| 2006 | G-CSF Mobilized Peripheral Blood Human Hematopoietic CD34+ Stem Cells Therapy for Acute Stroke: Preliminary Results
| Korean Journal of Cerebrovascular Surgery (대한뇌혈관외과학회지) |
| 2011 | Gap junctions contribute to astrocytic resistance against zinc toxicity | BRAIN RESEARCH BULLETIN |
| 1995 | Gastrin 유발 위점막 손상에 대한 Nicotine의 보호 효과
| Korean Journal of Pharmacology(대한약리학잡지) |
| 2019 | Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis | Human Genetics |
| 2005 | Gene SNPs and mutations in clinical genetic testing: Haplotype-based testing and analysis | MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS |
| 2021 | Generation of a more efficient prime editor 2 by addition of the Rad51 DNA-binding domain
| NATURE COMMUNICATIONS |
| 2022 | Generation of mutation-corrected induced pluripotent stem cell lines derived from adrenoleukodystrophy patient by using homology directed repair
| STEM CELL RESEARCH |
| 2016 | Generation of ΔF508-CFTR T84 cell lines by CRISPR/Cas9-mediated genome editing | BIOTECHNOLOGY LETTERS |
| 2023 | Genetic Characteristics and Audiological Performance After Cochlear Implantation in Patients With Incomplete Partition Type III
| CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY |
| 2020 | Genetic Inheritance of Late-Onset, Down-Sloping Hearing Loss and Its Implications for Auditory Rehabilitation | EAR AND HEARING |
| 2017 | Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population
| SCIENTIFIC REPORTS |
| 2020 | Genetic risk factors associated with NAFLD
| Hepatoma Research |
| 2015 | Genetic testing of Korean familial hypercholesterolemia using whole-exome sequencing
| PLOS ONE |
| 2009 | Genetic variation in the promoter region of chitinase 3-like 1 is associated with atopy. | AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE |
| 2013 | Genetic Variations of ABCC2 Gene Associated with Adverse Drug Reactions to Valproic Acid in Korean Epileptic Patients
| Genomics & Informatics |
| 2017 | Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract
| INVESTIGATIVE AND CLINICAL UROLOGY |
| 2020 | Genome-scale screening of deubiquitinase subfamily identifies USP3 as a stabilizer of Cdc25A regulating cell cycle in cancer | CELL DEATH AND DIFFERENTIATION |
| 2022 | Genome-wide association study identifies TNFSF15 associated with childhood asthma | ALLERGY |
| 2020 | Genomic Landscape and Mutational Spectrum of ADAMTS Family Genes in Mendelian Disorders Based on Gene Evidence Review for Variant Interpretation
| BIOMOLECULES |
| 2017 | Glutamatergic stimulation of the left dentate gyrus abolishes depressive-like behaviors in a rat learned helplessness paradigm | NEUROIMAGE |
