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    "Bielak, LF"的相關文件 

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    顯示 13 項.

    類別 日期 題名 關聯 檔案
    [鍾仁華] 期刊論文 2024-10-09 Rare variant contribution to the heritability of coronary artery disease -
    [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 -
    [熊昭] 期刊論文 2023-02 Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing -
    [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 -
    [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 2022-10-12 A saturated map of common genetic variants associated with human height -
    [邱燕楓] 期刊論文 2021-06 The trans-ancestral genomic architecture of glycemic traits -
    [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 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 2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease -
    [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 2020-09 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale -

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