How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report

by Ohi, Kazutaka, Hashimoto, Ryota, Yamamori, Hidenaga, Yasuda, Yuka, Fujimoto, Michiko, Nakatani, Noriko, Kamino, Kouzin, Takeda, Masatoshi
Published 2013

Sensory cognitive abnormalities of pain in autism spectrum disorder: a case–control study

by Yasuda, Yuka, Hashimoto, Ryota, Nakae, Aya, Kang, Hongling, Ohi, Kazutaka, Yamamori, Hidenaga, Fujimoto, Michiko, Hagihira, Satoshi, Takeda, Masatoshi
Published 2016

Neuromelanin Magnetic Resonance Imaging Reveals Increased Dopaminergic Neuron Activity in the Substantia Nigra of Patients with Schizophrenia

by Watanabe, Yoshiyuki, Tanaka, Hisashi, Tsukabe, Akio, Kunitomi, Yuki, Nishizawa, Mitsuo, Hashimoto, Ryota, Yamamori, Hidenaga, Fujimoto, Michiko, Fukunaga, Masaki, Tomiyama, Noriyuki
Published 2014

The impact of the genome-wide supported variant in the cyclin M2 gene on gray matter morphology in schizophrenia

by Ohi, Kazutaka, Hashimoto, Ryota, Yamamori, Hidenaga, Yasuda, Yuka, Fujimoto, Michiko, Umeda-Yano, Satomi, Fukunaga, Masaki, Watanabe, Yoshiyuki, Iwase, Masao, Kazui, Hiroaki, Takeda, Masatoshi
Published 2013

A Naturally Occurring Null Variant of the NMDA Type Glutamate Receptor NR3B Subunit Is a Risk Factor of Schizophrenia

by Matsuno, Hitomi, Ohi, Kazutaka, Hashimoto, Ryota, Yamamori, Hidenaga, Yasuda, Yuka, Fujimoto, Michiko, Yano-Umeda, Satomi, Saneyoshi, Takeo, Takeda, Masatoshi, Hayashi, Yasunori
Published 2015

Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes

by Ohi, Kazutaka, Hashimoto, Ryota, Ikeda, Masashi, Yamamori, Hidenaga, Yasuda, Yuka, Fujimoto, Michiko, Umeda-Yano, Satomi, Fukunaga, Masaki, Fujino, Haruo, Watanabe, Yoshiyuki, Iwase, Masao, Kazui, Hiroaki, Iwata, Nakao, Weinberger, Daniel R., Takeda, Masatoshi
Published 2015

Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder

by Hashimoto, Ryota, Nakazawa, Takanobu, Tsurusaki, Yoshinori, Yasuda, Yuka, Nagayasu, Kazuki, Matsumura, Kensuke, Kawashima, Hitoshi, Yamamori, Hidenaga, Fujimoto, Michiko, Ohi, Kazutaka, Umeda-Yano, Satomi, Fukunaga, Masaki, Fujino, Haruo, Kasai, Atsushi, Hayata-Takano, Atsuko, Shintani, Norihito, Takeda, Masatoshi, Matsumoto, Naomichi, Hashimoto, Hitoshi
Published 2016

Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series

by Yasuda, Yuka, Hashimoto, Ryota, Fukai, Ryoko, Okamoto, Nobuhiko, Hiraki, Yoko, Yamamori, Hidenaga, Fujimoto, Michiko, Ohi, Kazutaka, Taniike, Masako, Mohri, Ikuko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Saitsu, Hirotomo, Matsumoto, Naomichi, Miyake, Noriko, Takeda, Masatoshi
Published 2014