國家衛生研究院 NHRI:Items for Author
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    Items for Author "Guo, X" 

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    Showing 31 items.

    Collection Date Title Relation Bitstream
    [張俊彥] 期刊論文 2000-03-01 Unique biochemical, cytotoxic, and antitumor activity of camptothecin and 4 beta-amino-4'-O-demethylepipodophyllotoxin conjugates -
    [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 -
    [張憶壽] 期刊論文 2016-09-12 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals -
    [熊昭] 會議論文/會議摘要 2017-12 Whole genome sequence association analysis of sleep-disordered breathing traits in trans-omics for precision medicine (topmed) -
    [熊昭] 期刊論文 2023-02 Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing -
    [熊昭] 期刊論文 2017-07 Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci -
    [熊昭] 期刊論文 2017-07 Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms -
    [熊昭] 期刊論文 2017-05 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels -
    [熊昭] 期刊論文 2015-04-01 Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene -
    [熊昭] 期刊論文 2014-10 Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index -
    [熊昭] 期刊論文 2013-03-21 Trans-ethnic fine-mapping of lipid loci Identifies population-specific signals and allelic heterogeneity that increases the trait variance explained -
    [許志成] 期刊論文 2017-09-04 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease -
    [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 -
    [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 -
    [邱燕楓] 期刊論文 2019-10-31 Associations of autozygosity with a broad range of human phenotypes -
    [邱燕楓] 期刊論文 2016-03-16 Genetics of coronary artery disease in Taiwan: A cardiometabochip study by the TAICHI consortium -
    [邱燕楓] 期刊論文 2013-12 Trans-ethnic fine mapping identifies a novel independent locus at the 3′ end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population -
    [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 2023-12-14 Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores -
    [鍾仁華] 期刊論文 2023-06-08 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake -
    [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 2022-08-22 Whole genome association study of the plasma metabolome identifies metabolites linked to cardiometabolic disease in black individuals -
    [鍾仁華] 期刊論文 2022-08-01 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 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 2021-03-11 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 -

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