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Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Open accessAbstract
Schizophrenia is an idiopathic mental disorder with a heritable component and a substantial public health impact. We conducted a multi-stage genome-wide association study (GWAS) for schizophrenia beginning with a Swedish national sample (5,001 cases and 6,243 controls) followed by meta-analysis with previous schizophrenia GWAS (8,832 cases and 12,067 controls) and finally by replication of SNPs in 168 genomic regions in independent samples (7,413 cases, 19,762 controls and 581 parent-offspring trios). We identified 22 loci associated at genome-wide significance; 13 of these are new, and 1 was previously implicated in bipolar disorder. Examination of candidate genes at these loci suggests the involvement of neuronal calcium signaling. We estimate that 8,300 independent, mostly common SNPs (95% credible interval of 6,300-10,200 SNPs) contribute to risk for schizophrenia and that these collectively account for at least 32% of the variance in liability. Common genetic variation has an important role in the etiology of schizophrenia, and larger studies will allow more detailed understanding of this disorder.
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“This is further supported by studies showing substantial effects on schizophrenia risk of CNVs39 and rare damaging coding variants in genes with similar functions, including some of the same genes (SCHEMA; companion paper).”
From Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) · cites this paper as [39]
In the citing paper
“Psychiatric cases with a diagnosis of schizophrenia or bipolar disorder were ascertained from the Swedish National Hospital Discharge Register as described in previous studies9,50, which captures all inpatient hospitalizations. Controls were randomly selected from population registers.”
From Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia (2016) · cites this paper as [50]
In the citing paper
“replicating a couple of common variants associations previously observed for this cohort50”
From Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia (2016) · cites this paper as [50]
In the citing paper
“We integrate these considerations with results from recent genetic studies showing genetic susceptibility for schizophrenia associated with genes encoding for PNN components, matrix-regulating molecules and immune system factors.”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Ripke et al., 2013
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“recent evidence linking genes encoding structural constituents of PNNs and those that regulate their formation to schizophrenia”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Ripke et al., 2013
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“Interestingly, a recent genome-wide association study has identified MMP16 as a schizophrenia risk gene (Ripke et al., 2013).”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Ripke et al., 2013
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Self-citationGenetics of Cardiac Electrical Disease
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Self-citationAssociation analyses of 249,796 individuals reveal 18 new loci associated with body mass index
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Flagged first, then by citations
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Research works printed but not linked: 1
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Cited by
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Biological insights from 108 schizophrenia-associated genetic loci
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Self-citation
Metadata
- Authors
- Multicenter Genetic Studies of Schizophrenia Consortium, Ripke, S., Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2, O'Dushlaine, C., Chambert, K., Moran, J. L., Kähler, A. K., Akterin, S., Bergen, S. E., Collins, A. L., Crowley, J. J., Fromer, M., Kim, Y., Lee, S. H., Magnusson, P. K. E., Sanchez, N., Stahl, E. A., Williams, S., Wray, N. R., Xia, K., Bettella, F., Borglum, A. D., Bulik-Sullivan, B. K., Cormican, P., Craddock, N., de Leeuw, C., Durmishi, N., Gill, M., Golimbet, V., Hamshere, M. L., Holmans, P., Hougaard, D. M., Kendler, K. S., Lin, K., Morris, D. W., Mors, O., Mortensen, P. B., Neale, B. M., O'Neill, F. A., Owen, M. J., Milovancevic, M. P., Posthuma, D., Powell, J., Richards, A. L., Riley, B. P., Ruderfer, D., Rujescu, D., Sigurdsson, E., Silagadze, T., Smit, A. B., Stefansson, H., Steinberg, S., Suvisaari, J., Tosato, S., Verhage, M., Walters, J. T., Bramon, E., Corvin, A. P., O'Donovan, M. C., Stefansson, K., Scolnick, E., Purcell, S., McCarroll, S. A., Sklar, P., Hultman, C. M., & Sullivan, P. F.
- Affiliations
- Broad Institute (US)
- University of North Carolina at Chapel Hill (US)
- Karolinska Institutet (SE)
- The University of Queensland (AU)
- Icahn School of Medicine at Mount Sinai (US)
- deCODE Genetics (Iceland) (IS)
- Massachusetts General Hospital (US)
- Trinity College Dublin (IE)
- Cardiff University (GB)
- PHI University Psychiatric Clinic - Skopje (MK)
- Statens Serum Institut (DK)
- Virginia Commonwealth University (US)
- King's College London (GB)
- Aarhus University Hospital (DK)
- Aarhus University (DK)
- University of Belgrade (RS)
- Martin Luther University Halle-Wittenberg (DE)
- Tbilisi State Medical University (GE)
- Vrije Universiteit Amsterdam (NL)
- Finnish Institute for Health and Welfare (FI)
- University of Verona (IT)
- Corresponding author
- Sullivan, Patrick F
- ORCID
- Ripke, Stephan
- Moran, Jennifer L
- Kähler, Anna K
- Bergen, Sarah E
- Fromer, Menachem
- Kim, Yunjung
- Lee, Sang Hong
- Magnusson, Patrik K E
- Stahl, Eli A
- Williams, Stephanie
- Wray, Naomi R
- Xia, Kai
- Bettella, Francesco
- Bulik-Sullivan, Brendan K
- Craddock, Nick
- Gill, Michael
- Hamshere, Marian L
- Holmans, Peter
- Kendler, Kenneth S
- Lin, Kuang
- Morris, Derek W
- Mors, Ole
- Mortensen, Preben B
- Neale, Benjamin M
- Owen, Michael J
- Powell, John
- Richards, Alexander L
- Riley, Brien P
- Ruderfer, Douglas
- Rujescu, Dan
- Silagadze, Teimuraz
- Smit, August B
- Steinberg, Stacy
- Suvisaari, Jaana
- Tosato, Sarah
- Verhage, Matthijs
- Walters, James T
- Bramon, Elvira
- Corvin, Aiden P
- Scolnick, Edward
- Purcell, Shaun
- McCarroll, Steven A
- Sklar, Pamela
- Sullivan, Patrick F
- Venue
- Nature Genetics
- Published
- 2013-08-25
- Volume
- 45
- Issue
- 10
- Pages
- 1150-1159
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- PMC
- PMC3827979
- OpenAlex
- W2115807273
- Cited by
- 1,496
- References
- 101
- Citations by year
- 2026: 22 · 2025: 42 · 2024: 51 · 2023: 49 · 2022: 87 · 2021: 102 · 2020: 103 · 2019: 115 · 2018: 127 · 2017: 158 · 2016: 184 · 2015: 217 · 2014: 207 · 2013: 30
- FWCI
- 150.69
- Type
- journal article
- Language
- en
- Open access
- green
- research.vu.nl
- Licence
- other-oa
- www.springer.com/tdm (tdm)
- Locations
- Nature Genetics (publishedVersion)
- PubMed (publishedVersion)
- Discovery Research Portal (University of Dundee) (publishedVersion)
- Pure Amsterdam UMC (publishedVersion)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- VU Research Portal (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
- QUT ePrints (Queensland University of Technology) (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- Research Online (University of Wollongong) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- CLOK (University of Central Lancashire) (submittedVersion)
- Research Publications (Maastricht University) (submittedVersion, other-oa)
- UCL Discovery (University College London) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Minerva Access (University of Melbourne) (submittedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- Research Portal (Queen's University Belfast) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- RUNE (Research UNE) (submittedVersion)
- Hirsla (Landspítali University Hospital) (submittedVersion)
- STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) (submittedVersion)
- Research Publications (Maastricht University) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Funders
- Aarhus Universitet
- Wellcome Trust (085475/Z/08/Z, 095552/Z/11/Z, 085475, 095552, 090532, 085475/B/08/Z)
- Cancer Research UK
- National Institute for Health and Care Research (NF-SI-0507-10379, PDA/02/06/016)
- European Commission (223423)
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (645-000-003)
- Lundbeckfonden
- Karolinska Institutet
- Vetenskapsrådet (R01 MH077139)
- H. Lundbeck A/S
- Stanley Center for Psychiatric Research, Broad Institute
- Strategic Research Council
- National Institute of Mental Health (R01MH077139, K01MH094406, U01MH094421, R01MH083094, R01MH095034, MH077139)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Keywords
- schizophrenia, genetic susceptibility loci, single nucleotide polymorphisms, bipolar disorder, neuronal calcium signaling, candidate genes, heritability, genetic susceptibility, parent-offspring trios, meta-analysis
- MeSH terms
- Female, Humans, Male, Schizophrenia, Sweden, Case-Control Studies, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Genome-Wide Association Study
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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