Citation Impact
Citing Papers
CRISPR–Cas9 Structures and Mechanisms
2017 StandoutNobel
The study of the relation of DNA repair pathway genes SNPs and the sensitivity to radiotherapy and chemotherapy of NSCLC
2016
Risk factors for lung cancer worldwide
2016
Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement
2014 Standout
Genetic effects on gene expression across human tissues
2017 StandoutNature
From loss to loneliness: The relationship between bereavement and depressive symptoms.
2015
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
2018 Standout
Recent progress and prospects in Sasang constitutional medicine: A traditional type of physiome-based treatment
2014
Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations
2016 StandoutNobel
Genome editing in cardiovascular diseases
2016
Incidence, prevalence, and predictors of chemotherapy-induced peripheral neuropathy: A systematic review and meta-analysis
2014 Standout
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation
2016
Data Mining Algorithms and Techniques in Mental Health: A Systematic Review
2018 Standout
Multimodal biomedical AI
2022 Standout
Meta-Analysis Derived (MAD) Transcriptome of Psoriasis Defines the “Core” Pathogenesis of Disease
2012
Data Mining in Healthcare and Biomedicine: A Survey of the Literature
2011
A tutorial on regularized partial correlation networks.
2018 Standout
Nasopharyngeal carcinoma
2015 Standout
Tutorial: a guide to performing polygenic risk score analyses
2020
Hereditary gene mutations in Korean patients with isolated erythrocytosis
2014
Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights
2018
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
Problematic assumptions have slowed down depression research: why symptoms, not syndromes are the way forward
2015
10 Years of GWAS Discovery: Biology, Function, and Translation
2017 Standout
Proteasome Inhibitors with Photocontrolled Activity
2014 StandoutNobel
Widespread transcription at neuronal activity-regulated enhancers
2010 StandoutNature
Molecular aspects of fructose metabolism and metabolic disease
2021
Metastatic non-small cell lung cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
2018 Standout
Inflammation in obesity, diabetes, and related disorders
2022 Standout
Chemotherapy‐induced peripheral neurotoxicity: A critical analysis
2013
Psoriasis Pathogenesis and Treatment
2019 Standout
Immunology of Psoriasis
2014 Standout
Nanotechnology for Multimodal Synergistic Cancer Therapy
2017 Standout
A network theory of mental disorders
2017 Standout
An Evolutionary Algorithm Approach to Optimal Ensemble Classifiers for DNA Microarray Data Analysis
2008
A survey on ensemble learning
2019 Standout
Reactive Oxygen Species (ROS)-Based Nanomedicine
2019 Standout
The Traditional Medicine and Modern Medicine from Natural Products
2016 Standout
ProSOM: core promoter prediction based on unsupervised clustering of DNA physical profiles
2008
Multigene pathway‐based analyses identify nasopharyngeal carcinoma risk associations for cumulative adverse effects of TERT‐CLPTM1L and DNA double‐strand breaks repair
2014
Works of Hong‐Hee Won being referenced
No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study
2019
Genetic association study of individual symptoms in depression
2012
A Genome-Wide Scan for the Sasang Constitution in a Korean Family Suggests Significant Linkage at Chromosomes 8q11.22–23 and 11q22.1–3
2009
Polymorphic markers associated with severe oxaliplatin‐induced, chronic peripheral neuropathy in colon cancer patients
2011
The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations
2011
Differentially expressed genes in human peripheral blood as potential markers for statin response
2011
EnsemPro: An ensemble approach to predicting transcription start sites in human genomic DNA sequences
2008
Cataloging Coding Sequence Variations in Human Genome Databases
2008
Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease
2015
Myocardial Infarction–Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries
2015
DATA MINING FOR GENE EXPRESSION PROFILES FROM DNA MICROARRAY
2003
Multiple Associated Variants Increase the Heritability Explained for Plasma Lipids and Coronary Artery Disease
2014
A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia
2011
Cancer classification using ensemble of neural networks with multiple significant gene subsets
2006