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    Items for Author "Mitchell, BD" 

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    Showing 14 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 2020-10 Inherited causes of clonal haematopoiesis in 97,691 whole genomes -
    [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 2018-12 Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries -
    [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.] -
    [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 -
    [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 -
    [鍾仁華] 期刊論文 2024-10-09 Rare variant contribution to the heritability of coronary artery disease -
    [鍾仁華] 期刊論文 2024-05-30 Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores -
    [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 2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals -
    [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 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 2020-09 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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