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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.
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.
Identification of Ethnically Specific Genetic Variations in Pan-Asian Ethnos
Jin Ok Yang, Sohyun Hwang, Woo-Yeon Kim, Seong-Jin Park, Sang Cheol Kim, Kiejung Park, Byungwook Lee
Genomics Inform. 2014;12(1):42-47.   Published online March 31, 2014
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Web-Based Database and Viewer of East Asian Copy Number Variations
Ji-Hong Kim, Hae-Jin Hu, Yeun-Jun Chung
Genomics Inform. 2012;10(1):65-67.   Published online March 31, 2012
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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.
Identifying Copy Number Variants under Selection in Geographically Structured Populations Based on F-statistics
Hae-Hiang Song, Hae-Jin Hu, In-Hae Seok, Yeun-Jun Chung
Genomics Inform. 2012;10(2):81-87.   Published online June 30, 2012
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A Genome-wide Association Study of Copy Number Variation in Hematological Parameters in the Korean Population.
Ka Kyung Kim, Yoon Shin Cho, Nam H Cho, Chol Shin, Jong Won Kim
Genomics Inform. 2010;8(3):122-130.
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.
Genome Architecture and Its Roles in Human Copy Number Variation
Lu Chen, Weichen Zhou, Ling Zhang, Feng Zhang
Genomics Inform. 2014;12(4):136-144.   Published online December 31, 2014
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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.
Genome-wide Survey of Copy Number Variants Associated with Blood Pressure and Body Mass Index in a Korean Population.
Sanghoon Moon, Young Jin Kim, Yun Kyoung Kim, Dong Joon Kim, Ji Young Lee, Min Jin Go, Young Ah Shin, Chang Bum Hong, Bong Jo Kim
Genomics Inform. 2011;9(4):152-160.
Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data
Soon-Young Kim, Ji-Hong Kim, Yeun-Jun Chung
Genomics Inform. 2012;10(3):194-199.   Published online September 28, 2012
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Identification of a Copy Number Variation on Chromosome 20q13.12 Associated with Osteoporotic Fractures in the Korean Population
Tae-Joon Park, Mi Yeong Hwang, Sanghoon Moon, Joo-Yeon Hwang, Min Jin Go, Bong-Jo Kim
Genomics Inform. 2016;14(4):216-221.   Published online December 31, 2016
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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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