2009 | A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase gene. | 고정민 |
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 |
2009 | A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. | 조남한 |
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 |
2008 | A polymorphism in the zinc transporter gene SLC30A8 confers resistance against posttransplantation diabetes mellitus in renal allograft recipients. | 한승진 |
2006 | A polymorphism of MS4A2 (- 109T > C) encoding the beta-chain of the high-affinity immunoglobulin E receptor (FcepsilonR1beta) is associated with a susceptibility to aspirin-intolerant asthma. | 김승현, 서창희, 남동호, 박해심 |
2017 | A Role of the ABCC4 Gene Polymorphism in Airway Inflammation of Asthmatics | 반가영, 박해심, 김승현 |
2011 | A synonymous variation in protease-activated receptor-2 is associated with atopy in Korean children. | 박해심, 김승현 |
2016 | AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II | 손영배 |
2009 | Adenosine deaminase and adenosine receptor polymorphisms in aspirin-intolerant asthma. | 김승현, 예영민, 박해심 |
2011 | Age-dependent association of the polymorphisms in the mitochondria-shaping gene, OPA1, with blood pressure and hypertension in Korean population. | 진현석, 정선용 |
2009 | Allelic variants of CD40 and CD40L genes interact to promote antibiotic-induced cutaneous allergic reactions. | 박해심 |
2009 | Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. | 김승현, 박해심 |
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 |
2008 | Analysis of high-affinity IgE receptor (FcepsilonR1) polymorphisms in patients with aspirin-intolerant chronic urticaria. | 김승현, 예영민, 박해심 |
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 | 김순선, 김기범, 조진희, 조성원, 정재연 |
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. | 정재연, 조성원, 함기백, 김진홍 |
2009 | Association between CRHR1 polymorphism and improved lung function in response to inhaled corticosteroid in patients with COPD. | 신승수 |
2007 | Association between polymorphisms in prostanoid receptor genes and aspirin-intolerant asthma. | 김승현, 박해심 |
2009 | Association of common type 2 diabetes risk gene variants and posttransplantation diabetes mellitus in renal allograft recipients in Korea. | 한승진 |
2009 | Association of CRTH2 gene polymorphisms with the required dose of antihistamines in patients with chronic urticaria. | 김승현, 예영민, 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, 진현정, 남영희, 박해심 |
2010 | Association of interleukin-18 gene polymorphisms with hepatitis B virus clearance. | 정재연, 조성원, 이기명, 신성재, 김진홍 |
2008 | Association of lipoprotein lipase (LPL) single nucleotide polymorphisms with type 2 diabetes mellitus. | 조남한 |
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, 최길순, 예영민, 박해심 |
2015 | Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. | 김정현, 박은국, 김범택, 정선용 |
2017 | Association of the miR-196a2, miR-146a, and miR-499 Polymorphisms with Asthma Phenotypes in a Korean Population | 박해심, 김승현 |
2008 | Association of three sets of high-affinity IgE receptor (FcepsilonR1) polymorphisms with aspirin-intolerant asthma. | 김승현, 예영민, 박해심 |
2011 | Association of thromboxane A2 receptor (TBXA2R) gene polymorphism in patients with aspirin-intolerant acute urticaria. | 김승현, 김주희, 예영민, 박해심 |
2005 | Association of thromboxane A2 receptor gene polymorphism with the phenotype of acetyl salicylic acid-intolerant asthma. | 김승현, 박해심 |
2006 | Association of TNF-alpha genetic polymorphism with HLA DPB1*0301. | 김승현, 예영민, 박해심 |
2009 | Association of TNF-alpha promoter polymorphisms with aspirin-induced urticaria. | 김승현, 서창희, 박해심 |
2006 | Association of TNFA promoter region haplotype in Behçet's Disease. | 이은소 |
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 | Association studies of -3081(A/T) polymorphism of norepinephrine transporter gene with attention deficit/hyperactivity disorder in Korean population. | 이순영 |
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. | 이은소, 이성낙 |
2009 | C-reactive protein gene polymorphisms in disease susceptibility and clinical manifestations of Korean systemic lupus erythematosus. | 김현아, 김승현, 박해심, 서창희 |
2012 | Characterization of a vancomycin-resistant Enterococcus faecium outbreak caused by 2 genetically different clones at a neonatal intensive care unit | 이위교, 박일중 |
2017 | Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis | 손영배 |
2009 | Comparison of human papillomavirus detection and typing by hybrid capture 2, linear array, DNA chip, and cycle sequencing in cervical swab samples. | 이정필 |
2011 | Comparison of multiplex restriction fragment mass polymorphism and sequencing analyses for detecting entecavir resistance in chronic hepatitis B. | 조성원 |
2007 | Cytotoxic T lymphocyte-associated antigen-4 gene polymorphisms confer susceptibility to atopic asthma in Korean children. | 김승현, 박해심 |
2009 | Difference in nutritional risk between mild cognitive impairment group and normal cognitive function elderly group. | 홍창형 |
2015 | Differential effects of white matter hyperintensity on geriatric depressive symptoms according to APOE-ε4 status. | 장기중, 홍창형, 강대용, 이윤환, 정영기, 임기영, 노재성, 손상준 |
2010 | Discrete change in volatile anesthetic sensitivity in mice with inactivated tandem pore potassium ion channel TRESK. | 채윤정 |
2009 | Effect of beta2-adrenergic receptor polymorphism in asthma control of patients receiving combination treatment. | 김승현, 예영민, 박해심 |
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 |