Author

Jinsei Jung

Yonsei UniversityORCID 0000-0003-1906-6969Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:database / resource· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Heon Yung GeeiD· 2 shared Ae-Young HeriD· 1 shared Asta BlažytėiD· 1 shared BongHee LeeiD· 1 shared Borah KimiD· 1 shared Byung-Joo HamiD· 1 shared Chan-Mo YangiD· 1 shared Chang Geun KimiD· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Heon Yung GeeORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintNov 17, 2025

10,239 whole genomes with multiomic and clinical health information as the Korean Multiomics Reference dataset

Kyungwhan An, Sungwon Jeon, Yoonsung Kwon…·Jong Bhak

The paper introduces Korea10K, a large genomic dataset of 10,239 Korean genomes with multiomic and clinical data, enabling population-specific variant imputation and insights into genomic-epigenomic regulation.

1 citation

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJun 16, 2025

Rare Missense Variants in MYO7A and OTOP2 Genes in a South Korean Meniere Disease Cohort

Mai T. Pham, Pablo Cruz‐Granados, Seung Hyun Jang…·Jose Antonio Lopez-Escamez

The paper identifies rare missense variants in OTOP2 and MYO7A genes in a South Korean Meniere disease cohort, suggesting their potential pathogenic roles.

DOI 10.1101/2025.06.16.25329383

humanwhole-exome sequencing

𝕏 PostBluesky