| 2015 | | On the Estimation of Heritability with Family-Based and Population-Based Samples. | 조남한 |
| 2013 | | Osteogenesis imperfecta type V: clinical and radiographic manifestations in mutation confirmed patients. | 김옥화 |
| 2020 | | Osteopontin contributes to late-onset asthma phenotypes in adult asthma patients | 김승현, 박해심 |
| 2014 | | Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene. | 김옥화 |
| 2012 | | PAPSS2 mutations cause autosomal recessive brachyolmia | 김옥화 |
| 2010 | | Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome. | 고정민, 배기수 |
| 2011 | | Pulmonary manifestations in Proteus syndrome: pulmonary varicosities and bullous lung disease. | 김옥화 |
| 2004 | | Reduction in glycopeptide resistance in vancomycin-resistant enterococci as a result of vanA cluster rearrangements. | 이위교, 임영애, 조성란, 허지영 |
| 2014 | | Risk factors for asthma-related healthcare use: longitudinal analysis using the NHI claims database in a Korean asthma cohort. | 남동호 |
| 2016 | | Risk of the Development of Diabetes and Cardiovascular Disease in Metabolically Healthy Obese People: The Korean Genome and Epidemiology Study | 조남한 |
| 2018 | | Role of clusterin/progranulin in toluene diisocyanate-induced occupational asthma | 김승현, 박해심, 신유섭, 예영민 |
| 2022 | | Serum Amyloid A1: A Biomarker for Neutrophilic Airway Inflammation in Adult Asthmatic Patients | 박해심, 신유섭, 최영우 |
| 2016 | | Shifting p53-induced senescence to cell death by TIS21(/BTG2/Pc3) gene through posttranslational modification of p53 protein | 유민숙, 임인경 |
| 2014 | | Similar clinical characteristics of familial and sporadic inflammatory bowel disease in South Korea. | 정숙희 |
| 2014 | | Single nucleotide polymorphisms associated with abnormal coronary microvascular function. | 최병주 |
| 2003 | | Sonic hedgehog and FGF8 collaborate to induce dopaminergic phenotypes in the Nurr1-overexpressing neural stem cell. | 김승업, 이명애, 이용범 |
| 2005 | | Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency. | 정윤석 |
| 2019 | | T helper 1 and 2 stimuli induce distinct phenotypes in gingival fibroblasts | 지숙 |
| 1998 | | The cDNA cloning and ontogeny of mouse alpha-synuclein. | 곽병주, 조은혜 |
| 2023 | | The First Korean Family of Spinocerebellar Ataxia 21 (ATX-TMEM240) with Facial Dystonic Phenotype | 박동규, 윤정한 |
| 2014 | | The role of classical and alternative macrophages in the immunopathogenesis of herpes simplex virus-induced inflammation in a mouse model. | 손성향 |
| 2014 | | The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype. | 김승현, 박해심, 예영민 |
| 2017 | | The Ubiquitin-like with PHD and Ring Finger Domains 1 (UHRF1)/DNA Methyltransferase 1 (DNMT1) Axis Is a Primary Regulator of Cell Senescence | 우현구, 윤계순, 이영경 |
| 2005 | | Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas. | 김대중, 이관우 |
| 2017 | | TIS21(/BTG2) inhibits doxorubicin-induced stress fiber-vimentin networks via Nox4-ROS-ABI2-DRF-linked signal cascade | 유민숙, 임인경 |
| 2002 | | Tissue engineered tracheal prosthesis with acceleratedly cultured homologous chondrocytes as an alternative of tracheal reconstruction. | 민병현, 이철주, 최호 |
| 2020 | | Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma | 우현구 |
| 2018 | | Transcriptomic and histopathological analysis of cholangiolocellular differentiation trait in intrahepatic cholangiocarcinoma | 권소미, 우현구, 지별아 |
| 2022 | | Transferability of Alzheimer Disease Polygenic Risk Score Across Populations and Its Association with Alzheimer Disease-Related Phenotypes | 문소영, 손상준, 홍창형 |
| 2010 | | TRPV4-pathy, a novel channelopathy affecting diverse systems. | 김옥화 |
| 2005 | | Two distinct modes of cell death induced by doxorubicin: apoptosis and cell death through mitotic catastrophe accompanied by senescence-like phenotype. | 김욱환, 손성향, 윤계순, 최경숙 |
| 2014 | | Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA. | 정주용 |
