English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 864369      Online Users : 533
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 "Redline, S" 

    Return to Browse by Author

    Showing 15 items.

    Collection Date Title Relation Bitstream
    [熊昭] 會議論文/會議摘要 2017-12 Whole genome sequence association analysis of sleep-disordered breathing traits in trans-omics for precision medicine (topmed) -
    [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 -
    [熊昭] 期刊論文 2020-10 Inherited causes of clonal haematopoiesis in 97,691 whole genomes -
    [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.] -
    [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 2022-01-27 Upregulated heme biosynthesis increases obstructive sleep apnea severity: A pathway-based Mendelian randomization study -
    [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 2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals -
    [張憶壽] 期刊論文 2022-10-27 A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies -
    [鍾仁華] 期刊論文 2022-12-23 Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies -
    [鍾仁華] 期刊論文 2023-04-12 Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis -
    [許惠恒] 期刊論文 2023-06-29 Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study -
    [許惠恒] 期刊論文 2023-10-05 Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study -
    [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 2024-05-30 Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores -

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