Sungyun Kang
Biochemistry, Genetics and Molecular Biology · Indiana University
Publications
35
Citations
485
Est. group size
—
Recurring co-author estimate
Active years
11
Publishing since 2015
Sungyun Kang studies how DNA is organized and regulated inside cells, focusing on proteins such as CTCF and its testis-specific counterpart BORIS that shape the 3D folding of the genome and control gene activity. A recurring theme is how these proteins govern chromatin looping and gene regulation, particularly in male germ cells and sperm development (spermatogenesis).
Publication activity has been low and intermittent over the past decade, with a cluster of output around 2016–2017 and 2020–2021 and several years with no listed publications.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- The combined action of CTCF and its testis-specific paralog BORIS is essential for spermatogenesis
Nature Communications · 2021
- The combined action of CTCF and its testis-specific paralog BORIS is essential for spermatogenesis
bioRxiv (Cold Spring Harbor Laboratory) · 2021
- CTCF mediates chromatin looping via N-terminal domain-dependent cohesin retention
2020
- CTCF mediates chromatin looping via N-terminal domain-dependent cohesin retention
Proceedings of the National Academy of Sciences · 2020
- Testis-specific transcriptional regulators selectively occupy BORIS-bound CTCF target regions in mouse male germ cells
Scientific Reports · 2017
- Correction: Corrigendum: Testis-specific transcriptional regulators selectively occupy BORIS-bound CTCF target regions in mouse male germ cells
Scientific Reports · 2017
- ATP-degrading ENPP1 is required for survival (or persistence) of long-lived plasma cells
Scientific Reports · 2017
- Additional file 4: Fig. S4. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 12: Fig. S11. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 7: Fig. S7. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 5: Fig. S5. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 5: Fig. S5. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 1: Fig. S1. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 8: Fig. S8. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Additional file 6: Fig. S6. of Comparative analyses of CTCF and BORIS occupancies uncover two distinct classes of CTCF binding genomic regions
Figshare · 2016
- Figshare×22
- Scientific Reports×3
- bioRxiv (Cold Spring Harbor Laboratory)×2
- Proceedings of the National Academy of Sciences×1
- Nature Communications×1
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 11, 2026.
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