研究者詳細 - 久島　周

論文 - 久島　周

分割表示 117 件中 81 - 100 件目／全件表示 >>

Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia

Sobue, A; Kushima, I; Nagai, T; Shan, W; Kohno, T; Aleksic, B; Aoyama, Y; Mori, D; Arioka, Y; Kawano, N; Yamamoto, M; Hattori, M; Nabeshima, T; Yamada, K; Ozaki, N

SCIENTIFIC REPORTS 8 巻 2018年8月

Three lines of induced pluripotent stem cells derived from a 15q11.2-q13.1 duplication syndrome patient

Arioka, Y; Kushima, I; Mori, D; Ozaki, N

STEM CELL RESEARCH 31 巻頁： 240 - 243 2018年8月

Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant

Arioka, Y; Shishido, E; Kubo, H; Kushima, I; Yoshimi, A; Kimura, H; Ishizuka, K; Aleksic, B; Maeda, T; Ishikawa, M; Kuzumaki, N; Okano, H; Mori, D; Ozaki, N

TRANSLATIONAL PSYCHIATRY 8 巻 2018年7月

Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion

Arioka, Y; Kushima, I; Kubo, H; Mori, D; Ozaki, N

STEM CELL RESEARCH 30 巻頁： 81 - 84 2018年7月

Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion. 査読有り

Arioka Y, Kushima I, Kubo H, Mori D, Ozaki N.

Stem Cell Res. 2018年5月

Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder

Takata, A; Miyake, N; Tsurusaki, Y; Fukai, R; Miyatake, S; Koshimizu, E; Kushima, I; Okada, T; Morikawa, M; Uno, Y; Ishizuka, K; Nakamura, K; Tsujii, M; Yoshikawa, T; Toyota, T; Okamoto, N; Hiraki, Y; Hashimoto, R; Yasuda, Y; Saitoh, S; Ohashi, K; Sakai, Y; Ohga, S; Hara, T; Kato, M; Nakamura, K; Ito, A; Seiwa, C; Shirahata, E; Osaka, H; Matsumoto, A; Takeshita, S; Tohyama, J; Saikusa, T; Matsuishi, T; Nakamura, T; Tsuboi, T; Kato, T; Suzuki, T; Saitsu, H; Nakashima, M; Mizuguchi, T; Tanaka, F; Mori, N; Ozaki, N; Matsumoto, N

CELL REPORTS 22 巻 ( 3 ) 頁： 734 - 747 2018年1月

Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility

Yu, YJ; Lin, YN; Takasaki, Y; Wang, CY; Kimura, H; Xing, JR; Ishizuka, K; Toyama, M; Kushima, I; Mori, D; Arioka, Y; Uno, Y; Shiino, T; Nakamura, Y; Okada, T; Morikawa, M; Ikeda, M; Iwata, N; Okahisa, Y; Takaki, M; Sakamoto, S; Someya, T; Egawa, J; Usami, M; Kodaira, M; Yoshimi, A; Oya-Ito, T; Aleksic, B; Ohno, K; Ozaki, N

TRANSLATIONAL PSYCHIATRY 8 巻 2018年1月

IDENTIFICATION OF RARE DISRUPTIVE VARIANTS IN VOLTAGE-GATED CHANNEL GENES (CACNA1C, CACNA1D, CACNA1S, CACNA1I) IN JAPANESE SAMPLES OF SCHIZOPHRENIA AND AUTISM SPECTRUM DISORDER USING ION TORRENT PGM PLATFORM

Wang, C; Kimura, H; Xing, J; Ishizuka, K; Kushima, I; Arioka, Y; Yoshimi, A; Nakamura, Y; Shiino, Y; Oya, Y; Takasaki, Y; Aleksic, B; Mori, D; Ozaki, N

EUROPEAN NEUROPSYCHOPHARMACOLOGY 27 巻頁： S341 - S342 2017年10月

MUTATION SCREENING OF THE PCDH15 GENE IN PATIENTS SUFFERING FROM AUTISM SPECTRUM DISORDERS AND SCHIZOPHRENIA

Ishizuka, K; Wang, CY; Kimura, H; Xing, JR; Kushima, I; Arioka, Y; Yoshimi, A; Nakamura, Y; Oya-Ito, T; Takasaki, Y; Uno, Y; Okada, T; Mori, D; Aleksic, B; Ozaki, N

EUROPEAN NEUROPSYCHOPHARMACOLOGY 27 巻頁： S162 - S163 2017年10月

Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

Lim, ET; Uddin, M; De Rubeis, S; Chan, Y; Kamumbu, AS; Zhang, XC; D'Gama, AM; Kim, SN; Hill, RS; Goldberg, AP; Poultney, C; Minshew, NJ; Kushima, I; Aleksic, B; Ozaki, N; Parellada, M; Arango, C; Penzol, MJ; Carracedo, A; Kolevzon, A; Hultman, CM; Weiss, LA; Fromer, M; Chiocchetti, AG; Freitag, CM; Church, GM; Scherer, SW; Buxbaum, JD; Walsh, CA

NATURE NEUROSCIENCE 20 巻 ( 9 ) 頁： 1217 - + 2017年9月

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility

Kimura, H; Fujita, Y; Kawabata, T; Ishizuka, K; Wang, C; Iwayama, Y; Okahisa, Y; Kushima, I; Morikawa, M; Uno, Y; Okada, T; Ikeda, M; Inada, T; Branko, A; Mori, D; Yoshikawa, T; Iwata, N; Nakamura, H; Yamashita, T; Ozaki, N

TRANSLATIONAL PSYCHIATRY 7 巻 2017年8月

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders

Ishizuka, K; Fujita, Y; Kawabata, T; Kimura, H; Iwayama, Y; Inada, T; Okahisa, Y; Egawa, J; Usami, M; Kushima, I; Uno, Y; Okada, T; Ikeda, M; Aleksic, B; Mori, D; Someya, T; Yoshikawa, T; Iwata, N; Nakamura, H; Yamashita, T; Ozaki, N

TRANSLATIONAL PSYCHIATRY 7 巻 2017年8月

High-resolution copy number variation analysis of schizophrenia in Japan 査読有り

Kushima I, Aleksic B, Nakatochi M, Shimamura T, Shiino T, Yoshimi A, Kimura H, Takasaki Y, Wang C, Xing J, Ishizuka K, Oya-Ito T, Nakamura Y, Arioka Y, Maeda T, Yamamoto M, Yoshida M, Noma H, Hamada S, Morikawa M, Uno Y, Okada T, Iidaka T, Iritani S, Yamamoto T, Miyashita M, Kobori A, Arai M, Itokawa M, Cheng MC, Chuang YA, Chen CH, Suzuki M, Takahashi T, Hashimoto R, Yamamori H, Yasuda Y, Watanabe Y, Nunokawa A, Someya T, Ikeda M, Toyota T, Yoshikawa T, Numata S, Ohmori T, Kunimoto S, Mori D, Iwata N, Ozaki N.

Molecular Psychiatry 22 巻 ( 3 ) 頁： 430-440 2017年3月

High-resolution copy number variation analysis of schizophrenia in Japan

Kushima, I; Aleksic, B; Nakatochi, M; Shimamura, T; Shiino, T; Yoshimi, A; Kimura, H; Takasaki, Y; Wang, C; Xing, J; Ishizuka, K; Oya-Ito, T; Nakamura, Y; Arioka, Y; Maeda, T; Yamamoto, M; Yoshida, M; Noma, H; Hamada, S; Morikawa, M; Uno, Y; Okada, T; Iidaka, T; Iritani, S; Yamamoto, T; Miyashita, M; Kobori, A; Arai, M; Itokawa, M; Cheng, MC; Chuang, YA; Chen, CH; Suzuki, M; Takahashi, T; Hashimoto, R; Yamamori, H; Yasuda, Y; Watanabe, Y; Nunokawa, A; Someya, T; Ikeda, M; Toyota, T; Yoshikawa, T; Numata, S; Ohmori, T; Kunimoto, S; Mori, D; Iwata, N; Ozaki, N

MOLECULAR PSYCHIATRY 22 巻 ( 3 ) 頁： 430 - 440 2017年3月

Possible involvement of a cell adhesion molecule, Migfilin, in brain development and pathogenesis of autism spectrum disorders. 査読有り

Ishizuka K, Tabata H, Ito H, Kushima I, Noda M, Yoshimi A, Usami M, Watanabe K, Morikawa M, Uno Y, Okada T, Mori D, Aleksic B, Ozaki N, Nagata KI.

J Neurosci Res. 2017年

Copy number variant in the region of adenosine kinase (ADK) and its possible contribution to schizophrenia susceptibility. 査読有り

Kimura H, Kushima I, Yohimi A, Aleksic B, Ozaki N.

Int J Neuropsychopharmacol. 2017年

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. 査読有り

Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, Ikeda M, Iwata N, Levinson DF, Gejman PV, Shi J, Sanders AR, Duan J, Willis J, Sisodiya S, Costain G, Werge TM, Degenhardt F, Giegling I, Rujescu D, Hreidarsson SJ, Saemundsen E, Ahn JW, Ogilvie C, Girirajan SD, Stefansson H, Stefansson K, O'Donovan MC, Owen MJ, Bassett A, Kirov G.

PLoS Genet. 12 巻 ( 5 ) 頁： e1005993 2016年5月

Contribution of autosomal rare and de novo variants to sex differences in autism 査読有り国際共著

Mahmoud Koko, F Kyle Satterstrom; Autism Sequencing Consortium; APEX consortium; Varun Warrier, Hilary Martin

Am J Hum Genet 112 巻 ( 3 ) 頁： 599 - 614 2025年3月

Association Analysis of Rare CNTN5 Variants With Autism Spectrum Disorder in a Japanese Population 査読有り

Hadi, AF; Arta, RK; Kushima, I; Egawa, J; Watanabe, Y; Ozaki, N; Someya, T

NEUROPSYCHOPHARMACOLOGY REPORTS 45 巻 ( 1 ) 2025年3月

Proposal for a Novel Classification of Patients With Enlarged Ventricles and Cognitive Impairment Based on Data-Driven Analysis of Neuroimaging Results in Patients With Psychiatric Disorders 査読有り

Yasuda, Y; Ito, S; Matsumoto, J; Okada, N; Onitsuka, T; Ikeda, M; Kushima, I; Sumiyoshi, C; Fukunaga, M; Nemoto, K; Miura, K; Hashimoto, N; Ohi, K; Takahashi, T; Sasabayashi, D; Koeda, M; Yamamori, H; Fujimoto, M; Takano, H; Hasegawa, N; Narita, H; Yamamoto, M; Tha, KK; Kikuchi, M; Kamishikiryo, T; Itai, E; Okubo, Y; Tateno, A; Nakamura, M; Kubota, M; Igarashi, H; Hirano, Y; Okada, G; Miyata, J; Numata, S; Abe, O; Yoshimura, R; Nakagawa, S; Yamasue, H; Ozaki, N; Kasai, K; Hashimoto, R

NEUROPSYCHOPHARMACOLOGY REPORTS 45 巻 ( 1 ) 2025年3月

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