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Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
Wang C, Horigane SI, Wakamori M, Ueda S, Kawabata T, Fujii H, Kushima I, Kimura H, Ishizuka K, Nakamura Y, Iwayama Y, Ikeda M, Iwata N, Okada T, Aleksic B, Mori D, Yoshida T, Bito H, Yoshikawa T, Takemoto-Kimura S, Ozaki N. Wang C, et al. Transl Psychiatry. 2022 Feb 26;12(1):84. doi: 10.1038/s41398-022-01851-y. Transl Psychiatry. 2022. PMID: 35220405 Free PMC article.
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. Kushima I, et al. Among authors: wang c. Mol Psychiatry. 2017 Mar;22(3):430-440. doi: 10.1038/mp.2016.88. Epub 2016 May 31. Mol Psychiatry. 2017. PMID: 27240532
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. Kimura H, et al. Among authors: wang c. Transl Psychiatry. 2017 Aug 22;7(8):e1214. doi: 10.1038/tp.2017.170. Transl Psychiatry. 2017. PMID: 28892071 Free PMC article.
Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia.
Wang C, Koide T, Kimura H, Kunimoto S, Yoshimi A, Nakamura Y, Kushima I, Banno M, Kawano N, Takasaki Y, Xing J, Noda Y, Mouri A, Aleksic B, Ikeda M, Okada T, Iidaka T, Inada T, Iwata N, Ozaki N. Wang C, et al. Schizophr Res. 2014 Aug;157(1-3):149-56. doi: 10.1016/j.schres.2014.04.032. Epub 2014 May 28. Schizophr Res. 2014. PMID: 24878430
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.
Kimura H, Tsuboi D, Wang C, Kushima I, Koide T, Ikeda M, Iwayama Y, Toyota T, Yamamoto N, Kunimoto S, Nakamura Y, Yoshimi A, Banno M, Xing J, Takasaki Y, Yoshida M, Aleksic B, Uno Y, Okada T, Iidaka T, Inada T, Suzuki M, Ujike H, Kunugi H, Kato T, Yoshikawa T, Iwata N, Kaibuchi K, Ozaki N. Kimura H, et al. Among authors: wang c. Schizophr Bull. 2015 May;41(3):744-53. doi: 10.1093/schbul/sbu147. Epub 2014 Oct 20. Schizophr Bull. 2015. PMID: 25332407 Free PMC article.
Glia-related genes and their contribution to schizophrenia.
Wang C, Aleksic B, Ozaki N. Wang C, et al. Psychiatry Clin Neurosci. 2015 Aug;69(8):448-61. doi: 10.1111/pcn.12290. Epub 2015 Apr 7. Psychiatry Clin Neurosci. 2015. PMID: 25759284 Free article. Review.
Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
Takasaki Y, Koide T, Wang C, Kimura H, Xing J, Kushima I, Ishizuka K, Mori D, Sekiguchi M, Ikeda M, Aizawa M, Tsurumaru N, Iwayama Y, Yoshimi A, Arioka Y, Yoshida M, Noma H, Oya-Ito T, Nakamura Y, Kunimoto S, Aleksic B, Uno Y, Okada T, Ujike H, Egawa J, Kuwabara H, Someya T, Yoshikawa T, Iwata N, Ozaki N. Takasaki Y, et al. Among authors: wang c. Sci Rep. 2016 Sep 12;6:33311. doi: 10.1038/srep33311. Sci Rep. 2016. PMID: 27616045 Free PMC article.
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