Y. S. Hyun

发表

Inheritance of Charcot–Marie–Tooth disease 1A with rare nonrecurrent genomic rearrangement

N. Kim, H. Jeon, Byung-Ok Choi, 2011, neurogenetics.

Complete mitochondrial genome of Parupeneus barberinus (Perciformes, Mullidae): mitogenome characterization and phylogenetic analysis

Seung-Hyun Jung, Hyun-ju Hwang, Y. S. Hyun, 2017, Mitochondrial DNA. Part B, Resources.

Charcot‐Marie‐Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families

Deok‐Ho Kim, H. Koo, H. Kim, 2015, Annals of human genetics.

Wide phenotypic variations in Charcot-Marie-Tooth 1A neuropathy with rare copy number variations on 17p12

H. Koo, Byung-Ok Choi, Y. S. Hyun, 2011 .

Phylogenetic analysis of mitochondrial DNA control region in the swimming crab, portunus trituberculatus

Sun Wha Park, Y. S. Hyun, K. Chung, 2009 .

Characterization of 20 microsatellite loci by multiplex PCR in swimming crab, Portunus trituberculatus

Y. S. Hyun, K. Chung, G. Min, 2013, Genes & Genomics.

Rare variants in methionyl‐ and tyrosyl‐tRNA synthetase genes in late‐onset autosomal dominant Charcot–Marie–Tooth neuropathy

Chanil Park, H. Park, Y. S. Hyun, 2014, Clinical genetics.

ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy

Ji Eun Lee, H. Kim, Won Min Mo, 2016, Annals of neurology.

Two recessive intermediate Charcot‐Marie‐Tooth patients with GDAP1 mutations

H. Koo, Byung-Ok Choi, J. Yoo, 2011, Journal of the peripheral nervous system : JPNS.

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy

H. Koo, G. Kwak, Won Min Mo, 2016, PLoS genetics.

Clinico-genetics in Korean Charcot-Marie-Tooth disease type 2Z with MORC2 mutations.

Byung-Ok Choi, Y. Hong, Y. S. Hyun, 2016, Brain : a journal of neurology.

A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth disease

H. Koo, Byung-Ok Choi, Y. Hong, 2013, BMC Medical Genetics.

DGAT2 Mutation in a Family with Autosomal‐Dominant Early‐Onset Axonal Charcot‐Marie‐Tooth Disease

J. Kim, Ji Eun Lee, H. Koo, 2016, Human mutation.

A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14

S. Züchner, Jong-Won Kim, H. Koo, 2011, Human mutation.

Identification of Genetic Causes of Inherited Peripheral Neuropathies by Targeted Gene Panel Sequencing

G. Kwak, Byung-Ok Choi, Y. Hong, 2016, Molecules and cells.

Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases

K. Seong, H. Jeon, Byung-Ok Choi, 2010, Experimental & Molecular Medicine.

Exome sequencing is an efficient tool for genetic screening of Charcot–Marie–Tooth Disease

Byung-Ok Choi, Y. S. Hyun, K. Chung, 2012, Human mutation.

Development of polymorphic microsatellite markers for Cymbidium goeringii (Orchidaceae).

Joonki Kim, Y. S. Hyun, K. Chung, 2012, American journal of botany.

Analysis of Microsatellite Loci for Swimming Crab Portunus trituberculatus Populations in the Korean Side of the Yellow Sea

H. Kim, Y. S. Hyun, K. Chung, 2013 .

MPZ mutation in an early-onset Charcot-Marie-Tooth disease type 1B family by genome-wide linkage analysis.

H. Koo, Byung-Ok Choi, Jae-Won Hyun, 2011, International journal of molecular medicine.

A cohort study of MFN2 mutations and phenotypic spectrums in Charcot–Marie–Tooth disease 2A patients

H. Park, Y. S. Hyun, K. Chung, 2015, Clinical genetics.

Development of 21 polymorphic microsatellite markers for the black-banded sea krait, Laticauda semifasciata (Elapidae: Laticaudinae), and cross-species amplification for two other congeneric species

Daesik Park, Y. S. Hyun, M. Toda, 2017, Genes & Genomics.

Characterization of 20 microsatellite loci by multiplex PCR in swimming crab, Portunus trituberculatus

Y. S. Hyun, K. Chung, G. Min, 2013, Genes & Genomics.

Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.

Min Goo Lee, J. Lee, H. Koo, 2013, JAMA neurology.

Novel Compound Heterozygous Nonsense PRX Mutations in a Korean Dejerine-Sottas Neuropathy Family

H. Koo, Byung-Ok Choi, Y. Hong, 2014, Journal of clinical neurology.

A family with axonal sensorimotor polyneuropathy with TUBB3 mutation.

Ji Hoon Park, H. Koo, Byung-Ok Choi, 2015, Molecular medicine reports.

Clinical and histopathological study of Charcot-Marie-Tooth neuropathy with a novel S90W mutation in BSCL2

H. Koo, H. Chung, Y. S. Hyun, 2013, neurogenetics.

Rapid development and characterization of microsatellite markers for the sandhopper Trinorchestia longiramus Jo, 1988 (Amphipoda, Talitridae) in Korea using a 454 pyrosequencing approach

Y. S. Hyun, Sumin Oh, Jiyoung Woo, 2016 .

Abnormal detection of Y-STR alleles at DYS385 from female DNA in forensic casework and interchromosomal insertional translocation of P4 palindrome (HSFY/DYS385) from AZFb region.

Y. S. Hyun, Dong-ho Choi, Soon-hee Kim, 2019, Legal medicine.

A Brain Atlas of the Long Arm Octopus, Octopus minor

Seung-Hyun Jung, I. Whang, Y. S. Hyun, 2018, Experimental neurobiology.

Population genetics of insertion-deletion polymorphisms in South Koreans using Investigator DIPplex kit.

K. Seong, Y. S. Hyun, K. Chung, 2014, Forensic science international. Genetics.

Exome Sequencing Reveals a Novel PRPS1 Mutation in a Family with CMTX5 without Optic Atrophy

Byung-Ok Choi, Y. Hong, Sung-Hee Kim, 2013, Journal of clinical neurology.

Isolation and characterization of 20 polynucleotide microsatellite markers in a vulnerable Korean snail, Ellobium chinense, using 454 pyrosequencing

Y. S. Hyun, Sumin Oh, Jiyoung Woo, 2017, Genes & Genomics.

Two recessive intermediate Charcot‐Marie‐Tooth patients with GDAP1 mutations

H. Koo, Byung-Ok Choi, J. Yoo, 2011, Journal of the peripheral nervous system : JPNS.