User profiles for Raehun Jung
Raehoon JeongHarvard University Verified email at g.harvard.edu Cited by 23 |
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues
Homeodomains (HDs) are the second largest class of DNA binding domains (DBDs) among
eukaryotic sequence-specific transcription factors (TFs) and are the TF structural class with …
eukaryotic sequence-specific transcription factors (TFs) and are the TF structural class with …
Blood cell traits' GWAS loci colocalization with variation in PU. 1 genomic occupancy prioritizes causal noncoding regulatory variants
R Jeong, ML Bulyk - Cell genomics, 2023 - cell.com
Genome-wide association studies (GWASs) have uncovered numerous trait-associated loci
across the human genome, most of which are located in noncoding regions, making …
across the human genome, most of which are located in noncoding regions, making …
Pharmacokinetic Comparison Between a Fixed-Dose Combination of Atorvastatin/Omega-3-Acid Ethyl Esters and the Corresponding Loose Combination in Healthy …
…, DC Ha, RH Jung, MG Han, WT Jung… - Drug Design …, 2024 - Taylor & Francis
Purpose Statins are widely used in combination with omega-3 fatty acids for the treatment of
patients with dyslipidemia. The aim of this study was to compare the pharmacokinetic (PK) …
patients with dyslipidemia. The aim of this study was to compare the pharmacokinetic (PK) …
Chromatin accessibility variation provides insights into missing regulation underlying immune-mediated diseases
R Jeong, ML Bulyk - BioRxiv, 2024 - pmc.ncbi.nlm.nih.gov
Most genetic loci associated with complex traits and diseases through genome-wide
association studies (GWAS) are noncoding, suggesting that the causal variants likely have gene …
association studies (GWAS) are noncoding, suggesting that the causal variants likely have gene …
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays
…, EE Foster, L Berube, WM Chan, BJ Barry, R Jeong… - …, 2024 - pmc.ncbi.nlm.nih.gov
Purpose: To functionally evaluate novel human sequence-derived candidate genes and
variants for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs). Methods: …
variants for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs). Methods: …
Meta-analysis reveals transcription factors and DNA binding domain variants associated with congenital heart defect and orofacial clef
R Jeong, ML Bulyk - medRxiv, 2025 - medrxiv.org
Many structural birth defect patients lack genetic diagnoses because there are many disease
genes as yet to be discovered. We applied a gene burden test incorporating de novo …
genes as yet to be discovered. We applied a gene burden test incorporating de novo …
A Fast Actuation Mechanism and Energy-Effective Driving Method for Pulse-Closers
J Yoon, R Jung, Y Kim, SJ Ye… - IEEE Transactions on …, 2022 - ieeexplore.ieee.org
When a recloser detects fault currents in electric power distribution lines, it breaks the line and
then restores the line after several fault tests. To check whether fault remains, the recloser …
then restores the line after several fault tests. To check whether fault remains, the recloser …
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays
Purpose: To functionally evaluate novel human sequence-derived candidate genes and
variants for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs). Methods: …
variants for unsolved ocular congenital cranial dysinnervation disorders (oCCDDs). Methods: …
DNA binding analysis of rare variants in homeodomains reveals novel homeodomain specificity-determining residues
Homeodomains (HDs) are the second largest class of DNA binding domains (DBDs) among
eukaryotic sequence-specific transcription factors (TFs) and play important roles in …
eukaryotic sequence-specific transcription factors (TFs) and play important roles in …
Colocalization of blood cell traits GWAS associations and variation in PU. 1 genomic occupancy prioritizes causal noncoding regulatory variants
R Jeong, ML Bulyk - bioRxiv, 2023 - pmc.ncbi.nlm.nih.gov
Genome-wide association studies (GWAS) have uncovered numerous trait-associated loci
across the human genome, most of which are located in noncoding regions, making …
across the human genome, most of which are located in noncoding regions, making …