Inoue, Yushi

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

Kushima, I., Aleksic, B., Nakatochi, M., Shimamura, T., Okada, T., Uno, Y., Morikawa, M., Ishizuka, K., Shiino, T., Kimura, H., et al. (2018) · Cell Reports

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

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De novo mutations of voltage-gated sodium channel α II gene SCN2A in intractable epilepsies

Ogiwara, I., Ito, K., Sawaishi, Y., Osaka, H., Mazaki, E., Inoue, I., Montal, M., Hashikawa, T., Shike, T., Fujiwara, T., et al. (2009) · Neurology

Epilepsy research and treatmentIon channel regulation and function

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A Nonsense Mutation of the Sodium Channel Gene SCN2A in a Patient with Intractable Epilepsy and Mental Decline

Kamiya, K., Kaneda, M., Sugawara, T., Mazaki, E., Okamura, N., Montal, M., Makita, N., Tanaka, M., Fukushima, K., Fujiwara, T., et al. (2004) · The Journal of Neuroscience

Epilepsy research and treatmentIon channel regulation and function

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Elfn1 recruits presynaptic mGluR7 in trans and its loss results in seizures

Tomioka, N. H., Yasuda, H., Miyamoto, H., Hatayama, M., Morimura, N., Matsumoto, Y., Suzuki, T., Odagawa, M., Odaka, Y. S., Iwayama, Y., et al. (2014) · Nature Communications

Neuroscience and Neuropharmacology ResearchEpilepsy research and treatment

Cited by 113