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Detection Technique for Stator Inter-Turn Faults in BLDC Motors Based on Third-Harmonic Components of Line Currents

IEEE transactions on industry applications, 2017-01, Vol.53 (1), p.143-150

2017

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Guidelines for Laboratory Diagnosis of Coronavirus Disease 2019 (COVID-19) in Korea

Annals of Laboratory Medicine, 2020, 40(5), , pp.351-360

2020

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Copy‐number analysis by base‐level normalization: An intuitive visualization tool for evaluating copy number variations

Clinical genetics, 2023-01, Vol.103 (1), p.35-44

2023

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Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy

Epilepsia (Copenhagen), 2024-03, Vol.65 (3), p.766-778

2024

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ctDNA predicts clinical T1a to pathological T3a upstaging after partial nephrectomy

Cancer science, 2024-05, Vol.115 (5), p.1680-1687

2024

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Genome-wide CpG island methylation and intergenic demethylation propensities vary among different tumor sites

Nucleic acids research, 2016-02, Vol.44 (3), p.1105-1117

2016

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Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples

Clinica chimica acta, 2024-06, Vol.560, p.119703-119703, Article 119703

2024

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Surface and subsurface dispersal of radioactive materials from Fukushima by subpolar gyre and intermediate waters in the North Pacific

Scientific reports, 2024-03, Vol.14 (1), p.5055-5055, Article 5055

2024

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Real‐world data on prognostic value of measurable residual disease assessment by fragment analysis or next‐generation sequencing in multiple myeloma

British journal of haematology, 2022-08, Vol.198 (3), p.503-514

2022

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Applications of molecular barcode sequencing for the detection of low‐frequency variants in circulating tumour DNA from hepatocellular carcinoma

Liver international, 2022-10, Vol.42 (10), p.2317-2326

2022

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Disparate treatment outcomes according to presence of pathogenic mutations in West syndrome

Epilepsia (Copenhagen), 2021-07, Vol.62 (7), p.1656-1664

2021

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Whole exome sequencing identifies mutational signatures of vitreoretinal lymphoma

Haematologica (Roma), 2020-09, Vol.105 (9), p.e458-460

2020

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Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia

Scientific reports, 2020-08, Vol.10 (1), p.14297-14297, Article 14297

2020

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Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy

PloS one, 2019-06, Vol.14 (6), p.e0217521-e0217521

2019

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DYNC2H1 variants cause Leber congenital amaurosis without syndromic features

Clinical genetics, 2021-07, Vol.100 (1), p.111-113

2021

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Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy

Brain & development (Tokyo. 1979), 2020-06, Vol.42 (6), p.438-448

2020

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Immense variability in the sea surface temperature near macro tidal flat revealed by high-resolution satellite data (Landsat 8)

Scientific reports, 2022-01, Vol.12 (1), p.248-248, Article 248

2022

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Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing

Cancer cell international, 2023-05, Vol.23 (1), p.106-106, Article 106

2023

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Effect of Dispersing Carbon Nanotube in Aqueous Solution by Poly-Carboxylic-Based Surfactants on Mechanical and Microstructural Properties as Cementitious Composites

Materials, 2023-11, Vol.16 (21), p.6880

2023

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Early Detection Technique for Stator Winding Inter-Turn Fault in BLDC Motor Using Input Impedance

IEEE transactions on industry applications, 2015-01, Vol.51 (1), p.240-247

2015

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The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective

International journal of molecular sciences, 2023-02, Vol.24 (4), p.3297

2023

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The phenotype and treatment of SCN2A‐related developmental and epileptic encephalopathy

Epileptic disorders, 2020-10, Vol.22 (5), p.563-570

2020

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Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer

Cancer cell international, 2022-02, Vol.22 (1), p.82-82, Article 82

2022

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Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approaches

Hematological oncology, 2020-02, Vol.38 (1), p.82-88

2020

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A comparative study of next-generation sequencing and fragment analysis for the detection and allelic ratio determination of FLT3 internal tandem duplication

Diagnostic pathology, 2022-01, Vol.17 (1), p.14-8, Article 14

2022

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Detection Technique for Stator Inter-Turn Faults in BLDC Motors Based on Third-Harmonic Components of Line Currents

Guidelines for Laboratory Diagnosis of Coronavirus Disease 2019 (COVID-19) in Korea

Copy‐number analysis by base‐level normalization: An intuitive visualization tool for evaluating copy number variations

Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy

ctDNA predicts clinical T1a to pathological T3a upstaging after partial nephrectomy

Genome-wide CpG island methylation and intergenic demethylation propensities vary among different tumor sites

Comparison of exon-level copy number variants in CytoScan XON assay and next-generation sequencing in clinical samples

Surface and subsurface dispersal of radioactive materials from Fukushima by subpolar gyre and intermediate waters in the North Pacific

Real‐world data on prognostic value of measurable residual disease assessment by fragment analysis or next‐generation sequencing in multiple myeloma

Applications of molecular barcode sequencing for the detection of low‐frequency variants in circulating tumour DNA from hepatocellular carcinoma

Disparate treatment outcomes according to presence of pathogenic mutations in West syndrome

Whole exome sequencing identifies mutational signatures of vitreoretinal lymphoma

Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia

Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy

DYNC2H1 variants cause Leber congenital amaurosis without syndromic features

Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy

Immense variability in the sea surface temperature near macro tidal flat revealed by high-resolution satellite data (Landsat 8)

Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing

Effect of Dispersing Carbon Nanotube in Aqueous Solution by Poly-Carboxylic-Based Surfactants on Mechanical and Microstructural Properties as Cementitious Composites

Early Detection Technique for Stator Winding Inter-Turn Fault in BLDC Motor Using Input Impedance

The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective

The phenotype and treatment of SCN2A‐related developmental and epileptic encephalopathy

Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer

Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approaches

A comparative study of next-generation sequencing and fragment analysis for the detection and allelic ratio determination of FLT3 internal tandem duplication

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