| 2010 | Myotonic dystrophy type i combined with X-linked dominant Charcot-Marie-Tooth neuropathy | 구혜수; 최병옥; 최선영 | Article |
| 2011 | Two recessive intermediate Charcot-Marie-Tooth patients with GDAP1 mutations | 구혜수; 유정현; 최병옥 | Article |
| 2014 | Recessive C10orf2 mutations in a family with infantile-onset spinocerebellar ataxia, sensorimotor polyneuropathy, and myopathy | 구혜수; 유정현 | Article |
| 2013 | A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement | 구혜수; 유정현; 최병옥; 홍영빈 | Article |
| 2013 | A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L | 구혜수; 유정현; 최병옥 | Article |
| 2013 | Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease | 구혜수; 유정현; 최병옥 | Article |
| 2013 | Erratum: Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease (Nutrition and Metabolism) | 구혜수; 유정현; 최병옥 | Erratum |
| 2016 | A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy | 구혜수; 유정현 | 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 |
| 2011 | A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14 | 최경규; 구혜수; 박기덕; 유정현; 최병옥 | Article |
