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- Copy Number Variations in the Human Genome: Potential Source for Individual Diversity and Disease Association Studies.
- Tae Min Kim, Seon Hee Yim, Yeun Jun Chung
- Genomics Inform. 2008;6(1):1-7.
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- Replication of the Association between Copy Number Variation on 8p23.1 and Autism by Using ASD-specific BAC Array.
- Jung Hoon Woo, Song Ju Yang, Seon Hee Yim, Hae Jin Hu, Myung Ju Shin, Eun Hee Oh, Hyun Woong Kang, Seonyang Park, Yeun Jun Chung
- Genomics Inform. 2010;8(1):19-27.
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- No Association between Copy Number Variation of the TCRB Gene and the Risk of Autism Spectrum Disorder in the Korean Population.
- So Young Yang, Seon Hee Yim, Hae Jin Hu, Soon Ae Kim, Hee Jeong Yoo, Yeun Jun Chung
- Genomics Inform. 2010;8(2):76-80.
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- Current Status and Future Clinical Applications of Array.based Comparative Genomic Hybridization.
- Seon Hee Yim, Yeun Jun Chung
- Genomics Inform. 2004;2(3):113-120.
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- CGHscape: A Software Framework for the Detection and Visualization of Copy Number Alterations.
- Yong Bok Jeong, Tae Min Kim, Yeun Jun Chung
- Genomics Inform. 2008;6(3):126-129.
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- Comparison of the Affymetrix SNP Array 5.0 and Oligoarray Platforms for Defining CNV.
- Ji Hong Kim, Seung Hyun Jung, Hae Jin Hu, Seon Hee Yim, Yeun Jun Chung
- Genomics Inform. 2010;8(3):138-141.
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- Comparison of Normalization Methods for Defining Copy Number Variation Using Whole-genome SNP Genotyping Data.
- Ji Hong Kim, Seon Hee Yim, Yong Bok Jeong, Seong Hyun Jung, Hai Dong Xu, Seung Hun Shin, Yeun Jun Chung
- Genomics Inform. 2008;6(4):231-234.
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