國家衛生研究院 NHRI:Items for Author

國家衛生研究院 NHRI:Items for Author

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Items for Author "Palmer, ND"

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Showing 15 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	2021-04-12	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices	-
[熊昭] 期刊論文	2020-10	Inherited causes of clonal haematopoiesis in 97,691 whole genomes	-
[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	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	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	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	-

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