 scopus 로고    scopus 로고
    • An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk
    • Cheng Y, Quinn JF, Weiss LA. An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk. Hum Mol Genet 2013; 22: 1-13.
    • (2013) Hum Mol Genet , vol.22 , pp. 1-13
    • Cheng, Y.1    Quinn, J.F.2    Weiss, L.A.3
  • 48
    • 0142106373 scopus 로고    scopus 로고
    • How well is enzyme function conserved as a function of pairwise sequence identity?
    • Tian W, Skolnick J. How well is enzyme function conserved as a function of pairwise sequence identity? J Mol Biol 2003; 333: 863-882.
    • (2003) J Mol Biol , vol.333 , pp. 863-882
    • Tian, W.1    Skolnick, J.2
  • 49
    • 62349130698 scopus 로고    scopus 로고
    • Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
    • Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 2009; 10: R25.
    • (2009) Genome Biol , vol.10 , pp. R25
    • Langmead, B.1    Trapnell, C.2    Pop, M.3    Salzberg, S.L.4
  • 51
    • 65449136284 scopus 로고    scopus 로고
    • TopHat: Discovering splice junctions with RNA-Seq
    • Trapnell C, Pachter L, Salzberg SL. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics 2009; 25: 1105-1111.
    • (2009) Bioinformatics , vol.25 , pp. 1105-1111
    • Trapnell, C.1    Pachter, L.2    Salzberg, S.L.3
  • 52
    • 84876996918 scopus 로고    scopus 로고
    • TopHat2: Accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
    • Kim D, Pertea G, Trapnell C, Pimentel H, Kelley R, Salzberg SL. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol 2013; 14: R36.
    • (2013) Genome Biol , vol.14 , pp. R36
    • Kim, D.1    Pertea, G.2    Trapnell, C.3    Pimentel, H.4    Kelley, R.5    Salzberg, S.L.6
  • 53
    • 84883364264 scopus 로고    scopus 로고
    • Countbased differential expression analysis of RNA sequencing data using R and Bioconductor
    • Anders S, McCarthy DJ, Chen Y, Okoniewski M, Smyth GK, Huber W et al. Countbased differential expression analysis of RNA sequencing data using R and Bioconductor. Nat Protoc 2013; 8: 1765-1786.
    • (2013) Nat Protoc , vol.8 , pp. 1765-1786
    • Anders, S.1    McCarthy, D.J.2    Chen, Y.3    Okoniewski, M.4    Smyth, G.K.5    Huber, W.6
  • 54
    • 84864462544 scopus 로고    scopus 로고
    • A map of the cis-regulatory sequences in the mouse genome
    • Shen Y, Yue F, McCleary DF, Ye Z, Edsall L, Kuan S et al. A map of the cis-regulatory sequences in the mouse genome. Nature 2012; 488: 116-120.
    • (2012) Nature , vol.488 , pp. 116-120
    • Shen, Y.1    Yue, F.2    McCleary, D.F.3    Ye, Z.4    Edsall, L.5    Kuan, S.6
  • 55
    • 77951770756 scopus 로고    scopus 로고
    • BEDTools: A flexible suite of utilities for comparing genomic features
    • Quinlan AR, Hall IM. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 2010; 26: 841-842.
    • (2010) Bioinformatics , vol.26 , pp. 841-842
    • Quinlan, A.R.1    Hall, I.M.2
  • 59
    • 79958117256 scopus 로고    scopus 로고
    • MEME-ChIP: Motif analysis of large DNA datasets
    • Machanick P, Bailey TL. MEME-ChIP: motif analysis of large DNA datasets. Bioinformatics 2011; 27: 1696-1697.
    • (2011) Bioinformatics , vol.27 , pp. 1696-1697
    • MacHanick, P.1    Bailey, T.L.2
  • 60
    • 77951956867 scopus 로고    scopus 로고
    • Assigning roles to DNA regulatory motifs using comparative genomics
    • Buske F a, Boden M, Bauer DC, Bailey TL. Assigning roles to DNA regulatory motifs using comparative genomics. Bioinformatics 2010; 26: 860-866.
    • (2010) Bioinformatics , vol.26 , pp. 860-866
    • Buske, F.A.1    Boden, M.2    Bauer, D.C.3    Bailey, T.L.4
  • 62
    • 72649101692 scopus 로고    scopus 로고
    • A systematic approach to identify functional motifs within vertebrate developmental enhancers
    • Li Q, Ritter D, Yang N, Dong Z, Li H, Chuang JH et al. A systematic approach to identify functional motifs within vertebrate developmental enhancers. Dev Biol 2010; 337: 484-495.
    • (2010) Dev Biol , vol.337 , pp. 484-495
    • Li, Q.1    Ritter, D.2    Yang, N.3    Dong, Z.4    Li, H.5    Chuang, J.H.6
  • 63
    • 84908323329 scopus 로고    scopus 로고
    • 5th edn, University of Oregon Press: Eugene, Oregon
    • Westerfield M. The Zebrafish Book. 5th edn, University of Oregon Press: Eugene, Oregon, 2007.
    • (2007) The Zebrafish Book
    • Westerfield, M.1
  • 65
    • 25444488956 scopus 로고    scopus 로고
    • Transposon tools and methods in zebrafish
    • Kawakami K. Transposon tools and methods in zebrafish. Dev Dyn 2005; 234: 244-254.
    • (2005) Dev Dyn , vol.234 , pp. 244-254
    • Kawakami, K.1
  • 66
    • 0029057882 scopus 로고
    • Linked regularities in the development and evolution of mammalian brains
    • Finlay B, Darlington R. Linked regularities in the development and evolution of mammalian brains. Science 1995; 268: 1578-1584.
    • (1995) Science , vol.268 , pp. 1578-1584
    • Finlay, B.1    Darlington, R.2
  • 68
    • 0029135317 scopus 로고
    • Reduced size of corpus callosum in autism
    • Egaas B, Courchesne E, Saitoh O. Reduced size of corpus callosum in autism. Arch Neurol 1995; 52: 794-801.
    • (1995) Arch Neurol , vol.52 , pp. 794-801
    • Egaas, B.1    Courchesne, E.2    Saitoh, O.3
  • 69
    • 80755169819 scopus 로고    scopus 로고
    • Increased neuron number and head size in autism
    • Lainhart J, Lange N. Increased neuron number and head size in autism. JAMA J Am Med 2011; 306: 2031-2032.
    • (2011) JAMA J Am Med , vol.306 , pp. 2031-2032
    • Lainhart, J.1    Lange, N.2
  • 71
    • 13444256259 scopus 로고    scopus 로고
    • The homeodomain transcription factor Pitx3 facilitates differentiation of mouse embryonic stem cells into AHD2-expressing dopaminergic neurons
    • Chung S, Hedlund E, Hwang M, Kim DW, Shin B-S, Hwang D-Y et al. The homeodomain transcription factor Pitx3 facilitates differentiation of mouse embryonic stem cells into AHD2-expressing dopaminergic neurons. Mol Cell Neurosci 2005; 28: 241-252.
    • (2005) Mol Cell Neurosci , vol.28 , pp. 241-252
    • Chung, S.1    Hedlund, E.2    Hwang, M.3    Kim, D.W.4    Shin, B.-S.5    Hwang, D.-Y.6
  • 72
    • 38949210771 scopus 로고    scopus 로고
    • Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: A candidate gene analysis
    • Philippi A, Tores F, Carayol J, Rousseau F, Letexier M, Roschmann E et al. Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis. BMC Med Genet 2007; 8: 74.
    • (2007) BMC Med Genet , vol.8 , pp. 74
    • Philippi, A.1    Tores, F.2    Carayol, J.3    Rousseau, F.4    Letexier, M.5    Roschmann, E.6
  • 73
    • 43049100739 scopus 로고    scopus 로고
    • E2A proteins: Regulators of cell phenotype in normal physiology and disease
    • Slattery C, Ryan MP, McMorrow T. E2A proteins: regulators of cell phenotype in normal physiology and disease. Int J Biochem Cell Biol 2008; 40: 1431-1436.
    • (2008) Int J Biochem Cell Biol , vol.40 , pp. 1431-1436
    • Slattery, C.1    Ryan, M.P.2    McMorrow, T.3
  • 74
    • 0033980393 scopus 로고    scopus 로고
    • Helix-loop-helix proteins: Regulators of transcription in eucaryotic organisms
    • Massari M, Murre C. Helix-loop-helix proteins: regulators of transcription in eucaryotic organisms. Mol Cell Biol 2000; 20: 429-440.
    • (2000) Mol Cell Biol , vol.20 , pp. 429-440
    • Massari, M.1    Murre, C.2
  • 75
    • 19944401504 scopus 로고    scopus 로고
    • Mouse brain organization revealed through direct genome-scale TF expression analysis
    • Gray P a, Fu H, Luo P, Zhao Q, Yu J, Ferrari A et al. Mouse brain organization revealed through direct genome-scale TF expression analysis. Science 2004; 306: 2255-2257.
    • (2004) Science , vol.306 , pp. 2255-2257
    • Gray, P.A.1    Fu, H.2    Luo, P.3    Zhao, Q.4    Yu, J.5    Ferrari, A.6
  • 76
    • 0029815976 scopus 로고    scopus 로고
    • Tal-1 induces T cell acute lymphoblastic leukemia accelerated by casein kinase IIalpha
    • Kelliher M a, Seldin DC, Leder P. Tal-1 induces T cell acute lymphoblastic leukemia accelerated by casein kinase IIalpha. EMBO J 1996; 15: 5160-5166.
    • (1996) EMBO J , vol.15 , pp. 5160-5166
    • Kelliher, M.A.1    Seldin, D.C.2    Leder, P.3
  • 78
    • 84862777054 scopus 로고    scopus 로고
    • Lysine methylation of FOXO3 regulates oxidative stress-induced neuronal cell death
    • Xie Q, Hao Y, Tao L, Peng S, Rao C, Chen H et al. Lysine methylation of FOXO3 regulates oxidative stress-induced neuronal cell death. EMBO Rep 2012; 13: 371-377.
    • (2012) EMBO Rep , vol.13 , pp. 371-377
    • Xie, Q.1    Hao, Y.2    Tao, L.3    Peng, S.4    Rao, C.5    Chen, H.6
  • 79
    • 79955537355 scopus 로고    scopus 로고
    • Ribosomemediated specificity in Hox mRNA translation and vertebrate tissue patterning
    • Kondrashov N, Pusic A, Stumpf CR, Shimizu K, Hsieh AC, Xue S et al. Ribosomemediated specificity in Hox mRNA translation and vertebrate tissue patterning. Cell 2011; 145: 383-397.
    • (2011) Cell , vol.145 , pp. 383-397
    • Kondrashov, N.1    Pusic, A.2    Stumpf, C.R.3    Shimizu, K.4    Hsieh, A.C.5    Xue, S.6
  • 80
    • 84870918057 scopus 로고    scopus 로고
    • The phosphodiesterase-4 (PDE4) inhibitor rolipram decreases ethanol seeking and consumption in alcohol-preferring Fawn-Hooded rats
    • Wen R-T, Zhang M, Qin W-J, Liu Q, Wang W-P, Lawrence AJ et al. The phosphodiesterase-4 (PDE4) inhibitor rolipram decreases ethanol seeking and consumption in alcohol-preferring Fawn-Hooded rats. Alcohol Clin Exp Res 2012; 36: 2157-2167.
    • (2012) Alcohol Clin Exp Res , vol.36 , pp. 2157-2167
    • Wen, R.-T.1    Zhang, M.2    Qin, W.-J.3    Liu, Q.4    Wang, W.-P.5    Lawrence, A.J.6
  • 81
    • 65549088448 scopus 로고    scopus 로고
    • Expression of GABA(B) receptors is altered in brains of subjects with autism
    • Fatemi SH, Folsom TD, Reutiman TJ, Thuras PD. Expression of GABA(B) receptors is altered in brains of subjects with autism. Cerebellum 2009; 8: 64-69.
    • (2009) Cerebellum , vol.8 , pp. 64-69
    • Fatemi, S.H.1    Folsom, T.D.2    Reutiman, T.J.3    Thuras, P.D.4
  • 82
    • 80955177065 scopus 로고    scopus 로고
    • GABBR1 gene polymorphism (G1465A) is associated with temporal lobe epilepsy
    • Xi B, Chen J, Yang L, Wang W, Fu M, Wang C. GABBR1 gene polymorphism (G1465A) is associated with temporal lobe epilepsy. Epilepsy Res 2011; 96: 58-63.
    • (2011) Epilepsy Res , vol.96 , pp. 58-63
    • Xi, B.1    Chen, J.2    Yang, L.3    Wang, W.4    Fu, M.5    Wang, C.6
  • 83
    • 84855849489 scopus 로고    scopus 로고
    • GABAergic gene expression in postmortem hippocampus from alcoholics and cocaine addicts; Corresponding findings in alcohol-naive P and NP rats
    • Enoch M-A, Zhou Z, Kimura M, Mash DC, Yuan Q, Goldman D. GABAergic gene expression in postmortem hippocampus from alcoholics and cocaine addicts; corresponding findings in alcohol-naive P and NP rats. PLoS ONE 2012; 7: e29369.
    • (2012) PLoS ONE , vol.7 , pp. e29369
    • Enoch, M.-A.1    Zhou, Z.2    Kimura, M.3    Mash, D.C.4    Yuan, Q.5    Goldman, D.6
  • 85
    • 0028921396 scopus 로고
    • Distribution of a brain-specific proteoglycan, neurocan, and the corresponding mRNA during the formation of barrels in the rat somatosensory cortex
    • Watanabe E, Aono S, Matsui F, Yamada Y, Naruse I, Oohira a. Distribution of a brain-specific proteoglycan, neurocan, and the corresponding mRNA during the formation of barrels in the rat somatosensory cortex. Eur J Neurosci 1995; 7: 547-554.
    • (1995) Eur J Neurosci , vol.7 , pp. 547-554
    • Watanabe, E.1    Aono, S.2    Matsui, F.3    Yamada, Y.4    Naruse, I.5    Oohira, A.6
  • 86
    • 79952485391 scopus 로고    scopus 로고
    • Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder
    • Cichon S, Muhleisen TW, Degenhardt F a, Mattheisen M, Miro X, Strohmaier J et al. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet 2011; 88: 372-381.
    • (2011) Am J Hum Genet , vol.88 , pp. 372-381
    • Cichon, S.1    Muhleisen, T.W.2    Degenhardt, F.A.3    Mattheisen, M.4    Miro, X.5    Strohmaier, J.6
  • 87
    • 84861527496 scopus 로고    scopus 로고
    • Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder
    • Muhleisen TW, Mattheisen M, Strohmaier J, Degenhardt F, Priebe L, Schultz CC et al. Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr Res 2012; 138: 69-73.
    • (2012) Schizophr Res , vol.138 , pp. 69-73
    • Muhleisen, T.W.1    Mattheisen, M.2    Strohmaier, J.3    Degenhardt, F.4    Priebe, L.5    Schultz, C.C.6
  • 88
    • 0031983653 scopus 로고    scopus 로고
    • Neurexins: Three genes and 1001 products
    • Missler M, Sudhof T. Neurexins: three genes and 1001 products. Trends Genet 1998; 14: 20-26.
    • (1998) Trends Genet , vol.14 , pp. 20-26
    • Missler, M.1    Sudhof, T.2
  • 90
    • 79851473886 scopus 로고    scopus 로고
    • A highresolution anatomical atlas of the transcriptome in the mouse embryo
    • Diez-Roux G, Banfi S, Sultan M, Geffers L, Anand S, Rozado D et al. A highresolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol 2011; 9: e1000582.
    • (2011) PLoS Biol , vol.9 , pp. e1000582
    • Diez-Roux, G.1    Banfi, S.2    Sultan, M.3    Geffers, L.4    Anand, S.5    Rozado, D.6
  • 91
    • 79960261603 scopus 로고    scopus 로고
    • Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects
    • Carayol J, Sacco R, Tores F, Rousseau F, Lewin P, Hager J et al. Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects. Biol Psychiatry 2011; 70: 880-887.
    • (2011) Biol Psychiatry , vol.70 , pp. 880-887
    • Carayol, J.1    Sacco, R.2    Tores, F.3    Rousseau, F.4    Lewin, P.5    Hager, J.6
  • 92
    • 84876442861 scopus 로고    scopus 로고
    • The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population
    • Yang W, Liu J, Zheng F, Jia M, Zhao L, Lu T et al. The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population. PLoS ONE 2013; 8: e61021.
    • (2013) PLoS ONE , vol.8 , pp. e61021
    • Yang, W.1    Liu, J.2    Zheng, F.3    Jia, M.4    Zhao, L.5    Lu, T.6


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