Browsing byKeyword : Genetic Association Studies

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Showing results 1 to 32 of 32

Publication YearTitleAJOU
Author
2014Additive effect between IL-13 polymorphism and cesarean section delivery/prenatal antibiotics use on atopic dermatitis: a birth cohort study (COCOA).이수영
2009Allelic variants of CD40 and CD40L genes interact to promote antibiotic-induced cutaneous allergic reactions.박해심
2013An interstitial, apparently-balanced chromosomal insertion in the etiology of Langer-Giedion syndrome in an Asian family.김옥화
2011Association between variable number tandem repeats within the 3' flanking region of the interleukin-6 gene and systemic lupus erythematosus in Korean patients.김현아김승현서창희
2014Association of a microRNA-323b polymorphism with the persistence of hepatitis B virus infection by the enhancement of viral replication정재연조성원
2019Association of Asian mitochondrial DNA haplogroup B with new development of knee osteoarthritis in Koreans조남한
2013Association of guanosine triphosphate cyclohydrolase 1 gene polymorphisms with fibromyalgia syndrome in a Korean population.김현아
2017Association of the miR-196a2, miR-146a, and miR-499 Polymorphisms with Asthma Phenotypes in a Korean Population박해심김승현
2010Association of vascular endothelial growth factor polymorphisms with nonproliferative and proliferative diabetic retinopathy.이관우
2016Association-heterogeneity mapping identifies an Asian-specific association of the GTF2I locus with rheumatoid arthritis서창희
2017Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype손영배
2013Clinical consequences in truncating mutations in exon 34 of NOTCH2: report of six patients with Hajdu-Cheney syndrome and a patient with serpentine fibula polycystic kidney syndrome.정윤석김옥화
2011Combined pharmacogenetic effect of ADCY9 and ADRB2 gene polymorphisms on the bronchodilator response to inhaled combination therapy.김승현예영민박해심
2013Dietary intake and breast cancer among carriers and noncarriers of BRCA mutations in the Korean Hereditary Breast Cancer Study.정용식
2015Dipeptidyl-peptidase 10 as a genetic biomarker for the aspirin-exacerbated respiratory disease phenotype.김승현예영민박해심
2011Effect of Toll-like receptor 4 gene polymorphisms on work-related respiratory symptoms and sensitization to wheat flour in bakery workers.김승현박해심
2014Exonic variants associated with development of aspirin exacerbated respiratory diseases.박해심
2011Exploring genomic profiles of hepatocellular carcinoma우현구
2015Identification and in vivo functional characterization of novel compound heterozygous BMP1 variants in osteogenesis imperfecta.손영배
2016Imputing Variants in HLA-DR Beta Genes Reveals That HLA-DRB1 Is Solely Associated with Rheumatoid Arthritis and Systemic Lupus Erythematosus서창희
2010Interleukin 6 gene polymorphisms are associated with systemic lupus erythematosus in Koreans.김현아김승현박해심서창희
2010Linkage and association studies of joint morbidity from rheumatoid arthritis.민경복
2013Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.손영배정선용김현주
2017No association between estrogen receptor gene polymorphisms and premature thelarche in girls이해상윤종서황진순
2018Nonsynonymous Variants in PAX4 and GLP1R Are Associated With Type 2 Diabetes in an East Asian Population조남한
2014Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.김옥화
2012Response to growth hormone therapy in children with Noonan syndrome: correlation with or without PTPN11 gene mutation황진순
2011Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes.김옥화
2014Single nucleotide polymorphisms associated with abnormal coronary microvascular function.최병주
2010The genetic association of the FPRL1 promoter polymorphism with chronic urticaria in a Korean population.김승현박해심
2012TRPV4-pathy manifesting both skeletal dysplasia and peripheral neuropathy: a report of three patients김옥화
2011Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.김옥화
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