Journal article
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
- Abstract:
- Here we conducted a large-scale genetic association analysis of educational attainment in a sample of approximately 1.1 million individuals and identify 1,271 independent genome-wide-significant SNPs. For the SNPs taken together, we found evidence of heterogeneous effects across environments. The SNPs implicate genes involved in brain-development processes and neuron-to-neuron communication. In a separate analysis of the X chromosome, we identify 10 independent genome-wide-significant SNPs and estimate a SNP heritability of around 0.3% in both men and women, consistent with partial dosage compensation. A joint (multi-phenotype) analysis of educational attainment and three related cognitive phenotypes generates polygenic scores that explain 11–13% of the variance in educational attainment and 7–10% of the variance in cognitive performance. This prediction accuracy substantially increases the utility of polygenic scores as tools in research.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Access Document
- Files:
-
-
(Preview, Accepted manuscript, pdf, 346.6KB, Terms of use)
-
- Publisher copy:
- 10.1038/s41588-018-0147-3
Authors
- Publisher:
- Nature Publishing Group
- Journal:
- Nature Genetics More from this journal
- Volume:
- 50
- Pages:
- 1112–1121
- Publication date:
- 2018-07-23
- Acceptance date:
- 2018-04-30
- DOI:
- EISSN:
-
1546-1718
- ISSN:
-
1061-4036
- Pubs id:
-
pubs:891702
- UUID:
-
uuid:60aef5be-468b-47e9-a561-4302e40b2ae0
- Local pid:
-
pubs:891702
- Source identifiers:
-
891702
- Deposit date:
-
2018-07-30
- ARK identifier:
Terms of use
- Copyright holder:
- Lee, et al
- Copyright date:
- 2018
- Notes:
- © Lee, et al 2018. This is the author accepted manuscript following peer review version of the article. The final version is available online from Nature Publishing Group at: 10.1038/s41588-018-0147-3
If you are the owner of this record, you can report an update to it here: Report update to this record