메뉴 건너뛰기




Volumn 162, Issue 2, 2013, Pages 177-182

Schizophrenia two-hit hypothesis in velo-cardio facial syndrome

Author keywords

22qDS; CNV; Schizophrenia; VCFS

Indexed keywords

ARTICLE; AUTISM; BIPOLAR DISORDER; CONTROLLED STUDY; EPILEPSY; GENE DELETION; HUMAN; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; MOLECULAR GENETICS; PHENOTYPE; PRIORITY JOURNAL; PSYCHOSIS; SCHIZOAFFECTIVE PSYCHOSIS; SCHIZOPHRENIA; VELOCARDIOFACIAL SYNDROME;

EID: 84874126964     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32129     Document Type: Article
Times cited : (21)

References (35)
  • 2
    • 57049132697 scopus 로고    scopus 로고
    • Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome
    • Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW. 2008. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Hum Mol Genet 17(24):4045-4053.
    • (2008) Hum Mol Genet , vol.17 , Issue.24 , pp. 4045-4053
    • Bassett, A.S.1    Marshall, C.R.2    Lionel, A.C.3    Chow, E.W.4    Scherer, S.W.5
  • 3
    • 77955379566 scopus 로고    scopus 로고
    • Copy number variations in schizophrenia: Critical review and new perspectives on concepts of genetics and disease
    • Bassett AS, Scherer SW, Brzustowicz LM. 2010. Copy number variations in schizophrenia: Critical review and new perspectives on concepts of genetics and disease. Am J Psychiatry 167(8):899-914.
    • (2010) Am J Psychiatry , vol.167 , Issue.8 , pp. 899-914
    • Bassett, A.S.1    Scherer, S.W.2    Brzustowicz, L.M.3
  • 4
    • 80054848222 scopus 로고    scopus 로고
    • Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: A susceptibility region for neurological dysfunction including developmental and language delay
    • Burnside RD, Pasion R, Mikhail FM, Carroll AJ, Robin NH, Youngs EL, Gadi IK, Keitges E, Jaswaney VL, Papenhausen PR, et al. 2011. Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: A susceptibility region for neurological dysfunction including developmental and language delay. Hum Genet 130:517-528.
    • (2011) Hum Genet , vol.130 , pp. 517-528
    • Burnside, R.D.1    Pasion, R.2    Mikhail, F.M.3    Carroll, A.J.4    Robin, N.H.5    Youngs, E.L.6    Gadi, I.K.7    Keitges, E.8    Jaswaney, V.L.9    Papenhausen, P.R.10
  • 8
    • 77956314679 scopus 로고    scopus 로고
    • Induction of sodium channel Na(x) (SCN7A) expression in rat and human hippocampus in temporal lobe epilepsy
    • Gorter JA, Zurolo E, Iyer A, Fluiter K, van Vliet EA, Baayen JC, Aronica E. 2010. Induction of sodium channel Na(x) (SCN7A) expression in rat and human hippocampus in temporal lobe epilepsy. Epilepsia 51(9):1791-1800.
    • (2010) Epilepsia , vol.51 , Issue.9 , pp. 1791-1800
    • Gorter, J.A.1    Zurolo, E.2    Iyer, A.3    Fluiter, K.4    van Vliet, E.A.5    Baayen, J.C.6    Aronica, E.7
  • 11
    • 11144339384 scopus 로고    scopus 로고
    • Long-range control of gene expression: Emerging mechanisms and disruption in disease
    • Kleinjan DA, van Heyningen V. 2005. Long-range control of gene expression: Emerging mechanisms and disruption in disease. Am J Hum Genet 76(1):8-32.
    • (2005) Am J Hum Genet , vol.76 , Issue.1 , pp. 8-32
    • Kleinjan, D.A.1    van Heyningen, V.2
  • 13
    • 79952710338 scopus 로고    scopus 로고
    • Copy number variants in schizophrenia: Confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications
    • Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J, Zhang N, Mowry BJ, Olincy A, Amin F, et al. 2011. Copy number variants in schizophrenia: Confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry 168(3):302-316.
    • (2011) Am J Psychiatry , vol.168 , Issue.3 , pp. 302-316
    • Levinson, D.F.1    Duan, J.2    Oh, S.3    Wang, K.4    Sanders, A.R.5    Shi, J.6    Zhang, N.7    Mowry, B.J.8    Olincy, A.9    Amin, F.10
  • 16
    • 0032882849 scopus 로고    scopus 로고
    • High rates of schizophrenia in adults with velo-cardio-facial syndrome
    • Murphy KC, Jones LA, Owen MJ. 1999. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch Gen Psychiatry 56(10):940-945.
    • (1999) Arch Gen Psychiatry , vol.56 , Issue.10 , pp. 940-945
    • Murphy, K.C.1    Jones, L.A.2    Owen, M.J.3
  • 20
    • 79956304666 scopus 로고    scopus 로고
    • Translocation breakpoint at 7q31 associated with tics: Further evidence for IMMP2L as a candidate gene for Tourette syndrome
    • Patel C, Cooper-Charles L, McMullan DJ, Walker JM, Davison V, Morton J. 2011. Translocation breakpoint at 7q31 associated with tics: Further evidence for IMMP2L as a candidate gene for Tourette syndrome. Eur J Hum Genet 19(6):634-639.
    • (2011) Eur J Hum Genet , vol.19 , Issue.6 , pp. 634-639
    • Patel, C.1    Cooper-Charles, L.2    McMullan, D.J.3    Walker, J.M.4    Davison, V.5    Morton, J.6
  • 21
    • 75449083775 scopus 로고    scopus 로고
    • Terminal 3p deletions in two families-Correlation between molecular karyotype and phenotype
    • Pohjola P, de Leeuw N, Penttinen M, Kaariainen H. 2010. Terminal 3p deletions in two families-Correlation between molecular karyotype and phenotype. Am J Med Genet A 152A(2):441-446.
    • (2010) Am J Med Genet A , vol.152 A , Issue.2 , pp. 441-446
    • Pohjola, P.1    de Leeuw, N.2    Penttinen, M.3    Kaariainen, H.4
  • 24
    • 81855178259 scopus 로고    scopus 로고
    • De novo rates and selection of schizophrenia-associated copy number variants
    • Rees E, Moskvina V, Owen MJ, O'Donovan MC, Kirov G. 2011. De novo rates and selection of schizophrenia-associated copy number variants. Biol Psychiatry 70:1109-1114.
    • (2011) Biol Psychiatry , vol.70 , pp. 1109-1114
    • Rees, E.1    Moskvina, V.2    Owen, M.J.3    O'Donovan, M.C.4    Kirov, G.5
  • 27
    • 43349097737 scopus 로고    scopus 로고
    • No significant association of 14 candidate genes with schizophrenia in a large european ancestry sample: Implications for psychiatric genetics
    • Sanders AR, Duan J, Levinson DF, Shi J, He D, Hou C, Burrell GJ, Rice JP, Nertney DA, Olincy A, et al. 2008. No significant association of 14 candidate genes with schizophrenia in a large european ancestry sample: Implications for psychiatric genetics. Am J Psychiatry 165:497-506.
    • (2008) Am J Psychiatry , vol.165 , pp. 497-506
    • Sanders, A.R.1    Duan, J.2    Levinson, D.F.3    Shi, J.4    He, D.5    Hou, C.6    Burrell, G.J.7    Rice, J.P.8    Nertney, D.A.9    Olincy, A.10
  • 28
    • 44149115417 scopus 로고    scopus 로고
    • Velo-cardio-facial syndrome: 30 years of study
    • Shprintzen RJ. 2008. Velo-cardio-facial syndrome: 30 years of study. Dev Disabil Res Rev 14(1):3-10.
    • (2008) Dev Disabil Res Rev , vol.14 , Issue.1 , pp. 3-10
    • Shprintzen, R.J.1
  • 32
    • 35948984173 scopus 로고    scopus 로고
    • PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
    • Wang K, Li M, Hadley D, Liu R, Glessner J, Grant SF, Hakonarson H, Bucan M. 2007. PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Res 17(11):1665-1674.
    • (2007) Genome Res , vol.17 , Issue.11 , pp. 1665-1674
    • Wang, K.1    Li, M.2    Hadley, D.3    Liu, R.4    Glessner, J.5    Grant, S.F.6    Hakonarson, H.7    Bucan, M.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.