Author

In Gyeong Koh

Korea UniversityORCID 0009-0008-8228-1622Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:differential expression· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Approach:deep learning· 1 Approach:experimental assay· 1

Frequent Co-Authors

Joon‐Yong AniD· 3 shared Donna M. WerlingiD· 2 shared Hyeji LeeiD· 2 shared Il Bin KimiD· 2 shared Jihae LeeiD· 2 shared Yujin KimiD· 2 shared Chanhee KimiD· 1 shared Daekee LeeiD· 1 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersBioinformatics

Joon‐Yong AnORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BioinformaticsbioRxivPreprintAug 26, 2026

AI-driven framework modeling perturbation in brain organoids reveals candidate genes for autism

In Gyeong Koh, Eunhyong Chang, Young Seok Choi…·Joon‐Yong An

The paper uses an AI-driven framework to model perturbations in brain organoids and identifies candidate genes for autism using genomic and clinical data.

2 citations

humanscRNA-seq

𝕏 PostBluesky

NeuroscienceExperimental & Molecular MedicinePeer-reviewedOct 3, 2024

An integrative single-cell atlas to explore the cellular and temporal specificity of neurological disorder genes during human brain development

Seoyeon Kim, Jihae Lee, In Gyeong Koh…·Joon‐Yong An

The paper constructs a single-cell atlas of developing human brains to analyze the temporal and cellular specificity of neurological disorder genes across 393,060 cells.

44 citationstop 2%

humanscRNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicineBriefings in BioinformaticsPeer-reviewedMay 23, 2024

CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data

Yujin Kim, Minwoo Jeong, In Gyeong Koh…·Joon‐Yong An

CWAS-Plus identifies noncoding variant associations in whole-genome sequencing data using cell-type-specific functional data, finding links to autism and Alzheimer's disease.

17 citationstop 4%

humanwhole-genome sequencing

𝕏 PostBluesky