國家衛生研究院 NHRI:作者相關文件

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"Kooperberg, C"的相關文件

類別	日期	題名	關聯
[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	2016-06-13	Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome	-
[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	2021-04-12	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices	-
[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	2013-03-21	Trans-ethnic fine-mapping of lipid loci Identifies population-specific signals and allelic heterogeneity that increases the trait variance explained	-
[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	-
[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	2022-08-01	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	2021-02-10	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	-
[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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