2024 | Novel Clinical Anatomical Consideration of the Superficial and Deep Layers of the Deep Temporal Fascia | PLASTIC AND RECONSTRUCTIVE SURGERY |
2023 | Sonoanatomy and an ultrasound scanning protocol of the intramuscular innervation pattern of the infraspinatus muscle | REGIONAL ANESTHESIA AND PAIN MEDICINE |
2023 | Evaluating intramuscular neural distribution in the cricopharyngeus muscle for injecting botulinum toxin | AURIS NASUS LARYNX |
2022 | Novel Anatomical Proposal for Botulinum Neurotoxin Injection Targeting Lateral Canthal Rhytids
| TOXINS |
2022 | The Superficial Temporal Artery and Zygomatico-Orbital Artery: Superficial Arterial Distribution of the Anterior Temple Area
| BIOMED RESEARCH INTERNATIONAL |
2020 | Extracellular vesicles derived from macrophages display glycyl-tRNA synthetase 1 and exhibit anti-cancer activity
| JOURNAL OF EXTRACELLULAR VESICLES |
2016 | Ecological changes in oral microcosm biofilm during maturation
| JOURNAL OF BIOMEDICAL OPTICS |
2016 | First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
| JOURNAL OF CLINICAL NEUROLOGY |
2016 | Clinical assessment of oral malodor using autofluorescence of tongue coating | PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY |
2015 | Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1 | NEUROMUSCULAR DISORDERS |
2015 | Genome-wide association study of recalcitrant atopic dermatitis in Korean children | JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY |
2015 | Genetic association between VEGF polymorphisms and BRONJ in the Korean population | ORAL DISEASES |
2015 | Clinical features of familial hypercholesterolemia in Korea: Predictors of pathogenic mutations and coronary artery disease - A study supported by the Korean Society of Lipidology and Atherosclerosis | ATHEROSCLEROSIS |
2015 | Evaluation of polygenic cause in Korean patients with familial hypercholesterolemia - A study supported by Korean Society of Lipidology and Atherosclerosis | ATHEROSCLEROSIS |
2015 | GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy | EPILEPSY RESEARCH |
2015 | Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis
| PLOS ONE |
2015 | Targeted next-generation sequencing for the genetic diagnosis of dysferlinopathy | NEUROMUSCULAR DISORDERS |
2015 | Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing
| PLOS ONE |
2015 | microDuMIP: target-enrichment technique for microarray-based duplex molecular inversion probes
| NUCLEIC ACIDS RESEARCH |
2015 | Phase II clinical and exploratory biomarker study of dacomitinib in patients with recurrent and/or metastatic squamous cell carcinoma of head and neck | CLINICAL CANCER RESEARCH |
2014 | Perturbation of NCOA6 Leads to Dilated Cardiomyopathy | CELL REPORTS |
2014 | Identification of somatic mutations in EGFR/KRAS/ALK-negative lung adenocarcinoma in never-smokers
| GENOME MEDICINE |
2014 | Whole-Genome Analysis in Korean Patients with Autoimmune Myasthenia Gravis
| YONSEI MEDICAL JOURNAL |
2014 | A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
2013 | Proximal Dominant Hereditary Motor and Sensory Neuropathy With Proximal Dominance Association With Mutation in the TRK-Fused Gene | JAMA NEUROLOGY |
2013 | Genetic Variations of ABCC2 Gene Associated with Adverse Drug Reactions to Valproic Acid in Korean Epileptic Patients
| Genomics & Informatics |
2013 | Association between CDH13 Variants and Cardiometabolic and Vascular Phenotypes in a Korean Population
| YONSEI MEDICAL JOURNAL |
2013 | Pharmacogenetic determinants associated with sunitinib-induced toxicity and ethnic difference in Korean metastatic renal cell carcinoma patients | CANCER CHEMOTHERAPY AND PHARMACOLOGY |
2013 | Pharmacogenomic Assessment of Outcomes of Pemetrexed-Treated Patients with Adenocarcinoma of the Lung
| YONSEI MEDICAL JOURNAL |
2013 | Association of genetic variation in chitotriosidase with atopy in Korean children | ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY |
2013 | Fibroblast Growth Factor Receptor 1 Gene Amplification Is Associated With Poor Survival and Cigarette Smoking Dosage in Patients With Resected Squamous Cell Lung Cancer | JOURNAL OF CLINICAL ONCOLOGY |
2012 | EGFR polymorphism as a predictor of clinical outcome in advanced lung cancer patients treated with EGFR-TKI
| YONSEI MEDICAL JOURNAL |
2012 | Activation of IL-6R/JAK1/STAT3 signaling induces de novo resistance to irreversible EGFR inhibitors in non-small cell lung cancer with T790M resistance mutation | MOLECULAR CANCER THERAPEUTICS |
2012 | TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS |
2011 | A synonymous variation in protease-activated receptor-2 is associated with atopy in Korean children | JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY |
2010 | Association between cystic fibrosis transmembrane conductance regulator gene mutations and susceptibility for childhood asthma in Korea
| YONSEI MEDICAL JOURNAL |
2010 | MRP1 polymorphisms associated with citalopram response in patients with major depression | JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY |
2010 | A nonsynonymous variation in MRP2/ABCC2 is associated with neurological adverse drug reactions of carbamazepine in patients with epilepsy. | PHARMACOGENETICS AND GENOMICS |
2010 | Selective inhibition of MDR1 (ABCB1) by HM30181 increases oral bioavailability and therapeutic efficacy of paclitaxel. | EUROPEAN JOURNAL OF PHARMACOLOGY |
2010 | The L441P mutation of cystic fibrosis transmembrane conductance regulator and its molecular pathogenic mechanisms in a Korean patient with cystic fibrosis
| JOURNAL OF KOREAN MEDICAL SCIENCE |
2009 | Genetic variation in the promoter region of chitinase 3-like 1 is associated with atopy. | AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE |
2007 | MRP2 haplotypes confer differential susceptibility to toxic liver injury | PHARMACOGENETICS AND GENOMICS |
2007 | Dynamic regulation of cystic fibrosis transmembrane conductance regulator by competitive interactions of molecular adaptors
| JOURNAL OF BIOLOGICAL CHEMISTRY |
2005 | Gene SNPs and mutations in clinical genetic testing: Haplotype-based testing and analysis | MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS |
2004 | Inhibitory regulation of cystic fibrosis transmembrane conductance regulator anion-transporting activities by Shank2
| JOURNAL OF BIOLOGICAL CHEMISTRY |
2003 | A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases
| HUMAN MOLECULAR GENETICS |