Author

Sung Kweon Cho

Ajou UniversityORCID 0000-0002-5929-7932Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Byung Gon KimiD· 1 shared Cheryl Ann WinkleriD· 1 shared Daeui ParkiD· 1 shared Do Hyeon ChaiD· 1 shared Gi Tae Kim· 1 shared Heekyung Kho· 1 shared Heon Yung GeeiD· 1 shared Hohyeon Lee· 1 shared

Activity by Year

2018-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 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

1 shared paperNeuroscience

Byung Gon KimORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Novel mouse model of cerebral microbleeds created by Crispr/Cas9-mediated Col4a1 deletion in adult brain microvessels

Hyunmi Kim, Yeojin Seo, Heekyung Kho, Shivani Shailendrakumar Singh, Jina Lee, Hohyeon Lee, Ji-Won Hwang, Tae‐Ryong Riew, Seungyon Koh, Jun Young Choi, Hyun Woong Roh, Sang Joon Son, Gi Tae Kim, Sung Kweon Cho, Hyun‐Seok Jin, , Byung Gon Kim

This study creates a novel mouse model of cerebral microbleeds by deleting Col4a1 in adult brain microvessels, showing progressive CMB burden and cognitive decline.

bioRxiv · Jun 22, 2025 · PreprintNeuroscience

Genetic predisposition to hypouricemia on whole-exome sequencing analysis and its utilities in primary screening purposes

Do Hyeon Cha, Heon Yung Gee, Raúl E. Cachau, Jong Mun Choi, Daeui Park, Sun Ha Jee, Seungho Ryu, Kyeong Kyu Kim, Cheryl Ann Winkler, Sung Kweon Cho

This paper uses whole-exome sequencing to identify genetic markers for hypouricemia and shows that screening two SNPs can detect 87.7% of cases.

bioRxiv · Nov 8, 2018 · PreprintGenetics