Common variant at 16p11.2 conferring risk of psychosis

S. Steinberg, S. de Jong, M. Mattheisen, J. Costas, D. Demontis, S. Jamain, O. P. H. Pietiläinen, K. Lin, S. Papiol, J. Huttenlocher, E. Sigurdsson, E. Vassos, I. Giegling, R. Breuer, G. Fraser, N. Walker, I. Melle, S. Djurovic, I. Agartz, A. Tuulio-HenrikssonJ. Suvisaari, Jouko Lönnqvist, T. Paunio, L. Olsen, T. Hansen, A. Ingason, M. Pirinen, E. Strengman, D. M. Hougaard, T. Orntoft, M. Didriksen, M. V. Hollegaard, M. Nordentoft, L. Abramova, V. Kaleda, M. Arrojo, J. Sanjuan, C. Arango, B. Etain, F. Bellivier, A. Meary, F. Schuerhoff, A. Szoke, M. Ribolsi, V. Magni, A. Siracusano, S. Sperling, K. Rehnstrom, Leena Helena Kilpinen, A. Palotie, GROUP, Wellcome Trust Case Control Consor

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalMolecular Psychiatry
Volume19
Issue number1
Pages (from-to)108-114
Number of pages7
ISSN1359-4184
DOIs
Publication statusPublished - Jan 2014
MoE publication typeA1 Journal article-refereed

Fields of Science

  • association
  • bipolar disorder
  • cross-disorder
  • schizophrenia
  • 16p11.2
  • GENOME-WIDE ASSOCIATION
  • BIPOLAR-DISORDER
  • GENE-EXPRESSION
  • SCHIZOPHRENIA
  • LOCUS
  • DISEASE
  • MICRODELETIONS
  • AUTISM
  • METAANALYSIS
  • PHENOTYPES
  • 3111 Biomedicine
  • 3124 Neurology and psychiatry

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