English
|
正體中文
|
简体中文
|
Items with full text/Total items : 12145/12927 (94%)
Visitors : 923034 Online Users : 1024
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by
NTU Library IR team.
Scope
All of NHRI
Institute of Molecular and Genomic Medicine
Institute of Biotechnology and Pharmaceutical Research
Institute of Biomedical Engineering and Nanomedicine
Immunology Research Center
Center for Neuropsychiatric Research
Institute of Cellular and Systems Medicine
National Institute of Infectious Diseases and Vaccinology
Institute of Population Health Sciences
National Institute of Cancer Research
National Institute of Environmental Health Sciences
National Mosquito-Borne Diseases Control Research Center
National Center for Geriatrics and Welfare Research
Forum
Center of Biomedical Resource
NHRI Graduate Student Program
Core Instrument Center
Pathology Core Laboratory
Laboratory Animal Center
Administrative Units
圖書館
Tips:
please add "double quotation mark" for query phrases to get precise results
please goto advance search for comprehansive author search
Adv. Search
Home
‧
Login
‧
Upload
‧
Help
‧
About
‧
Administer
NHRI
>
Items for Author
Loading...
Category
Loading community tree, please wait....
Year
Loading year class tree, please wait....
Items for Author "Redline, S"
Return to Browse by Author
Showing 15 items.
Collection
Date
Title
Relation
Bitstream
[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
-
[熊昭] 期刊論文
2021-04-12
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices
-
[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
-
[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
2023-12-14
Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores
-
[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
2022-12-23
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
-
[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
-
[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
-
[熊昭] 期刊論文
2022-01-27
Upregulated heme biosynthesis increases obstructive sleep apnea severity: A pathway-based Mendelian randomization study
-
[鍾仁華] 期刊論文
2022-10-11
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
-
[熊昭] 會議論文/會議摘要
2017-12
Whole genome sequence association analysis of sleep-disordered breathing traits in trans-omics for precision medicine (topmed)
-
DSpace Software
Copyright © 2002-2004
MIT
&
Hewlett-Packard
/
Enhanced by
NTU Library IR team
Copyright ©
-
Feedback