Genome-wide association study identifies five new schizophrenia loci

Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium; Stephan Ripke; Alan R Sanders; Kenneth S Kendler; Douglas F Levinson; Pamela Sklar; Peter A Holmans; Dan-Yu Lin; Jubao Duan; Roel A Ophoff; Ole A Andreassen; Edward Scolnick; Sven Cichon; David St Clair; Aiden Corvin; Hugh Gurling; Thomas Werge; Dan Rujescu; Douglas H R Blackwood; Carlos N Pato; Anil K Malhotra; Shaun Purcell; Frank Dudbridge; Benjamin M Neale; Lizzy Rossin; Peter M Visscher; Danielle Posthuma; Douglas M Ruderfer; Ayman Fanous; Hreinn Stefansson; Stacy Steinberg; Bryan J Mowry; Vera Golimbet; Marc De Hert; Erik G Jönsson; István Bitter; Olli P H Pietiläinen; David A Collier; Sarah Tosato; Ingrid Agartz; Margot Albus; Madeline Alexander; Richard L Amdur; Farooq Amin; Nicholas Bass; Sarah E Bergen; Donald W Black; Thomas Hansen; Alan W Maclean; Kevin A McGhee; Andrew McIntosh

doi:10.1038/ng.940

Genome-wide association study identifies five new schizophrenia loci

Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Stephan Ripke, Alan R Sanders, Kenneth S Kendler, Douglas F Levinson, Pamela Sklar, Peter A Holmans, Dan-Yu Lin, Jubao Duan, Roel A Ophoff, Ole A Andreassen, Edward Scolnick, Sven Cichon, David St Clair, Aiden Corvin, Hugh Gurling, Thomas Werge, Dan Rujescu, Douglas H R Blackwood, Carlos N PatoAnil K Malhotra, Shaun Purcell, Frank Dudbridge, Benjamin M Neale, Lizzy Rossin, Peter M Visscher, Danielle Posthuma, Douglas M Ruderfer, Ayman Fanous, Hreinn Stefansson, Stacy Steinberg, Bryan J Mowry, Vera Golimbet, Marc De Hert, Erik G Jönsson, István Bitter, Olli P H Pietiläinen, David A Collier, Sarah Tosato, Ingrid Agartz, Margot Albus, Madeline Alexander, Richard L Amdur, Farooq Amin, Nicholas Bass, Sarah E Bergen, Donald W Black, Thomas Hansen, Alan W Maclean, Kevin A McGhee, Andrew McIntosh

Research output: Contribution to journal › Article › peer-review

Abstract

We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856 individuals of European ancestry and a stage 2 replication sample of 29,839 independent subjects. The combined stage 1 and 2 analysis yielded genome-wide significant associations with schizophrenia for seven loci, five of which are new (1p21.3, 2q32.3, 8p23.2, 8q21.3 and 10q24.32-q24.33) and two of which have been previously implicated (6p21.32-p22.1 and 18q21.2). The strongest new finding (P = 1.6 × 10(-11)) was with rs1625579 within an intron of a putative primary transcript for MIR137 (microRNA 137), a known regulator of neuronal development. Four other schizophrenia loci achieving genome-wide significance contain predicted targets of MIR137, suggesting MIR137-mediated dysregulation as a previously unknown etiologic mechanism in schizophrenia. In a joint analysis with a bipolar disorder sample (16,374 affected individuals and 14,044 controls), three loci reached genome-wide significance: CACNA1C (rs4765905, P = 7.0 × 10(-9)), ANK3 (rs10994359, P = 2.5 × 10(-8)) and the ITIH3-ITIH4 region (rs2239547, P = 7.8 × 10(-9)).

Original language	English
Pages (from-to)	969-76
Number of pages	8
Journal	Nature Genetics
Volume	43
Issue number	10
DOIs	https://doi.org/10.1038/ng.940
Publication status	Published - 2011

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10.1038/ng.940

Genome-wide association study identifies five new schizophrenia loci
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Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Ripke, S., Sanders, A. R., Kendler, K. S., Levinson, D. F., Sklar, P., Holmans, P. A., Lin, D.-Y., Duan, J., Ophoff, R. A., Andreassen, O. A., Scolnick, E., Cichon, S., St Clair, D., Corvin, A., Gurling, H., Werge, T., Rujescu, D., Blackwood, D. H. R., ... McIntosh, A. (2011). Genome-wide association study identifies five new schizophrenia loci. Nature Genetics, 43(10), 969-76. https://doi.org/10.1038/ng.940

@article{a01912ad80834c279ceadbf85e5334df,

title = "Genome-wide association study identifies five new schizophrenia loci",

abstract = "We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856 individuals of European ancestry and a stage 2 replication sample of 29,839 independent subjects. The combined stage 1 and 2 analysis yielded genome-wide significant associations with schizophrenia for seven loci, five of which are new (1p21.3, 2q32.3, 8p23.2, 8q21.3 and 10q24.32-q24.33) and two of which have been previously implicated (6p21.32-p22.1 and 18q21.2). The strongest new finding (P = 1.6 × 10(-11)) was with rs1625579 within an intron of a putative primary transcript for MIR137 (microRNA 137), a known regulator of neuronal development. Four other schizophrenia loci achieving genome-wide significance contain predicted targets of MIR137, suggesting MIR137-mediated dysregulation as a previously unknown etiologic mechanism in schizophrenia. In a joint analysis with a bipolar disorder sample (16,374 affected individuals and 14,044 controls), three loci reached genome-wide significance: CACNA1C (rs4765905, P = 7.0 × 10(-9)), ANK3 (rs10994359, P = 2.5 × 10(-8)) and the ITIH3-ITIH4 region (rs2239547, P = 7.8 × 10(-9)).",

author = "\{Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium\} and Stephan Ripke and Sanders, \{Alan R\} and Kendler, \{Kenneth S\} and Levinson, \{Douglas F\} and Pamela Sklar and Holmans, \{Peter A\} and Dan-Yu Lin and Jubao Duan and Ophoff, \{Roel A\} and Andreassen, \{Ole A\} and Edward Scolnick and Sven Cichon and \{St Clair\}, David and Aiden Corvin and Hugh Gurling and Thomas Werge and Dan Rujescu and Blackwood, \{Douglas H R\} and Pato, \{Carlos N\} and Malhotra, \{Anil K\} and Shaun Purcell and Frank Dudbridge and Neale, \{Benjamin M\} and Lizzy Rossin and Visscher, \{Peter M\} and Danielle Posthuma and Ruderfer, \{Douglas M\} and Ayman Fanous and Hreinn Stefansson and Stacy Steinberg and Mowry, \{Bryan J\} and Vera Golimbet and \{De Hert\}, Marc and J{\"o}nsson, \{Erik G\} and Istv{\'a}n Bitter and Pietil{\"a}inen, \{Olli P H\} and Collier, \{David A\} and Sarah Tosato and Ingrid Agartz and Margot Albus and Madeline Alexander and Amdur, \{Richard L\} and Farooq Amin and Nicholas Bass and Bergen, \{Sarah E\} and Black, \{Donald W\} and Thomas Hansen and Maclean, \{Alan W\} and McGhee, \{Kevin A\} and Andrew McIntosh",

year = "2011",

doi = "10.1038/ng.940",

language = "English",

volume = "43",

pages = "969--76",

journal = "Nature Genetics",

publisher = "Nature Publishing Group",

number = "10",

}

Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium, Ripke, S, Sanders, AR, Kendler, KS, Levinson, DF, Sklar, P, Holmans, PA, Lin, D-Y, Duan, J, Ophoff, RA, Andreassen, OA, Scolnick, E, Cichon, S, St Clair, D, Corvin, A, Gurling, H, Werge, T, Rujescu, D, Blackwood, DHR, Pato, CN, Malhotra, AK, Purcell, S, Dudbridge, F, Neale, BM, Rossin, L, Visscher, PM, Posthuma, D, Ruderfer, DM, Fanous, A, Stefansson, H, Steinberg, S, Mowry, BJ, Golimbet, V, De Hert, M, Jönsson, EG, Bitter, I, Pietiläinen, OPH, Collier, DA, Tosato, S, Agartz, I, Albus, M, Alexander, M, Amdur, RL, Amin, F, Bass, N, Bergen, SE, Black, DW, Hansen, T, Maclean, AW, McGhee, KA & McIntosh, A 2011, 'Genome-wide association study identifies five new schizophrenia loci', Nature Genetics, vol. 43, no. 10, pp. 969-76. https://doi.org/10.1038/ng.940

TY - JOUR

T1 - Genome-wide association study identifies five new schizophrenia loci

AU - Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium

AU - Ripke, Stephan

AU - Sanders, Alan R

AU - Kendler, Kenneth S

AU - Levinson, Douglas F

AU - Sklar, Pamela

AU - Holmans, Peter A

AU - Lin, Dan-Yu

AU - Duan, Jubao

AU - Ophoff, Roel A

AU - Andreassen, Ole A

AU - Scolnick, Edward

AU - Cichon, Sven

AU - St Clair, David

AU - Corvin, Aiden

AU - Gurling, Hugh

AU - Werge, Thomas

AU - Rujescu, Dan

AU - Blackwood, Douglas H R

AU - Pato, Carlos N

AU - Malhotra, Anil K

AU - Purcell, Shaun

AU - Dudbridge, Frank

AU - Neale, Benjamin M

AU - Rossin, Lizzy

AU - Visscher, Peter M

AU - Posthuma, Danielle

AU - Ruderfer, Douglas M

AU - Fanous, Ayman

AU - Stefansson, Hreinn

AU - Steinberg, Stacy

AU - Mowry, Bryan J

AU - Golimbet, Vera

AU - De Hert, Marc

AU - Jönsson, Erik G

AU - Bitter, István

AU - Pietiläinen, Olli P H

AU - Collier, David A

AU - Tosato, Sarah

AU - Agartz, Ingrid

AU - Albus, Margot

AU - Alexander, Madeline

AU - Amdur, Richard L

AU - Amin, Farooq

AU - Bass, Nicholas

AU - Bergen, Sarah E

AU - Black, Donald W

AU - Hansen, Thomas

AU - Maclean, Alan W

AU - McGhee, Kevin A

AU - McIntosh, Andrew

PY - 2011

Y1 - 2011

N2 - We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856 individuals of European ancestry and a stage 2 replication sample of 29,839 independent subjects. The combined stage 1 and 2 analysis yielded genome-wide significant associations with schizophrenia for seven loci, five of which are new (1p21.3, 2q32.3, 8p23.2, 8q21.3 and 10q24.32-q24.33) and two of which have been previously implicated (6p21.32-p22.1 and 18q21.2). The strongest new finding (P = 1.6 × 10(-11)) was with rs1625579 within an intron of a putative primary transcript for MIR137 (microRNA 137), a known regulator of neuronal development. Four other schizophrenia loci achieving genome-wide significance contain predicted targets of MIR137, suggesting MIR137-mediated dysregulation as a previously unknown etiologic mechanism in schizophrenia. In a joint analysis with a bipolar disorder sample (16,374 affected individuals and 14,044 controls), three loci reached genome-wide significance: CACNA1C (rs4765905, P = 7.0 × 10(-9)), ANK3 (rs10994359, P = 2.5 × 10(-8)) and the ITIH3-ITIH4 region (rs2239547, P = 7.8 × 10(-9)).

AB - We examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856 individuals of European ancestry and a stage 2 replication sample of 29,839 independent subjects. The combined stage 1 and 2 analysis yielded genome-wide significant associations with schizophrenia for seven loci, five of which are new (1p21.3, 2q32.3, 8p23.2, 8q21.3 and 10q24.32-q24.33) and two of which have been previously implicated (6p21.32-p22.1 and 18q21.2). The strongest new finding (P = 1.6 × 10(-11)) was with rs1625579 within an intron of a putative primary transcript for MIR137 (microRNA 137), a known regulator of neuronal development. Four other schizophrenia loci achieving genome-wide significance contain predicted targets of MIR137, suggesting MIR137-mediated dysregulation as a previously unknown etiologic mechanism in schizophrenia. In a joint analysis with a bipolar disorder sample (16,374 affected individuals and 14,044 controls), three loci reached genome-wide significance: CACNA1C (rs4765905, P = 7.0 × 10(-9)), ANK3 (rs10994359, P = 2.5 × 10(-8)) and the ITIH3-ITIH4 region (rs2239547, P = 7.8 × 10(-9)).

UR - https://www.scopus.com/pages/publications/80053384370

U2 - 10.1038/ng.940

DO - 10.1038/ng.940

M3 - Article

C2 - 21926974

VL - 43

SP - 969

EP - 976

JO - Nature Genetics

JF - Nature Genetics

IS - 10

ER -

Genome-wide association study identifies five new schizophrenia loci

Abstract

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