Jeong-Hyun Kim

发表

The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice

Hyungtae Kim, Jeong-Sun Seo, U. Yoon, 2005, Nucleic acids research.

Gene expression profiling: canonical molecular changes and clinicopathological features in sporadic colorectal cancers.

Seon-Young Kim, Jeong-Hyun Kim, Jin-Cheon Kim, 2008, World journal of gastroenterology.

DNA Methylation and gene expression patterns are widely altered in fetal growth restriction and associated with FGR development

Jeong-Hyun Kim, Kwoneel Kim, J. Kim, 2021, Animal cells and systems.

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.

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.

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

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

A PHLDB1 variant associated with the nonfunctional pituitary adenoma

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

Association between the oxytocin receptor gene polymorphism (rs53576) and bulimia nervosa.

J. Treasure, Y. Kim, Jae-Gook Shin, 2015, European eating disorders review : the journal of the Eating Disorders Association.

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.

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

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

Integrative multi‐omics approach for mechanism of humidifier disinfectant‐associated lung injury

S. Hong, Sang-Bum Hong, Seong-Jin Choi, 2021, Clinical and translational medicine.

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.

Immune Enhancing Effect of Houttuyniae Herba on Mouse Macrophage

Yoon-Sang Kim, Jeong-Hyun Kim, E. Lim, 2012 .

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.

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.

Functional Role of the Polymorphic 647 T/C Variant of ENT1 (SLC29A1) and Its Association with Alcohol Withdrawal Seizures

J. Biernacka, D. Mrazek, C. Colby, 2011, PloS one.

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.

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.

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.

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 .

Prenatal PM2.5 exposure/vitamin D- associated early persistent atopic dermatitis via placental methylation.

Mi-Young Lee, H. Won, Jisun Yoon, 2020, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Gene expression profile of necrotizing enterocolitis model in neonatal mice.

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

New variations of the EDNRB gene and its association with sporadic Hirschsprung's disease in Korea.

Hyungtae Kim, Jong-Won Kim, Jeong-Meen Seo, 2006, Journal of pediatric 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.

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.

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.

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.

Association Analysis of SLC6A20 Polymorphisms With Hirschsprung Disease

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

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.

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.

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

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

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

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

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.

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.

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 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 of FANCC polymorphisms with FEV1 decline in aspirin exacerbated respiratory disease

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

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.

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.

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.

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.

Differential Methylation of the Oxytocin Receptor Gene in Patients with Anorexia Nervosa: A Pilot Study

Mi Jeong Kim, J. Treasure, Y. Kim, 2014, PloS one.

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.

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.

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 .

Novel mutations of RET gene in Korean patients with sporadic Hirschsprung's disease.

Jong-Won Kim, Jeong-Meen Seo, S. Lee, 2006, Journal of pediatric surgery.

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

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

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.

Sequence variations of the human MPDZ gene and association with alcoholism in subjects with European ancestry.

E. Wieben, J. Biernacka, D. Mrazek, 2009, Alcoholism, clinical and experimental research.

Potential association between ITPKC genetic variations and Hirschsprung disease

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

Association of IL13 genetic polymorphisms with atopic dermatitis

Yoon Mee Park, S. Hong, K. Kim, 2020, Annals of Allergy, Asthma & Immunology.

Association of IL-13 genetic polymorphisms with atopic dermatitis: fine mapping and haplotype analysis.

Yoon Mee Park, S. Hong, K. Kim, 2020, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

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

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

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.

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

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

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

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

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

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

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.

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.

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.

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.

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.

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.

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.

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.

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.