English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 925502      Online Users : 741
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 "Palmer, ND" 

    Return to Browse by Author

    Showing 15 items.

    Collection Date Title Relation Bitstream
    [鍾仁華] 期刊論文 2023-04-12 Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis -
    [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 2021-10-05 A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response -
    [鍾仁華] 期刊論文 2021-11-02 A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response[Erratum:Nature Genetics. 202 Oct 05;53(10):1504-1516.] -
    [熊昭] 期刊論文 2021-04-12 Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices -
    [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.] -
    [鍾仁華] 期刊論文 2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease -
    [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 2024-10-09 Rare variant contribution to the heritability of coronary artery disease -
    [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 2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals -
    [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 -

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