H. Cheong

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

A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease

H. Shin, H. Cheong, J. Sul, 2014, PloS one.

Screening of Dihydropyrimidine Dehydrogenase Genetic Variants by Direct Sequencing in Different Ethnic Groups

H. Shin, H. Cheong, S. Han, 2013, Journal of Korean medical science.

Polymorphisms in the leptin receptor (LEPR)—putative association with obesity and T2DM

H. Shin, H. Cheong, Jong-Young Lee, 2006, Journal of Human Genetics.

A PHLDB1 variant associated with the nonfunctional pituitary adenoma

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

A genome-wide association analysis of chromosomal aberrations and Hirschsprung disease.

H. Shin, H. Cheong, W. Park, 2016, Translational research : the journal of laboratory and clinical medicine.

TPX2 Induces Mitotic Survival via BCL2L1 Induction Through YAP1 Protein Stabilization in Human Embryonic Stem Cells

H. Shin, H. Cheong, S. Kim, 2021 .

Comprehensive Variant Screening of the UGT Gene Family

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

MYLK polymorphism associated with blood eosinophil level among asthmatic patients in a Korean population

H. Shin, S. Uh, H. Cheong, 2009, Molecules and cells.

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

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

Two independent variants of epidermal growth factor receptor associated with risk of glioma in a Korean population

H. Shin, H. Cheong, Jong-Hee Chang, 2022, Scientific Reports.

Association of RANBP1 haplotype with smooth pursuit eye movement abnormality

H. Shin, H. Cheong, Jaeuk Hwang, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-Wide and Follow-Up Studies Identify CEP68 Gene Variants Associated with Risk of Aspirin-Intolerant Asthma

H. Shin, S. Uh, H. Cheong, 2010, PloS one.

Growth hormone-releasing hormone (GHRH) polymorphisms associated with carcass traits of meat in Korean cattle

H. Shin, H. Cheong, T. Park, 2006, BMC Genetics.

A sequence variant on 17q21 is associated with age at onset and severity of asthma

D. Postma, I. Hall, D. Gudbjartsson, 2010, European Journal of Human Genetics.

TPX2 prompts mitotic survival via the induction of BCL2L1 through YAP1 protein stabilization in human embryonic stem cells

H. Shin, H. Cheong, S. Kim, 2023, Experimental & Molecular Medicine.

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.

Direct sequencing and comprehensive screening of genetic polymorphisms on CYP2 family genes (CYP2A6, CYP2B6, CYP2C8, and CYP2E1) in five ethnic populations

H. Shin, H. Cheong, Jeong-Hyun Kim, 2014, Archives of Pharmacal Research.

CXCR3 polymorphisms associated with risk of asthma.

H. Shin, S. Uh, H. Cheong, 2005, Biochemical and biophysical research communications.

Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.

H. Shin, H. Cheong, Jong-Young Lee, 2010, Ophthalmology.

Putative association of DNA methyltransferase 1 (DNMT1) polymorphisms with clearance of HBV infection.

H. Shin, H. Cheong, Y. Kim, 2009, BMB reports.

Cytidine deaminase polymorphisms and worse treatment response in normal karyotype AML

H. Shin, H. Cheong, Hyung-Lae Kim, 2015, Journal of Human Genetics.

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.

Lack of association of RAD51 genetic variations with hepatitis B virus clearance and occurrence of hepatocellular carcinoma in a Korean population

H. Shin, H. Cheong, Y. Kim, 2011, Journal of medical virology.

Leptin polymorphisms associated with carcass traits of meat in korean cattle

H. Shin, H. Cheong, Sung-Jong Oh, 2006 .

Association Analysis of SERPINB5 Polymorphisms with HBV Clearance and HCC Occurrence in a Korean Population

H. Shin, H. Cheong, Y. Kim, 2010 .

Titin-cap (TCAP) polymorphisms associated with marbling score of beef.

H. Cheong, H. D. Shin, I. Cheong, 2007, Meat science.

Association analysis of signal transducer and activator of transcription 4 (STAT4) polymorphisms with asthma

H. Shin, H. Cheong, Choon-Sik Park, 2005, Journal of Human Genetics.

Genome-wide methylation profiling of the bronchial mucosa of asthmatics: relationship to atopy

H. Shin, H. Cheong, Choon-Sik Park, 2013, BMC Medical Genetics.

Genetic variants in the HLA-G region are associated with Kawasaki disease.

Jong-Keuk Lee, Young Mi Hong, Mi-Jin Kang, 2008, Human immunology.

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 .

The genetic effect of copy number variations on the risk of alcoholism in a Korean population.

H. Shin, H. Cheong, M. Jung, 2012, Alcoholism, clinical and experimental research.

The Genetic Effect of Copy Number Variations on the Risk of Type 2 Diabetes in a Korean Population

H. Shin, H. Cheong, Jong-Young Lee, 2011, PloS one.

articlePositive Association between Aspirin-Intolerant Asthma and Genetic Polymorphisms of FSIP 1 : a Case-Case Study

H. Shin, S. Uh, H. Cheong, 2015 .

Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid.

H. Shin, S. Uh, H. Cheong, 2014, Clinica chimica acta; international journal of clinical chemistry.

Putative association between UBE2E2 polymorphisms and the risk of gestational diabetes mellitus

H. Shin, H. Cheong, Sung-Hoon Kim, 2013, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Potential Association Between ANXA4 Polymorphisms and Aspirin-exacerbated Respiratory Disease

H. Shin, S. Uh, H. Cheong, 2012, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Potential Association of DCBLD2 Polymorphisms with Fall Rates of FEV1 by Aspirin Provocation in Korean Asthmatics

H. Shin, S. Uh, H. Cheong, 2012, Journal of Korean medical science.

Possible Association of SLC22A2 Polymorphisms with Aspirin-Intolerant Asthma

H. Shin, S. Uh, H. Cheong, 2011, International Archives of Allergy and Immunology.

Lack of association between FOS polymorphisms and clearance of HBV infection as well as HCC occurrence

H. Shin, H. Cheong, Y. Kim, 2011, Genes & Genomics.

No association of TF gene polymorphisms with hepatitis B virus Clearance and hepatocellular carcinoma occurrence in a Korean population

H. Shin, H. Cheong, Y. Kim, 2011, Genes & Genomics.

Association analysis of UBE3C polymorphisms in Korean aspirin-intolerant asthmatic patients.

H. Shin, S. Uh, H. Cheong, 2010, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Positive Association between Aspirin-Intolerant Asthma and Genetic Polymorphisms of FSIP1: a Case-Case Study

H. Shin, S. Uh, H. Cheong, 2010, BMC pulmonary medicine.

Identification of DNA methylation markers for lineage commitment of in vitro hepatogenesis.

H. Shin, H. Cheong, Mirang Kim, 2011, Human molecular genetics.

Frequent Amplification of CENPF, GMNN and CDK13 Genes in Hepatocellular Carcinomas

H. Shin, H. Cheong, S. Chi, 2012, PloS one.

Genetic polymorphisms in the Rb-binding zinc finger gene RIZ and the risk of lung cancer.

H. Shin, H. Cheong, Hai-rim Shin, 2007, Carcinogenesis.

Identification of copy number variations and common deletion polymorphisms in cattle

H. Shin, H. Cheong, J. Bae, 2010, BMC Genomics.

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population.

H. Shin, H. Cheong, Sangsoo Kim, 2008, Biochemical and biophysical research communications.

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

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

Lack of Association of BIRC5 Polymorphisms with Clearance of HBV Infection and HCC Occurrence in a Korean Population

H. Shin, H. Cheong, Y. Kim, 2009 .

Association of common promoter polymorphisms of MCP1 with hepatitis B virus clearance

H. Shin, H. Cheong, Y. Kim, 2006, Experimental & Molecular Medicine.

Polymorphisms in interleukin 8 and its receptors (IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts

Young Hun Kim, Bermseok Oh, Kuchan Kimm, 2006, Journal of Human Genetics.

A single nucleotide polymorphism in CAPN1 associated with marbling score in Korean cattle

H. Shin, H. Cheong, J. Bae, 2008, BMC Genetics.

Highly Polymorphic Bovine Leptin Gene

H. Shin, H. Cheong, B. H. Cho, 2005 .

Development of discrimination SNP markers for Hanwoo (Korean native cattle).

H. Cheong, H. D. Shin, L. Kim, 2013, Meat science.

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.

Determination of DPYD Enzyme Activity in Korean Population

H. Shin, H. Cheong, Joong-Gon Shin, 2015, Therapeutic drug monitoring.

Genome-Wide Association Study of Ulcerative Colitis in Koreans Suggests Extensive Overlapping of Genetic Susceptibility With Caucasians

H. Shin, H. Cheong, D. Kang, 2013, Inflammatory bowel diseases.

Genetic associations of common deletion polymorphisms in families with Avellino corneal dystrophy.

H. Shin, H. Cheong, Jong-Young Lee, 2009, Biochemical and biophysical research communications.

Gene expression profile of necrotizing enterocolitis model in neonatal mice.

H. Shin, H. Cheong, Sung-Eun Jung, 2015, International journal of surgery.

Direct sequencing and comprehensive screening of genetic polymorphisms on CYP2 family genes (CYP2A6, CYP2B6, CYP2C8, and CYP2E1) in five ethnic populations

H. Shin, H. Cheong, Jeong-Hyun Kim, 2015, Archives of pharmacal research.

A Genome-Wide Association Study of Total Serum and Mite-Specific IgEs in Asthma Patients

Joon Seol Bae, Choon-Sik Park, H. Shin, 2013, PloS one.

Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality

H. Shin, H. Cheong, Chul-Soo Park, 2009, Journal of Human Genetics.

SPP1 polymorphisms associated with HBV clearance and HCC occurrence.

H. Shin, H. Cheong, Y. Kim, 2007, International journal of epidemiology.

Putative Association of ITGB1 Haplotype with the Clearance of HBV Infection

H. Shin, H. Cheong, Y. Kim, 2010 .

Prediction of cholesterol ratios within a Korean population

H. Shin, H. Cheong, Jin Sol Lee, 2018, Royal Society Open Science.

Association of APOE genotype with lipid profiles and type 2 diabetes mellitus in a Korean population

H. Shin, H. Cheong, Jung Yeon Seo, 2021, Genes & Genomics.

Effect of Diffuse Panbronchiolitis Critical Region 1 Polymorphisms on the Risk of Aspirin-Exacerbated Respiratory Disease in Korean Asthmatics

H. Shin, S. Uh, H. Cheong, 2012, Respiratory Care.

A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31–32 region and asthma

H. Shin, S. Uh, H. Cheong, 2010, Journal of Human Genetics.

A possible association of EMID2 polymorphisms with aspirin hypersensitivity in asthma

H. Shin, H. Cheong, Choon-Sik Park, 2010, Immunogenetics.

Genetic Analysis of Complement Component 9 (C9) Polymorphisms with Clearance of Hepatitis B Virus Infection

H. Shin, H. Cheong, Y. Kim, 2011, Digestive Diseases and Sciences.

HLA-DRA Polymorphisms associated with Risk of Nasal Polyposis in Asthmatic Patients

H. Shin, S. Uh, H. Cheong, 2012, American journal of rhinology & allergy.

Lack of Association between CD58 Genetic Variations and Aspirin-Exacerbated Respiratory Disease in a Korean Population

H. Shin, S. Uh, H. Cheong, 2011, The Journal of asthma : official journal of the Association for the Care of Asthma.

Association of IL-17RB gene polymorphism with asthma.

H. Shin, S. Uh, H. Cheong, 2009, Chest.

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

P. Sham, P. Tam, A. Chakravarti, 2016, Human molecular genetics.

TPX2 Amplification-Driven Aberrant Mitosis in Culture Adapted Human Embryonic Stem Cells with gain of 20q11.21

H. Shin, H. Cheong, Chang-Young Jang, 2021, Stem Cell Reviews and Reports.

Identification of Polymorphisms in CYP2E1 Gene and Association Analysis among Chronic HBV Patients

H. Shin, H. Cheong, Y. Kim, 2009 .

Genetic Association of PARP15 Polymorphisms with Clinical Outcome of Acute Myeloid Leukemia in a Korean Population.

H. Shin, H. Cheong, K. Ahn, 2016, Genetic testing and molecular biomarkers.

Epigenome-Wide Association Analysis of Differentially Methylated Signals in Blood Samples of Patients with Non-Small-Cell Lung Cancer

H. Shin, H. Cheong, W. Kim, 2019, Journal of clinical medicine.

Single nucleotide polymorphisms in fibroblast growth factor 23 gene, FGF23, are associated with prostate cancer risk

H. Cheong, J. Oh, S. Myung, 2014, BJU international.

Lack of Association between PRNP M129V Polymorphism and Multiple Sclerosis, Mild Cognitive Impairment, Alcoholism and Schizophrenia in a Korean Population

H. Shin, H. Cheong, H. Kim, 2010, Disease markers.

Common interleukin 10 polymorphism associated with decreased risk of tuberculosis

H. Shin, H. Cheong, B. Park, 2005, Experimental & Molecular Medicine.

Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication

H. Shin, H. Cheong, I. Choi, 2013, Human Genetics.

Lack of association of HLA-DRA polymorphisms with aspirin exacerbated respiratory disease in a Korean population

H. Shin, S. Uh, H. Cheong, 2011, Genes & Genomics.

Association analysis of G72/G30 polymorphisms with schizophrenia in the Korean population

H. Shin, H. Cheong, Chul-Soo Park, 2007, Schizophrenia Research.

Sotos syndrome associated with Hirschsprung’s disease: a new case and exome-sequencing analysis

H. Shin, H. Cheong, Jeong-Hyun Kim, 2017, Pediatric Research.

Association of Interleukin-18 Gene Polymorphisms with Hepatitis B Virus Clearance

H. Shin, H. Cheong, B. Oh, 2010, Digestive Diseases and Sciences.

WDR46 is a Genetic Risk Factor for Aspirin-Exacerbated Respiratory Disease in a Korean Population

H. Shin, S. Uh, H. Cheong, 2012, Allergy, asthma & immunology research.

A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.

H. Shin, H. Cheong, Y. Kim, 2013, Human molecular genetics.

HDAC10 promoter polymorphism associated with development of HCC among chronic HBV patients.

H. Shin, H. Cheong, Choon-Sik Park, 2007, Biochemical and biophysical research communications.

Polymorphisms of the Reg1α Gene and Early Onset Type 2 Diabetes in the Korean Population

H. Shin, H. Cheong, Jong-Young Lee, 2010, Korean diabetes journal.

SLC29A1 (ENT1) polymorphisms and outcome of complete remission in acute myeloid leukemia

Sung-Soo Yoon, Youngil Koh, H. Shin, 2016, Cancer Chemotherapy and Pharmacology.

Association analysis of C6 genetic variations and aspirin hypersensitivity in Korean asthmatic patients.

H. Shin, S. Uh, H. Cheong, 2011, Human immunology.

A Functional SNP of the Interleukin-18 Gene Is Associated with the Presence of Hepatocellular Carcinoma in Hepatitis B Virus-Infected Patients

H. Shin, H. Cheong, B. Oh, 2009, Digestive Diseases and Sciences.

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 genetic polymorphisms in FABP3 and FABP4 and putative association with back fat thickness in Korean native cattle.

H. Shin, H. Cheong, Seoae Cho, 2008, BMB reports.

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.

Screening for 392 polymorphisms in 141 pharmacogenes.

H. Shin, H. Cheong, M. Chung, 2014, Biomedical reports.

Association study of genetic variations in microRNAs with the risk of hepatitis B-related liver diseases.

H. Shin, H. Cheong, Y. Kim, 2012, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

MCM7 polymorphisms associated with the AML relapse and overall survival

H. Shin, H. Cheong, K. Ahn, 2016, Annals of Hematology.

Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population

H. Shin, H. Cheong, Choon-Sik Park, 2013, Human Genetics.

Association between HTR7 genetic polymorphisms and alcohol dependence, using the alcohol use disorders identification test (AUDIT).

H. Shin, H. Cheong, J. Bae, 2014, Alcoholism, clinical and experimental research.

Association of SLC6A12 variants with aspirin‐intolerant asthma in a Korean population

H. Shin, S. Uh, H. Cheong, 2010, Annals of human genetics.

Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication

H. Shin, H. Cheong, I. Choi, 2013, Human Genetics.

Genetic association analysis of CIITA variations with nasal polyp pathogenesis in asthmatic patients.

H. Shin, S. Uh, H. Cheong, 2013, Molecular medicine reports.

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

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

ADFP promoter polymorphism associated with marbling score in Korean cattle.

H. Shin, H. Cheong, J. Bae, 2009, BMB reports.

Association Analysis between Insulin-like Growth Factor Binding Protein 3 (IGFBP3) Polymorphisms and Carcass Traits in Cattle

H. Shin, H. Cheong, I. Cheong, 2008 .

Identification of variants in cyclin D1 (CCND1) and B-Cell CLL/lymphoma 2 (BCL2)

H. Shin, H. Cheong, Yong-Sun Kim, 2004, Journal of Human Genetics.

Association of the variants in AGT gene with modified drug response in Korean aspirin-intolerant asthma patients.

H. Shin, H. Cheong, Choon-Sik Park, 2011, Pulmonary pharmacology & therapeutics.

RNA-Seq for Gene Expression Profiling of Human Necrotizing Enterocolitis: a Pilot Study

H. Shin, H. Cheong, Sung-Eun Jung, 2017, Journal of Korean medical science.

No associations of polymorphisms in ADPRT with hepatitis B virus clearance and hepatocellular carcinoma occurrence in a Korean population

H. Shin, H. Cheong, Y. Kim, 2011, Hepatology research : the official journal of the Japan Society of Hepatology.

Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients

H. Cheong, S. Debette, W. Ryu, 2022, Annals of neurology.

Gene profile of fibroblasts identify relation of CCL8 with idiopathic pulmonary fibrosis

H. Shin, S. Uh, H. Cheong, 2017, Respiratory Research.

Polymorphisms in FOXO Gene Family and Association Analysis with BMI

H. Shin, H. Cheong, Jung Hye Kim, 2006, Obesity.

Genetic diversity and divergence among Korean cattle breeds assessed using a BovineHD single-nucleotide polymorphism chip

H. Shin, H. Cheong, C. Cho, 2018, Asian-Australasian journal of animal sciences.

Putative association of GPC5 polymorphism with the risk of inflammatory demyelinating diseases

H. Shin, H. Cheong, H. Kim, 2013, Journal of the Neurological Sciences.

KIF3A, a Cilia Structural Gene on Chromosome 5q31, and Its Polymorphisms Show an Association with Aspirin Hypersensitivity in Asthma

H. Shin, S. Uh, H. Cheong, 2011, Journal of Clinical Immunology.

Difference of copy number variation in blood of patients with lung cancer

H. Cheong, W. Kim, Seon-Sook Han, 2020, The International journal of biological markers.

CD55 polymorphisms and risk of aspirin‑exacerbated respiratory disease.

H. Shin, S. Uh, H. Cheong, 2012, Molecular medicine reports.

CD 55 polymorphisms and risk of aspirin ‐ exacerbated respiratory disease

H. Shin, H. Cheong, Choon-Sik Park, 2022 .

Identification of genetic polymorphisms in bovine mitochondrial deoxyribonucleic acid.

H. Cheong, H. D. Shin, J. Bae, 2010, Journal of animal science.

The association of 5-alpha reductase type 2 (SRD5A2) gene polymorphisms with prostate cancer in a Korean population

H. Cheong, S. Myung, H. J. Kim, 2015, Korean journal of urology.

Discovery of donor genotype associated with long-term survival of patients with hematopoietic stem cell transplantation in refractory acute myeloid leukemia

Ju Han Kim, H. Cheong, Hyung-Lae Kim, 2018, Leukemia & lymphoma.

Association analysis of IL7R polymorphisms with inflammatory demyelinating diseases.

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

Lack of association between CD226 genetic variants and inflammatory demyelinating diseases in Korean population.

H. Shin, H. Cheong, H. Kim, 2013, Neuro endocrinology letters.

Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica

H. Shin, H. Cheong, Hyun-Young Park, 2010, Neurobiology of Disease.

DCBLD2 Gene Variations Correlate with Nasal Polyposis in Korean Asthma Patients

H. Shin, S. Uh, H. Cheong, 2012, Lung.

Association of CACNG6 polymorphisms with aspirin-intolerance asthmatics in a Korean population

H. Shin, S. Uh, H. Cheong, 2010, BMC Medical Genetics.

Effects of genetic polymorphisms of UCP2 and UCP3 on very low calorie diet-induced body fat reduction in Korean female subjects.

H. Shin, H. Cheong, Y. Yoon, 2007, Biochemical and biophysical research communications.

BMI prediction within a Korean population

H. Shin, H. Cheong, Jin Sol Lee, 2017, PeerJ.

Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women

Jong Yong Lee, H. Shin, H. Cheong, 2006, Journal of Human Genetics.

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.

Genetic analysis of primary open-angle glaucoma-related risk alleles in a Korean population: the GLAU-GENDISK study

Dong Myung Kim, H. Cheong, K. Park, 2020, British Journal of Ophthalmology.

Genetic association analysis of ERBB4 polymorphisms with the risk of schizophrenia and SPEM abnormality in a Korean population

H. Shin, H. Cheong, Chul-Soo Park, 2012, Brain Research.

Potential association between ITPKC genetic variations and Hirschsprung disease

H. Shin, H. Cheong, Hyun-Young Kim, 2017, Molecular Biology Reports.

Screening of Genetic Polymorphisms of CYP3A4 and CYP3A5 Genes

H. Shin, H. Cheong, S. Han, 2013, The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology.

Screening of Genetic Polymorphisms of CYP 3 A 4 and CYP 3 A 5 Genes

H. Shin, H. Cheong, S. Han, 2013 .

Expression efficiency of NAT2 haplotypes in a Korean population.

H. Shin, H. Cheong, Jin Sol Lee, 2016, Genes & genetic systems.

Genome-wide detection of allelic gene expression in hepatocellular carcinoma cells using a human exome SNP chip.

H. Cheong, Jong-Keuk Lee, Yon Mi Park, 2014, Gene.

The association between KL polymorphism and prostate cancer risk in Korean patients

H. Cheong, S. Myung, H. J. Kim, 2014, Molecular Biology Reports.

NT5C3 polymorphisms and outcome of first induction chemotherapy in acute myeloid leukemia

H. Shin, H. Cheong, K. Ahn, 2014, Pharmacogenetics and genomics.

Lack of association between AQP4 polymorphisms and risk of inflammatory demyelinating disease in a Korean population.

H. Shin, H. Cheong, H. Kim, 2014, Gene.

KIF1B polymorphisms associated with the risk of inflammatory demyelinating disease in Korean population

H. Shin, H. Cheong, H. Kim, 2014, Genes & Genomics.

Global DNA Methylation Pattern of Fibroblasts in Idiopathic Pulmonary Fibrosis.

H. Shin, H. Cheong, Choon-Sik Park, 2019, DNA and cell biology.

Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study

Dong Myung Kim, H. Cheong, T. Nakazawa, 2020, Scientific Reports.

Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus

H. Shin, H. Cheong, Sung-Hoon Kim, 2011, BMC Medical Genetics.

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

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

Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage

Ituro Inoue, Joon Seol Bae, H. Shin, 2010, Journal of Human Genetics.

Genome-Wide Profiling of Structural Genomic Variations in Korean HapMap Individuals

H. Shin, H. Cheong, J. Bae, 2010, PloS one.

Direct sequencing for comprehensive screening of LDLR genetic polymorphisms among five ethnic populations

H. Shin, H. Cheong, Jeong-Hyun Kim, 2015, Genes & Genomics.

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.

TREX1 polymorphisms associated with autoantibodies in patients with systemic lupus erythematosus

H. Shin, H. Cheong, S. Bae, 2008, Rheumatology International.

Possible role of EMID2 on nasal polyps pathogenesis in Korean asthma patients

H. Shin, S. Uh, H. Cheong, 2012, BMC Medical Genetics.

Association analysis of monocyte chemotactic protein-3 (MCP3) polymorphisms with asthmatic phenotypes.

H. Shin, S. Uh, H. Cheong, 2005, Journal of biochemistry and molecular biology.

Genetic analysis between FGD6 and aspirin exacerbated respiratory disease in a Korean population

H. Shin, S. Uh, H. Cheong, 2011, Genes & Genomics.

Genetic polymorphisms in the transforming growth factor beta‐induced gene associated with BMI

Y. J. Kim, H. Shin, H. Cheong, 2005, Human mutation.

Screening of genetic variations of SLC15A2, SLC22A1, SLC22A2 and SLC22A6 genes

H. Shin, H. Cheong, J. Bae, 2011, Journal of Human Genetics.

Genetic variations in KIFC1 and the risk of aspirin exacerbated respiratory disease in a Korean population: an association analysis

H. Shin, S. Uh, H. Cheong, 2012, Molecular Biology Reports.

A possible association between ZNRD1 and aspirin-induced airway bronchoconstriction in a Korean population.

H. Shin, H. Cheong, Choon-Sik Park, 2012, Journal of investigational allergology & clinical immunology.

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.

Functional Study of Haplotypes in UGT1A1 Promoter to Find a Novel Genetic Variant Leading to Reduced Gene Expression

H. Shin, H. Cheong, M. Chung, 2015, Therapeutic drug monitoring.

Lack of association between IRAK2 genetic variants and aspirin exacerbated respiratory disease

H. Shin, H. Cheong, Choon-Sik Park, 2013, Genes & Genomics.

Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population

H. Shin, H. Cheong, Choon-Sik Park, 2012, Human Genetics.

Genetic variations in KIFC1 and the risk of aspirin exacerbated respiratory disease in a Korean population: an association analysis

H. Shin, S. Uh, H. Cheong, 2011, Molecular Biology Reports.

CCND2 polymorphisms associated with clearance of HBV Infection

H. Shin, H. Cheong, Y. Kim, 2010, Journal of Human Genetics.

The association between KL polymorphism and prostate cancer risk in Korean patients

H. Cheong, S. Myung, H. J. Kim, 2014, Molecular Biology Reports.