scispace - formally typeset
H

Hwahyung Lee

Publications -  8
Citations -  877

Hwahyung Lee is an academic researcher. The author has contributed to research in topics: Trichostatin A & Cancer epigenetics. The author has an hindex of 8, co-authored 8 publications receiving 689 citations.

Papers
More filters
Journal ArticleDOI

An anatomic transcriptional atlas of human glioblastoma

TL;DR: The Ivy Glioblastoma Atlas is presented, an anatomically based transcriptional atlas of human gliOBlastoma that aligns individual histologic features with genomic alterations and gene expression patterns, thus assigning molecular information to the most important morphologic hallmarks of the tumor.
Journal ArticleDOI

Genome-Wide Analysis of Epigenetic Silencing Identifies BEX1 and BEX2 as Candidate Tumor Suppressor Genes in Malignant Glioma

TL;DR: Using an integrated approach, this experimental paradigm provides a powerful new method for the identification of epigenetically silenced genes with potential function as tumor suppressors, biomarkers for disease diagnosis and detection, and therapeutically reversible modulators of critical regulatory pathways important in glioma pathogenesis.
Journal ArticleDOI

Comprehensive Analysis of MGMT Promoter Methylation: Correlation with MGMT Expression and Clinical Response in GBM

TL;DR: A new classification scheme utilizing methylation data from across the entire MGMT promoter is proposed and an analysis based on this approach, which is called 3R classification, is predictive of progression-free survival.
Journal ArticleDOI

Dickkopf-1 is an epigenetically silenced candidate tumor suppressor gene in medulloblastoma.

TL;DR: W whole-genome microarray analysis yielded 714 up-regulated genes in immortalized medulloblastoma cell line D283 on treatment with histone deacetylase (HDAC) inhibitor trichostatin A (TSA).
Journal ArticleDOI

Exploration of the gene fusion landscape of glioblastoma using transcriptome sequencing and copy number data

TL;DR: This study highlights the prevalence of gene fusions as one of the major genomic abnormalities in GBM as a small subset of patients with fusions of receptor tyrosine kinases can benefit from existing FDA approved drugs and drugs available in various clinical trials.