Author
Kihoon Han
Korea UniversityORCID 0000-0002-5925-2152Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
Click to filter author papersSignature Assays, Organisms & Methods
Click to filter · or open tagActivity by Year
2020-2026 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 36 mutual co-author links5 papers
Recent·Most cited
- NeurosciencebioRxivPreprintDOI 10.64898/2026.10.27.762134
- NeuroscienceExperimental & Molecular MedicinePeer-reviewed
Asymmetric distribution of mitochondrial Ca2+ regulators specifies compartment-specific mitochondrial function and neuronal development
Dong Cheol Jang, Su Yeon Kim, Won Seok Kim…·Seok‐Kyu Kwon
The paper identifies compartment-specific mitochondrial Ca2+ dynamics in neurons and their molecular regulators, showing how these differences affect neuronal development.
DOI 10.1038/s12276-026-01803-2 - NeurosciencebioRxivPreprint
Longitudinal deep phenotyping in a mouse model of West syndrome reveals temporal dynamics of synapse remodeling, gliosis, and proteomic and lipidomic changes during seizure evolution
Ruiying Ma, Muwon Kang, Gyu Hyun Kim…·Kihoon Han
This study uses longitudinal multi-omic analyses of a mouse model to show seizure evolution in West syndrome involves synaptic remodeling, gliosis, and proteomic/lipidomic changes over time.
DOI 10.1101/2025.05.06.652352 - NeuroscienceFrontiers in Molecular NeurosciencePeer-reviewed
Neuronal mitochondrial morphology is significantly affected by both fixative and oxygen level during perfusion
Su Yeon Kim, Klaudia Strucinska, Bertha Osei…·Tommy L. Lewis
This study identifies fixation and oxygen levels during perfusion as critical factors affecting neuronal mitochondrial morphology in vitro and in vivo.
- GeneticsGenome ResearchPeer-reviewed
Co-expression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders
Kaifang Pang, Li Wang, Wei Wang…·Zhandong Liu
The paper identifies a convergent defect in neural progenitor cell transitions during fetal development associated with autism and epilepsy using single-cell RNA sequencing and gene co-expression analysis.