| 2011 | | A functional promoter polymorphism of the human IL18 gene is associated with aspirin-induced urticaria. | 김승현, 박해심 |
| 2013 | | A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder. | 우현구 |
| 2014 | | A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation. | 정주용 |
| 2017 | | A Role of the ABCC4 Gene Polymorphism in Airway Inflammation of Asthmatics | 김승현, 박해심, 반가영 |
| 2011 | | A synonymous variation in protease-activated receptor-2 is associated with atopy in Korean children. | 김승현, 박해심 |
| 2016 | | AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II | 손영배 |
| 2011 | | Age-dependent association of the polymorphisms in the mitochondria-shaping gene, OPA1, with blood pressure and hypertension in Korean population. | 정선용, 진현석 |
| 2012 | | AMPK γ2 subunit gene PRKAG2 polymorphism associated with cognitive impairment as well as diabetes in old age | 홍창형 |
| 2015 | | An HLA-C amino-acid variant in addition to HLA-B*27 confers risk for ankylosing spondylitis in the Korean population. | 서창희 |
| 2021 | | Apolipoprotein E ε4 is not associated with cognitive impairment in patients with idiopathic REM sleep behavior disorder | 김태준 |
| 2005 | | Association analysis of cysteinyl-leukotriene receptor 2 (CYSLTR2) polymorphisms with aspirin intolerance in asthmatics. | 박해심 |
| 2010 | | Association analysis of N-acetyl transferase-2 polymorphisms with aspirin intolerance among asthmatics. | 박해심 |
| 2005 | | Association analysis of signal transducer and activator of transcription 4 (STAT4) polymorphisms with asthma. | 박해심 |
| 2012 | | Association between apolipoprotein E genotype, chronic liver disease, and hepatitis B virus | 김기범, 김순선, 정재연, 조성원, 조진희 |
| 2016 | | Association between catechol-O-methyl transferase gene polymorphisms and fibromyalgia in a Korean population: A case-control study | 김현아 |
| 2006 | | Association between chronic hepatitis B virus infection and interleukin-10, tumor necrosis factor-alpha gene promoter polymorphisms. | 김진홍, 정재연, 조성원, 함기백 |
| 2007 | | Association between polymorphisms in prostanoid receptor genes and aspirin-intolerant asthma. | 김승현, 박해심 |
| 2012 | | Association of GNLY genetic polymorphisms with chronic liver disease in a Korean population | 정재연, 조성원 |
| 2013 | | Association of guanosine triphosphate cyclohydrolase 1 gene polymorphisms with fibromyalgia syndrome in a Korean population. | 김현아 |
| 2011 | | Association of interleukin 10 promoter polymorphism at -819 T>C with aspirin-induced urticaria in a Korean population. | 김승현, 남영희, 박해심, 진현정 |
| 2015 | | Association of P2RY12 polymorphisms with eosinophil and platelet activation in patients with aspirin-exacerbated respiratory disease. | 김승현, 박해심 |
| 2014 | | Association of polymorphism in microRNA 604 with susceptibility to persistent hepatitis B virus infection and development of hepatocellular carcinoma. | 정재연, 조성원 |
| 2010 | | Association of the CCR3 gene polymorphism with aspirin exacerbated respiratory disease. | 김승현, 박해심, 예영민, 최길순 |
| 2015 | | Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. | 김범택, 김정현, 박은국, 정선용 |
| 2017 | | Association of the miR-196a2, miR-146a, and miR-499 Polymorphisms with Asthma Phenotypes in a Korean Population | 김승현, 박해심 |
| 2011 | | Association of thromboxane A2 receptor (TBXA2R) gene polymorphism in patients with aspirin-intolerant acute urticaria. | 김승현, 김주희, 박해심, 예영민 |
| 2005 | | Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma. | 김승현, 박해심 |
| 2021 | | Association of TLR 9 gene polymorphisms with remission in patients with rheumatoid arthritis receiving TNF-α inhibitors and development of machine learning models | 정주양 |
| 2015 | | Association of TNFSF15 polymorphisms in Korean children with Crohn's disease. | 장주영 |
| 2015 | | Association of VARS2-SFTA2 polymorphisms with the risk of chronic hepatitis B in a Korean population. | 정재연, 조성원 |
| 2010 | | Autosomal recessive multiple epiphyseal dysplasia in a Korean girl caused by novel compound heterozygous mutations in the DTDST (SLC26A2) gene. | 김옥화 |
| 2003 | | Behçet's disease: the first Mongolian case in literature showing HLA B51, MICA gene type *5/*6. | 이성낙, 이은소 |
| 2012 | | Characterization of a vancomycin-resistant Enterococcus faecium outbreak caused by 2 genetically different clones at a neonatal intensive care unit | 박일중, 이위교 |
| 2017 | | Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis | 손영배 |
| 2011 | | Comparison of multiplex restriction fragment mass polymorphism and sequencing analyses for detecting entecavir resistance in chronic hepatitis B. | 조성원 |
| 2021 | | Cortical thickness is differently associated with ALDH2 rs671 polymorphism according to level of amyloid deposition | 노현웅, 박범희, 손상준, 정재연, 최진욱, 하재호, 홍창형 |
| 2015 | | Differential effects of white matter hyperintensity on geriatric depressive symptoms according to APOE-ε4 status. | 강대용, 노재성, 손상준, 이윤환, 임기영, 장기중, 정영기, 홍창형 |
| 2010 | | Discrete change in volatile anesthetic sensitivity in mice with inactivated tandem pore potassium ion channel TRESK. | 채윤정 |
| 2012 | | Effect of interleukin-18 gene polymorphisms on sensitization to wheat flour in bakery workers | 김승현, 박해심 |
| 2015 | | Effect of rivastigmine or memantine add-on therapy is affected by butyrylcholinesterase genotype in patients with probable Alzheimer's disease. | 문소영 |
| 2015 | | Effects of MBL2 polymorphisms in patients with diisocyanate-induced occupational asthma. | 김승현, 박해심, 예영민 |
| 2022 | | Effects of RETN polymorphisms on treatment response in rheumatoid arthritis patients receiving TNF-α inhibitors and utilization of machine-learning algorithms | 김현아, 정주양 |
| 2014 | | Exonic variants associated with development of aspirin exacerbated respiratory diseases. | 박해심 |
| 2015 | | FcγRIIB Gene Polymorphisms Are Associated with Disease Risk and Clinical Manifestations of Systemic Lupus Erythematosus in Koreans. | 김현아, 서창희, 정주양 |
| 2021 | | Gene polymorphisms in leptin and its receptor and the response to growth hormone treatment in patients with idiopathic growth hormone deficiency | 심영석 |
| 2011 | | Genetic basis of congenital and infantile nephrotic syndromes. | 배기수 |
| 2016 | | Genetic polymorphisms in the Wnt/beta-catenin pathway genes as predictors of tumor development and survival in patients with hepatitis B virus-associated hepatocellular carcinoma | 김순선, 노충균, 신성재, 유병무, 이광재, 이기명, 정재연, 조성원, 조효정 |
| 2017 | | Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases | 박해심 |
| 2010 | | Genetic variations in the sodium balance-regulating genes ENaC, NEDD4L, NDFIP2 and USP2 influence blood pressure and hypertension. | 진현석 |
| 2011 | | Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men | 조남한 |
| 1996 | | Genotype Distribution of Hepatitis C Virus in Patients with Liver Disease | 김진홍, 함기백 |
| 2006 | | Genotypes and Clinical Characteristics of BK Virus in Kidney Transplant Recipients | 김미정, 김흥수, 박지은, 송영수, 신규태, 정혁준, 정희선 |
| 2014 | | Hepatitis C virus attenuates interferon-induced major histocompatibility complex class I expression and decreases CD8+ T cell effector functions. | 윤사라, 최용준 |
| 2015 | | High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. | 서창희 |
| 2016 | | High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry | 서창희 |
| 2017 | | HLA-A*31:01 and lamotrigine-induced severe cutaneous adverse drug reactions in a Korean population | 박해심 |
| 2020 | | HLAs associated with perampanel-induced psychiatric adverse effects in a Korean population | 김태준 |
| 2005 | | Homocysteine levels--before and after methionine loading--in 51 Dutch families. | 이순영 |
| 2019 | | Identification of a Novel Frameshift Variant of POU3F4 and Genetic Counseling of Korean Incomplete Partition Type III Subjects Based on Detailed Genotypes | 장정훈, 정연훈 |
| 2011 | | Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach. | 김현주, 정선용 |
