| 2008 | Genetic characteristics of 207 microsatellite markers in the Korean population and in other Asian populations | 원용진 | Article |
| 2020 | Gravitational-wave Constraints on the Equatorial Ellipticity of Millisecond Pulsars | 김정리 | Article |
| 2004 | Hereditary neuropathy with liability to pressure palsies (HNPP) patients of Korean ancestry with chromosome 17p11.2-p12 deletion | 박기덕; 최병옥 | Article |
| 2018 | Impairment of PPARα and the fatty acid oxidation pathway aggravates renal fibrosis during aging | 오구택 | Article |
| 2009 | Infectious mononucleosis hepatitis in young adults: Two case reports | 유권; 정성애; 조민선; 심기남; 김태헌 | Article |
| 2011 | Inheritance of Charcot-Marie-tooth disease 1A with rare nonrecurrent genomic rearrangement | 최병옥 | Article |
| 2013 | Missense mutations of mitofusin 2 in axonal Charcot-Marie-Tooth neuropathy: Polymorphic or incomplete penetration? | 최병옥 | Article |
| 2015 | Molecular genetic diagnosis of a bethlem myopathy family with an autosomal-dominant COL6A1 mutation, as evidenced by exome sequencing | 박형준 | Article |
| 2011 | MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis | 최경규; 구혜수; 박기덕; 유정현; 최병옥 | Article |
| 2004 | Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot-Marie-Tooth neuropathy patients. | 최경규; 최병옥 | Article |
| 2010 | Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases | 최병옥 | Article |
| 2013 | Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease | 구혜수; 유정현; 최병옥 | Article |
| 2007 | Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families | 최병옥 | Article |
| 2010 | Myotonic dystrophy type i combined with X-linked dominant Charcot-Marie-Tooth neuropathy | 구혜수; 최병옥; 최선영 | Article |
| 2019 | Narrow-band search for gravitational waves from known pulsars using the second LIGO observing run | 김정리 | Article |
| 2008 | NEFL Pro22Arg mutation in Charcot-Marie-Tooth disease type 1 | 최병옥 | Article |
| 2015 | Novel compound heterozygous nonsense prx mutations in a korean dejerine-sottas neuropathy family | 구혜수 | Article |
| 2023 | Open Data from the Third Observing Run of LIGO, Virgo, KAGRA, and GEO | 김정리 | Article |
| 2011 | Primary adenosquamous cell carcinoma of the pancreas: A case report with a review of the Korean literature | 성순희; 유권; 정성애; 조민선; 심기남 | Article |
| 2013 | Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene | 구혜수; 박기덕; 유정현; 최병옥; 정성철 | Article |
| 2013 | Proximal lower-limb weakness in Charcot-Marie-Tooth disease - Reply | 유정현 | Letter |
| 2007 | Rapid diagnosis of CMT1A duplications and HNPP deletions by multiplex microsatellite PCR | 최병옥 | Article |
| 2013 | Rare variants in methionyl- and tyrosyl-tRNA synthetase genes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy | 최병옥 | Article in Press |
| 2014 | Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy | 구혜수; 유정현 | Article |
| 2022 | Search for continuous gravitational waves from 20 accreting millisecond x-ray pulsars in O3 LIGO data | 김정리 | Article |
| 2022 | Search for Gravitational Waves Associated with Gamma-Ray Bursts Detected by Fermi and Swift during the LIGO-Virgo Run O3b | 김정리 | Article |
| 2022 | Search for intermediate-mass black hole binaries in the third observing run of Advanced LIGO and Advanced Virgo | 전건상; 김정리 | Article |
| 2021 | Search for Lensing Signatures in the Gravitational-Wave Observations from the First Half of LIGO-Virgo's Third Observing Run | 김정리 | Article |
| 2019 | Search for Multimessenger Sources of Gravitational Waves and High-energy Neutrinos with Advanced LIGO during Its First Observing Run, ANTARES, and IceCube | 김정리 | Article |
| 2019 | Search for Subsolar Mass Ultracompact Binaries in Advanced LIGO's Second Observing Run | 김정리 | Article |
