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    "Beer, R"的相关文件  

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    显示 14 项.

    类别 日期 题名 關聯 档案
    [鍾仁華] 期刊論文 2023-07-07 Clonal haematopoiesis and risk of chronic liver disease[Erratum:Nature. 2023 Apr 12;616(7958):747-754.] -
    [鍾仁華] 期刊論文 2023-04-12 Clonal haematopoiesis and risk of chronic liver 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 -
    [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 2022-08-22 Whole genome association study of the plasma metabolome identifies metabolites linked to cardiometabolic disease in black individuals -
    [鍾仁華] 期刊論文 2022-03-07 Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data -
    [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.] -
    [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 2021-06-15 Genome sequencing unveils a regulatory landscape of platelet reactivity -
    [鍾仁華] 期刊論文 2021-06-09 Variant-specific inflation factors for assessing population stratification at the phenotypic variance level -
    [熊昭] 期刊論文 2020-04-01 Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries[Erratum: Nature Communications. 2018 Dec;9:Article number 2606.] -
    [熊昭] 期刊論文 2018-08-23 Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries[Erratum: Nature Communications. 2018 Dec;9:Article number 2606.] -
    [熊昭] 期刊論文 2018-08-23 Deep-coverage whole genome sequences and blood lipids among 16,324 individuals -
    [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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