ScholarWorks@Hanyang University: Koh, In Song

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Koh, In Song (고인송)

COLLEGE OF MEDICINE (DEPARTMENT OF PHYSIOLOGY)

Research Area: 생리학, 생명정보학, 시스템의학

Tel 02-2220-0615
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single nucleotide polymorphism:7||Single nucleotide polymorphism:5||Haplotype:4||haplotype:4||Aspirinintolerant asthma:4||Hepatocellular carcinoma:3||Schizophrenia:3||SNP:3||Korean:3||Polymorphism:3||single nucleotide polymorphism (SNP):2||Bioinformatics:2||Exome sequencing:2||enteric nervous system:2||RNASeq:2||overweight:2||Hepatitis B virus:2||obesity:2||Single nucleotide polymorphism (SNP):2||Singlenucleotide polymorphism:2||DtyrosyltRNA deacylase 1:1||Database:1||Deletion:1||Diffusion tensor imaging:1||EMID2:1||Epistatic interaction:1||Ethnic diversity:1||Frontal executive dysfunction:1||Functional variants:1||Gender:1||Gene–ferritin interaction:1||Gene Expression:1||Gene expression:1||Genetic factor:1||Genomewide association study:1||Genomewide association study (GWAS):1||Genomewide gene–environment interaction:1||HCC:1||HLADQ:1||Haplotypes:1||Highdensity lipoproteincholesterol:1||Hirschsprung:1||Hirschsprung disease:1||Human microbiome:1||IL11:1||Imputation:1||Inherited mutation:1||Interaction:1||Juvenile myoclonic epilepsy:1||KARE:1||KIAA1377:1||Korean specific:1||Lipoprotein:1||Lowfrequency variant:1||MRI:1||Menarche:1||Menopause:1||Metabolism:1||Metagenomics:1||MicroRNA:1||MicroRNAs:1||Missing heritability:1||Monomelic amyotrophy:1||NGS:1||Necrotizing Enterocolitis:1||Neuregulin 1:1||Next generation sequencing:1||Organic aniontransporting peptide genes:1||PDE4B:1||Pharmacogenetics:1||PreBcell leukemia transcription factor 1 (PBX1):1||Prospective study:1||RAD51, HBV:1||RANBP1:1||RASSF1A:1||RTN4R:1||SLC6A20:1||SNPwinter:1||SPEM abnormality:1||STAT4:1||STK10:1||Smooth pursuit eye movement:1||Solute carrier family 22, member 2:1||Structural variation:1||Support vector machine:1||Systems toxicology:1||THR beta:1||TREM2:1||Toxicogenomics:1||Type 2 diabetes:1||USH2A:1||Unmapped region:1||Variants:1||White matter integrity:1||Whole genome sequencing:1||age:1||aspirin exacerbated respiratory disease (AERD):1||aspirinintolerant asthma:1||association study:1||autophagy:1||biclustering:1||body height:1||body mass index:1||brain volume:1||breast cancer:1||cell proliferation:1||colon cancer:1||cyclin B1:1||differentially expressed gene:1||docetaxel:1||endometrial cancer:1||follicle stimulating hormone:1||fynrelated kinase:1||gene expression profiling:1||genomewide association study:1||hepatitis B virus:1||hepatocellular carcinoma:1||hypoxiainducible factor 1:1||interaction:1||interferon receptor 1:1||interferon receptor 2:1||linkage disequilibrium:1||lipids:1||lipoprotein lipase:1||lipoproteins:1||magnetic resonance imaging:1||methylation:1||miRHunter:1||microRNA (miRNA):1||microsatellite instability:1||ovarian follicle:1||overweight/obesity:1||polymorphism:1||primary ovarian failure:1||ratio of control to case:1||retinitis pigmentosa:1||schizophrenia:1||sex:1||simulated data:1||single nucleotide polymorphism, haplotype:1||singlenucleotide polymorphism:1||smooth pursuit eye movement:1||statistical power:1||1000 Genomes Project:1||tuberculosis:1||ADPRT:1||ATF6B:1||Aggregation of lowfrequency variants:1||Aging:1||Albumin:1||Alternative Splicing:1||Alternative splicing:1||Alzheimer disease:1||Alzheimer’s disease:1||Association study:1||Blood pressure:1||Blood urea nitrogen (BUN):1||Brain volume:1||C5orf42:1||C6:1||Chronic hepatitis B virus:1||Chronic kidney disease (CKD):1||Combined computational method:1||Complement component 9:1||

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