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Human gain-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of atherogenic lipoproteins Cell Genomics 2023;3:100339 |
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Rare coding variants in 35 genes associate with circulating lipid levels - a multi-ancestry analysis of 170,000 exomes AMERICAN JOURNAL OF HUMAN GENETICS 2022 Jan,109(1):81-96 |
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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation NATURE GENETICS 2022 May,54(5):560-572 |
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Shared genetic architectures of subjective well-being in East Asian and European ancestry populations Nature Human Behaviour 2022 May,6(7):1014-1026 |
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids AMERICAN JOURNAL OF HUMAN GENETICS 2022 Aug,109(8):1366-1387 |
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Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals HUMAN MOLECULAR GENETICS 2022 Aug,30(8):716-726 |
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The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians Nature Communications 2022 Nov,13(1):6642 |
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Analyzing the Korean Reference Genome with meta-imputation increased the imputation accuracy and spectrum of rare variants in the Korean population Frontiers in Genetics 2022 Nov,13:1008646 |
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Genome-Wide Association Studies Identify Two Novel Loci Conferring Susceptibility to Diabetic Retinopathy in Japanese Patients with Type 2 Diabetes HUMAN MOLECULAR GENETICS 2021 May,30(8):716-726 |
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Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes Nature Communications 2021 Jun,12(1):3505 |
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The Trans-Ancestral Genomic Architecture of Glycemic Traits NATURE GENETICS 2021 Jun,53(6):840-860 |
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Genetic variants shape rheumatoid arthritis-specific transcriptomic features in CD4+ T cells through differential DNA methylation, explaining a substantial proportion of heritability ANNALS OF THE RHEUMATIC DISEASES 2021 Jul,80(7):876-883 |
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Unraveling the Genomic Architecture of the CYP3A Locus and ADME Genes for Personalized Tacrolimus Dosing TRANSPLANTATION 2021 Oct,105(10):2213-2225 |
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Expanding the clinical phenotype and genetic spectrum of PURA-related neurodevelopmental disorders BRAIN AND DEVELOPMENT 2021 Oct,43(9):912-918 |
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Validation and genetic heritability estimation of known T2D related variants in the Korean population Genomics & Informatics 2021 Dec,19(4):e37 |
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Identification of type 2 diabetes loci in 433,540 East Asian indiciduals NATURE 2020 May,582(7811):240-245 |
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Integrated Analysis of Tissue-Specific Promoter Methylation and Gene Expression Profile in Complex Diseases International Journal of Molecular Sciences 2020 July,21(14):5056 |
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Obesity susceptible novel DNA methylation marker on regulatory region of inflammation gene: Results from the Korea Epigenome Study (KES) BMJ Open Diabetes Research and Care 2020 Aug,8(1):e001338 |
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GEN2VCF: A converter for human genome imputation output format to VCF format Genes & Genomics 2020 Oct,42(10):1163-1168 |
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Metabolomics profiles associated with diabetic retinopathy in type 2 diabetes patients PLoS One 2020 Oct,15(10):e0241365 |
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Putative positive role of inflammatory genes in fat deposition supported by altered gene expression in purified human adipocytes and preadipocytes from lean and obese adipose tissues Journal of Translational Medicine 2020 Nov,18:433 |
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Identification of metabolic markers predictive of prediabetes in a Korean population Scientific Reports 2020 Dec,10:22009 |
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The Korea Biobank Array: Design and Identification of coding variants associated with blood biochemical Traits Scientific Reports 2019 Feb,9:1382 |
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The genetic and epigenetic association of LDL Receptor Related Protein 1B (LRP1B) gene with obesity related traits from childhood obesity Scientific Reports 2019 Feb,9:1815 |
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Epigenetic analysis in rheumatoid arthritis synoviocytes EXPERIMENTAL AND MOLECULAR MEDICINE 2019 Feb,51(2):22 |
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The association of genetically controlled CpG methylation(cg158269425) of protein tyrosine phosphatase, receptor type N2 (PTPRN2) with childhood obesity Scientific Reports 2019 Mar,9:4855: |
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls NATURE 2019 Jun,570(7759):71-76 |
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Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups GENETIC EPIDEMIOLOGY 2019 Sep,43(6):617-628 |
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Programmable nuclease-based integration into novel extragenic genomic safe harbor identified from Korean population-based CNV analysis Molecular Therapy-Oncolytics 2019 Sep,14:253-265 |
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Identification of novel non-synonymous variants associated with type 2 diabetes-related metabolites in Korean population BIOSCIENCE REPORTS 2019 Oct,39(10):BSR20190078 |
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Metabolomics profiles associated with HbA1c levels in patients with type 2 diabetes PLoS One 2019 Nov,:e0224274 |
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Recapitulation of previously reported associations for type 2 diabetes and metabolic traits in the 126K East Asians Genomics & Informatics 2019 Dec,17(4):e48 |
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