4.8 Article

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

期刊

NATURE GENETICS
卷 50, 期 3, 页码 381-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41588-018-0059-2

关键词

-

资金

  1. European Union's Seventh Framework Programme [279227]
  2. Medical Research Council (MRC) Centre [MR/L010305/1, G0800509, MR/L011794/1]
  3. European Community's Seventh Framework Programme [HEALTH-F2-2010-241909]
  4. German Research Foundation (DFG) [FOR2107 DA1151/5-1, SFB-TRR58, C09]
  5. Interdisciplinary Center for Clinical Research (IZKF) of the medical faculty of Munster [Dan3/012/17]
  6. National Health and Medical Research Council (NHMRC) [1078901, 105363]
  7. Agencia Estatal de Investigacion (AEI) [CGL2016-75904-C2-1-P]
  8. Xunta de Galicia [ED431C 2016-037]
  9. Fondo Europeo de Desarrollo Regional (FEDER)
  10. Lundbeck Foundation [R102-A9118, R155-2014-1724]
  11. Stanley Medical Research Institute, an advanced grant from the European Research Council [294838]
  12. Danish Strategic Research Council
  13. Aarhus University
  14. Wellcome Trust [076113, WT091310, 06854/Z/02/Z, 083270, 076113/C/04/Z, 10436/Z/14/Z, 088262/Z/09/Z]
  15. UK MRC [G0000934]
  16. Juvenile Diabetes Research Foundation (JDRF)
  17. European Union [HEALTH-F4-2007-201413]
  18. National Institute for Health Research (NIHR) programme [RP-PG-0310-1002]
  19. Chief Scientist Office of the Scottish government Health Directorates [CZD/16/6]
  20. Scottish Funding Council [HR03006]
  21. MRC [G0901245-G0500079]
  22. National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  23. National Institute of Allergy and Infectious Diseases (NIAID)
  24. National Human Genome Research Institute (NHGRI)
  25. National Institute of Child Health and Human Development (NICHD)
  26. JDRF
  27. NIHR
  28. King's College London
  29. Australian NHMRC [241944, 339462, 389875, 389891, 389892, 389927, 389938, 442915, 442981, 496675, 496739, 552485, 552498, 613602, 613608, 613674, 619667]
  30. Australian Research Council [FT0991360, FT0991022]
  31. FP-5 GenomEUtwin Project [QLG2-CT-2002-01254]
  32. US National Institutes of Health (NIH) [AA07535, AA10248, AA13320, AA13321, AA13326, AA14041, MH66206, DA12854, DA019951]
  33. Center for Inherited Disease Research (Baltimore, MD, USA)
  34. NIH [HD044454, HD059215]
  35. Alzheimer's Research UK (ARUK)
  36. Welsh government
  37. ARUK
  38. Alzheimer's Society
  39. Ulster Garden Villages
  40. Northern Ireland RD Office
  41. Royal College of Physicians/Dunhill Medical Trust
  42. NIH
  43. Barnes Jewish Foundation
  44. Charles and Joanne Knight Alzheimer's Research Initiative
  45. German Federal Ministry of Education and Research (BMBF), Competence Network Dementia and Competence Network Degenerative Dementia
  46. Alfried Krupp von Bohlen und Halbach-Stiftung
  47. National Health and Medical Research Council of Australia [613674] Funding Source: NHMRC
  48. Lundbeck Foundation [R155-2014-1724, R248-2017-2003] Funding Source: researchfish
  49. Medical Research Council [MR/L023784/2, MR/L010305/1, MR/P005748/1, MR/K026992/1, UKDRI-3003, MC_UU_00007/10, G19/2] Funding Source: researchfish
  50. MQ Mental Health Research [MQDS16/36] Funding Source: researchfish
  51. MRC [MR/P005748/1, MR/L023784/2, MC_UU_00007/10, UKDRI-3003, G19/2, MR/L011794/1] Funding Source: UKRI
  52. Wellcome Trust [088262/Z/09/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Schizophrenia is a debilitating psychiatric condition often associated with poor quality of life and decreased life expectancy. Lack of progress in improving treatment outcomes has been attributed to limited knowledge of the underlying biology, although large-scale genomic studies have begun to provide insights. We report a new genome-wide association study of schizophrenia (11,260 cases and 24,542 controls), and through meta-analysis with existing data we identify 50 novel associated loci and 145 loci in total. Through integrating genomic fine-mapping with brain expression and chromosome conformation data, we identify candidate causal genes within 33 loci. We also show for the first time that the common variant association signal is highly enriched among genes that are under strong selective pressures. These findings provide new insights into the biology and genetic architecture of schizophrenia, highlight the importance of mutation-intolerant genes and suggest a mechanism by which common risk variants persist in the population.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据