English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 923193      Online Users : 925
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
    •  Adv. Search
    Home ‧ Login ‧ Upload ‧ Help ‧ About ‧ Administer Goto mobile version

    Category

    Loading community tree, please wait....

    Year

    Loading year class tree, please wait....

    Items for Author "Kardia, SLR" 

    Return to Browse by Author

    Showing 12 items.

    Collection Date Title Relation Bitstream
    [熊昭] 期刊論文 2023-02 Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing -
    [熊昭] 期刊論文 2021-04-12 Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices -
    [熊昭] 期刊論文 2020-10 Inherited causes of clonal haematopoiesis in 97,691 whole genomes -
    [邱燕楓] 期刊論文 2023-08-22 Whole genome sequencing analysis of body mass index identifies novel african ancestry-specific risk allele -
    [鍾仁華] 期刊論文 2024-05-30 Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores -
    [鍾仁華] 期刊論文 2023-12-14 Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores -
    [鍾仁華] 期刊論文 2023-04-12 Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis -
    [鍾仁華] 期刊論文 2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals -
    [鍾仁華] 期刊論文 2022-08-01 Insights from a large-scale whole-genome sequencing study of systolic blood pressure, diastolic blood pressure, and hypertension -
    [鍾仁華] 期刊論文 2021-03-11 Inherited causes of clonal haematopoiesis in 97,691 whole genomes[Erratum:Nature. 2020 Oct;586(7831):763-768.] -
    [鍾仁華] 期刊論文 2021-02-10 Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program -
    [鍾仁華] 期刊論文 2020-09 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale -

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