A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits von Cho, Eun Young, Lee, Mi Hee, Park, Man Suk, Han, Bok-Ghee, Clarke, Geraldine, Oh, Bermseok, Cho, Yoon Shin, Go, Min Jin, Kim, Dong-Joon, Ahn, Younjhin, Shin, Chol, McCarthy, Mark I, Jang, Hye-Yoon, Lee, Jong-Koo, Cardon, Lon, Heo, Jee Yeon, Lee, Jong-Keuk, Oh, Ji Hee, Min, Haesook, Lee, Jong-Eun, Ban, Hyo-Jeong, Kim, Jun-Woo, Lee, Jong-Young, Kim, Young Jin, Kim, Hyung-Lae, Park, Ji Wan, Cha, Seung-Hun, Han, Hye Ree, Yoon, Dankyu, Park, Miey, Cho, Nam H, Park, Taesung

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Hygiene Hypothesis as the Etiology of Kawasaki Disease: Dysregulation of Early B Cell Development von Lee, Jong-Keuk

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Response to "Familial Intracranial Aneurysm Requires Not Only Whole-Exome Sequencing, But Also Mitochondrial DNA Sequencing" von Suh, Dae Chul, Lee, Jong-Keuk, Seo, Eul-Ju

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Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm von Song, Yunsun, Lee, Jong-Keuk, Lee, Jin-Ok, Kwon, Boseong, Seo, Eul-Ju, Suh, Dae Chul

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Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease von Kwon, Young-Chang, Kim, Jae-Jung, Yun, Sin Weon, Yu, Jeong Jin, Yoon, Kyung Lim, Lee, Kyung-Yil, Kil, Hong-Ryang, Kim, Gi Beom, Han, Myung-Ki, Song, Min Seob, Lee, Hyoung Doo, Ha, Kee-Soo, Sohn, Sejung, Ebata, Ryota, Hamada, Hiromichi, Suzuki, Hiroyuki, Ito, Kaoru, Onouchi, Yoshihiro, Hong, Young Mi, Jang, Gi Young, Lee, Jong-Keuk

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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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Identification of 15 loci influencing height in a Korean population von Kim, Jae-Jung, Lee, Hae-In, Park, Taesung, Kim, Kyunga, Lee, Jong-Eun, Cho, Nam Han, Shin, Chol, Cho, Yoon Shin, Lee, Jong-Young, Han, Bok-Ghee, Yoo, Han-Wook, Lee, Jong-Keuk

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A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease von Kim, Jae-Jung, Yun, Sin Weon, Yu, Jeong Jin, Yoon, Kyung Lim, Lee, Kyung-Yil, Kil, Hong-Ryang, Kim, Gi Beom, Han, Myung-Ki, Song, Min Seob, Lee, Hyoung Doo, Ha, Kee Soo, Sohn, Sejung, Johnson, Todd A, Takahashi, Atsushi, Kubo, Michiaki, Tsunoda, Tatsuhiko, Ito, Kaoru, Onouchi, Yoshihiro, Hong, Young Mi, Jang, Gi Young, Lee, Jong-Keuk

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Identification of SAMD9L as a susceptibility locus for intravenous immunoglobulin resistance in Kawasaki disease by genome-wide association analysis von Kim, Jae-Jung, Yun, Sin Weon, Yu, Jeong Jin, Yoon, Kyung Lim, Lee, Kyung-Yil, Kil, Hong-Ryang, Kim, Gi Beom, Han, Myung-Ki, Song, Min Seob, Lee, Hyoung Doo, Ha, Kee Soo, Sohn, Sejung, Ebata, Ryota, Hamada, Hiromichi, Suzuki, Hiroyuki, Ito, Kaoru, Onouchi, Yoshihiro, Hong, Young Mi, Jang, Gi Young, Lee, Jong-Keuk

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Rare Neurovascular Diseases in Korea: Classification and Related Genetic Variants von Song, Yunsun, Kwon, Boseong, Al-Abdulwahhab, Abdulrahman Hamed, Nam, Yeo Kyoung, Ahn, Yura, Jeong, So Yeong, Seo, Eul Ju, Lee, Jong Keuk, Suh, Dae Chul

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Joint Identification of Multiple Genetic Variants via Elastic‐Net Variable Selection in a Genome‐Wide Association Analysis von Cho, Seoae, Kim, Kyunga, Kim, Young Jin, Lee, Jong‐Keuk, Cho, Yoon Shin, Lee, Jong‐Young, Han, Bok‐Ghee, Kim, Heebal, Ott, Jurg, Park, Taesung

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A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease von Kim, Jae-Jung, Hong, Young Mi, Sohn, Saejung, Jang, Gi Young, Ha, Kee-Soo, Yun, Sin Weon, Han, Myung Ki, Lee, Kyung-Yil, Song, Min Seob, Lee, Hyoung Doo, Kim, Dong Soo, Lee, Jong-Eun, Shin, Eun-Soon, Jang, Ji-Hyun, Lee, Yeon-Su, Kim, Sook-Young, Lee, Jong-Young, Han, Bok-Ghee, Wu, Jer-Yuarn, Kim, Kwi-Joo, Park, Young-Mi, Seo, Eul-Joo, Park, In-Sook, Lee, Jong-Keuk

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Association of the IL16 Asn1147Lys polymorphism with intravenous immunoglobulin resistance in Kawasaki disease von Kim, Hea-Ji, Kim, Jae-Jung, Yun, Sin Weon, Yu, Jeong Jin, Yoon, Kyung Lim, Lee, Kyung-Yil, Kil, Hong-Ryang, Kim, Gi Beom, Han, Myung-Ki, Song, Min Seob, Lee, Hyoung Doo, Ha, Kee Soo, Hong, Young Mi, Jang, Gi Young, Lee, Jong-Keuk

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IgA Levels Are Associated with Coronary Artery Lesions in Kawasaki Disease von Kim, Jae Jung, Kim, Hea Ji, Yu, Jeong Jin, Yun, Sin Weon, Lee, Kyung Yil, Yoon, Kyung Lim, Kil, Hong Ryang, Kim, Gi Beom, Han, Myung Ki, Song, Min Seob, Lee, Hyoung Doo, Jun, Hyun Ok, Ha, Kee Soo, Hong, Young Mi, Jang, Gi Young, Lee, Jong Keuk

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A Haplotype at the COL9A2 Gene Locus Contributes to the Genetic Risk for Lumbar Spinal Stenosis in the Korean Population von HYUN, Seung-Jae, PARK, Borae G, RHIM, Seung-Chul, CHAE WAN BAE, LEE, Jong-Keuk, ROH, Sung-Woo, JEON, Sang-Ryong

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Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis von Kim, Jae-Jung, Park, Young-Mi, Yoon, Dankyu, Lee, Kyung-Yil, Seob Song, Min, Doo Lee, Hyoung, Kim, Kwi-Joo, Park, In-Sook, Nam, Hyo-Kyoung, Weon Yun, Sin, Ki Han, Myung, Mi Hong, Young, Young Jang, Gi, Lee, Jong-Keuk

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Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height von Kim, Jae-Jung, Park, Young-Mi, Baik, Kyu-Heum, Choi, Hye-Yeon, Yang, Gap-Seok, Koh, InSong, Hwang, Jung-Ah, Lee, Jieun, Lee, Yeon-Su, Rhee, Hwanseok, Kwon, Tae Soo, Han, Bok-Ghee, Heath, Karen E., Inoue, Hiroshi, Yoo, Han-Wook, Park, Kiejung, Lee, Jong-Keuk

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Novel Classification and Pathogenetic Analysis of Hypoganglionosis and Adult-Onset Hirschsprung’s Disease von Do, Mi Young, Myung, Seung-Jae, Park, Hyo-Jin, Chung, Jun-Won, Kim, In-Wha, Lee, Sun Mi, Yu, Chang Sik, Lee, Hye Kyung, Lee, Jong-Keuk, Park, Young Soo, Jang, Se Jin, Kim, Hye Jin, Ye, Byong Duk, Byeon, Jeong-Sik, Yang, Suk-Kyun, Kim, Jin-Ho

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Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease von Khor, Chiea Chuen, Davila, Sonia, Breunis, Willemijn B, Lee, Yi-Ching, Shimizu, Chisato, Wright, Victoria J, Yeung, Rae S M, Tan, Dennis E K, Sim, Kar Seng, Wang, Jie Jin, Wong, Tien Yin, Pang, Junxiong, Mitchell, Paul, Cimaz, Rolando, Dahdah, Nagib, Cheung, Yiu-Fai, Huang, Guo-Ying, Yang, Wanling, Park, In-Sook, Lee, Jong-Keuk, Wu, Jer-Yuarn, Levin, Michael, Burns, Jane C, Burgner, David, Kuijpers, Taco W, Hibberd, Martin L

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Single-Exome sequencing identified a novel RP2 mutation in a child with X-linked retinitis pigmentosa von Lim, Hassol, BS, MD, PhD, Park, Young-Mi, MS, Lee, Jong-Keuk, PhD, Taek Lim, Hyun, MD, PhD

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