H. Shin

H. Shin, Shin-Yoon Kim, E. Park, 2005, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

TPX2 Amplification-Driven Aberrant Mitosis in Long-Term Cultured Human Embryonic Stem Cells

H. Shin, H. Cheong, Chang-Young Jang, 2021, bioRxiv.

Meta-analysis of six genes (BDNF, DRD1, DRD3, DRD4, GRIN2B and MAOA) involved in neuroplasticity and the risk for alcohol dependence.

H. Shin, D. Forero, D. Kim, 2015, Drug and alcohol dependence.

TGFBR3 Polymorphisms and Its Haplotypes Associated with Chronic Hepatitis B Virus Infection and Age of Hepatocellular Carcinoma Occurrence

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

CD58 polymorphisms associated with the risk of neuromyelitis optica in a Korean population

H. Shin, H. Kim, J. Bae, 2014, BMC Neurology.

High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci.

P. Gregersen, Y. Okada, S. Eyre, 2015, Annals of the rheumatic diseases.

Brain-metastatic triple-negative breast cancer cells regain growth ability by altering gene expression patterns.

D. Noh, H. Shin, S. Paek, 2013, Cancer genomics & proteomics.

Association between Bone Mineral Density and LDL Receptor-Related Protein 5 Gene Polymorphisms in Young Korean Men

H. Shin, Shin-Yoon Kim, G. Kim, 2004, Journal of Korean medical science.

Functional polymorphism in aldehyde dehydrogenase-2 gene associated with risk of tuberculosis

H. Shin, H. Cheong, Choon-Sik Park, 2014, BMC Medical Genetics.

Common MCL1 polymorphisms associated with risk of tuberculosis.

H. Shin, H. Cheong, B. Park, 2008, BMB reports.

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

H. Shin, S. Bang, Hye-Soon Lee, 2013, Arthritis and rheumatism.

Different genetic effect of PXK on systemic lupus erythematosus in the Korean population

H. Shin, S. Bang, Hye-Soon Lee, 2010, Rheumatology International.

Different Genetic Effects of Interferon Regulatory Factor 5 (IRF5) Polymorphisms on Systemic Lupus Erythematosus in a Korean Population

H. Shin, S. Bae, Soo Ok Lee, 2008, The Journal of Rheumatology.

Replication of the genetic effects of IFN regulatory factor 5 (IRF5) on systemic lupus erythematosus in a Korean population

H. Shin, S. Bae, Soo Ok Lee, 2007, Arthritis research & therapy.

SLC12A3 (solute carrier family 12 member [sodium/chloride] 3) polymorphisms are associated with end-stage renal disease in diabetic nephropathy.

H. Shin, C. Ahn, K. Park, 2006, Diabetes.

Association analysis of interleukin 5 receptor alpha subunit (IL5RA) polymorphisms and asthma

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

Genome-wide DNA methylation profiles of maternal peripheral blood and placentas: potential risk factors for preeclampsia and validation of GRK5

H. Shin, H. Cheong, Jeong-Hyun Kim, 2017, Genes & Genomics.

Cox-2 and IL-10 Polymorphisms and Association with Squamous Cell Carcinoma of The Head and Neck in a Korean Sample

H. Shin, Seung Hwan Lee, C. Park, 2010, Journal of Korean medical science.

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.

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

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

Exonic Variants Associated with Development of Aspirin Exacerbated Respiratory Diseases

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

Selective Elimination of Culture-Adapted Human Embryonic Stem Cells with BH3 Mimetics

H. Shin, S. Moon, Wankyu Kim, 2018, Stem cell reports.

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.

Association analysis of ILVBL gene polymorphisms with aspirin-exacerbated respiratory disease in asthma

H. Shin, Choon-Sik Park, H. Chang, 2017, BMC Pulmonary Medicine.

Effects of UCP2 and UCP3 Variants on the Manifestation of Overweight in Korean Children

H. Shin, J. Kang, J. Song, 2009, Obesity.

A Single Nucleotide Polymorphism on the Promoter of eotaxin1 Associates with Its mRNA Expression and Asthma Phenotypes

H. Shin, S. Uh, Choon-Sik Park, 2005 .

Association between Genetic Polymorphisms in Hepatocyte Nuclear Factor 4α and Type 2 Diabetes in Koreans

H. Shin, H. Choi, S. Kwak, 2006 .

Association of KCNQ1 polymorphisms with the gestational diabetes mellitus in Korean women.

H. Shin, Sung-Hoon Kim, Sunmin Park, 2010, The Journal of clinical endocrinology and metabolism.

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.

The effects of uncoupling protein 3 haplotypes on obesity phenotypes and very low-energy diet-induced changes among overweight Korean female subjects.

H. Shin, Y. Yoon, Kil-Soo Kim, 2006, Metabolism: clinical and experimental.

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.

Genetic effect of CysLTR2 polymorphisms on its mRNA synthesis and stabilization

H. Shin, S. Uh, Choon-Sik Park, 2009, BMC Medical Genetics.

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

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

Lack of association of GPRA (G protein-coupled receptor for asthma susceptibility) haplotypes with high serum IgE or asthma in a Korean population.

H. Shin, Choon-Sik Park, K. Park, 2004, The Journal of allergy and clinical immunology.

Comprehensive Variant Screening of the UGT Gene Family

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

Association of PTGER gene family polymorphisms with aspirin intolerant asthma in Korean asthmatics.

H. Shin, S. Uh, Choon-Sik Park, 2010, BMB reports.

Association between a TGFbeta1 promoter polymorphism and rhinosinusitis in aspirin-intolerant asthmatic patients.

H. Shin, Choon-Sik Park, J. Holloway, 2007, Respiratory medicine.

Association analysis of cysteinyl-leukotriene receptor 2 (CYSLTR2) polymorphisms with aspirin intolerance in asthmatics

H. Shin, Choon-Sik Park, Hae‐Sim Park, 2005, Pharmacogenetics and genomics.

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

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

Association of TNF-alpha promoter polymorphisms with the clearance of hepatitis B virus infection.

H. Shin, Jung-Hwan Yoon, Y. Kim, 2003, Human molecular genetics.

Highly polymorphic human CYP4A11 gene

H. Shin, B. H. Cho, B. Park, 2005, Journal of Human Genetics.

2-1 Genetic Effects on Urinary 1 -Hydroxypyrene Levels in a

H. Shin, T. Kawamoto, H. Kim, 2003 .

Genetic polymorphisms in peroxisome proliferator-activated receptor delta associated with obesity.

H. Shin, K. Park, Y. Cho, 2004, Diabetes.

Associations between TMEM196 polymorphisms and NSAID-exacerbated respiratory disease in asthma

H. Shin, Choon-Sik Park, Jong-Sook Park, 2019, Pharmacogenetics and genomics.

Identification of novel SNPs in the interleukin 6 receptor gene (IL6R)

Jun Yeun Kim, H. Shin, J. Jung, 2003, Human mutation.

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

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

Identification of Novel SNPs in Bovine Insulin-like Growth Factor Binding Protein-3 (IGFBP3) Gene

Jun Yeun Kim, H. Shin, Sung-Jong Oh, 2005 .

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.

A highly sensitive and specific genetic marker to diagnose aspirin-exacerbated respiratory disease using a genome-wide association study.

H. Shin, S. Uh, Choon-Sik Park, 2012, DNA and cell biology.

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.

Genetic association analysis of CNR1 and CNR2 polymorphisms with schizophrenia in a Korean population

H. Shin, Jaeuk Hwang, Chul-Soo Park, 2014, Psychiatric Genetics.

Interleukin 3 (IL3) polymorphisms associated with decreased risk of asthma and atopy

H. Shin, S. Uh, Choon-Sik Park, 2004, Journal of Human Genetics.

Association analysis of novel TBX21 variants with asthma phenotypes

H. Shin, Choon-Sik Park, S. Hong, 2003, Human mutation.

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.

mRNA Expression and Asthma Phenotypes Promoter of eotaxin1 Associates with Its A Single Nucleotide Polymorphism on the

H. Shin, S. Uh, Choon-Sik Park, 2013 .

Association of eotaxin-2 gene polymorphisms with plasma eotaxin-2 concentration

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

A Single Nucleotide Polymorphism on the Promoter of eotaxin1 Associates with Its mRNA Expression and Asthma Phenotypes1

H. Shin, S. Uh, Choon-Sik Park, 2005, The Journal of Immunology.

Expression and Asthma Phenotypes Associates with Its eotaxin 1 Promoter of A Single Nucleotide Polymorphism

H. Shin, S. Uh, Choon-Sik Park, 2005 .

Association of Eotaxin gene family with asthma and serum total IgE.

H. Shin, Choon-Sik Park, J. Jung, 2003, Human molecular genetics.

Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes

H. Ostrer, D. Goldstein, X. Estivill, 2007 .

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.

Association analysis of RGS7BP gene polymorphisms with aspirin intolerance in asthmatic patients.

H. Shin, S. Uh, Choon-Sik Park, 2011, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Polymorphisms near Interleukin 28B Gene Are Not Associated with Hepatitis B Virus Clearance, Hepatitis B e Antigen Clearance and Hepatocellular Carcinoma Occurrence

H. Shin, Y. Kim, Jeong‐Hoon Lee, 2013, Intervirology.

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

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

Genetic Association of CHRNB3 and CHRNA6 Gene Polymorphisms with Nicotine Dependence Syndrome Scale in Korean Population

H. Shin, Min Kwon, D. Kim, 2014, Psychiatry investigation.

Cytidine deaminase polymorphisms and worse treatment response in normal karyotype AML

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

Association of Polymorphism in Pri-microRNAs-371-372-373 with the Occurrence of Hepatocellular Carcinoma in Hepatitis B Virus Infected Patients

H. Shin, Y. Kim, Jeong‐Hoon Lee, 2012, PloS one.

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.

Interleukin 10 haplotype associated with increased risk of hepatocellular carcinoma.

Ji Hyun Jung, H. Shin, J. Jung, 2003, Human molecular genetics.

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 .

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.

PRMT8 Controls the Pluripotency and Mesodermal Fate of Human Embryonic Stem Cells By Enhancing the PI3K/AKT/SOX2 Axis

H. Shin, Su-Jae Lee, S. Moon, 2017, Stem cells.

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

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

Association analysis of peroxisome proliferator-activated receptors gamma gene polymorphisms with asprin hypersensitivity in asthmatics

H. Shin, S. Uh, Choon-Sik Park, 2009, Allergy, asthma & immunology research.

Association of peroxisome proliferator-activated receptor-gamma gene polymorphisms with the development of asthma.

H. Shin, Choon-Sik Park, Ji-yeon Lee, 2009, Respiratory medicine.

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

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

Targeted Next-Generation Sequencing at Copy-Number Breakpoints for Personalized Analysis of Rearranged Ends in Solid Tumors

H. Shin, Jong-Yeon Shin, Seong-Yeol Park, 2014, PloS one.

Microphthalmia-associated transcription factor polymorphisms and association with bone mineral density of the proximal femur in postmenopausal women.

Jong Yong Lee, H. Shin, B. Oh, 2007, Molecules and cells.

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 TP53 polymorphisms with lung cancer in a Korean population

H. Shin, Hae-Yun Jung, Jun Suk Kim, 2008, Journal of Human Genetics.

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.

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.

Single nucleotide polymorphisms in bone turnover-related genes in Koreans: ethnic differences in linkage disequilibrium and haplotype

H. Shin, Jong-Young Lee, B. Oh, 2007, BMC Medical Genetics.

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.

Potential Association of DDR1 Genetic Variant with FEV1 Decline by Aspirin Provocation in Asthmatics

H. Shin, S. Uh, Choon-Sik Park, 2012, The Journal of asthma : official journal of the Association for the Care of Asthma.

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.

Putative association of SMAPIL polymorphisms with risk of aspirin intolerance in asthmatics

H. Shin, S. Uh, Choon-Sik Park, 2010, The Journal of asthma : official journal of the Association for the Care of Asthma.

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.

Sequence variants of toll-like receptor 4 (TLR4) and the risk of prostate cancer in Korean men

H. Shin, Wun-Jae Kim, S. Myung, 2012, World Journal of Urology.

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.

Identification of novel variants in transforming growth factor‐beta 1 (TGFB1) gene and association analysis with bone mineral density

H. Shin, I. Han, B. Park, 2003, Human mutation.

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 .

TNFR1 promoter -329G/T polymorphism results in allele-specific repression of TNFR1 expression.

H. Shin, Y. S. Kim, B. Oh, 2008, Biochemical and biophysical research communications.

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 .

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.

Association of Polymorphism in MicroRNA 604 with Susceptibility to Persistent Hepatitis B Virus Infection and Development of Hepatocellular Carcinoma

H. Shin, Y. Kim, J. Cheong, 2014, Journal of Korean medical science.

A Single Nucleotide Polymorphism within the Acetyl-Coenzyme A Carboxylase Beta Gene Is Associated with Proteinuria in Patients with Type 2 Diabetes

T. Hansen, O. Pedersen, Yusuke Nakamura, 2010, PLoS genetics.

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.

Genetic Effects of FTO and MC4R Polymorphisms on Body Mass in Constitutional Types

H. Shin, Imhoi Koo, S. Choi, 2011, Evidence-based complementary and alternative medicine : eCAM.

Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci.

Bok-Ghee Han, Jan Freudenberg, Young Mo Kang, 2011, Arthritis and rheumatism.

Gene expression profile of necrotizing enterocolitis model in neonatal mice.

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

Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population

H. Shin, Chul-Soo Park, B. Kim, 2011, Psychiatry Research.

Implication of Genetic Variants Near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in Type 2 Diabetes and Obesity in 6,719 Asians

H. Shin, M. Ng, J. Chan, 2008, Diabetes.

Association of tumor necrosis factor polymorphisms with asthma and serum total IgE.

H. Shin, Choon-Sik Park, J. Jung, 2004, Human molecular genetics.

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.

Association analysis of NOX5 polymorphisms with Hirschsprung disease.

H. Shin, Hyun-Young Kim, K. Park, 2019, Journal of pediatric surgery.

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 .

Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans.

Cue Hyunkyu Lee, H. Shin, Jianjun Liu, 2016, Gastroenterology.

Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans

H. Shin, D. Kang, Jianjun Liu, 2016, Inflammatory Bowel Diseases.

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.

X Chromosome-wide Association Study Identifies a Susceptibility Locus for Inflammatory Bowel Disease in Koreans

H. Shin, B. Han, B. Ye, 2017, Journal of Crohn's & colitis.

Immunochip Analysis Identification of 6 Additional Susceptibility Loci for Crohn's Disease in Koreans

H. Shin, K. Taylor, J. Rotter, 2015, Inflammatory bowel diseases.

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.

A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B

Yusuke Nakamura, Tatsuhiko Tsunoda, Philippe Froguel, 2010, Nature Genetics.

Generation of Cloned Transgenic Cats Expressing Red Fluorescence Protein1

Bon Chul Koo, H. Shin, I. Kong, 2008, Biology of reproduction.

Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease

H. Shin, Hyun-Young Kim, K. Park, 2016, Journal of pediatric gastroenterology and nutrition.

IGF2 polymorphisms are associated with hepatitis B virus clearance and hepatocellular carcinoma.

H. Shin, Y. Kim, C. Kim, 2006, Biochemical and biophysical research communications.

Identification of single nucleotide polymorphisms in the tumor necrosis factor (TNF) and TNF receptor superfamily in the Korean population.

Bermseok Oh, Hung-Tae Kim, Kuchan Kimm, 2004, Human immunology.

Lack of association between Poly(ADP-ribose) polymerase (PARP) polymorphisms and rheumatoid arthritis in a Korean population

H. Shin, S. Bang, S. Bae, 2010, Rheumatology International.

Putative Role of Functional Interferon Regulatory Factor 5 (IRF5) Polymorphism in Rheumatoid Arthritis in a Korean Population

H. Shin, S. Bae, J. Bae, 2008, The Journal of Rheumatology.

Putative Association of Fas and FasL Gene Polymorphisms with Clinical Outcomes of Hepatitis B Virus Infection

H. Shin, Y. Kim, Y. Jung, 2007, Intervirology.

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 interleukin-6 promoter variant with bone mineral density in pre-menopausal women

H. Shin, Jeong-Sun Seo, J. Jung, 2003, Journal of Human Genetics.

Association of IL-17RB gene polymorphism with asthma.

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

Association of Genetic Variants of NLRP4 with Exacerbation of Asthma: The Effect of Smoking.

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

Association of single nucleotide polymorphisms on Interleukin 17 receptor A (IL17RA) gene with aspirin hypersensitivity in asthmatics.

H. Shin, S. Uh, Choon-Sik Park, 2013, Human immunology.

Ethnic specificity of lupus-associated loci identified in a genome-wide association study in Korean women

H. Shin, S. Bang, Hye-Soon Lee, 2013, Annals of the rheumatic diseases.

Lack of association between interleukin 23 receptor gene polymorphisms and rheumatoid arthritis susceptibility

H. Shin, S. Bae, J. Bae, 2009, Rheumatology International.

In vitro production and initiation of pregnancies in inter-genus nuclear transfer embryos derived from leopard cat (Prionailurus bengalensis) nuclei fused with domestic cat (Felis silverstris catus) enucleated oocytes.

H. Shin, Hyosang Lee, I. Kong, 2006, Theriogenology.

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 .

Polymorphisms in fatty acid-binding protein-3 (FABP3) - putative association with type 2 diabetes mellitus.

H. Shin, K. Park, Y. Cho, 2003, Human mutation.

Comparison of commonly used ICR stocks and the characterization of Korl:ICR

H. Shin, M. Chung, Mi Gyeong Kim, 2017, Laboratory animal research.

Association analyses of DNA methyltransferase-1 (DNMT1) polymorphisms with systemic lupus erythematosus

H. Shin, S. Bae, Yong-Wook Park, 2004, Journal of Human Genetics.

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.

Effect of serum starvation on the efficiency of nuclear transfer using odd-eyed white cat fibroblasts.

H. Shin, I. Kong, Nam-Hyung Kim, 2007, Theriogenology.

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.

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.

ADH Cluster Genes, Genome-Wide Association Studies, and Alcohol Dependence

H. Shin, B. Park, 2016 .

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.

Common DNase I polymorphism associated with autoantibody production among systemic lupus erythematosus patients.

H. Shin, Hye-Soon Lee, S. Bae, 2004, Human molecular genetics.

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

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

Association Analysis between (AAT)n Repeats in the Cannabinoid Receptor 1 Gene and Schizophrenia in a Korean Population

H. Shin, Jaeuk Hwang, J. Bae, 2014 .

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.

Independent Association of Tumor Necrosis Factor Polymorphism with Type 1 Diabetes Susceptibility

H. Shin, Yongsoo Park, Seiwon Yang, 2008, Annals of the New York Academy of Sciences.

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.

XPD Polymorphisms and Risk of Squamous Cell Carcinoma of the Head and Neck in a Korean Sample

H. Shin, Seung Hwan Lee, C. Park, 2010, Clinical and experimental otorhinolaryngology.

Association of DNA repair gene XRCC1 polymorphisms with head and neck cancer in Korean population

H. Shin, H. Lee, C. Park, 2004, International journal of cancer.

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.

Methionine synthase reductase polymorphisms are associated with serum osteocalcin levels in postmenopausal women

H. Shin, J. Hong, Shin-Yoon Kim, 2006, Experimental & Molecular Medicine.

5' UTR polymorphism of dopamine receptor D1 (DRD1) associated with severity and temperament of alcoholism.

H. Shin, D. Kim, Y. Cheon, 2007, Biochemical and biophysical research communications.

Screening for 392 polymorphisms in 141 pharmacogenes.

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

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

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

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.

Association analysis of member RAS oncogene family gene polymorphisms with aspirin intolerance in asthmatic patients.

H. Shin, Choon-Sik Park, Jong-Sook Park, 2014, DNA and cell biology.

MCM7 polymorphisms associated with the AML relapse and overall survival

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

Association of polymorphism in MicroRNA 219‐1 with clearance of hepatitis B virus infection

H. Shin, Y. Kim, J. Cheong, 2013, Journal of medical virology.

H. Shin, Choon-Sik Park, Hae‐Sim Park, 2004, Human Genetics.

Association of thromboxane A2 receptor (TBXA2R) with atopy and asthma.

H. Shin, Choon-Sik Park, J. Jung, 2003, The Journal of allergy and clinical immunology.

Association Analysis Between FILIP1 Polymorphisms and Aspirin Hypersensitivity in Korean Asthmatics

H. Shin, S. Uh, Choon-Sik Park, 2012, Allergy, asthma & immunology research.

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

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

Contribution of the OBSCN nonsynonymous variants to aspirin exacerbated respiratory disease susceptibility in Korean population.

H. Shin, S. Uh, Choon-Sik Park, 2012, DNA and cell biology.

Association analysis of formyl peptide receptor 2 (FPR2) polymorphisms and Aspirin exacerbated respiratory diseases

H. Shin, S. Uh, Choon-Sik Park, 2012, Journal of Human Genetics.

Association of FANCC polymorphisms with FEV1 decline in aspirin exacerbated respiratory disease

H. Shin, S. Uh, Choon-Sik Park, 2012, Molecular Biology Reports.

Association analysis of thromboxane A synthase 1 gene polymorphisms with aspirin intolerance in asthmatic patients.

Se-Min Park, Jong-Sook Park, Choon-Sik Park, 2011, Pharmacogenomics.

Association of polymorphisms in thromboxane A2 receptor and thromboxane A synthase 1 with cerebral infarction in a Korean population.

H. Shin, Choon-Sik Park, H. Chang, 2009, BMB reports.

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 of genetic polymorphisms in CD40 with susceptibility to SLE in the Korean population.

H. Shin, S. Bae, Y. Joo, 2013, Rheumatology.

[Tumor necrosis factor-alpha and interleukin-10 gene polymorphisms in Korean patients with inflammatory bowel disease].

Ji Won Kim, H. Shin, H. Jung, 2003, The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi.

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 N-acetyl transferase-2 polymorphisms with aspirin intolerance among asthmatics.

H. Shin, S. Uh, Choon-Sik Park, 2010, Pharmacogenomics.

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 .

MCP-1 and RANTES Polymorphisms in Korean Diabetic End-Stage Renal Disease

H. Shin, C. Ahn, K. Park, 2007, Journal of Korean medical science.

Association of interleukin 10 haplotype with low bone mineral density in Korean postmenopausal women.

H. Shin, I. Han, Joon-Shik Shin, 2004, Journal of biochemistry and molecular biology.

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.

Genetic Polymorphisms in Peroxisome Proliferator-Activated Receptor δ Associated With Obesity

H. Shin, K. Park, Y. Cho, 2004 .

Genetic interactions model among Eotaxin gene polymorphisms in asthma

Choon-Sik Park, H. Shin, S. Uh, 2008, 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.

Genetic effect of CCR3 and IL5RA gene polymorphisms on eosinophilia in asthmatic patients.

H. Shin, S. Uh, Choon-Sik Park, 2007, The Journal of allergy and clinical immunology.

ADH1B and ALDH2 polymorphisms and their associations with increased risk of squamous cell carcinoma of the head and neck in the Korean population.

H. Shin, Seung Hwan Lee, C. Park, 2011, Oral oncology.

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.

The effects of UCP-1 polymorphisms on obesity phenotypes among Korean female subjects.

H. Shin, Y. Yoon, Kil-Soo Kim, 2005, Biochemical and biophysical research communications.

Associations between polymorphisms in the mitochondrial uncoupling proteins (UCPs) with T2DM.

H. Shin, B. Oh, K. Park, 2008, Clinica chimica acta; international journal of clinical chemistry.

Association of a microRNA‐323b polymorphism with the persistence of hepatitis B virus infection by the enhancement of viral replication

H. Shin, J. Cheong, J. Yoon, 2014, Journal of viral hepatitis.

Association between interleukin 6 promoter variants and chronic hepatitis B progression

H. Shin, J. Jung, Y. Kim, 2003, Experimental & Molecular Medicine.

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.

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.

Regulatory Effect of Common Promoter Polymorphisms on the Expression of the 11β-Hydroxysteroid Dehydrogenase Type 1 Gene

H. Shin, B. Oh, S. Kwak, 2009, Hormone Research in Paediatrics.

Association between colony-stimulating factor 1 receptor gene polymorphisms and asthma risk

H. Shin, S. Uh, Choon-Sik Park, 2010, Human Genetics.

Putative association of RUNX1 polymorphisms with IgE levels in a Korean population

H. Shin, S. Uh, Choon-Sik Park, 2006, Experimental & Molecular Medicine.

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.

Association analysis of DTD1 gene variations with aspirin-intolerance in asthmatics.

H. Shin, S. Uh, Choon-Sik Park, 2011, International journal of molecular medicine.

ADAM33 Gene Polymorphisms are Associated with the Risk of Idiopathic Pulmonary Fibrosis

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

Genetic association analysis of TAP1 and TAP2 polymorphisms with aspirin exacerbated respiratory disease and its FEV1 decline

H. Shin, S. Uh, Choon-Sik Park, 2011, Journal of Human Genetics.

Genetic association of DRD2 polymorphisms with anxiety scores among alcohol-dependent patients.

H. Shin, D. Kim, Y. Cheon, 2008, Biochemical and biophysical research communications.

Association analysis of FABP1 gene polymorphisms with aspirin-exacerbated respiratory disease in asthma

H. Shin, Choon-Sik Park, Hye-Rim Shin, 2014, Experimental lung research.

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 .

Polymorphisms of ADIPOR1 and ADIPOR2 are associated with phenotypes of type 2 diabetes in Koreans

H. Shin, B. Oh, K. Park, 2009, Clinical endocrinology.

Association analysis of sphingomyelinase 2 polymorphisms for the extrinsic type of atopic dermatitis in Koreans.

H. Shin, Jong-Young Lee, B. Han, 2007, Journal of dermatological science.

Polymorphisms in the ghrelin gene are associated with serum high-density lipoprotein cholesterol level and not with type 2 diabetes mellitus in Koreans.

H. Shin, H. Choi, K. Park, 2006, The Journal of clinical endocrinology and metabolism.

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.

Polymorphisms and haplotypes of integrinalpha1 (ITGA1) are associated with bone mineral density and fracture risk in postmenopausal Koreans.

H. Shin, Jong-Young Lee, B. Oh, 2007, Bone.

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.

Angiotensin-Converting Enzyme (ACE) Gene Polymorphisms are Associated with Idiopathic Pulmonary Fibrosis

H. Shin, S. Uh, Choon-Sik Park, 2013, Lung.

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.

Replication of Genetic Effects of FTO Polymorphisms on BMI in a Korean Population

H. Shin, S. Choi, J. Y. Kim, 2008, Obesity.

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.

Association of the ins/del polymorphisms of uncoupling protein 2 (UCP2) with BMI in a Korean population.

H. Shin, Won Kim, B. Park, 2008, Biochemical and biophysical research communications.

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.

Association of IL-15 Polymorphisms with Bone Mineral Density in Postmenopausal Korean Women

H. Shin, Jong-Young Lee, B. Oh, 2009, Calcified Tissue International.

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.

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

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

[Association of interleukin-12 gene polymorphism with persistence of hepatitis B virus infection and hepatocellular carcinoma].

H. Shin, Jin Sun Park, J. Cheong, 2007, The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi.

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.

Gender-Specific Associations between CHGB Genetic Variants and Schizophrenia in a Korean Population

H. Shin, Jaeuk Hwang, Chul-Soo Park, 2017, Yonsei medical journal.

Global DNA Methylation Pattern of Fibroblasts in Idiopathic Pulmonary Fibrosis.

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

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.

Lack of Associations of Neuregulin 1 Variations with Schizophrenia and Smooth Pursuit Eye Movement Abnormality in a Korean Population

H. Shin, B. Cha, Jaeuk Hwang, 2012, Journal of Molecular Neuroscience.

Association of ZDHHC8 polymorphisms with smooth pursuit eye movement abnormality

H. Shin, Chul-Soo Park, B. Kim, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Association analyses of the INSIG2 polymorphism in the obesity and cholesterol levels of Korean populations

H. Shin, Imhoi Koo, S. Choi, 2009, BMC Medical Genetics.

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.

A promoter SNP rs4073T>A in the common allele of the interleukin 8 gene is associated with the development of idiopathic pulmonary fibrosis via the IL-8 protein enhancing mode

H. Shin, S. Uh, Choon-Sik Park, 2011, Respiratory research.

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.

DNase II polymorphisms associated with risk of renal disorder among systemic lupus erythematosus patients

H. Shin, Hye-Soon Lee, S. Bae, 2005, Journal of Human Genetics.

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.

Effect of single nucleotide polymorphisms within the interleukin-4 promoter on aspirin intolerance in asthmatics and interleukin-4 promoter activity

H. Shin, S. Uh, Choon-Sik Park, 2010, Pharmacogenetics and genomics.

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.

HNF1B polymorphism associated with development of prostate cancer in Korean patients.

H. Shin, Wonyong Kim, S. Myung, 2011, Urology.

Association of FLT3 Polymorphisms With Low BMD and Risk of Osteoporotic Fracture in Postmenopausal Women

H. Shin, Jong-Young Lee, B. Oh, 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean women

H. Shin, Jong-Young Lee, B. Oh, 2007, Journal of Human Genetics.

Associations of catalase gene polymorphisms with bone mineral density and bone turnover markers in postmenopausal women

Jong Yong Lee, H. Shin, B. Oh, 2006, Journal of Medical Genetics.

No association between interleukin 23 receptor gene polymorphisms and systemic lupus erythematosus

H. Shin, S. Bae, J. Bae, 2009, Rheumatology International.

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.

Association analysis of tapasin polymorphisms with aspirin-exacerbated respiratory disease in asthmatics

H. Shin, S. Uh, Choon-Sik Park, 2013, Pharmacogenetics and genomics.

Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.

H. Ostrer, D. Goldstein, X. Estivill, 1998, American journal of human genetics.

Association of TNF-α promoter polymorphisms with the clearance of hepatitis B virus infection

H. Shin, Y. Kim, C. Kim, 2003 .

Genome-Wide Association Study of Rheumatoid Arthritis in Koreans: Population-Specific Loci as Well as Overlap With European Susceptibility Loci

Annette Lee, P. Gregersen, H. Shin, 2011 .

Genome‐wide methylation profile of nasal polyps: relation to aspirin hypersensitivity in asthmatics

H. Shin, Mi-Ae Kim, C. Park, 2011, Allergy.

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

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

Cox-2 and IL-10 Polymorphisms and Association with Squamous Cell Carcinoma of The Head and Neck in a Korean Sample

H. Shin, Seung Hwan Lee, C. Park, 2010, Journal of Korean medical science.

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

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

Multifactor-dimensionality reduction shows a two-locus interaction associated with Type 2 diabetes mellitus

J. H. Moore, H. Shin, M. Ritchie, 2004, Diabetologia.

Associations of CD6, TNFRSF1A and IRF8 polymorphisms with risk of inflammatory demyelinating diseases

H. Shin, J. Bae, J. Kim, 2013, Neuropathology and applied neurobiology.

Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease

H. Shin, Hyun-Young Kim, K. Park, 2015, Neonatology.

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

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

Polymorphisms of ATF6B Are Potentially Associated With FEV1 Decline by Aspirin Provocation in Asthmatics

H. Shin, S. Uh, Choon-Sik Park, 2013, Allergy, asthma & immunology research.

Lack of association of fragile histidine triad (FHIT) polymorphisms with lung cancer in the Korean population

H. Shin, S. Oh, Hae-Yun Jung, 2007, 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.

MERTK polymorphisms associated with risk of haematological disorders among Korean SLE patients.

H. Shin, H. D. Shin, Y. Sung, 2007, Rheumatology.

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.

Potential association of VAMP5 polymorphisms with total colonic aganglionosis in Hirschsprung disease

H. Shin, Jeong-Hyun Kim, Joong-Gon Shin, 2016, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

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.

No association between CCL2 gene polymorphisms and risk of inflammatory demyelinating diseases in a Korean population.

H. Shin, H. Kim, H. D. Shin, 2014, Tissue antigens.

Association study of DKK2 polymorphisms with alcohol dependence and alcohol-related harm.

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

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.

Deletion variants of RABGAP1L, 10q21.3, and C4 are associated with the risk of systemic lupus erythematosus in Korean women.

H. Shin, S. Bang, Hye-Soon Lee, 2013, Arthritis and rheumatism.

Association of TWIST1 gene polymorphisms with bone mineral density in postmenopausal women

H. Shin, M. Go, J. Lee, 2010, Osteoporosis International.

Peroxisome proliferator-activated receptor gamma coactivator 1 alpha promoter polymorphisms are associated with early-onset type 2 diabetes mellitus in the Korean population

J. H. Kim, H. Shin, Y. M. Cho, 2005, Diabetologia.

Genetic restriction of HIV-1 pathogenesis to AIDS by promoter alleles of IL10.

J. Goedert, J. Stephens, S. O’Brien, 2000, Proceedings of the National Academy of Sciences of the United States of America.

PRMT8 Controls the Pluripotency and Mesodermal Fate of Human Embryonic Stem Cells By Enhancing the PI3K/AKT/SOX2 Axis

H. Shin, Su-Jae Lee, S. Moon, 2017, Stem cells.

ADAM33 polymorphism: association with bronchial hyper‐responsiveness in Korean asthmatics

H. Shin, S. Uh, S. Holgate, 2004, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

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.

Genome‐wide methylation profile of nasal polyps: relation to aspirin hypersensitivity in asthmatics

H. Shin, Mi-Ae Kim, H. S. Cheong, 2011, Allergy.

Gene expression profile of necrotizing enterocolitis model in neonatal mice.

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

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

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

Association of CHRM2 polymorphisms with severity of alcohol dependence

H. Shin, J. Bae, Tae-Cheon Kang, 2011, Genes, brain, and behavior.

Association analyses of the INSIG2 polymorphism in the obesity and cholesterol levels of Korean populations

H. Shin, Imhoi Koo, S. Choi, 2009, BMC Medical Genetics.

Association of KCNQ1 polymorphisms with the gestational diabetes mellitus in Korean women.

H. Shin, Sung-Hoon Kim, Sunmin Park, 2010, The Journal of clinical endocrinology and metabolism.

Undifferentiated embryonal sarcoma of the liver in a child: A whole exome sequencing analysis.

H. Shin, Hyunjin Park, Jeong-Hyun Kim, 2017, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Identification of copy number variations and common deletion polymorphisms in cattle

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

Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population

H. Shin, T. Kim, Y. M. Cho, 2009, Diabetologia.

A promoter nucleotide variant of the dendritic cell-specific DCNP1 associates with serum IgE levels specific for dust mite allergens among the Korean asthmatics

H. Shin, J. Lee, B. Oh, 2007, Genes and Immunity.