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Epigenetic interplay between methylation and miRNA in bladder cancer: focus on isoform expression
BMC genomics, 2021-10, Vol.22 (1), p.1-754, Article 754
2021
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Leveraging deep phenotyping from health check-up cohort with 10,000 Korean individuals for phenome-wide association study of 136 traits
Scientific reports, 2022-02, Vol.12 (1), p.1930-1930, Article 1930
2022
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Deep learning imaging phenotype can classify metabolic syndrome and is predictive of cardiometabolic disorders
Journal of translational medicine, 2024-05, Vol.22 (1), p.434-434, Article 434
2024
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Min-redundancy and max-relevance multi-view feature selection for predicting ovarian cancer survival using multi-omics data
BMC medical genomics, 2018-09, Vol.11 (Suppl 3), p.71-71, Article 71
2018
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Genetic Analysis Reveals Rare Variants in T-Cell Response Gene MR1 Associated with Poor Overall Survival after Urothelial Cancer Diagnosis
Cancers, 2021-04, Vol.13 (8), p.1864
2021
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Population-dependent Intron Retention and DNA Methylation in Breast Cancer
Molecular cancer research, 2018-03, Vol.16 (3), p.461-469
2018
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Association between genetic risk and adherence to healthy lifestyle for developing age-related hearing loss
BMC medicine, 2024-03, Vol.22 (1), p.141-141, Article 141
2024
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Long-term cardiovascular outcomes of gestational diabetes mellitus: a prospective UK Biobank study
Cardiovascular diabetology, 2022-10, Vol.21 (1), p.221-221, Article 221
2022
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Polygenic risk for type 2 diabetes, lifestyle, metabolic health, and cardiovascular disease: a prospective UK Biobank study
Cardiovascular diabetology, 2022-07, Vol.21 (1), p.131-131, Article 131
2022
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Identification of epigenetic interactions between miRNA and DNA methylation associated with gene expression as potential prognostic markers in bladder cancer
BMC medical genomics, 2017-05, Vol.10 (Suppl 1), p.30-30, Article 30
2017
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Polygenic risk score-based phenome-wide association study of head and neck cancer across two large biobanks
BMC medicine, 2024-03, Vol.22 (1), p.120-13, Article 120
2024
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Exome-Wide Rare Variant Analysis From the DiscovEHR Study Identifies Novel Candidate Predisposition Genes for Endometrial Cancer
Frontiers in oncology, 2019-07, Vol.9, p.574-574
2019
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The effects of alternative splicing on miRNA binding sites in bladder cancer
PloS one, 2018-01, Vol.13 (1), p.e0190708-e0190708
2018
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An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer
Scientific reports, 2019-11, Vol.9 (1), p.17173-17173, Article 17173
2019
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Prognostic Effect of Inflammatory Genes on Stage I-III Colorectal Cancer-Integrative Analysis of TCGA Data
Cancers, 2021-02, Vol.13 (4), p.751
2021
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Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer's disease
BMC medical genomics, 2018-09, Vol.11 (Suppl 3), p.76-76, Article 76
2018
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Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer
Scientific reports, 2020-02, Vol.10 (1), p.2481-2481, Article 2481
2020
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Reliability of microarray analysis for studying periodontitis: low consistency in 2 periodontitis cohort data sets from different platforms and an integrative meta-analysis
Journal of Periodontal & Implant Science, 2021, 51(1), , pp.18-29
2021
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Increasing the Density of Laboratory Measures for Machine Learning Applications
Journal of clinical medicine, 2020-12, Vol.10 (1), p.103
2020
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A Network-Based Analysis of Disease Complication Associations for Obstetric Disorders in the UK Biobank
Journal of personalized medicine, 2021-12, Vol.11 (12), p.1382
2021
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Quality Control Procedures for Genome‐Wide Association Studies
Current protocols, 2022-11, Vol.2 (11), p.e603-n/a
2022
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Associations between polygenic risk of coronary artery disease and type 2 diabetes, lifestyle, and cardiovascular mortality: A prospective UK Biobank study
Frontiers in cardiovascular medicine, 2022-08, Vol.9, p.919374
2022
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Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
BMC medical genomics, 2019-05, Vol.12 (1), p.59-59, Article 59
2019
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Correction to: Systematic characterization of germline variants from the DiscovEHR study endometrial carcinoma population
BMC medical genomics, 2019-05, Vol.12 (1), p.65-65, Article 65
2019
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Dissecting the clinical relevance of polygenic risk score for obesity-a cross-sectional, longitudinal analysis
International Journal of Obesity, 2022-09, Vol.46 (9), p.1686-1693
2022
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