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    Items for Author "Aguet, F" 

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    Showing 15 items.

    Collection Date Title Relation Bitstream
    [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 -
    [熊昭] 期刊論文 2022-01-27 Upregulated heme biosynthesis increases obstructive sleep apnea severity: A pathway-based Mendelian randomization study -
    [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 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 -
    [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 -
    [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 -

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