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Volumn 77, Issue 9, 2015, Pages 766-768

DSM-5 and psychiatric genetics - Round hole, meet square peg

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; BRAIN DEVELOPMENT; BRAIN DYSFUNCTION; CHROMATIN ASSEMBLY AND DISASSEMBLY; COMPULSION; DIGEORGE SYNDROME; DSM-5; EFFECT SIZE; GENE LOCUS; GENETIC DISORDER; GENETIC HETEROGENEITY; GENETIC RISK; GENETIC VARIABILITY; GENETICS; HUMAN; INTELLIGENCE QUOTIENT; NONHUMAN; NOTE; PHENOTYPE; PRIORITY JOURNAL; TRANSLATIONAL RESEARCH; FEMALE; MALE;

EID: 84926355300     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2015.02.031     Document Type: Note
Times cited : (7)

References (10)
  • 1
    • 84926358552 scopus 로고    scopus 로고
    • A genomewide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
    • P. Chaste, L. Klei, S.J. Sanders, V. Hus, M.T. Murtha, and J.K. Lowe A genomewide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Biol Psychiatry 77 2015 775 784
    • (2015) Biol Psychiatry , vol.77 , pp. 775-784
    • Chaste, P.1    Klei, L.2    Sanders, S.J.3    Hus, V.4    Murtha, M.T.5    Lowe, J.K.6
  • 3
    • 84871371945 scopus 로고    scopus 로고
    • The autism sequencing consortium: Large-scale, high-throughput sequencing in autism spectrum disorders
    • J.D. Buxbaum, M.J. Daly, B. Devlin, T. Lehner, K. Roeder, and M.W. State The autism sequencing consortium: Large-scale, high-throughput sequencing in autism spectrum disorders Neuron 76 2012 1052 1056
    • (2012) Neuron , vol.76 , pp. 1052-1056
    • Buxbaum, J.D.1    Daly, M.J.2    Devlin, B.3    Lehner, T.4    Roeder, K.5    State, M.W.6
  • 8
    • 84912101541 scopus 로고    scopus 로고
    • The contribution of de novo coding mutations to autism spectrum disorder
    • I. Iossifov, S.J. Sanders, M. Ronemus, N. Krumm, and D. Levy The contribution of de novo coding mutations to autism spectrum disorder Nature 515 2014 216 221
    • (2014) Nature , vol.515 , pp. 216-221
    • Iossifov, I.1    Sanders, S.J.2    Ronemus, M.3    Krumm, N.4    Levy, D.5
  • 9
    • 84879001958 scopus 로고    scopus 로고
    • De novo mutations in histone-modifying genes in congenital heart disease
    • S. Zaidi, M. Choi, H. Wakimoto, L. Ma, J. Jiang, and J.D. Overton De novo mutations in histone-modifying genes in congenital heart disease Nature 498 2013 220 223
    • (2013) Nature , vol.498 , pp. 220-223
    • Zaidi, S.1    Choi, M.2    Wakimoto, H.3    Ma, L.4    Jiang, J.5    Overton, J.D.6
  • 10
    • 77957118061 scopus 로고    scopus 로고
    • The ESSENCE in child psychiatry: Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations
    • C. Gillberg The ESSENCE in child psychiatry: Early Symptomatic Syndromes Eliciting Neurodevelopmental Clinical Examinations Res Dev Disabil 31 2010 1543 1551
    • (2010) Res Dev Disabil , vol.31 , pp. 1543-1551
    • Gillberg, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.