Author

Hyoungseok Jeon

Seoul National University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Murim ChoiiD· 2 shared Anna ChoiD· 1 shared Byung Chan LimiD· 1 shared Byungsoo Kang· 1 shared Eum Ji Kim· 1 shared Eun Young JeoniD· 1 shared Eunha KimiD· 1 shared Hyuna KimiD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 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

2 shared papersNeuroscience

Murim ChoiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Distinct prefrontal projections conversely orchestrate social competition and hierarchy

Tae-Yong Choi, Hyoungseok Jeon, Sejin Jeong, Eum Ji Kim, Jeongseop Kim, Yun Ha Jeong, Byungsoo Kang, Murim Choi, Ja Wook Koo

The paper identifies distinct mPFC projections that encode social winning and losing behaviors and shows Pou3f1 expression in mPFC-VTA neurons regulates social hierarchy.

Neuron · Dec 11, 2023Peer-reviewedNeuroscience

Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population

Youngha Lee, Soojin Park, Jin Sook Lee, Soo Yeon Kim, Jaeso Cho, Yongjin Yoo, Sangmoon Lee, Taekyeong Yoo, Moses Lee, Jieun Seo, Jeongeun Lee, Jana Kneissl, Jean Lee, Hyoungseok Jeon, Eun Young Jeon, , Jong‐Hee Chae

The paper identifies pathogenic variants in 57.5% of 553 undiagnosed neurodevelopmental patients, revealing a high proportion of recessive variants and their potential for carrier screening.

Scientific Reports · Jan 29, 2020Peer-reviewedGenetics