Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study by Egawa, Jun, Hoya, Satoshi, Watanabe, Yuichiro, Nunokawa, Ayako, Shibuya, Masako, Ikeda, Masashi, Inoue, Emiko, Okuda, Shujiro, Kondo, Kenji, Saito, Takeo, Kaneko, Naoshi, Muratake, Tatsuyuki, Igeta, Hirofumi, Iwata, Nakao, Someya, Toshiyuki

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Rare FBXO18 variations and risk of schizophrenia: Whole‐exome sequencing in two parent‐affected offspring trios followed by resequencing and case–control studies by Hoya, Satoshi, Watanabe, Yuichiro, Hishimoto, Akitoyo, Nunokawa, Ayako, Inoue, Emiko, Igeta, Hirofumi, Otsuka, Ikuo, Shibuya, Masako, Egawa, Jun, Sora, Ichiro, Someya, Toshiyuki

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Rare heterozygous truncating variations and risk of autism spectrum disorder: Whole‐exome sequencing of a multiplex family and follow‐up study in a Japanese population by Inoue, Emiko, Watanabe, Yuichiro, Egawa, Jun, Sugimoto, Atsunori, Nunokawa, Ayako, Shibuya, Masako, Igeta, Hirofumi, Someya, Toshiyuki

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Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese pop... by Egawa, Jun, Watanabe, Yuichiro, Wang, Chenyao, Inoue, Emiko, Sugimoto, Atsunori, Sugiyama, Toshiro, Igeta, Hirofumi, Nunokawa, Ayako, Shibuya, Masako, Kushima, Itaru, Orime, Naoki, Hayashi, Taketsugu, Okada, Takashi, Uno, Yota, Ozaki, Norio, Someya, Toshiyuki

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Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population by Takasaki, Yuto, Koide, Takayoshi, Wang, Chenyao, Kimura, Hiroki, Xing, Jingrui, Kushima, Itaru, Ishizuka, Kanako, Mori, Daisuke, Sekiguchi, Mariko, Ikeda, Masashi, Aizawa, Miki, Tsurumaru, Naoko, Iwayama, Yoshimi, Yoshimi, Akira, Arioka, Yuko, Yoshida, Mami, Noma, Hiromi, Oya-Ito, Tomoko, Nakamura, Yukako, Kunimoto, Shohko, Aleksic, Branko, Uno, Yota, Okada, Takashi, Ujike, Hiroshi, Egawa, Jun, Kuwabara, Hitoshi, Someya, Toshiyuki, Yoshikawa, Takeo, Iwata, Nakao, Ozaki, Norio

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Interleukin 1 beta gene and risk of schizophrenia: detailed case-control and family-based studies and an updated meta-analysis by Shibuya, Masako, Watanabe, Yuichiro, Nunokawa, Ayako, Egawa, Jun, Kaneko, Naoshi, Igeta, Hirofumi, Someya, Toshiyuki

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Association of rs2129575 in the tryptophan hydroxylase 2 gene with clinical phenotypes of autism spectrum disorders by Egawa, Jun, Watanabe, Yuichiro, Endo, Taro, Someya, Toshiyuki

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Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case–control study by Lo, Tzuyao, Kushima, Itaru, Kimura, Hiroki, Aleksic, Branko, Okada, Takashi, Kato, Hidekazu, Inada, Toshiya, Nawa, Yoshihiro, Torii, Youta, Yamamoto, Maeri, Kimura, Ryo, Funabiki, Yasuko, Kosaka, Hirotaka, Numata, Shusuke, Kasai, Kiyoto, Sasaki, Tsukasa, Yokoyama, Shigeru, Munesue, Toshio, Hashimoto, Ryota, Yasuda, Yuka, Fujimoto, Michiko, Usami, Masahide, Itokawa, Masanari, Arai, Makoto, Ohi, Kazutaka, Someya, Toshiyuki, Watanabe, Yuichiro, Egawa, Jun, Takahashi, Tsutomu, Suzuki, Michio, Yamasue, Hidenori, Iwata, Nakao, Ikeda, Masashi, Ozaki, Norio

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Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population by Inoue, Emiko, Watanabe, Yuichiro, Xing, Jingrui, Kushima, Itaru, Egawa, Jun, Okuda, Shujiro, Hoya, Satoshi, Okada, Takashi, Uno, Yota, Ishizuka, Kanako, Sugimoto, Atsunori, Igeta, Hirofumi, Nunokawa, Ayako, Sugiyama, Toshiro, Ozaki, Norio, Someya, Toshiyuki

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Possible association between the oxytocin receptor gene and N‐acetylaspartate of the right medial temporal lobe in autism spectrum disorders by Egawa, Jun, Watanabe, Yuichiro, Endo, Taro, Kitamura, Hideaki, Someya, Toshiyuki

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Association between OXTR and clinical phenotypes of autism spectrum disorders by Egawa, Jun, Watanabe, Yuichiro, Endo, Taro, Tamura, Ryu, Masuzawa, Naio, Someya, Toshiyuki

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Oxytocin receptor (OXTR) gene and risk of schizophrenia: Case-control and family-based analyses and meta-analysis in a Japanese population by Watanabe, Yuichiro, Kaneko, Naoshi, Nunokawa, Ayako, Shibuya, Masako, Egawa, Jun, Someya, Toshiyuki

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Supportive evidence for the association between the Gln2Pro polymorphism in the SIGMAR1 gene and schizophrenia in the Japanese population: A case–control study and an updated meta-... by Watanabe, Yuichiro, Nunokawa, Ayako, Kaneko, Naoshi, Shibuya, Masako, Egawa, Jun, Someya, Toshiyuki

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Rare PDCD11 variations are not associated with risk of schizophrenia in Japan by Hoya, Satoshi, Watanabe, Yuichiro, Hishimoto, Akitoyo, Nunokawa, Ayako, Kaneko, Naoshi, Muratake, Tatsuyuki, Shinmyo, Naofumi, Otsuka, Ikuo, Okuda, Shujiro, Inoue, Emiko, Igeta, Hirofumi, Shibuya, Masako, Egawa, Jun, Orime, Naoki, Sora, Ichiro, Someya, Toshiyuki

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Resequencing and association analysis of MIR137 with schizophrenia in a Japanese population by Egawa, Jun, Nunokawa, Ayako, Shibuya, Masako, Watanabe, Yuichiro, Kaneko, Naoshi, Igeta, Hirofumi, Someya, Toshiyuki

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A detailed association analysis between the tryptophan hydroxylase 2 ( TPH2 ) gene and autism spectrum disorders in a Japanese population by Egawa, Jun, Watanabe, Yuichiro, Nunokawa, Ayako, Endo, Taro, Kaneko, Naoshi, Tamura, Ryu, Sugiyama, Toshiro, Someya, Toshiyuki

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Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population by Egawa, Jun, Watanabe, Yuichiro, Shibuya, Masako, Endo, Taro, Sugimoto, Atsunori, Igeta, Hirofumi, Nunokawa, Ayako, Inoue, Emiko, Someya, Toshiyuki

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Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility by Nawa, Yoshihiro, Kimura, Hiroki, Mori, Daisuke, Kato, Hidekazu, Toyama, Miho, Furuta, Sho, Yu, Yanjie, Ishizuka, Kanako, Kushima, Itaru, Aleksic, Branko, Arioka, Yuko, Morikawa, Mako, Okada, Takashi, Inada, Toshiya, Kaibuchi, Kozo, Ikeda, Masashi, Iwata, Nakao, Suzuki, Michio, Okahisa, Yuko, Egawa, Jun, Someya, Toshiyuki, Nishimura, Fumichika, Sasaki, Tsukasa, Ozaki, Norio

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Influence of the 5-HTR1A C-1019G polymorphism on clinical phenotypes of autism spectrum disorders by Egawa, Jun, Endo, Taro, Tamura, Ryu, Masuzawa, Naio, Fukui, Naoki, Sugai, Takuro, Someya, Toshiyuki

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Developmental prosopagnosia referred to outpatient psychiatric service by Kitamura, Hideaki, Egawa, Jun, Someya, Toshiyuki

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