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BMC Medical Genetics|October 13, 2020
Pathogenic NF1 truncating mutation and copy number alterations in a dedifferentiated liposarcoma with multiple lung metastasis: a case reportYoon-Seob Kim, Sun Shin, Seung-Hyun Jung, et al.
The Korean Journal of Internal Medicine|May 22, 2015
Clinical implications of copy number variations in autoimmune disordersSeon-Hee Yim, Seung-Hyun Jung, Boram Chung, et al.
BMC Bioinformatics|May 3, 2022
tReasure: R-based GUI package analyzing tRNA expression profiles from small RNA sequencing dataJin-Ok Lee, Jiyon Chu, Gyuyeon Jang, et al.
Genomics & Informatics|October 30, 2012
Identifying Copy Number Variants under Selection in Geographically Structured Populations Based on F-statisticsHae-Hiang Song, Hae-Jin Hu, In-Hae Seok, et al.
Genomics & Informatics|February 24, 2015
MAP: Mutation Arranger for Defining Phenotype-Related Single-Nucleotide VariantIn-Pyo Baek, Yong-Bok Jeong, Seung-Hyun Jung, et al.
Experimental & Molecular Medicine|November 19, 2025
RPS24 microexon isoform as a novel biomarker for estrogen receptor-positive breast cancer progression and therapeutic resistanceJiyeon Park, Dahye Nam, Seung-Hyun Jung, et al.
The Journal of Dermatology|September 19, 2022
Genomic landscape of multiple Bowen's disease using whole-exome sequencingYoon-Seob Kim, Gyeong Sin Park, Chul Hwan Bang, et al.
International Journal of Molecular Sciences|May 7, 2025
Single-Cell RNA Sequencing of Baseline Immune Profiles After Third Vaccination Associated with Subsequent SARS-CoV-2 Infection in Naïve IndividualsHyunhye Kang, Junseong Park, Hyunjoo Bae, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 22, 2007
Germline methylation patterns inferred from local nucleotide frequency of repetitive sequences in the human genomeTae-Min Kim, Yeun-Jun Chung, Mun-Gan Rhyu, et al.
BMC Bioinformatics|November 21, 2007
Inferring biological functions and associated transcriptional regulators using gene set expression coherence analysisTae-Min Kim, Yeun-Jun Chung, Mun-Gan Rhyu, et al.
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