S. Seo

发表

Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015

Seung Jun Lee, B. S. Yu, S. Y. Kim, 2016, Emerging infectious diseases.

A novel strategy for interpreting the T-SPOT.TB test results read by an ELISPOT plate imager

Seong-Wook Lee, K. Park, J. Park, 2019, PloS one.

Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A

Kyung Jin Ahn, S. Y. Kim, Sung Im Cho, 2017, Annals of laboratory medicine.

Relationship among genetic polymorphism of SLCO1B1, rifampicin exposure and clinical outcomes in patients with active pulmonary tuberculosis

Jong Sun Park, Jae-Yong Chung, K. Park, 2021, British journal of clinical pharmacology.

Viral RNA in Blood as Indicator of Severe Outcome in Middle East Respiratory Syndrome Coronavirus Infection

Seung Jun Lee, S. Y. Kim, Sung Im Cho, 2016, Emerging infectious diseases.

Evaluation of a Real-Time Reverse Transcription-PCR (RT-PCR) Assay for Detection of Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in Clinical Samples from an Outbreak in South Korea in 2015

B. S. Yu, Sung Im Cho, M. Seong, 2017, Journal of Clinical Microbiology.

Universal Screening for Lynch Syndrome Compared with Pedigree-Based Screening: 10-Year Experience in a Tertiary Hospital

H. Lee, Min Hyun Kim, Duck-Woo Kim, 2022, Cancer research and treatment.

PRRT2 mutation in Korean patients with paroxysmal kinesigenic dyskinesia: A clinico-genetic analysis

Young Eun Kim, J. Yun, B. Jeon, 2014 .

Diverse Phenotypic Expression of Cardiomyopathies in a Family with TNNI3 p.Arg145Trp Mutation

C. Ki, M. Seong, S. Park, 2017, Korean circulation journal.

Non-Homologous End Joining Repair Mechanism-Mediated Deletion of CHD7 Gene in a Patient with Typical CHARGE Syndrome

Seung Jun Lee, Sung Im Cho, M. Seong, 2014, Annals of laboratory medicine.

Pitfalls of Multiple Ligation-Dependent Probe Amplifications in Detecting DMD Exon Deletions or Duplications.

Seung Jun Lee, J. Y. Kim, S. Y. Kim, 2016, The Journal of molecular diagnostics : JMD.

Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing

M. Seong, S. Park, Jee-Soo Lee, 2022, Scientific Reports.

Evaluation of a Fully Automated, Rapid Detection System for CYP2C19 and UGT1A1 Genotyping

Seung Jun Lee, Sung Im Cho, M. Seong, 2014 .

Performance of two commercially available BCR-ABL1 quantification assays that use an international reporting scale

Seung Jun Lee, Min Jin Kim, J. Y. Kim, 2016, Clinical chemistry and laboratory medicine.

Genetics of Aldosterone-Producing Adenoma in Korean Patients

Young Shin Song, M. Seong, A. Hong, 2016, PloS one.

Current Issues, Challenges, and Future Perspectives of Genetic Counseling in Korea

Namhee Kim, Jongha Yoo, S. Seo, 2022, Annals of laboratory medicine.

Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma

Seung Jun Lee, Ji‐Hyun Lee, M. Seong, 2016, BMC Medical Genetics.

Immunohistochemical Staining to Identify Concomitant Systemic Mastocytosis in Acute Myeloid Leukemia with RUNX1::RUNX1T1

M. Seong, J. Lee, B. Kim, 2022, Annals of laboratory medicine.

Clinical applications of next‐generation sequencing‐based gene panel in patients with muscular dystrophy: Korean experience

Sung Im Cho, M. Seong, S. Park, 2016, Clinical genetics.

Effects of interleukin-4 and interleukin-12B gene polymorphisms on hepatitis B virus vaccination.

Sohee Oh, Hyunwoong Park, J. Chang, 2017, Annals of hepatology.

Novel COL2A1 Variant (c.619G>A, p.Gly207Arg) Manifesting as a Phenotype Similar to Progressive Pseudorheumatoid Dysplasia and Spondyloepiphyseal Dysplasia, Stanescu Type

R. Pauli, N. Sobreira, M. Seong, 2015, Human mutation.

The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV alleles.

P. Stankiewicz, J. Lupski, J. Scull, 2014, American journal of human genetics.

Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia

Seung Jun Lee, J. Y. Kim, Sung Im Cho, 2015, Journal of the Neurological Sciences.

MutationalspectrumoftheSPASTandATL1genesinKoreanpatientswith hereditary spastic paraplegia

M. Seong, J. Sung, Seong-Ho Kang, 2015 .

A Case of Myosin-heavy-chain-9 (MYH9) Gene Mutation Confirmed May-Hegglin Anomaly: 11-year Follow-up

D. Kim, M. Seong, J. Shim, 2016 .

Replication‐Based Rearrangements Are a Common Mechanism for SNCA Duplication in Parkinson's Disease

J. Tainer, Han-Joon Kim, A. Bacolla, 2020, Movement disorders : official journal of the Movement Disorder Society.

Digital polymerase chain reaction for detecting c-MYC copy number gain in tissue and cell-free plasma samples of colorectal cancer patients

H. Lee, W. Kim, Duck-Woo Kim, 2019, Scientific Reports.

Single nucleotide polymorphisms in the TGF-β1 gene are associated with polycystic ovary syndrome susceptibility and characteristics: a study in Korean women

E. Roh, Sue Shin, E. Song, 2016, Journal of Assisted Reproduction and Genetics.

Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome

Hyun-Young Kim, Sung-Eun Jung, S. Lee, 2018, Annals of laboratory medicine.

Chimerism monitoring after allogeneic hematopoietic stem cell transplantation using quantitative real-time PCR of biallelic insertion/deletion polymorphisms.

J. Y. Kim, M. Seong, S. Park, 2014, The Journal of molecular diagnostics : JMD.

Tissue miR-200c-3p and circulating miR-1290 as potential prognostic biomarkers for colorectal cancer

H. Lee, Duck-Woo Kim, Heung-Kwon Oh, 2022, Scientific reports.

Long-Term Quality Control Program Plan for Cord Blood Banks in Korea: A Pilot Study for Cryopreservation Stability

Sohee Oh, B. Kim, E. Roh, 2016, Annals of laboratory medicine.

A case report and literature review of Fanconi Anemia (FA) diagnosed by genetic testing

Seung Jun Lee, M. Seong, S. Park, 2015, Italian Journal of Pediatrics.

Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center

Seung Jun Lee, Sung Im Cho, M. Seong, 2017, Muscle & nerve.

Whole Exome Sequencing Identifies Novel Genetic Alterations in Patients with Pheochromocytoma/Paraganglioma.

Sung Im Cho, M. Seong, S. Park, 2020, Endocrinology and metabolism.

Plasma CC‐chemokine ligand 28 level is correlated with hematopoietic stem cells in human cord blood

Sohee Oh, Hyunwoong Park, E. Roh, 2015, Transfusion.

Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.

Seung Jun Lee, Sung Im Cho, M. Seong, 2015, Investigative ophthalmology & visual science.

Usefulness of a Microcolumn Agglutination Card for Neonates

S. Song, K. Park, Junghan Song, 2010 .

Comparative analysis of HER2 copy number between plasma and tissue samples in gastric cancer using droplet digital PCR

Sang-Hoon Ahn, D. Park, H. Lee, 2020, Scientific Reports.

Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR).

Sung Im Cho, M. Seong, S. Park, 2016, Investigative ophthalmology & visual science.

Diagnostic application of an extensive gene panel for Leber congenital amaurosis with severe genetic heterogeneity.

Seung Jun Lee, J. Y. Kim, Sung Im Cho, 2015, The Journal of molecular diagnostics : JMD.

Clinical Staging and Genetic Profiling of Korean Patients with Primary Lymphedema Using Whole-Exome Sequencing: Preliminary Results

M. Seong, S. Park, Jee-Soo Lee, 2022 .

Identification of novel mutations in the VPS33B gene involved in arthrogryposis, renal dysfunction, and cholestasis syndrome

M. Seong, J. Ko, S. Park, 2015, Clinical genetics.

Comprehensive Study of Microsatellite Instability Testing and Its Comparison With Immunohistochemistry in Gastric Cancers

Sang-Hoon Ahn, D. Park, H. Lee, 2023, Journal of gastric cancer.

Localization of Quantitative Trait Loci for Bone Mineral Density on Chromosome 13 in the Mongolian Population

S. Seo, Seoiyoung Ahn, Jong-Il Kim, 2009 .