國家衛生研究院 NHRI:Items for Author
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    Items for Author "Rich, SS" 

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    Showing 39 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 2023-02 Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing -
    [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 2021-04-12 Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices -
    [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.] -
    [熊昭] 期刊論文 2018-08-23 Deep-coverage whole genome sequences and blood lipids among 16,324 individuals -
    [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 -
    [許惠恒] 期刊論文 2024-07-11 A global initiative to deliver precision health in diabetes -
    [許惠恒] 期刊論文 2024-04-20 Effective interventions in preventing gestational diabetes mellitus: A systematic review and meta-analysis -
    [許惠恒] 期刊論文 2024-04-06 Islet autoantibodies as precision diagnostic tools to characterize heterogeneity in type 1 diabetes: A systematic review -
    [許惠恒] 期刊論文 2024-03-26 Genotype-stratified treatment for monogenic insulin resistance: a systematic review[Erratum:Communications Medicine. 2023 Oct 05;3:Article number 134.] -
    [許惠恒] 期刊論文 2023-12-18 Refining the diagnosis of gestational diabetes mellitus: a systematic review and meta-analysis -
    [許惠恒] 期刊論文 2023-10-05 Precision gestational diabetes treatment: A systematic review and meta-analyses -
    [許惠恒] 期刊論文 2023-10-05 Participant characteristics in the prevention of gestational diabetes as evidence for precision medicine: A systematic review and meta-analysis -
    [許惠恒] 期刊論文 2023-10-05 Impact of individual and environmental factors on dietary or lifestyle interventions to prevent type 2 diabetes development: A systematic review -
    [許惠恒] 期刊論文 2023-10-05 Genotype-stratified treatment for monogenic insulin resistance: a systematic review -
    [許惠恒] 期刊論文 2023-10-05 Disease-modifying therapies and features linked to treatment response in type 1 diabetes prevention: A systematic review -
    [許惠恒] 期刊論文 2023-10-05 Utility and precision evidence of technology in the treatment of type 1 diabetes: A systematic review -
    [許惠恒] 期刊論文 2023-10-05 The use of precision diagnostics for monogenic diabetes: A systematic review and expert opinion -
    [許惠恒] 期刊論文 2023-10-05 Treatment effect heterogeneity following type 2 diabetes treatment with GLP1-receptor agonists and SGLT2-inhibitors: A systematic review -
    [許惠恒] 期刊論文 2023-10-05 Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine -
    [許惠恒] 期刊論文 2023-10-05 Precision subclassification of type 2 diabetes: A systematic review -
    [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 2023-12-14 Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores -
    [鍾仁華] 期刊論文 2023-04-12 Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis -
    [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 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 2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease -
    [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 -
    [鍾仁華] 期刊論文 2016-12-15 Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci -

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