Author

S-A Lim

Seoul National UniversityORCID 0000-0002-4137-1671Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Alessandro SerrettiiD· 1 shared Bernhard Theodor BauneiD· 1 shared Byung-Chul Lee· 1 shared Cantas AleviD· 1 shared Cathryn M. LewisiD· 1 shared Chiara FabbriiD· 1 shared Chris Wai Hang LoiD· 1 shared Chul‐Hwan LeeiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alessandro SerrettiORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Mtf2 Safeguards Naïve Pluripotency by Restricting Trophectoderm Competence

Seong-Min Kim, S-A Lim, Seong-Kyun Lim, Yeon-Joon Chu, Jiwon Bu, Young-Woo Won, Keun-Tae Kim, Hanbyeol Kim, Cantas Alev, Murim Choi, Chul‐Hwan Lee, Hyuk‐Jin Cha

This study identifies Mtf2 as an epigenetic barrier that maintains naive pluripotency by restricting trophectoderm competence in embryonic stem cells.

bioRxiv · Jun 14, 2026 · PreprintDevelopmental Biology

Trans-ancestry genome-wide association meta-analysis of antidepressant response to selective serotonin reuptake inhibitors in clinical studies of depression

Ke Hu, Chris Wai Hang Lo, Swapnil Awasthi, Oliver Pain, Madhurbain Singh, Yeeun Ahn, Katherine Jean Aitchison, Bernhard Theodor Baune, Joanna M. Biernacka, Guido Bondolfi, Tania Carrillo‐Roa, Hong Choi, Darina Czamara, Katharina Domschke, Chiara Fabbri, , Cathryn M. Lewis

This study performs a trans-ancestry GWAS of SSRI response in depression, finding suggestive associations and enrichment in serotonergic pathways but no genome-wide significant variants.

medRxiv · Jun 4, 2026 · PreprintGenetic & Genomic Medicine