國家衛生研究院 NHRI:Items for Author

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Items for Author "Chung, RH"

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Showing 69 items.

Collection	Date	Title	Relation
[鍾仁華] 期刊論文	2024-12	Latent space representation of electronic health records for clustering dialysis-associated kidney failure subtypes	-
[劉玉麗] 期刊論文	2024-10-30	Association of bone turnover markers and craving reduction in patients with alcohol use disorder during withdrawal: Exploring the role of bone-brain axis	-
[鍾仁華] 期刊論文	2024-10-10	Clustering-based risk stratification of prediabetes populations: Insights from the Taiwan and UK Biobanks	-
[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	2024-10	Using large language model (LLM) to identify high-burden informal caregivers in long-term care	-
[許志成] 期刊論文	2024-07	Pulse pressure is associated with decline in physical function in older adults	-
[鍾仁華] 期刊論文	2024-06-26	Understanding and alleviating informal caregiver burden through the development and validation of a caregiver strain index-based model in Taiwan	-
[鍾仁華] 期刊論文	2024-06	Classifying Alzheimer's disease and normal subjects using machine learning techniques and genetic-environmental features	-
[鍾仁華] 期刊論文	2024-05-30	Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores	-
[許志成] 會議論文/會議摘要	2024-05	A linear relationship of ankle-brachial systolic blood pressure index for cognitive function decline among older adults without peripheral artery disease: The halst study	-
[許志成] 會議論文/會議摘要	2024-05	Alcohol drinking may modify the association between Hdl-cholesterol and coronary calcium score in an older population	-
[劉玉麗] 期刊論文	2024-03	Changes of neurofilament light chain in patients with alcohol dependence following withdrawal and the genetic effect from ALDH2 Polymorphism	-
[鍾仁華] 期刊論文	2024-01-11	Evaluating polygenic risk scores for predicting cardiometabolic traits and disease risks in the Taiwan Biobank	-
[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	2023-12	Exploring concepts and trends in informal caregiver burden: Systematic review using citation network and content analysis	-
[鍾仁華] 會議論文/會議摘要	2023-10-24	Age trajectories of disability in middle and older age: A machine learning approach	-
[鍾仁華] 期刊論文	2023-09-16	Predicting long-term care service demands for cancer patients: A machine learning approach	-
[熊昭] 期刊論文	2023-06-16	Prevalence and predictive modeling of undiagnosed diabetes and impaired fasting glucose in Taiwan: A Taiwan Biobank study	-
[鍾仁華] 期刊論文	2023-06-08	Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake	-
[鍾仁華] 會議論文/會議摘要	2023-06	Assessing causality between carotid-femoral pulse wave velocity and cognitive function: A mendelian randomization study	-
[劉玉麗] 期刊論文	2023-01	Splice-site variants in the gene encoding GABA-A receptor delta subunit are associated with amphetamine use in patients under methadone maintenance treatment	-
[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	-
[許志成] 會議論文/會議摘要	2022-06	Pulse pressure associated with physical function decline and frailty syndrome progression	-
[劉玉麗] 期刊論文	2022-05	Association of the D-amino acid oxidase gene with methadone dose in heroin dependent patients under methadone maintenance treatment	-
[劉玉麗] 期刊論文	2022-01	Increase in plasma CCL11 (Eotaxin-1) in patients with alcohol dependence and changes during detoxification	-
[鍾仁華] 圖書	2021-10-29	Linkage disequilibrium and association analysis	-
[熊昭] 期刊論文	2021-07	Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose	-
[鍾仁華] 期刊論文	2021-06-15	Genome sequencing unveils a regulatory landscape of platelet reactivity	-
[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	2020-12-18	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease	-
[劉玉麗] 期刊論文	2020-10-22	CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption	-
[劉玉麗] 期刊論文	2020-06-18	Genetic variants in NECTIN4 encoding an adhesion molecule are associated with continued opioid use	-
[劉玉麗] 期刊論文	2020-04	Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence	-
[鍾仁華] 期刊論文	2020-02	pWGBSSimla: A profile-based whole-genome bisulfite sequencing data simulator incorporating methylation QTLs, allele-specific methylations and differentially methylated regions	-
[熊昭] 期刊論文	2020-02	Predicting lung cancer occurrence in never-smoking females in Asia: TNSF-SQ, a prediction model	-
[鍾仁華] 會議論文/會議摘要	2019-08	Genomewide sex-by-snp interaction scan identifies adgrv1 for the sex differences of opioid dependence in african american and supporting evidence in relations with treatment side effects in the asian population	-
[鍾仁華] 期刊論文	2019-05-01	A multi-omics data simulator for complex disease studies and its application to evaluate multi-omics data analysis methods for disease classification	-
[蔡慧如] 期刊論文	2019-03	Genetic loci determining total immunoglobulin E levels from birth through adulthood	-
[劉玉麗] 期刊論文	2018-10	GRK5 is associated with the regulation of methadone dosage in heroin dependence	-
[熊昭] 期刊論文	2018-06	IGF1 gene is associated with triglyceride levels in subjects with family history of hypertension from the SAPPHIRe and TWB projects	-
[鍾仁華] 期刊論文	2018-01	A powerful gene-based test accommodating common and low-frequency variants to detect both main effects and gene-gene interaction effects in case-control studies	-
[劉玉麗] 期刊論文	2017-11-16	Missense mutation at CLDN8 associated with a high plasma interferon gamma-inducible protein 10 level in methadone-maintained patients with urine test positive for morphine	-
[鍾仁華] 圖書	2017-10-05	Single marker family-based association analysis conditional on parental information	-
[許志成] 期刊論文	2017-09-04	Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease	-
[熊昭] 期刊論文	2017-08-08	Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population	-
[熊昭] 期刊論文	2017-07	Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms	-
[蔡慧如] 期刊論文	2017-04-04	Obesity disproportionately impacts lung volumes, airflow and exhaled nitric oxide in children	-
[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	-
[鍾仁華] 期刊論文	2016-10-18	A combined association test for rare variants using family and case-control data	-
[王聲昌] 會議論文/會議摘要	2016-10	Apoptosis pathway CASP10 gene associated with methadone dose and interacted with GRK5	-
[鍾仁華] 期刊論文	2016-09-13	Pathway analysis incorporating protein-protein interaction networks identified candidate pathways for the seven common diseases	-
[張憶壽] 期刊論文	2016-09-12	The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals	-
[鍾仁華] 期刊論文	2016-08-02	Cost-effectiveness analysis of different genetic testing strategies for lynch syndrome in Taiwan	-
[鍾仁華] 期刊論文	2016-07-08	GCORE-sib: An efficient gene-gene interaction tool for genome-wide association studies based on discordant sib pairs	-
[鍾仁華] 期刊論文	2016-06	An efficient gene-gene interaction test for genome-wide association studies in trio families	-
[鍾仁華] 期刊論文	2016-06	GESDB: A platform of simulation resources for genetic epidemiology studies	-
[鍾仁華] 期刊論文	2016-06	FamPipe: An automatic analysis pipeline for analyzing sequencing data in families for disease studies	-
[鍾仁華] 期刊論文	2016-02	SeqSIMLA2_exact: Simulate multiple disease sites in large pedigrees with given disease status for diseases with low prevalence	-
[鍾仁華] 期刊論文	2015-08-18	Effect of common genetic variants of growth arrest-specific 6 gene on insulin resistance, obesity and type 2 diabetes in an Asian population	-
[鍾仁華] 期刊論文	2015-05-15	A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families	-
[鍾仁華] 期刊論文	2015-01	SeqSIMLA2: Simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure	-
[鍾仁華] 期刊論文	2014-09-22	Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data	-
[鍾仁華] 會議論文/會議摘要	2014-06-17	Identification of rare variants for hypertension with incorporation of linkage information	-
[劉玉麗] 期刊論文	2014-04	The association of genetic polymorphisms in the kappa-opioid receptor 1 gene with body weight, alcohol use, and withdrawal symptoms in patients with methadone maintenance	-
[鍾仁華] 期刊論文	2013-09-04	Pathway-PDT: A flexible pathway analysis tool for nuclear families	-
[鍾仁華] 期刊論文	2013-06-20	SeqSIMLA: A sequence and phenotype simulation tool for complex disease studies	-
[鍾仁華] 會議論文/會議摘要	2013-04	PUPPI: A pathway analysis method using protein-protein interaction network for case-control data	-
[鍾仁華] 期刊論文	2012-05	A two-stage random forest-based pathway analysis method	-

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Items for Author "Chung, RH"