國家衛生研究院 NHRI:Item 3990099045/14600
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 12145/12927 (94%)
造訪人次 : 858832      線上人數 : 811
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧：
  • 您可在西文檢索詞彙前後加上"雙引號"，以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋，建議至進階搜尋限定作者欄位，可獲得較完整資料
    •  進階搜尋
    主頁 ‧ 登入 ‧ 上傳 ‧ 說明 ‧ 關於NHRI ‧ 管理 到手機版


    請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/14600


    題名: A saturated map of common genetic variants associated with human height
    作者: Yengo, L;Vedantam, S;Marouli, E;Sidorenko, J;Bartell, E;Sakaue, S;Graff, M;Eliasen, AU;Jiang, Y;Raghavan, S;Miao, J;Arias, JD;Graham, SE;Mukamel, RE;Spracklen, CN;Yin, X;Chen, SH;Ferreira, T;Highland, HH;Ji, Y;Karaderi, T;Lin, K;Lüll, K;Malden, DE;Medina-Gomez, C;Machado, M;Moore, A;Rüeger, S;Sim, X;Vrieze, S;Ahluwalia, TS;Akiyama, M;Allison, MA;Alvarez, M;Andersen, MK;Ani, A;Appadurai, V;Arbeeva, L;Bhaskar, S;Bielak, LF;Bollepalli, S;Bonnycastle, LL;Bork-Jensen, J;Bradfield, JP;Bradford, Y;Braund, PS;Brody, JA;Burgdorf, KS;Cade, BE;Cai, H;Cai, Q;Campbell, A;Cañadas-Garre, M.;et al.
    貢獻者: Institute of Population Health Sciences
    摘要: Common single-nucleotide polymorphisms (SNPs) are predicted to collectively explain 40-50% of phenotypic variation in human height, but identifying the specific variants and associated regions requires huge sample sizes(1). Here, using data from a genome-wide association study of 5.4 million individuals of diverse ancestries, we show that 12,111 independent SNPs that are significantly associated with height account for nearly all of the common SNP-based heritability. These SNPs are clustered within 7,209 non-overlapping genomic segments with a mean size of around 90 kb, covering about 21% of the genome. The density of independent associations varies across the genome and the regions of increased density are enriched for biologically relevant genes. In out-of-sample estimation and prediction, the 12,111 SNPs (or all SNPs in the HapMap 3 panel(2)) account for 40% (45%) of phenotypic variance in populations of European ancestry but only around 10-20% (14-24%) in populations of other ancestries. Effect sizes, associated regions and gene prioritization are similar across ancestries, indicating that reduced prediction accuracy is likely to be explained by linkage disequilibrium and differences in allele frequency within associated regions. Finally, we show that the relevant biological pathways are detectable with smaller sample sizes than are needed to implicate causal genes and variants. Overall, this study provides a comprehensive map of specific genomic regions that contain the vast majority of common height-associated variants. Although this map is saturated for populations of European ancestry, further research is needed to achieve equivalent saturation in other ancestries.
    日期: 2022-10-12
    關聯: Nature. 2022 Oct 12;610(7933):704-712.
    Link to: http://dx.doi.org/10.1038/s41586-022-05275-y
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0028-0836&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000866362700001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85139748621
    顯示於類別:[鍾仁華] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    PUB36224396.pdf19276KbAdobe PDF153檢視/開啟


    在NHRI中所有的資料項目都受到原著作權保護.

    TAIR相關文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋