FOXC2 Mutations in Familial and Sporadic Spinal Extradural Arachnoid Cyst

by 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
Published 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...

by 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
Published 2016

A novel FOXC2 mutation in spinal extradural arachnoid cyst

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

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

by 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
Published 2011

Identification of HOXD4 Mutations in Spinal Extradural Arachnoid Cyst

by 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
Published 2015

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

by 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.
Published 2015

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

by 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
Published 2013

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

by 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
Published 2016

Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations

by 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
Published 2016