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

Por Nakajima, Masahiro, Kou, Ikuyo, Ohashi, Hirofumi, Ikegawa, Shiro
Publicado no Am J Hum Genet (2016)

Asporin Expression Is Highly Regulated in Human Chondrocytes

Por Duval, Elise, Bigot, Nicolas, Hervieu, Magalie, Kou, Ikuyo, Leclercq, Sylvain, Galéra, Philippe, Boumediene, Karim, Baugé, Catherine
Publicado em 2011

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 no Hum Genome Var (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 em 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 no PLoS Genet (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 em 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 no PLoS One (2015)

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 em 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 no Nat Commun (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 no J Med Genet (2016)

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 no PLoS One (2016)

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 em 2013

A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis

Por 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
Publicado no Am J Hum Genet (2015)

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

Por 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
Publicado em 2013