國家衛生研究院 NHRI:Items for Author

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Items for Author "Correa, A"

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Showing 24 items.

Collection	Date	Title	Relation
[鍾仁華] 期刊論文	2023-04-12	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis	-
[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	-
[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	2021-11-02	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	2022-03-07	Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data	-
[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	2018-08-23	Deep-coverage whole genome sequences and blood lipids among 16,324 individuals	-
[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	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.]	-
[其他] 期刊論文	2019-12	Development of risk prediction equations for incident chronic kidney 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	2021-06-15	Genome sequencing unveils a regulatory landscape of platelet reactivity	-
[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	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	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	2020-12-18	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease	-
[熊昭] 期刊論文	2023-02	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing	-
[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	-
[熊昭] 期刊論文	2017-06	Protein truncating variants at the cholesteryl ester transfer protein gene and risk for coronary heart disease	-
[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	2021-06-09	Variant-specific inflation factors for assessing population stratification at the phenotypic variance level	-
[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	2022-10-11	Whole genome sequence analysis of blood lipid levels in >66,000 individuals	-

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Items for Author "Correa, A"