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分子與基因醫學研究所
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Items for Author "Aguet, F"
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Showing 15 items.
Collection
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Relation
Bitstream
[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.]
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[鍾仁華] 期刊論文
2023-04-12
Clonal haematopoiesis and risk of chronic liver disease
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[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
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[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
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[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
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[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.]
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[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
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[鍾仁華] 期刊論文
2021-06-15
Genome sequencing unveils a regulatory landscape of platelet reactivity
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[鍾仁華] 期刊論文
2021-06-09
Variant-specific inflation factors for assessing population stratification at the phenotypic variance level
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[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.]
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[鍾仁華] 期刊論文
2021-02-10
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
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[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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[熊昭] 期刊論文
2022-01-27
Upregulated heme biosynthesis increases obstructive sleep apnea severity: A pathway-based Mendelian randomization study
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[熊昭] 期刊論文
2020-10
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
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[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
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