Identification and Functional Characterization of RSPO2 as a Susceptibility Gene for Ossification of the Posterior Longitudinal Ligament of the Spine

nork Nakajima, Masahiro, Kou, Ikuyo, Ohashi, Hirofumi, Ikegawa, Shiro
Argitaratua izan da Am J Hum Genet (2016)

Asporin Expression Is Highly Regulated in Human Chondrocytes

nork Duval, Elise, Bigot, Nicolas, Hervieu, Magalie, Kou, Ikuyo, Leclercq, Sylvain, Galéra, Philippe, Boumediene, Karim, Baugé, Catherine
Argitaratua 2011

A novel FOXC2 mutation in spinal extradural arachnoid cyst

nork Ogura, Yoji, Fujibayashi, Shunsuke, Iida, Aritoshi, Kou, Ikuyo, Nakajima, Masahiro, Okada, Eijiro, Toyama, Yoshiaki, Iwanami, Akio, Ishii, Ken, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Argitaratua izan da Hum Genome Var (2015)

FOXC2 Mutations in Familial and Sporadic Spinal Extradural Arachnoid Cyst

nork Ogura, Yoji, Yabuki, Shoji, Iida, Aritoshi, Kou, Ikuyo, Nakajima, Masahiro, Kano, Hiroki, Shiina, Masaaki, Kikuchi, Shinichi, Toyama, Yoshiaki, Ogata, Kazuhiro, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Argitaratua 2013

Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis De...

nork Guo, Long, Yamashita, Hiroshi, Kou, Ikuyo, Takimoto, Aki, Meguro-Horike, Makiko, Horike, Shin-ichi, Sakuma, Tetsushi, Miura, Shigenori, Adachi, Taiji, Yamamoto, Takashi, Ikegawa, Shiro, Hiraki, Yuji, Shukunami, Chisa
Argitaratua izan da PLoS Genet (2016)

Common Variants in a Novel Gene, FONG on Chromosome 2q33.1 Confer Risk of Osteoporosis in Japanese

nork Kou, Ikuyo, Takahashi, Atsushi, Urano, Tomohiko, Fukui, Naoshi, Ito, Hideki, Ozaki, Kouichi, Tanaka, Toshihiro, Hosoi, Takayuki, Shiraki, Masataka, Inoue, Satoshi, Nakamura, Yusuke, Kamatani, Naoyuki, Kubo, Michiaki, Mori, Seijiro, Ikegawa, Shiro
Argitaratua 2011

Identification of HOXD4 Mutations in Spinal Extradural Arachnoid Cyst

nork Ogura, Yoji, Miyake, Noriko, Kou, Ikuyo, Iida, Aritoshi, Nakajima, Masahiro, Takeda, Kazuki, Fujibayashi, Shunsuke, Shiina, Masaaki, Okada, Eijiro, Toyama, Yoshiaki, Iwanami, Akio, Ishii, Ken, Ogata, Kazuhiro, Asahara, Hiroshi, Matsumoto, Naomichi, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Argitaratua izan da PLoS One (2015)

CELSR2 is a candidate susceptibility gene in idiopathic scoliosis

nork Einarsdottir, Elisabet, Grauers, Anna, Wang, Jingwen, Jiao, Hong, Escher, Stefan A., Danielsson, Aina, Simony, Ane, Andersen, Mikkel, Christensen, Steen Bach, Åkesson, Kristina, Kou, Ikuyo, Khanshour, Anas M., Ohlin, Acke, Wise, Carol, Ikegawa, Shiro, Kere, Juha, Gerdhem, Paul
Argitaratua izan da PLoS One (2017)

New Sequence Variants in HLA Class II/III Region Associated with Susceptibility to Knee Osteoarthritis Identified by Genome-Wide Association Study

nork Nakajima, Masahiro, Takahashi, Atsushi, Kou, Ikuyo, Rodriguez-Fontenla, Cristina, Gomez-Reino, Juan J., Furuichi, Tatsuya, Dai, Jin, Sudo, Akihiro, Uchida, Atsumasa, Fukui, Naoshi, Kubo, Michiaki, Kamatani, Naoyuki, Tsunoda, Tatsuhiko, Malizos, Konstantinos N., Tsezou, Aspasia, Gonzalez, Antonio, Nakamura, Yusuke, Ikegawa, Shiro
Argitaratua 2010

A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females

nork Sharma, Swarkar, Londono, Douglas, Eckalbar, Walter L., Gao, Xiaochong, Zhang, Dongping, Mauldin, Kristen, Kou, Ikuyo, Takahashi, Atsushi, Matsumoto, Morio, Kamiya, Nobuhiro, Murphy, Karl K., Cornelia, Reuel, Herring, John A., Burns, Dennis, Ahituv, Nadav, Ikegawa, Shiro, Gordon, Derek, Wise, Carol A.
Argitaratua izan da Nat Commun (2015)

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome

nork Hempel, Annmarie, Pagnamenta, Alistair T, Blyth, Moira, Mansour, Sahar, McConnell, Vivienne, Kou, Ikuyo, Ikegawa, Shiro, Tsurusaki, Yoshinori, Matsumoto, Naomichi, Lo-Castro, Adriana, Plessis, Ghislaine, Albrecht, Beate, Battaglia, Agatino, Taylor, Jenny C, Howard, Malcolm F, Keays, David, Sohal, Aman Singh, Kühl, Susanne J, Kini, Usha, McNeill, Alisdair
Argitaratua izan da J Med Genet (2016)

Screening of known disease genes in congenital scoliosis

nork Takeda, Kazuki, Kou, Ikuyo, Mizumoto, Shuji, Yamada, Shuhei, Kawakami, Noriaki, Nakajima, Masahiro, Otomo, Nao, Ogura, Yoji, Miyake, Noriko, Matsumoto, Naomichi, Kotani, Toshiaki, Sudo, Hideki, Yonezawa, Ikuho, Uno, Koki, Taneichi, Hiroshi, Watanabe, Kei, Shigematsu, Hideki, Sugawara, Ryo, Taniguchi, Yuki, Minami, Shohei, Nakamura, Masaya, Matsumoto, Morio, Watanabe, Kota, Ikegawa, Shiro
Argitaratua izan da Mol Genet Genomic Med (2018)

An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis

nork Ogura, Yoji, Takeda, Kazuki, Kou, Ikuyo, Khanshour, Anas, Grauers, Anna, Zhou, Hang, Liu, Gang, Fan, Yan-Hui, Zhou, Taifeng, Wu, Zhihong, Takahashi, Yohei, Matsumoto, Morio, Einarsdottir, Elisabet, Kere, Juha, Huang, Dongsheng, Qiu, Guixing, Xu, Leilei, Qiu, Yong, Wise, Carol A., Song, You-Qiang, Wu, Nan, Su, Peiqiang, Gerdhem, Paul, Watanabe, Kota, Ikegawa, Shiro
Argitaratua izan da Sci Rep (2018)

Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations

nork Wang, Zheng, Iida, Aritoshi, Miyake, Noriko, Nishiguchi, Koji M., Fujita, Kosuke, Nakazawa, Toru, Alswaid, Abdulrahman, Albalwi, Mohammed A., Kim, Ok-Hwa, Cho, Tae-Joon, Lim, Gye-Yeon, Isidor, Bertrand, David, Albert, Rustad, Cecilie F., Merckoll, Else, Westvik, Jostein, Stattin, Eva-Lena, Grigelioniene, Giedre, Kou, Ikuyo, Nakajima, Masahiro, Ohashi, Hirohumi, Smithson, Sarah, Matsumoto, Naomichi, Nishimura, Gen, Ikegawa, Shiro
Argitaratua izan da PLoS One (2016)

A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis

nork Kou, Ikuyo, Watanabe, Kota, Takahashi, Yohei, Momozawa, Yukihide, Khanshour, Anas, Grauers, Anna, Zhou, Hang, Liu, Gang, Fan, Yan-Hui, Takeda, Kazuki, Ogura, Yoji, Zhou, Taifeng, Iwasaki, Yusuke, Kubo, Michiaki, Wu, Zhihong, Matsumoto, Morio, Einarsdottir, Elisabet, Kere, Juha, Huang, Dongsheng, Qiu, Guixing, Qiu, Yong, Wise, Carol A., Song, You-Qiang, Wu, Nan, Su, Peiqiang, Gerdhem, Paul, Ikegawa, Shiro
Argitaratua izan da Sci Rep (2018)

Identification of a Susceptibility Locus for Severe Adolescent Idiopathic Scoliosis on Chromosome 17q24.3

nork Miyake, Atsushi, Kou, Ikuyo, Takahashi, Yohei, Johnson, Todd A., Ogura, Yoji, Dai, Jin, Qiu, Xusheng, Takahashi, Atsushi, Jiang, Hua, Yan, Huang, Kono, Katsuki, Kawakami, Noriaki, Uno, Koki, Ito, Manabu, Minami, Shohei, Yanagida, Haruhisa, Taneichi, Hiroshi, Hosono, Naoya, Tsuji, Taichi, Suzuki, Teppei, Sudo, Hideki, Kotani, Toshiaki, Yonezawa, Ikuho, Kubo, Michiaki, Tsunoda, Tatsuhiko, Watanabe, Kota, Chiba, Kazuhiro, Toyama, Yoshiaki, Qiu, Yong, Matsumoto, Morio, Ikegawa, Shiro
Argitaratua 2013

Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci

nork Khanshour, Anas M, Kou, Ikuyo, Fan, Yanhui, Einarsdottir, Elisabet, Makki, Nadja, Kidane, Yared H, Kere, Juha, Grauers, Anna, Johnson, Todd A, Paria, Nandina, Patel, Chandreshkumar, Singhania, Richa, Kamiya, Nobuhiro, Takeda, Kazuki, Otomo, Nao, Watanabe, Kota, Luk, Keith D K, Cheung, Kenneth M C, Herring, John A, Rios, Jonathan J, Ahituv, Nadav, Gerdhem, Paul, Gurnett, Christina A, Song, You-Qiang, Ikegawa, Shiro, Wise, Carol A
Argitaratua izan da Hum Mol Genet (2018)

A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis

nork Ogura, Yoji, Kou, Ikuyo, Miura, Shigenori, Takahashi, Atsushi, Xu, Leilei, Takeda, Kazuki, Takahashi, Yohei, Kono, Katsuki, Kawakami, Noriaki, Uno, Koki, Ito, Manabu, Minami, Shohei, Yonezawa, Ikuho, Yanagida, Haruhisa, Taneichi, Hiroshi, Zhu, Zezhang, Tsuji, Taichi, Suzuki, Teppei, Sudo, Hideki, Kotani, Toshiaki, Watanabe, Kota, Hosogane, Naobumi, Okada, Eijiro, Iida, Aritoshi, Nakajima, Masahiro, Sudo, Akihiro, Chiba, Kazuhiro, Hiraki, Yuji, Toyama, Yoshiaki, Qiu, Yong, Shukunami, Chisa, Kamatani, Yoichiro, Kubo, Michiaki, Matsumoto, Morio, Ikegawa, Shiro
Argitaratua izan da Am J Hum Genet (2015)

Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture

nork Hwang, Joo-Yeon, Lee, Seung Hun, Go, Min Jin, Kim, Beom-Jun, Kou, Ikuyo, Ikegawa, Shiro, Guo, Yan, Deng, Hong-Wen, Raychaudhuri, Soumya, Kim, Young Jin, Oh, Ji Hee, Kim, Youngdoe, Moon, Sanghoon, Kim, Dong-Joon, Koo, Heejo, Cha, My-Jung, Lee, Min Hye, Yun, Ji Young, Yoo, Hye-Sook, Kang, Young-Ah, Cho, Eun-Hee, Kim, Sang-Wook, Oh, Ki Won, Kang, Moo II, Son, Ho Young, Kim, Shin-Yoon, Kim, Ghi Su, Han, Bok-Ghee, Cho, Yoon Shin, Cho, Myeong-Chan, Lee, Jong-Young, Koh, Jung-Min
Argitaratua 2013

Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese

nork Kou, Ikuyo, Otomo, Nao, Takeda, Kazuki, Momozawa, Yukihide, Lu, Hsing-Fang, Kubo, Michiaki, Kamatani, Yoichiro, Ogura, Yoji, Takahashi, Yohei, Nakajima, Masahiro, Minami, Shohei, Uno, Koki, Kawakami, Noriaki, Ito, Manabu, Yonezawa, Ikuho, Watanabe, Kei, Kaito, Takashi, Yanagida, Haruhisa, Taneichi, Hiroshi, Harimaya, Katsumi, Taniguchi, Yuki, Shigematsu, Hideki, Iida, Takahiro, Demura, Satoru, Sugawara, Ryo, Fujita, Nobuyuki, Yagi, Mitsuru, Okada, Eijiro, Hosogane, Naobumi, Kono, Katsuki, Nakamura, Masaya, Chiba, Kazuhiro, Kotani, Toshiaki, Sakuma, Tsuyoshi, Akazawa, Tsutomu, Suzuki, Teppei, Nishida, Kotaro, Kakutani, Kenichiro, Tsuji, Taichi, Sudo, Hideki, Iwata, Akira, Sato, Tatsuya, Inami, Satoshi, Matsumoto, Morio, Terao, Chikashi, Watanabe, Kota, Ikegawa, Shiro
Argitaratua izan da Nat Commun (2019)