| 2007 | | Genetic counseling in Korean health care system | 김현주 |
| 2009 | | Genotypic and phenotypic analyses of Korean patients with syndromic craniosynostosis. | 유재은, 정선용, 박문성, 김현주, 윤수한 |
| 1999 | | Hepatopulmonary syndrome in Gaucher disease with right-to-left shunt: evaluation and measurement using Tc-99m MAA. | 박찬희, 한명호, 김현주 |
| 2010 | | Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26. | 김현주, 정선용, 정연훈, 김유찬 |
| 2011 | | Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach. | 정선용, 김현주 |
| 2008 | | Identification of differentially expressed genes related to NF1-associated malignant transformation from a patient with neurofibromatosis type 1. | 정선용, 한재호, 김현주 |
| 2012 | | Inhibition of Bcl-xL by ABT-737 enhances chemotherapy sensitivity in neurofibromatosis type 1-associated malignant peripheral nerve sheath tumor cells | 김보영, 진현석, 김현주, 한재호, 임현이, 정선용 |
| 2010 | | Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis type 1. | 정선용, 김현주 |
| 2008 | | Molecular diagnosis of fragile X syndrome in a female child | 정선용, 김현주 |
| 2008 | | Multiple endocrine neoplasia type 1 with multiple leiomyomas linked to a novel mutation in the MEN1 gene. | 정선용, 김현주 |
| 2013 | | Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1. | 손영배, 정선용, 김현주 |
| 2012 | | Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism | 정선용, 김현주 |
| 2006 | | Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta. | 김현주 |
| 2007 | | National survey for genetic counseling and demands for Professional genetic counselor | 정윤석, 김현주 |
| 2004 | | Novel and recurrent mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia. | 김현주 |
| 2013 | | Ocular Abnormality of Korean Patients with Molecular Genetically Confirmed Gaucher Disease | 김현주, 정선용 |
| 2010 | | Phenotypic and Cytogenetic Delineation of Six Korean Children with Kabuki Syndrome | 고정민, 김현주 |
| 2004 | | Pontine atrophy precedes cerebellar degeneration in spinocerebellar ataxia 7: MRI-based volumetric analysis. | 방오영, 이필휴, 김선용, 김현주, 허균 |
| 2011 | | SCA in Korea and its regional distribution: a multicenter analysis. | 용석우, 김현주 |
| 2007 | | Spinocerebellar ataxia 7 (SCA7) | 정선용, 김현주 |
| 2011 | | Strabismus and Poor Stereoacuity Associated with Kabuki Syndrome | 김현주 |
| 1998 | | Structurally abnormal type II collagen in a severe form of Kniest dysplasia caused by an exon 24 skipping mutation. | 김현주 |
| 2005 | | The effect of relaxation therapy on patient's pain following a total knee replacement | 김현주 |
| 2007 | | The spectrum of 5p deletion in Korean 20 patients with Cri du chat syndrome | 김현주 |
| 2006 | | The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1. | 정선용, 박상진, 김현주 |
| 2009 | | Two cases of acute myeloid leukemia with t(16;21)(p11;q22) and TLS/FUS-ERG fusion transcripts. | 박일중, 이현우, 박준성, 김효철, 김현주, 한재호, 조성란 |
| 2006 | | Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array. | 박상진, 정선용, 김현주 |
