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

Cite this

Steinberg, S., de Jong, S., Mattheisen, M., Costas, J., Demontis, D., Jamain, S., ... Wellcome Trust Case Control Consor (2014). Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19(1), 108-114. https://doi.org/10.1038/mp.2012.157
Steinberg, S. ; de Jong, S. ; Mattheisen, M. ; Costas, J. ; Demontis, D. ; Jamain, S. ; Pietiläinen, O. P. H. ; Lin, K. ; Papiol, S. ; Huttenlocher, J. ; Sigurdsson, E. ; Vassos, E. ; Giegling, I. ; Breuer, R. ; Fraser, G. ; Walker, N. ; Melle, I. ; Djurovic, S. ; Agartz, I. ; Tuulio-Henriksson, A. ; Suvisaari, J. ; Lönnqvist, Jouko ; Paunio, T. ; Olsen, L. ; Hansen, T. ; Ingason, A. ; Pirinen, M. ; Strengman, E. ; Hougaard, D. M. ; Orntoft, T. ; Didriksen, M. ; Hollegaard, M. V. ; Nordentoft, M. ; Abramova, L. ; Kaleda, V. ; Arrojo, M. ; Sanjuan, J. ; Arango, C. ; Etain, B. ; Bellivier, F. ; Meary, A. ; Schuerhoff, F. ; Szoke, A. ; Ribolsi, M. ; Magni, V. ; Siracusano, A. ; Sperling, S. ; Rehnstrom, K. ; Kilpinen, Leena Helena ; Palotie, A. ; GROUP ; Wellcome Trust Case Control Consor. / Common variant at 16p11.2 conferring risk of psychosis. In: Molecular Psychiatry. 2014 ; Vol. 19, No. 1. pp. 108-114.
@article{facb7e907c1841ac84e968560dea5c20,
title = "Common variant at 16p11.2 conferring risk of psychosis",
keywords = "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",
author = "S. Steinberg and {de Jong}, S. and M. Mattheisen and J. Costas and D. Demontis and S. Jamain and Pietil{\"a}inen, {O. P. H.} and K. Lin and S. Papiol and J. Huttenlocher and E. Sigurdsson and E. Vassos and I. Giegling and R. Breuer and G. Fraser and N. Walker and I. Melle and S. Djurovic and I. Agartz and A. Tuulio-Henriksson and J. Suvisaari and Jouko L{\"o}nnqvist and T. Paunio and L. Olsen and T. Hansen and A. Ingason and M. Pirinen and E. Strengman and Hougaard, {D. M.} and T. Orntoft and M. Didriksen and Hollegaard, {M. V.} and M. Nordentoft and L. Abramova and V. Kaleda and M. Arrojo and J. Sanjuan and C. Arango and B. Etain and F. Bellivier and A. Meary and F. Schuerhoff and A. Szoke and M. Ribolsi and V. Magni and A. Siracusano and S. Sperling and K. Rehnstrom and Kilpinen, {Leena Helena} and A. Palotie and GROUP and {Wellcome Trust Case Control Consor}",
year = "2014",
month = "1",
doi = "10.1038/mp.2012.157",
language = "English",
volume = "19",
pages = "108--114",
journal = "Molecular Psychiatry",
issn = "1359-4184",
publisher = "Nature Publishing Group",
number = "1",

}

Steinberg, S, de Jong, S, Mattheisen, M, Costas, J, Demontis, D, Jamain, S, Pietiläinen, OPH, Lin, K, Papiol, S, Huttenlocher, J, Sigurdsson, E, Vassos, E, Giegling, I, Breuer, R, Fraser, G, Walker, N, Melle, I, Djurovic, S, Agartz, I, Tuulio-Henriksson, A, Suvisaari, J, Lönnqvist, J, Paunio, T, Olsen, L, Hansen, T, Ingason, A, Pirinen, M, Strengman, E, Hougaard, DM, Orntoft, T, Didriksen, M, Hollegaard, MV, Nordentoft, M, Abramova, L, Kaleda, V, Arrojo, M, Sanjuan, J, Arango, C, Etain, B, Bellivier, F, Meary, A, Schuerhoff, F, Szoke, A, Ribolsi, M, Magni, V, Siracusano, A, Sperling, S, Rehnstrom, K, Kilpinen, LH, Palotie, A, GROUP & Wellcome Trust Case Control Consor 2014, 'Common variant at 16p11.2 conferring risk of psychosis', Molecular Psychiatry, vol. 19, no. 1, pp. 108-114. https://doi.org/10.1038/mp.2012.157

Common variant at 16p11.2 conferring risk of psychosis. / Steinberg, S.; de Jong, S.; Mattheisen, M.; Costas, J.; Demontis, D.; Jamain, S.; Pietiläinen, O. P. H.; Lin, K.; Papiol, S.; Huttenlocher, J.; Sigurdsson, E.; Vassos, E.; Giegling, I.; Breuer, R.; Fraser, G.; Walker, N.; Melle, I.; Djurovic, S.; Agartz, I.; Tuulio-Henriksson, A.; Suvisaari, J.; Lönnqvist, Jouko; Paunio, T.; Olsen, L.; Hansen, T.; Ingason, A.; Pirinen, M.; Strengman, E.; Hougaard, D. M.; Orntoft, T.; Didriksen, M.; Hollegaard, M. V.; Nordentoft, M.; Abramova, L.; Kaleda, V.; Arrojo, M.; Sanjuan, J.; Arango, C.; Etain, B.; Bellivier, F.; Meary, A.; Schuerhoff, F.; Szoke, A.; Ribolsi, M.; Magni, V.; Siracusano, A.; Sperling, S.; Rehnstrom, K.; Kilpinen, Leena Helena; Palotie, A.; GROUP; Wellcome Trust Case Control Consor.

In: Molecular Psychiatry, Vol. 19, No. 1, 01.2014, p. 108-114.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - Common variant at 16p11.2 conferring risk of psychosis

AU - Steinberg, S.

AU - de Jong, S.

AU - Mattheisen, M.

AU - Costas, J.

AU - Demontis, D.

AU - Jamain, S.

AU - Pietiläinen, O. P. H.

AU - Lin, K.

AU - Papiol, S.

AU - Huttenlocher, J.

AU - Sigurdsson, E.

AU - Vassos, E.

AU - Giegling, I.

AU - Breuer, R.

AU - Fraser, G.

AU - Walker, N.

AU - Melle, I.

AU - Djurovic, S.

AU - Agartz, I.

AU - Tuulio-Henriksson, A.

AU - Suvisaari, J.

AU - Lönnqvist, Jouko

AU - Paunio, T.

AU - Olsen, L.

AU - Hansen, T.

AU - Ingason, A.

AU - Pirinen, M.

AU - Strengman, E.

AU - Hougaard, D. M.

AU - Orntoft, T.

AU - Didriksen, M.

AU - Hollegaard, M. V.

AU - Nordentoft, M.

AU - Abramova, L.

AU - Kaleda, V.

AU - Arrojo, M.

AU - Sanjuan, J.

AU - Arango, C.

AU - Etain, B.

AU - Bellivier, F.

AU - Meary, A.

AU - Schuerhoff, F.

AU - Szoke, A.

AU - Ribolsi, M.

AU - Magni, V.

AU - Siracusano, A.

AU - Sperling, S.

AU - Rehnstrom, K.

AU - Kilpinen, Leena Helena

AU - Palotie, A.

AU - GROUP

AU - Wellcome Trust Case Control Consor

PY - 2014/1

Y1 - 2014/1

KW - association

KW - bipolar disorder

KW - cross-disorder

KW - schizophrenia

KW - 16p11.2

KW - GENOME-WIDE ASSOCIATION

KW - BIPOLAR-DISORDER

KW - GENE-EXPRESSION

KW - SCHIZOPHRENIA

KW - LOCUS

KW - DISEASE

KW - MICRODELETIONS

KW - AUTISM

KW - METAANALYSIS

KW - PHENOTYPES

KW - 3111 Biomedicine

KW - 3124 Neurology and psychiatry

U2 - 10.1038/mp.2012.157

DO - 10.1038/mp.2012.157

M3 - Article

VL - 19

SP - 108

EP - 114

JO - Molecular Psychiatry

JF - Molecular Psychiatry

SN - 1359-4184

IS - 1

ER -

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S et al. Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry. 2014 Jan;19(1):108-114. https://doi.org/10.1038/mp.2012.157