4.7 Article

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

期刊

NATURE NEUROSCIENCE
卷 19, 期 12, 页码 1563-1565

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nn.4404

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资金

  1. Knut and Alice Wallenberg Foundation [2015.0327]
  2. Swedish Research Council [2016-00250]
  3. Royal Netherlands Academy of Science [PAH/6635]
  4. Finnish Foundation for Cardiovascular Research
  5. National Human Genome Research Institute [U54 HG003067, R01 HG006855]
  6. National Institute of Mental Health [1U01MH105666-01, 1R01MH101244-02]
  7. National Institute of Diabetes and Digestive and Kidney Disease [1U54DK105566-02]
  8. Stanley Center for Psychiatric Research
  9. Alexander and Margaret Stewart Trust
  10. National Institutes of Mental Health [R01 MH077139, RC2 MH089905]
  11. Sylvan C. Herman Foundation
  12. EU [692145, 676550, 654248]
  13. Estonian Research Council [IUT20-60]
  14. NIASC
  15. EIT-Health
  16. NIH-BMI Grant [2R0IDK075787-06A1]
  17. EU through the European Regional Development Fund [2014-2020.4.01.15-0012 GENTRANSMED]
  18. Swedish Research Council [2016-00250] Funding Source: Swedish Research Council
  19. Forte [2016-00250] Funding Source: Forte

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Disruptive, damaging ultra-rare variants in highly constrained genes are enriched in individuals with neurodevelopmental disorders. In the general population, this class of variants was associated with a decrease in years of education (YOE). This effect was stronger among highly brain-expressed genes and explained more YOE variance than pathogenic copy number variation but less than common variants. Disruptive, damaging ultra-rare variants in highly constrained genes influence the determinants of YOE in the general population.

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