| 2014 | | Simultaneous determination of metoprolol and its metabolites, α-hydroxymetoprolol and O-desmethylmetoprolol, in human plasma by liquid chromatography with tandem mass spectrometry: Application to the pharmacokinetics of metoprolol associated with CYP2D6 genotypes. | 조두연 |
| 2003 | | Sources of polycyclic aromatic hydrocarbon exposure in non-occupationally exposed Koreans. | 장재연 |
| 2005 | | Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency. | 정윤석 |
| 2004 | | Subcellular localization and transcriptional repressor activity of HBx on p21(WAF1/Cip1) promoter is regulated by ERK-mediated phosphorylation. | 최경숙 |
| 2010 | | The common exon 3 polymorphism of the growth hormone receptor gene and the effect of growth hormone therapy on growth in Korean patients with Turner syndrome. | 고정민 |
| 2014 | | The effect of perinatal anxiety on bronchiolitis is influenced by polymorphisms in ROS-related genes. | 장형윤 |
| 2008 | | The effect of the ApoE genotype on the association between head circumference and cognition. | 홍창형 |
| 2019 | | The Liver X Receptor Is Upregulated in Monocyte-Derived Macrophages and Modulates Inflammatory Cytokines Based on LXRalpha Polymorphism | 김현아, 서창희, 정주양 |
| 2003 | | The origin of cells that repopulate patellar tendons used for reconstructing anterior cruciate ligaments in man. | 민병현 |
| 2006 | | The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1. | 김현주, 박상진, 정선용 |
| 2005 | | Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas. | 김대중, 이관우 |
| 2012 | | Transgenic mice expressing yellow fluorescent protein under control of the human tyrosine hydroxylase promoter | 이명애 |
| 2010 | | Type 2 Diabetes Genetic Association Database manually curated for the study design and odds ratio. | 진현석 |
| 2015 | | Underlying Mechanisms and Management of Refractory Gastroesophageal Reflux Disease | 이광재 |
| 2003 | | Urokinase receptor deficiency accelerates renal fibrosis in obstructive nephropathy. | 김흥수 |
| 2003 | | Urokinase receptor modulates cellular and angiogenic responses in obstructive nephropathy. | 김흥수 |
| 2008 | | VanB phenotype-vanA genotype Enterococcus faecium with heterogeneous expression of teicoplanin resistance. | 박일중, 이위교 |
| 2006 | | Which gene is a dominant predictor of response during FOLFOX chemotherapy for the treatment of metastatic colorectal cancer, the MTHFR or XRCC1 gene? | 김영배, 서광욱 |
| 2011 | | Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA). | 김옥화 |
| 2014 | | Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA. | 정주용 |
| 2011 | | Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type. | 김옥화 |
