Author

Hyojung Yoon

Nationwide Children's HospitalORCID 0000-0002-1376-9527Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:protein structure prediction· 1 Assay:proteomics· 1

Frequent Co-Authors

Tracy A. BedrosianiD· 3 shared Adam P. OstendorfiD· 2 shared Amanda RinglandiD· 2 shared Christopher R. PiersoniD· 2 shared Daniel C. KoboldtiD· 2 shared Diana ThomasiD· 2 shared Erin L. HeinzeniD· 2 shared Sahibjot SraniD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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3 shared papersNeuroscience

Tracy A. BedrosianORCID

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3 papers

Recent·Most cited

Disrupted O-GalNAc glycosylation as a mechanism and biomarker of SLC35A2-associated epilepsy

Robert G. Mealer, James J. Anderson, Sheridan L Smith, Brianna M. Masters, Samuel H. Barth, Kaitlyn D. J. Huizar, Sahibjot Sran, Hyojung Yoon, Amanda Ringland, Savannah Muron, MaryAnn E Bowyer, Alissa M. D’Gama, Annapurna Poduri, Hart G.W. Lidov, Edward Yang, , Tracy A. Bedrosian

This study identifies disrupted O-GalNAc glycosylation as a mechanism and biomarker for SLC35A2-associated epilepsy using mouse models and human tissue analysis.

bioRxiv · Mar 4, 2026 · PreprintNeuroscience

Loss of Slc35a2 alters development of the mouse cerebral cortex

Soad Elziny, Sahibjot Sran, Hyojung Yoon, Rachel R. Corrigan, John Page, Amanda Ringland, Anna Lanier, Sara Lapidus, James Foreman, Erin L. Heinzen, Philip H. Iffland, Peter B. Crino, Tracy A. Bedrosian

This study shows that disrupting Slc35a2 in mouse cortical neurons causes altered neuronal migration and reduced seizure threshold, contributing to MOGHE-like features.

Neuroscience Letters · Jun 22, 2024Peer-reviewedNeuroscience

Detection of brain somatic variation in epilepsy-associated developmental lesions

Tracy A. Bedrosian, Katherine E. Miller, Olivia E. Grischow, Kathleen M. Schieffer, Stephanie LaHaye, Hyojung Yoon, Anthony R. Miller, Jason B. Navarro, Jesse J. Westfall, Kristen Leraas, Samantha S. Choi, Rachel Williamson, James Fitch, Benjamin Kelly, Peter White, , Daniel C. Koboldt

The paper identifies somatic and germline genetic variations in brain tissue from children with epilepsy-associated developmental lesions, highlighting new candidate genes and structural variations.

Epilepsia · Jun 10, 2022Peer-reviewedGenetic & Genomic Medicine