Cytidine deaminase polymorphisms and worse treatment response in normal karyotype AML von Hyo Kim, Lyoung, Sub Cheong, Hyun, Koh, Youngil, Ahn, Kwang-Sung, Lee, Chansu, Kim, Hyung-Lae, Doo Shin, Hyoung, Yoon, Sung-Soo

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Expression efficiency of NAT2 haplotypes in a Korean population von Na, Han Sung, Lee, Jin Sol, Cheong, Hyun Sub, Shin, Hee Jung, Kang, Tae Sun, Park, Hyun Joo, Shin, Hyoung Doo, Chung, Myeon Woo

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Two independent variants of epidermal growth factor receptor associated with risk of glioma in a Korean population von Baek, In Ki, Cheong, Hyun Sub, Namgoong, Seok, Kim, Jeong-Hyun, Kang, Seok-Gu, Yoon, Seon-Jin, Kim, Se Hoon, Chang, Jong Hee, Kim, Lyoung Hyo, Shin, Hyoung Doo

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A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease von Kim, Jeong-Hyun, Cheong, Hyun Sub, Sul, Jae Hoon, Seo, Jeong-Meen, Kim, Dae-Yeon, Oh, Jung-Tak, Park, Kwi-Won, Kim, Hyun-Young, Jung, Soo-Min, Jung, Kyuwhan, Cho, Min Jeng, Bae, Joon Seol, Shin, Hyoung Doo

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TPX2 prompts mitotic survival via the induction of BCL2L1 through YAP1 protein stabilization in human embryonic stem cells von Kim, Yun-Jeong, Go, Young-Hyun, Jeong, Ho-Chang, Kwon, Eun-Ji, Kim, Seong-Min, Cheong, Hyun Sub, Kim, Wantae, Shin, Hyoung Doo, Lee, Haeseung, Cha, Hyuk-Jin

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Association analysis of RTEL1 variants with risk of adult gliomas in a Korean population von Namgoong, Suhg, Cheong, Hyun Sub, Kim, Jeong-Hyun, Kim, Lyoung Hyo, Seo, Jung Yeon, Kang, Seok-Gu, Yoon, Seon-Jin, Kim, Se Hoon, Chang, Jong Hee, Shin, Hyoung Doo

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Identification of copy number variations and common deletion polymorphisms in cattle von Bae, Joon Seol, Cheong, Hyun Sub, Kim, Lyoung Hyo, NamGung, Suk, Park, Tae Joon, Chun, Ji-Yong, Kim, Jason Yongha, Pasaje, Charisse Flerida A, Lee, Jin Sol, Shin, Hyoung Doo

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Possible role of EMID2 on nasal polyps pathogenesis in Korean asthma patients von Pasaje, Charisse Flerida Arnejo, Bae, Joon Seol, Park, Byung-Lae, Cheong, Hyun Sub, Kim, Jeong-Hyun, Jang, An-Soo, Uh, Soo-Taek, Park, Choon-Sik, Shin, Hyoung Doo

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Frequent amplification of CENPF, GMNN and CDK13 genes in hepatocellular carcinomas von Kim, Hye-Eun, Kim, Dae-Ghon, Lee, Kyung Jin, Son, Jang Geun, Song, Min-Young, Park, Young-Mi, Kim, Jae-Jung, Cho, Sung-Won, Chi, Sung-Gil, Cheong, Hyun Sub, Shin, Hyoung Doo, Lee, Sang-Wook, Lee, Jong-Keuk

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A genome-wide association study identified new variants associated with the risk of chronic hepatitis B von Kim, Yoon Jun, Kim, Hwi Young, Lee, Jeong-Hoon, Yu, Su Jong, Yoon, Jung-Hwan, Lee, Hyo-Suk, Kim, Chung Yong, Cheong, Jae Youn, Cho, Sung Won, Park, Neung Hwa, Park, Byung Lae, Namgoong, Seok, Kim, Lyoung Hyo, Cheong, Hyun Sub, Shin, Hyoung Doo

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Identification of genetic polymorphisms in FABP3 and FABP4 and putative association with back fat thickness in Korean native cattle von Cho, S.A. (Seoul National University, Seoul, Republic of Korea), Park, T.S. (Seoul National University, Seoul, Republic of Korea), Yoon, D.H. (National Livestock Research Institute, RDA, Suwon, Republic of Korea), Cheong, H.S. (SNP Genetics Inc., Seoul, Republic of Korea), Namgoong, S. (SNP Genetics Inc., Seoul, Republic of Korea), Park, B.L. (SNP Genetics Inc., Seoul, Republic of Korea), Lee, H.W. (SNP Genetics Inc., Seoul, Republic of Korea), Han, C.S. (SNP Genetics Inc., Seoul, Republic of Korea), Kim, E.M. (SNP Genetics Inc., Seoul, Republic of Korea), Cheong, I.C. (National Livestock Research Institute, RDA, Suwon, Republic of Korea), Kim, H.B. (Seoul National University, Seoul, Republic of Korea), Shin, H.D. (SNP Genetics Inc., Seoul, Republic of Korea), E-mail: hdshin@snp-genetics.com

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Association analysis of UBE3C polymorphisms in Korean aspirin-intolerant asthmatic patients von Lee, Jin Sol, BS, Kim, Jeong-Hyun, PhD, Bae, Joon Seol, PhD, Kim, Jason Yongha, BS, Park, Tae Joon, BS, Pasaje, Charisse Flerida, BS, Park, Byung-Lae, PhD, Cheong, Hyun Sub, MS, Park, Jong-Sook, MD, Uh, Soo-Taek, MD, Kim, Mi-Kyeong, MD, Choi, Inseon S., MD, Cho, Sang Heon, MD, Choi, Byoung Whui, MD, Park, Choon-Sik, MD, Shin, Hyoung Doo, PhD

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Association of APOE genotype with lipid profiles and type 2 diabetes mellitus in a Korean population von Seo, Jung Yeon, Youn, Byeong Ju, Cheong, Hyun Sub, Shin, Hyoung Doo

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Polymorphisms in the leptin receptor (LEPR)-putative association with obesity and T2DM von Park, Kyong Soo, Shin, Hyoung Doo, Park, Byung Lae, Cheong, Hyun Sub, Cho, Young Min, Lee, Hong Kyu, Lee, Jong-Young, Lee, Jong-Keuk, Oh, Bermseok, Kimm, Kuchan

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Screening of genetic variations of SLC15A2, SLC22A1, SLC22A2 and SLC22A6 genes von Cheong, Hyun Sub, Kim, Hae Deun, Na, Han Sung, Kim, Ji On, Kim, Lyoung Hyo, Kim, Seung Hee, Bae, Joon Seol, Chung, Myeon Woo, Shin, Hyoung Doo

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A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31-32 region and asthma von Kim, Jeong-Hyun, Cheong, Hyun Sub, Park, Byung-Lae, Bae, Joon Seol, Jung, Seok, Yoon, Sang-Hyuk, Park, Jong Sook, Jang, An Soo, Park, Sung Woo, Uh, Soo-Taek, Kim, Yong-Hoon, Hwang, Hyeon-Kyu, Park, Choon-Sik, Shin, Hyoung Doo

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Genome-wide and follow-up studies identify CEP68 gene variants associated with risk of aspirin-intolerant asthma von Kim, Jeong-Hyun, Park, Byung-Lae, Cheong, Hyun Sub, Bae, Joon Seol, Park, Jong Sook, Jang, An Soo, Uh, Soo-Taek, Choi, Jae-Sung, Kim, Yong-Hoon, Kim, Mi-Kyeong, Choi, Inseon S, Cho, Sang Heon, Choi, Byoung Whui, Park, Choon-Sik, Shin, Hyoung Doo

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The schizophrenia genetics knowledgebase: a comprehensive update of findings from candidate gene studies von Liu, Chenxing, Kanazawa, Tetsufumi, Tian, Ye, Mohamed Saini, Suriati, Mancuso, Serafino, Mostaid, Md Shaki, Takahashi, Atsushi, Zhang, Dai, Zhang, Fuquan, Yu, Hao, Doo Shin, Hyoung, Sub Cheong, Hyun, Ikeda, Masashi, Kubo, Michiaki, Iwata, Nakao, Woo, Sung-Il, Yue, Weihua, Kamatani, Yoichiro, Shi, Yongyong, Li, Zhiqiang, Everall, Ian, Pantelis, Christos, Bousman, Chad

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Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study von Kim, Yong Woo, Kim, Yu Jeong, Cheong, Hyun Sub, Shiga, Yukihiro, Hashimoto, Kazuki, Song, Yong Ju, Kim, Seok Hwan, Choi, Hyuk Jin, Nishiguchi, Koji M., Kawai, Yosuke, Nagasaki, Masao, Nakazawa, Toru, Park, Ki Ho, Kim, Dong Myung, Jeoung, Jin Wook

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Identification of Genome-wide Copy Number Variations and a Family-based Association Study of Avellino Corneal Dystrophy von Bae, Joon Seol, PhD, Cheong, Hyun Sub, MS, Chun, Ji-Yong, BS, Park, Tae Joon, BS, Kim, Ji-On, BS, Kim, Eun Mi, MS, Park, Miey, PhD, Kim, Dong-Joon, MS, Lee, Eun-Ju, PhD, Kim, Eung Kweon, MD, Lee, Jong-Young, PhD, Shin, Hyoung Doo, PhD

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