S. Namgoong

发表

Replication of genome wide association studies on hepatocellular carcinoma susceptibility loci of STAT4 and HLA-DQ in a Korean population.

H. Shin, H. Cheong, Y. Kim, 2015, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

Exonic Variants Associated with Development of Aspirin Exacerbated Respiratory Diseases

H. Shin, Choon-Sik Park, H. Chang, 2014, PloS one.

A PHLDB1 variant associated with the nonfunctional pituitary adenoma

Se Hoon Kim, H. Shin, H. Cheong, 2019, Journal of Neuro-Oncology.

Comprehensive Variant Screening of the UGT Gene Family

H. Shin, H. Cheong, S. Han, 2013, Yonsei medical journal.

Asian-specific 3’UTR variant in CDKN2B associated with risk of pituitary adenoma

H. Shin, H. Cheong, Jong-Hee Chang, 2022, Molecular Biology Reports.

Association of VARS2‐SFTA2 polymorphisms with the risk of chronic hepatitis B in a Korean population

H. Shin, H. Cheong, Jung-Hwan Yoon, 2015, Liver international : official journal of the International Association for the Study of the Liver.

Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population

H. Shin, H. Cheong, Y. Kim, 2018, Liver international : official journal of the International Association for the Study of the Liver.

Identification of additional EHMT2 variant associated with the risk of chronic hepatitis B by GWAS follow-up study

H. Shin, H. Cheong, Y. Kim, 2017, Genes & Immunity.

A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population

H. Shin, H. Cheong, Y. Kim, 2020, BMC medical genetics.

A Non-Synonymous Variant of Complement Factor B Associated with Risk of Chronic Hepatitis B in a Korean Population

H. Shin, H. Cheong, Y. Kim, 2020 .

Association study of polymorphisms in interferon-γ receptor genes with the risk of pulmonary tuberculosis.

H. Shin, S. Uh, Choon-Sik Park, 2015, Molecular medicine reports.

Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population

H. Shin, H. Cheong, Jong-Hee Chang, 2018, PloS one.

Comparison of genetic variations of the SLCO1B1, SLCO1B3, and SLCO2B1 genes among five ethnic groups.

H. Shin, H. Cheong, M. Chung, 2015, Environmental toxicology and pharmacology.

Potential association between TSGA13 variants and risk of total colonic aganglionosis in Hirschsprung disease.

Hyun-Young Kim, Jeong-Meen Seo, Jeong-Hyun Kim, 2019, Gene.

Genome‐wide association study with the risk of schizophrenia in a Korean population

H. Shin, H. Cheong, Jaeuk Hwang, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Identification of novel OCT4 genetic variant associated with the risk of chronic hepatitis B in a Korean population

H. Shin, H. Cheong, B. Ju, 2017, Liver international : official journal of the International Association for the Study of the Liver.

Association Analysis of Melanocortin 3 Receptor Polymorphisms with the Risk of Pulmonary Tuberculosis

H. Shin, S. Uh, Choon-Sik Park, 2014, Lung.

Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population

H. Shin, H. Cheong, Choon-Sik Park, 2014, Genomics & informatics.

Association analysis of IL7R polymorphisms with inflammatory demyelinating diseases.

H. Shin, H. Cheong, H. Kim, 2014, Molecular medicine reports.

Identification of additional EHMT2 variant associated with the risk of chronic hepatitis B by GWAS follow-up study

H. Shin, H. Cheong, Y. Kim, 2017, Genes & Immunity.

Investigating the potential genetic association between RANBP9 polymorphisms and the risk of schizophrenia.

H. Shin, H. Cheong, Jaeuk Hwang, 2015, Molecular medicine reports.

Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases.

H. Shin, H. Cheong, Choon-Sik Park, 2017, Allergy and asthma proceedings.

Association analysis of PDE4B polymorphisms with schizophrenia and smooth pursuit eye movement abnormality in a Korean population.

H. Shin, H. Cheong, Jaeuk Hwang, 2015, General physiology and biophysics.

Genome‐wide association study with the risk of schizophrenia in a Korean population

H. Shin, H. Cheong, Jaeuk Hwang, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.