| 2014 | | Neurotrophin 3 genotype and emotional adverse effects of osmotic-release oral system methylphenidate (OROS-MPH) in children with attention-deficit/hyperactivity disorder. | 신윤미 |
| 2013 | | No effect of the estrogen receptor α gene polymorphisms in the etiology of precocious puberty in girls. | 이해상, 황진순 |
| 2011 | | Norovirus infections in asymptomatic food handlers in elementary schools without norovirus outbreaks in some regions of Incheon, Korea. | 유준환 |
| 2010 | | Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family. | 김옥화 |
| 2005 | | Polymorphisms of high-affinity IgE receptor and histamine-related genes in patients with ASA-induced urticaria/angioedema. | 김승현, 남동호, 박해심, 서창희 |
| 2016 | | Polymorphisms of the TRPV2 and TRPV3 genes associated with fibromyalgia in a Korean population | 김현아 |
| 2010 | | Prevalence of the VNIc genotype of Cryptococcus neoformans in non-HIV-associated cryptococcosis in the Republic of Korea. | 이위교, 최영화 |
| 2007 | | RANTES, MCP-1, CCR2, CCR5, CXCR1 and CXCR4 gene polymorphisms are not associated with the outcome of hepatitis B virus infection: results from a large scale single ethnic population. | 김진홍, 정재연, 조성원 |
| 2004 | | Reduction in glycopeptide resistance in vancomycin-resistant enterococci as a result of vanA cluster rearrangements. | 이위교, 임영애, 조성란, 허지영 |
| 2010 | | Relationship between the diagnostic components of metabolic syndrome (MS) and cognition by ApoE genotype in the elderly. | 정영기, 홍창형 |
| 2012 | | Relationship of plasminogen activator inhibitor 1 gene 4G/5G polymorphisms to hypertension in Korean women | 김광민, 김규남, 김범택, 이득주, 조두연, 주남석 |
| 2015 | | Replication of genome wide association studies on hepatocellular carcinoma susceptibility loci of STAT4 and HLA-DQ in a Korean population. | 정재연, 조성원 |
| 2013 | | Risk factors for neurologic complications of hand, foot and mouth disease in the Republic of Korea, 2009. | 정다은 |
| 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 |
| 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 |
| 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 |
| 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 |
