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Issue Date Title Journals
2024-02 Personalized Biomarker-Based Umbrella Trial for Patients With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma: KCSG HN 15-16 TRIUMPH Trial Journal of Clinical Oncology
2024-01 Immunological subtyping of salivary gland cancer identifies histological origin-specific tumor immune microenvironment Npj Precision Oncology
2023-12 Comprehensive benchmarking and guidelines of mosaic variant calling strategies Nature Methods
2023-10 CanISO: a database of genomic and transcriptomic variations in domestic dog (Canis lupus familiaris) BMC Genomics
2023-09 Copy number aberrations in circulating tumor DNA enables prognosis prediction and molecular characterization of breast cancer Journal of the National Cancer Institute
2023-08 Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders Journal of Molecular Diagnostics
2023-07 Targeting Wnt/β-catenin-mediated upregulation of oncogenic NLGN3 suppresses cancer stem cells in glioblastoma Cell death & disease
2023-05 Genomic and transcriptomic profiling reveal molecular characteristics of parathyroid carcinoma EXPERIMENTAL AND MOLECULAR MEDICINE
2023-03 Human induced pluripotent stem cell line YCMi007-A generated from a dilated cardiomyopathy patient with a heterozygous dominant c.613C > T (p. Arg205Trp) variant of the TNNT2 gene STEM CELL RESEARCH
2022-10 Characterizing intrinsic molecular features of the immune subtypes of salivary mucoepidermoid carcinoma TRANSLATIONAL ONCOLOGY
2022-09 Analysis of low-level somatic mosaicism reveals stage and tissue-specific mutational features in human development PLoS genetics
2022-08 An induced pluripotent stem cell line (YCMi006-A) generated from a patient with hypertrophic cardiomyopathy who carries the ACTA1 mutation p.Ile343Met Stem Cell Research
2022-06 HLA-I-restricted CD8<sup>+</sup> T cell immunity may accelerate tumorigenesis in conjunction with VHL inactivation Iscience
2022-04 Tumor microenvironment-aware, single-transcriptome prediction of microsatellite instability in colorectal cancer using meta-analysis SCIENTIFIC REPORTS
2022-04 Insignificant effects of loss of heterozygosity in HLA in the efficacy of immune checkpoint blockade treatment GENES & GENOMICS
2022-04 Derivation of YCMi005-A, a human-induced pluripotent stem cell line, from a patient with dilated cardiomyopathy carrying missense variant in TPM1 (p. Glu192Lys) STEM CELL RESEARCH
2022-03 H-1 NMR based urinary metabolites profiling dataset of canine mammary tumors Scientific data
2022-03 Generation of a human induced pluripotent stem cell line YCMi004-A from a patient with dilated cardiomyopathy carrying a protein-truncating mutation of the Titin gene and its differentiation towards cardiomyocytes STEM CELL RESEARCH
2022-02 Establishment of reference standards for multifaceted mosaic variant analysis Scientific Data
2022-01 Genome-wide association study identifies TNFSF15 associated with childhood asthma ALLERGY
2021-12 Genomic and transcriptomic characterization of heterogeneous immune subgroups of microsatellite instability-high colorectal cancers Journal for ImmunoTherapy of Cancer
2021-10 Establishment of a novel human iPSC line (YCMi003-A) from a patient with dilated cardiomyopathy carrying genetic variant LMNA p.Asp364His. STEM CELL RESEARCH
2021-05 Comprehensive Analysis of Mutation-Based and Expressed Genes-Based Pathways in Head and Neck Squamous Cell Carcinoma PROCESSES
2021-04 Genomic landscape of extraordinary responses in metastatic breast cancer COMMUNICATIONS BIOLOGY
2021-03 Profiling of conditionally reprogrammed cell lines for in vitro chemotherapy response prediction of pancreatic cancer EBioMedicine
2021-02 Development of a program for in silico optimized selection of oligonucleotide-based molecular barcodes PLOS ONE
2020-11 An Improved, Assay Platform Agnostic, Absolute Single Sample Breast Cancer Subtype Classifier Cancers
2020-09 Wnt/β-catenin signaling pathway induces autophagy-mediated temozolomide-resistance in human glioblastoma CELL DEATH & DISEASE
2020-07 Cross-species oncogenic signatures of breast cancer in canine mammary tumors NATURE COMMUNICATIONS
2020-07 Prognostic value of cd200r1 mrna expression in head and neck squamous cell carcinoma Cancers
2020-05 Comparison of whole mitochondrial genome variants between hair shafts and reference samples using massively parallel sequencing INTERNATIONAL JOURNAL OF LEGAL MEDICINE
2020-04 Molecular subtypes of oropharyngeal cancer show distinct immune microenvironment related with immune checkpoint blockade response BRITISH JOURNAL OF CANCER
2019-11 Molecular characterization of lung adenocarcinoma from Korean patients using next generation sequencing PLOS ONE
2019-11 Impact of mouse contamination in genomic profiling of patient-derived models and best practice for robust analysis Genome Biology
2019-11 BAMixChecker: an automated checkup tool for matched sample pairs in NGS cohort BIOINFORMATICS
2019-08 Whole-exome and whole-transcriptome sequencing of canine mammary gland tumors Scientific Data
2019-07 Characteristic gene alterations in primary gastrointestinal T- and NK-cell lymphomas. LEUKEMIA
2019-04 A therapeutic strategy for chemotherapy-resistant gastric cancer via destabilization of both β-catenin and ras Cancers
2019-03 The use of technical replication for detection of low-level somatic mutations in next-generation sequencing NATURE COMMUNICATIONS
2019-01 Investigating the Feasibility of Targeted Next-Generation Sequencing to Guide the Treatment of Head and Neck Squamous Cell Carcinoma CANCER RESEARCH AND TREATMENT
2019-01 Molecular Diagnostic Assays and Clinicopathologic Implications of MET Exon 14 Skipping Mutation in Non–small-cell Lung Cancer CLINICAL LUNG CANCER
2018-12 Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylation Neurology: Genetics
2018-04 Neopepsee: accurate genome-level prediction of neoantigens by harnessing sequence and amino acid immunogenicity information ANNALS OF ONCOLOGY
2018-04 AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing BIOINFORMATICS
2018-03 Palmitate and minimally-modified low-density lipoprotein cooperatively promote inflammatory responses in macrophages. PLOS ONE
2018-03 Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy EPILEPSY RESEARCH
2018-02 Isoform specific gene expression analysis of KRAS in the prognosis of lung adenocarcinoma patients BMC BIOINFORMATICS
2017-12 Somatic mutation driven codon transition bias in human cancer SCIENTIFIC REPORTS
2017-11 Next-generation sequencing reveals novel resistance mechanisms and molecular heterogeneity in EGFR-mutant non-small cell lung cancer with acquired resistance to EGFR-TKIs LUNG CANCER
2017-05 In Silico Simulation of Signal Cascades in Biomedical Networks Based on the Production Rule System Lecture Notes in Computer Science
2017-03 Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia AMERICAN JOURNAL OF HUMAN GENETICS
2016-10 Vecuum: identification and filtration of false somatic variants caused by recombinant vector contamination BIOINFORMATICS
2016-08 ISOexpresso: a web-based platform for isoform-level expression analysis in human cancer BMC GENOMICS
2016-04 Pilot Study of a Next-Generation Sequencing-Based Targeted Anticancer Therapy in Refractory Solid Tumors at a Korean Institution PLOS ONE
2016-03 Next-generation sequencing reveals somatic mutations that confer exceptional response to everolimus ONCOTARGET
2016-03 Establishment and characterisation of patient-derived xenografts as paraclinical models for gastric cancer SCIENTIFIC REPORTS
2016-01 Exome sequencing reveals recurrent REV3L mutations in cisplatin-resistant squamous cell carcinoma of head and neck SCIENTIFIC REPORTS
2015-12 Analysis of Whole Transcriptome Sequencing Data: Workflow and Software Genomics & Informatics
2015-12 An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development NATURE MEDICINE
2015-08 SoloDel: a probabilistic model for detecting low-frequent somatic deletions from unmatched sequencing data BIOINFORMATICS
2015-05 Identification of genomic features in the classification of loss- and gain-of-function mutation BMC MEDICAL INFORMATICS AND DECISION MAKING
2015-05 Context-based resolution of semantic conflicts in biological pathways BMC MEDICAL INFORMATICS AND DECISION MAKING
2015-04 Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy NATURE MEDICINE
2014-09 A Systems Approach to Predict Oncometabolites via Context-Specific Genome-Scale Metabolic Networks PLOS COMPUTATIONAL BIOLOGY
2013-08 Virmid: accurate detection of somatic mutations with sample impurity inference GENOME BIOLOGY
2013-07 Reprever: resolving low-copy duplicated sequences using template driven assembly NUCLEIC ACIDS RESEARCH
2013-04 Evaluating genome architecture of a complex region via generalized bipartite matching BMC BIOINFORMATICS
2013-04 Wessim: a whole-exome sequencing simulator based on in silico exome capture BIOINFORMATICS
2012-08 De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly NATURE GENETICS
2011-12 Exploring molecular links between lymph node invasion and cancer prognosis in human breast cancer BMC SYSTEMS BIOLOGY
2011-01 Context-dependent transcriptional regulations between signal transduction pathways BMC BIOINFORMATICS
2009-03 Mining metastasis related genes by primary-secondary tumor comparisons from large-scale databases Bmc Bioinformatics
2008-08 Computational identification of significantly regulated metabolic reactions by integration of data on enzyme activity and gene expression BMB REPORTS
2007-11 BioCAD: an information fusion platform for bio-network inference and analysis BMC BIOINFORMATICS