| 2010 | | KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect. | 고정민, 황진순 |
| 2017 | | Makorin ring finger 3 gene analysis in Koreans with familial precocious puberty | 이해상 |
| 2007 | | Molecular cloning and characterization of a cytosolic heat shock protein 70 from Naegleria fowleri. | 권대호, 박선, 송경주, 신호준 |
| 2001 | | Molecular cloning and characterization of a gene encoding a 13.1 kDa antigenic protein of Naegleria fowleri. | 김형일, 박선, 신호준 |
| 2020 | | Molecular detection of free-living amoebae from Namhangang (southern Han River) in Korea | 손혜진, 신호준 |
| 2010 | | Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family. | 김옥화 |
| 2007 | | Novel complex class 1 integron bearing an ISCR1 element in an Escherichia coli isolate carrying the blaCTX-M-14 gene. | 이위교 |
| 2017 | | Pan-cancer analysis of systematic batch effects on somatic sequence variations | 우현구 |
| 2004 | | Presence of human mycoplasma DNA in gastric tissue samples from Korean chronic gastritis patients. | 김영배, 함기백 |
| 2010 | | Prevalence of the VNIc genotype of Cryptococcus neoformans in non-HIV-associated cryptococcosis in the Republic of Korea. | 이위교, 최영화 |
| 2019 | | Rapid diagnosis of bacterial meningitis by nanopore 16S amplicon sequencing: A pilot study | 김태준 |
| 2016 | | Resistance Mechanisms and Clinical Features of Fluconazole-Nonsusceptible Candida tropicalis Isolates Compared with Fluconazole-Less-Susceptible Isolates | 이위교 |
| 2019 | | Streptococcus koreensis sp. nov., Isolated from Human Subgingival Dental Plaque of Periodontitis Lesion | 지숙 |
| 2012 | | The first study on nucleotide-level identification of Hb Koriyama in a patient with severe hemolytic anemia | 박준은 |
| 2007 | | Three cases of xanthogranulomatous epididymitis caused by E. coli. | 주희재 |
| 2014 | | TSH signaling overcomes B-RafV600E-induced senescence in papillary thyroid carcinogenesis through regulation of DUSP6. | 김장희, 박태준, 소의영, 이정훈, 한재호 |
| 2012 | | Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidence | 손영배 |
| 2014 | | Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA. | 정주용 |
| 2011 | | Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type. | 김옥화 |
