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Volumn 72, Issue 8, 2012, Pages 617-619

Brain copy number variants and neuropsychiatric traits

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

EID: 84866599675     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2012.08.007     Document Type: Note
Times cited : (6)

References (10)
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    • Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders
    • T. Ye, B.K. Lipska, R. Tao, T.M. Hyde, L. Wang, C. Li Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders Biol Psychiatry 72 2012 651 654
    • (2012) Biol Psychiatry , vol.72 , pp. 651-654
    • Ye, T.1    Lipska, B.K.2    Tao, R.3    Hyde, T.M.4    Wang, L.5    Li, C.6
  • 2
    • 51649107515 scopus 로고    scopus 로고
    • Schizophrenia: Incriminating genomic evidence
    • J.R. Lupski Schizophrenia: incriminating genomic evidence Nature 455 2008 178 179
    • (2008) Nature , vol.455 , pp. 178-179
    • Lupski, J.R.1
  • 4
    • 77950461601 scopus 로고    scopus 로고
    • Origins and functional impact of copy number variation in the human genome
    • D.F. Conrad, D. Pinto, R. Redon, L. Feuk, O. Gokcumen, Y. Zhang Origins and functional impact of copy number variation in the human genome Nature 464 2010 704 712
    • (2010) Nature , vol.464 , pp. 704-712
    • Conrad, D.F.1    Pinto, D.2    Redon, R.3    Feuk, L.4    Gokcumen, O.5    Zhang, Y.6
  • 5
    • 80053549439 scopus 로고    scopus 로고
    • Clan genomics and the complex architecture of human disease
    • J.R. Lupski, J.W. Belmont, E. Boerwinkle, R.A. Gibbs Clan genomics and the complex architecture of human disease Cell 147 2011 32 43
    • (2011) Cell , vol.147 , pp. 32-43
    • Lupski, J.R.1    Belmont, J.W.2    Boerwinkle, E.3    Gibbs, R.A.4
  • 7
    • 84858434210 scopus 로고    scopus 로고
    • CNVs: Harbingers of a rare variant revolution in psychiatric genetics
    • D. Malhotra, J. Sebat CNVs: harbingers of a rare variant revolution in psychiatric genetics Cell 148 2012 1223 1241
    • (2012) Cell , vol.148 , pp. 1223-1241
    • Malhotra, D.1    Sebat, J.2
  • 8
    • 84861075586 scopus 로고    scopus 로고
    • KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
    • C. Golzio, J. Willer, M.E. Talkowski, E.C. Oh, Y. Taniguchi, S. Jacquemont KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant Nature 485 2012 363 367
    • (2012) Nature , vol.485 , pp. 363-367
    • Golzio, C.1    Willer, J.2    Talkowski, M.E.3    Oh, E.C.4    Taniguchi, Y.5    Jacquemont, S.6
  • 9
    • 76549129054 scopus 로고    scopus 로고
    • Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia
    • B. Crespi, P. Stead, M. Elliot Evolution in health and medicine Sackler colloquium: comparative genomics of autism and schizophrenia Proc Natl Acad Scis PNAS 107 Suppl 1 2010 1736 1741
    • (2010) Proc Natl Acad Scis PNAS , vol.107 , Issue.SUPPL. 1 , pp. 1736-1741
    • Crespi, B.1    Stead, P.2    Elliot, M.3
  • 10
    • 84860780495 scopus 로고    scopus 로고
    • De novo mutations revealed by whole-exome sequencing are strongly associated with autism
    • S.J. Sanders, M.T. Murtha, A.R. Gupta, J.D. Murdoch, M.J. Raubeson, A.J. Willsey De novo mutations revealed by whole-exome sequencing are strongly associated with autism Nature 485 2012 237 241
    • (2012) Nature , vol.485 , pp. 237-241
    • Sanders, S.J.1    Murtha, M.T.2    Gupta, A.R.3    Murdoch, J.D.4    Raubeson, M.J.5    Willsey, A.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.