| Comparative analyses of copy-number variation in autism spectrum disorder and schizophrenia reveal etiological overlap and biological insights I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Okada, Y Uno, ... Cell reports 24 (11), 2838-2856, 2018 | 212 | 2018 |
| Integrative analyses of de novo mutations provide deeper biological insights into autism spectrum disorder A Takata, N Miyake, Y Tsurusaki, R Fukai, S Miyatake, E Koshimizu, ... Cell reports 22 (3), 734-747, 2018 | 160 | 2018 |
| High-resolution copy number variation analysis of schizophrenia in Japan I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Shiino, A Yoshimi, ... Molecular psychiatry 22 (3), 430-440, 2017 | 132 | 2017 |
| Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders K Ishizuka, Y Fujita, T Kawabata, H Kimura, Y Iwayama, T Inada, ... Translational psychiatry 7 (8), e1184-e1184, 2017 | 70 | 2017 |
| Resequencing and association analysis of six PSD-95-related genes as possible susceptibility genes for schizophrenia and autism spectrum disorders J Xing, H Kimura, C Wang, K Ishizuka, I Kushima, Y Arioka, A Yoshimi, ... Scientific reports 6 (1), 1-8, 2016 | 67 | 2016 |
| Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility Y Yu, Y Lin, Y Takasaki, C Wang, H Kimura, J Xing, K Ishizuka, M Toyama, ... Translational psychiatry 8 (1), 12, 2018 | 55 | 2018 |
| ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk M Sekiguchi, A Sobue, I Kushima, C Wang, Y Arioka, H Kato, A Kodama, ... Translational psychiatry 10 (1), 247, 2020 | 43 | 2020 |
| Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant Y Arioka, E Shishido, H Kubo, I Kushima, A Yoshimi, H Kimura, K Ishizuka, ... Translational psychiatry 8 (1), 129, 2018 | 33 | 2018 |
| Cross-disorder analysis of genic and regulatory copy number variations in bipolar disorder, schizophrenia, and autism spectrum disorder I Kushima, M Nakatochi, B Aleksic, T Okada, H Kimura, H Kato, ... Biological psychiatry 92 (5), 362-374, 2022 | 32 | 2022 |
| A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility H Kimura, Y Fujita, T Kawabata, K Ishizuka, C Wang, Y Iwayama, ... Translational psychiatry 7 (8), e1214-e1214, 2017 | 29 | 2017 |
| Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia K Ishizuka, T Yoshida, T Kawabata, A Imai, H Mori, H Kimura, T Inada, ... Journal of neurodevelopmental disorders 12, 1-16, 2020 | 28 | 2020 |
| Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population Y Takasaki, T Koide, C Wang, H Kimura, J Xing, I Kushima, K Ishizuka, ... Scientific reports 6 (1), 33311, 2016 | 28 | 2016 |
| Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility. H Kimura, C Wang, K Ishizuka, J Xing, Y Takasaki, I Kushima, B Aleksic, ... Schizophrenia research 178 (1-3), 104-106, 2016 | 25 | 2016 |
| Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders K Ishizuka, H Kimura, C Wang, J Xing, I Kushima, Y Arioka, T Oya-Ito, ... PLoS One 11 (4), e0153224, 2016 | 20 | 2016 |
| Peripheral biomarkers of attention-deficit hyperactivity disorder: Current status and future perspective N Takahashi, K Ishizuka, T Inada Journal of Psychiatric Research 137, 465-470, 2021 | 16 | 2021 |
| Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia M Sawahata, D Mori, Y Arioka, H Kubo, I Kushima, K Kitagawa, A Sobue, ... Psychiatry and clinical neurosciences 74 (5), 318-327, 2020 | 15 | 2020 |
| Establishment of in-hospital clinical network for patients with neurofibromatosis type 1 in Nagoya University Hospital Y Nishida, K Ikuta, A Natsume, N Ishihara, M Morikawa, H Kidokoro, ... Scientific reports 11 (1), 11933, 2021 | 12 | 2021 |
| Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum … H Kato, I Kushima, D Mori, A Yoshimi, B Aleksic, Y Nawa, M Toyama, ... Translational psychiatry 10 (1), 421, 2020 | 12 | 2020 |
| Clinical features and long-term outcomes of living donors of liver transplantation who developed psychiatric disorders M Shizuku, H Kamei, H Kimura, N Kurata, K Jobara, A Yoshizawa, ... Annals of transplantation 25, e918500-1, 2020 | 12 | 2020 |
| Integrative analyses of de novo mutations provide deeper biological insights into autism spectrum disorder. Cell Rep 22: 734–747 A Takata, N Miyake, Y Tsurusaki, R Fukai, S Miyatake, E Koshimizu, ... | 10 | 2018 |
