Overview: Research on the Genetic Architecture of the Developing Cerebral Cortex in Norms and Diseases von Momoi, Mariko Y.

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Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to autism spectrum disorder von Fujita-Jimbo, Eriko, Yu, Zhi-Ling, Li, Hong, Yamagata, Takanori, Mori, Masato, Momoi, Takashi, Momoi, Mariko Y

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Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells von Fujita, Eriko, Tanabe, Yuko, Shiota, Akira, Ueda, Masatsugu, Suwa, Kiyotaka, Momoi, Mariko Y, Momoi, Takashi

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LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome von Matsumoto, Ayumi, Mizuno, Makoto, Hamada, Nanako, Nozaki, Yasuyuki, Jimbo, Eriko F, Momoi, Mariko Y, Nagata, Koh-ichi, Yamagata, Takanori

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Comment on: Risk of neuropsychiatric adverse events associated with the use of oseltamivir: a nationwide population-based case-crossover study von Ohkusa, Yasushi, Sugawara, Tamie, Taniguchi, Kiyosu, Miyazaki, Chiaki, Momoi, Mariko Y, Okabe, Nobuhiko

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CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder‐related mutation von Tanabe, Yuko, Fujita‐Jimbo, Eriko, Momoi, Mariko Y., Momoi, Takashi

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Clinically-oriented monitoring of acute effects of methylphenidate on cerebral hemodynamics in ADHD children using fNIRS von Monden, Yukifumi, Dan, Haruka, Nagashima, Masako, Dan, Ippeita, Kyutoku, Yasushi, Okamoto, Masako, Yamagata, Takanori, Momoi, Mariko Y, Watanabe, Eiju

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Impairment of social and emotional behaviors in Cadm1-knockout mice von Takayanagi, Yuki, Fujita, Eriko, Yu, Zhiling, Yamagata, Takanori, Momoi, Mariko Y., Momoi, Takashi, Onaka, Tatsushi

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A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellum von Fujita, Eriko, Tanabe, Yuko, Imhof, Beat A., Momoi, Mariko Y., Momoi, Takashi

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Role of Class III phosphoinositide 3‐kinase in the brain development: possible involvement in specific learning disorders von Inaguma, Yutaka, Matsumoto, Ayumi, Noda, Mariko, Tabata, Hidenori, Maeda, Akihiko, Goto, Masahide, Usui, Daisuke, Jimbo, Eriko F., Kikkawa, Kiyoshi, Ohtsuki, Mamitaro, Momoi, Mariko Y., Osaka, Hitoshi, Yamagata, Takanori, Nagata, Koh‐ichi

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Mutations in the gene encoding CADM1 are associated with autism spectrum disorder von Zhiling, Yu, Fujita, Eriko, Tanabe, Yuko, Yamagata, Takanori, Momoi, Takashi, Momoi, Mariko Y.

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MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus von Saito, Mari, Yamagata, Takanori, Matsumoto, Ayumi, Shiba, Yusuke, Nagashima, Masako, Taniguchi, Shuhei, Jimbo, Eriko, Momoi, Mariko Y

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Association of moderately abnormal behavior and administered neuraminidase inhibitors von Sugawara, Tamie, Ohkusa, Yasushi, Taniguchi, Kiyosu, Miyazaki, Chiaki, Momoi, Mariko Y., Okabe, Nobuhiko

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Severe abnormal behavior incidence after administration of neuraminidase inhibitors using the national database of medical claims von Nakamura, Yuuki, Sugawara, Tamie, Ohkusa, Yasushi, Taniguchi, Kiyosu, Miyazaki, Chiaki, Momoi, Mariko, Okabe, Nobuhiko

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Cytokine profiles of seventeen cytokines, growth factors and chemokines in cord blood and its relation to perinatal clinical findings von Takahashi, Naoto, Uehara, Ritei, Kobayashi, Mami, Yada, Yukari, Koike, Yasunori, Kawamata, Ryou, Odaka, Jun, Honma, Yoko, Momoi, Mariko Y.

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Life-Threatening Abnormal Behavior Incidence in 10-19 Year Old Patients Administered Neuraminidase Inhibitors von Nakamura, Yuuki, Sugawara, Tamie, Ohkusa, Yasushi, Taniguchi, Kiyosu, Miyazaki, Chiaki, Momoi, Mariko, Okabe, Nobuhiko

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Role of an adaptor protein Lin‐7B in brain development: possible involvement in autism spectrum disorders von Mizuno, Makoto, Matsumoto, Ayumi, Hamada, Nanako, Ito, Hidenori, Miyauchi, Akihiko, Jimbo, Eriko F., Momoi, Mariko Y., Tabata, Hidenori, Yamagata, Takanori, Nagata, Koh‐ichi

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Inquiry into some gap among oseltamivir use and severe abnormal behavior in Japanese children and adolescents with influenza von Ohkusa, Yasushi, Sugawara, Tamie, Taniguchi, Kiyosu, Miyazaki, Chiaki, Momoi, Mariko Y., Okabe, Nobuhiko

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Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder von Fujita, Eriko, Tanabe, Yuko, Momoi, Mariko Y., Momoi, Takashi

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Contiguous ABCD1 DXS1357E deletion syndrome: Report of an autopsy case von Iwasa, Mitsuaki, Yamagata, Takanori, Mizuguchi, Masashi, Itoh, Masayuki, Matsumoto, Ayumi, Hironaka, Mitsugu, Honda, Ayako, Momoi, Mariko Y., Shimozawa, Nobuyuki

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