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 |
2013 | SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3 | 김형래; 최경규; 구혜수; 유정현; 최병옥; 정성철 | Article |
2007 | Thymidylate synthase (TYMS) tandem repeat polymorphism: As a predictive genetic marker for the risk of Alzheimer's disease | 최병옥 | Article |
2005 | Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot-Marie-Tooth disease family | 김원기; 구혜수; 박기덕; 최병옥 | Article |
2012 | Two novel mutations of GARS in Korean families with distal hereditary motor neuropathy type v | 최병옥 | Article |
2011 | Two recessive intermediate Charcot-Marie-Tooth patients with GDAP1 mutations | 구혜수; 유정현; 최병옥 | Article |
2011 | Wide phenotypic variations in Charcot-Marie-Tooth 1A neuropathy with rare copy number variations on 17p12 | 구혜수; 최병옥 | Article |
2012 | X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans | 최경규; 박기덕; 최병옥; 김영화 | Article |