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-Henriksson; J. 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

doi:10.1038/mp.2012.157

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

Forskningsoutput: Tidskriftsbidrag › Artikel › Vetenskaplig › Peer review

Originalspråk	engelska
Tidskrift	Molecular Psychiatry
Volym	19
Nummer	1
Sidor (från-till)	108-114
Antal sidor	7
ISSN	1359-4184
DOI	https://doi.org/10.1038/mp.2012.157
Status	Publicerad - jan. 2014
MoE-publikationstyp	A1 Tidskriftsartikel-refererad

Vetenskapsgrenar

3111 Biomedicinska vetenskaper
3124 Neurologi och psykiatri

Åtkomst av dokument

10.1038/mp.2012.157

Citera det här

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., ... 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

@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 = jan,

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, nr. 1, s. 108-114. https://doi.org/10.1038/mp.2012.157

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 -