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Intron retention is a widespread mechanism of tumor-suppressor inactivation

Nature genetics, 2015-11, Vol.47 (11), p.1242-1248

2015

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Tracing Oncogene Rearrangements in the Mutational History of Lung Adenocarcinoma

Cell, 2019-06, Vol.177 (7), p.1842-1857.e21

2019

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Mutalisk: a web-based somatic MUTation AnaLyIS toolKit for genomic, transcriptional and epigenomic signatures

Nucleic acids research, 2018-07, Vol.46 (W1), p.W102-W108

2018

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Systematic Guidelines for Effective Utilization of COVID-19 Databases in Genomic, Epidemiologic, and Clinical Research

Viruses, 2023-03, Vol.15 (3), p.692

2023

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HSPA5 and FGFR1 genes in the mesenchymal subtype of glioblastoma can improve a treatment efficacy

Animal cells and systems, 2024, Vol.28 (1), p.216-227

2024

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Single-cell RNA sequencing of nc886, a non-coding RNA transcribed by RNA polymerase III, with a primer spike-in strategy

PloS one, 2024-08, Vol.19 (8), p.e0301562

2024

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Systematic investigation of cancer-associated somatic point mutations in SNP databases

Nature biotechnology, 2013-09, Vol.31 (9), p.787-789

2013

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Distinct genomic profiles of gestational choriocarcinoma, a unique cancer of pregnant tissues

Experimental and Molecular Medicine, 2020, 52(0), , pp.1-9

2020

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OGT and FLAD1 Genes Had Significant Prognostic Roles in Progressive Pathogenesis in Prostate Cancer

The world journal of men's health, 2023-07, Vol.41 (3), p.712

2023

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Aldehyde dehydrogenase is used by cancer cells for energy metabolism

Experimental & molecular medicine, 2016-11, Vol.48 (11), p.e272-e272

2016

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FIREVAT: finding reliable variants without artifacts in human cancer samples using etiologically relevant mutational signatures

Genome medicine, 2019-12, Vol.11 (1), p.81-81, Article 81

2019

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RhoGAP domain-containing fusions and PPAPDC1A fusions are recurrent and prognostic in diffuse gastric cancer

Nature communications, 2018-10, Vol.9 (1), p.4439-13, Article 4439

2018

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Genomic profile analysis of diffuse-type gastric cancers

Genome biology, 2014-04, Vol.15 (4), p.R55-R55

2014

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A retrospective single-centered, comprehensive targeted genetic sequencing analysis of prognostic survival using tissues from Korean patients with metastatic renal cell carcinoma after targeted therapy

Investigative and clinical urology, 2022-11, Vol.63 (6), p.602-611

2022

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Abstract 5413: AIVE, an artificial intelligence protein miner based on omics data to discover new cancer druggable candidates

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.5413-5413

Hong, Dongwan

2023

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Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals

Nature genetics, 2011-08, Vol.43 (8), p.745-752

2011

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Epithelial Splicing Regulatory Protein (ESPR1) Expression in an Unfavorable Prognostic Factor in Prostate Cancer Patients

Frontiers in oncology, 2020-10, Vol.10, p.556650-556650

2020

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FX: an RNA-Seq analysis tool on the cloud

Bioinformatics (Oxford, England), 2012-03, Vol.28 (5), p.721-723

2012

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Reply to Krupenko et al. Comment on “Lee et al. The Combination of Loss of ALDH1L1 Function and Phenformin Treatment Decreases Tumor Growth in KRAS-Driven Lung Cancer Cancers 2020, 12, 1382”

Cancers, 2021-05, Vol.13 (9), p.2238

2021

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Genomic characterization of clonal evolution during oropharyngeal carcinogenesis driven by human papillomavirus 16

BMB reports, 2018-11, Vol.51 (11), p.584-589

2018

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Reference-unbiased copy number variant analysis using CGH microarrays

Nucleic acids research, 2010-11, Vol.38 (20), p.e190-e190

2010

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TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology

Nucleic acids research, 2011-01, Vol.39 (Database issue), p.D883-D888

2011

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Clonal dynamics in early human embryogenesis inferred from somatic mutation

Nature (London), 2021-09, Vol.597 (7876), p.393-397

2021

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Extraction of Informative Genes from Multiple Microarray Data Integrated by Rank-Based Approach

IEICE Transactions on Information and Systems, 2011/04/01, Vol.E94.D(4), pp.841-854

2011

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Intron retention is a widespread mechanism of tumor-suppressor inactivation

Tracing Oncogene Rearrangements in the Mutational History of Lung Adenocarcinoma

Mutalisk: a web-based somatic MUTation AnaLyIS toolKit for genomic, transcriptional and epigenomic signatures

Systematic Guidelines for Effective Utilization of COVID-19 Databases in Genomic, Epidemiologic, and Clinical Research

HSPA5 and FGFR1 genes in the mesenchymal subtype of glioblastoma can improve a treatment efficacy

Single-cell RNA sequencing of nc886, a non-coding RNA transcribed by RNA polymerase III, with a primer spike-in strategy

Systematic investigation of cancer-associated somatic point mutations in SNP databases

Distinct genomic profiles of gestational choriocarcinoma, a unique cancer of pregnant tissues

OGT and FLAD1 Genes Had Significant Prognostic Roles in Progressive Pathogenesis in Prostate Cancer

Aldehyde dehydrogenase is used by cancer cells for energy metabolism

FIREVAT: finding reliable variants without artifacts in human cancer samples using etiologically relevant mutational signatures

RhoGAP domain-containing fusions and PPAPDC1A fusions are recurrent and prognostic in diffuse gastric cancer

Genomic profile analysis of diffuse-type gastric cancers

Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

A retrospective single-centered, comprehensive targeted genetic sequencing analysis of prognostic survival using tissues from Korean patients with metastatic renal cell carcinoma after targeted therapy

Abstract 5413: AIVE, an artificial intelligence protein miner based on omics data to discover new cancer druggable candidates

Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals

Epithelial Splicing Regulatory Protein (ESPR1) Expression in an Unfavorable Prognostic Factor in Prostate Cancer Patients

FX: an RNA-Seq analysis tool on the cloud

Reply to Krupenko et al. Comment on “Lee et al. The Combination of Loss of ALDH1L1 Function and Phenformin Treatment Decreases Tumor Growth in KRAS-Driven Lung Cancer Cancers 2020, 12, 1382”

Genomic characterization of clonal evolution during oropharyngeal carcinogenesis driven by human papillomavirus 16

Reference-unbiased copy number variant analysis using CGH microarrays

TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology

Clonal dynamics in early human embryogenesis inferred from somatic mutation

Extraction of Informative Genes from Multiple Microarray Data Integrated by Rank-Based Approach

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