A novel FOXC2 mutation in spinal extradural arachnoid cyst

por Ogura, Yoji, Fujibayashi, Shunsuke, Iida, Aritoshi, Kou, Ikuyo, Nakajima, Masahiro, Okada, Eijiro, Toyama, Yoshiaki, Iwanami, Akio, Ishii, Ken, Nakamura, Masaya, Matsumoto, Morio, Ikegawa, Shiro
Publicado 2015

FOXC2 Mutations in Familial and Sporadic Spinal Extradural Arachnoid Cyst

por 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
Publicado 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...

por 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
Publicado 2016

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

por 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
Publicado 2011

Identification of HOXD4 Mutations in Spinal Extradural Arachnoid Cyst

por 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
Publicado 2015

CELSR2 is a candidate susceptibility gene in idiopathic scoliosis

por 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
Publicado 2017

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

por 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
Publicado 2010

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

por 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.
Publicado 2015

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

por 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
Publicado 2016

Screening of known disease genes in congenital scoliosis

por 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
Publicado 2018

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

por 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
Publicado 2018

Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations

por 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
Publicado 2016

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

por 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
Publicado 2018

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

por 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
Publicado 2013

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

por 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
Publicado 2019