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Latent space representation of electronic health records for clustering dialysis-associated kidney failure subtypes |
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Association of bone turnover markers and craving reduction in patients with alcohol use disorder during withdrawal: Exploring the role of bone-brain axis |
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Clustering-based risk stratification of prediabetes populations: Insights from the Taiwan and UK Biobanks |
Journal of Diabetes Investigation. 2024 Oct 10;Article in Press. |
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Rare variant contribution to the heritability of coronary artery disease |
Nature Communications. 2024 Oct 09;15:Article number 8741. |
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Using large language model (LLM) to identify high-burden informal caregivers in long-term care |
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Pulse pressure is associated with decline in physical function in older adults |
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Understanding and alleviating informal caregiver burden through the development and validation of a caregiver strain index-based model in Taiwan |
BMC Geriatrics. 2024 Jun 26;24:Article number 558. |
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Classifying Alzheimer's disease and normal subjects using machine learning techniques and genetic-environmental features |
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Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores |
Scientific Reports. 2024 May 30;14:Article number 12436. |
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Changes of neurofilament light chain in patients with alcohol dependence following withdrawal and the genetic effect from ALDH2 Polymorphism |
European Archives of Psychiatry and Clinical Neuroscience. 2024 Mar;274(2):423-432. |
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Evaluating polygenic risk scores for predicting cardiometabolic traits and disease risks in the Taiwan Biobank |
HGG Advances. 2024 Jan 11;5(1):Article number 100260. |
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Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores |
medRxiv. 2023 Dec 14;Article in Press. |
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Exploring concepts and trends in informal caregiver burden: Systematic review using citation network and content analysis |
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Predicting long-term care service demands for cancer patients: A machine learning approach |
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Clonal haematopoiesis and risk of chronic liver disease[Erratum:Nature. 2023 Apr 12;616(7958):747-754.] |
Nature. 2023 Jul 07;619(7970):Article number E47. |
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Prevalence and predictive modeling of undiagnosed diabetes and impaired fasting glucose in Taiwan: A Taiwan Biobank study |
BMJ Open Diabetes Research and Care. 2023 Jun 16;11(3):Article number e003423. |
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Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake |
Nature Genetics. 2023 Jun 08;55(6):973-983. |
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Clonal haematopoiesis and risk of chronic liver disease |
Nature. 2023 Apr 12;616(7958):747-754. |
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Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis |
Nature. 2023 Apr 12;616:755-763. |
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Splice-site variants in the gene encoding GABA-A receptor delta subunit are associated with amphetamine use in patients under methadone maintenance treatment |
International Journal of Molecular Sciences. 2023 Jan;24(1):Article number 721. |
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Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies |
Nature Genetics. 2022 Dec 23;55:154-164. |
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A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies |
Nature Methods. 2022 Oct 27;19:1599-1611. |
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A saturated map of common genetic variants associated with human height |
Nature. 2022 Oct 12;610(7933):704-712. |
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Whole genome sequence analysis of blood lipid levels in >66,000 individuals |
Nature Communications. 2022 Oct 11;13:Article number 5995. |
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Whole genome association study of the plasma metabolome identifies metabolites linked to cardiometabolic disease in black individuals |
Nature Communications. 2022 Aug 22;13:Article number 4923. |
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Insights from a large-scale whole-genome sequencing study of systolic blood pressure, diastolic blood pressure, and hypertension |
Hypertension. 2022 Aug 1;79(8):1656-1667. |
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Association of the D-amino acid oxidase gene with methadone dose in heroin dependent patients under methadone maintenance treatment |
Journal of Human Genetics. 2022 May;67(5):273-278. |
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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data |
Nature Genetics. 2022 Mar 07;54(3):263-273. |
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Increase in plasma CCL11 (Eotaxin-1) in patients with alcohol dependence and changes during detoxification |
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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.] |
Nature Genetics. 2021 Nov 02;53(12):1722. |
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A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response |
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Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose |
Diabetologia. 2021 Jul;64(7):1613-1625. |
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Genome sequencing unveils a regulatory landscape of platelet reactivity |
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program |
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Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease |
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CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption |
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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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Genetic variants in NECTIN4 encoding an adhesion molecule are associated with continued opioid use |
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Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence |
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pWGBSSimla: A profile-based whole-genome bisulfite sequencing data simulator incorporating methylation QTLs, allele-specific methylations and differentially methylated regions |
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Predicting lung cancer occurrence in never-smoking females in Asia: TNSF-SQ, a prediction model |
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A multi-omics data simulator for complex disease studies and its application to evaluate multi-omics data analysis methods for disease classification |
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Genetic loci determining total immunoglobulin E levels from birth through adulthood |
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GRK5 is associated with the regulation of methadone dosage in heroin dependence |
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IGF1 gene is associated with triglyceride levels in subjects with family history of hypertension from the SAPPHIRe and TWB projects |
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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 |
Frontiers in Genetics. 2018 Jan;8:Article number 228. |
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