BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 27058588)

  • 1. Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.
    Ishizuka K; Kimura H; Wang C; Xing J; Kushima I; Arioka Y; Oya-Ito T; Uno Y; Okada T; Mori D; Aleksic B; Ozaki N
    PLoS One; 2016; 11(4):e0153224. PubMed ID: 27058588
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    Transl Psychiatry; 2022 Feb; 12(1):84. PubMed ID: 35220405
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    Transl Psychiatry; 2017 Aug; 7(8):e1184. PubMed ID: 28763059
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    Transl Psychiatry; 2017 Aug; 7(8):e1214. PubMed ID: 28892071
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
    Ishizuka K; Yoshida T; Kawabata T; Imai A; Mori H; Kimura H; Inada T; Okahisa Y; Egawa J; Usami M; Kushima I; Morikawa M; Okada T; Ikeda M; Branko A; Mori D; Someya T; Iwata N; Ozaki N
    J Neurodev Disord; 2020 Sep; 12(1):25. PubMed ID: 32942984
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of SHANK2 Pathogenic Variants in a Chinese Uygur Population with Schizophrenia.
    Zhang H; Wang D; Chen J; Li X; Yi Q; Shi Y
    J Mol Neurosci; 2021 Jan; 71(1):1-8. PubMed ID: 32897530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    Sci Rep; 2016 Sep; 6():33311. PubMed ID: 27616045
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    Schizophr Bull; 2015 May; 41(3):744-53. PubMed ID: 25332407
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility.
    Nawa Y; Kimura H; Mori D; Kato H; Toyama M; Furuta S; Yu Y; Ishizuka K; Kushima I; Aleksic B; Arioka Y; Morikawa M; Okada T; Inada T; Kaibuchi K; Ikeda M; Iwata N; Suzuki M; Okahisa Y; Egawa J; Someya T; Nishimura F; Sasaki T; Ozaki N
    Hum Genome Var; 2020 Nov; 7(1):37. PubMed ID: 33298905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population.
    Lo T; Kushima I; Aleksic B; Kato H; Nawa Y; Hayashi Y; Otgonbayar G; Kimura H; Arioka Y; Mori D; Ozaki N
    Int Rev Psychiatry; 2022 Feb; 34(2):154-167. PubMed ID: 35699097
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.
    Kato H; Kushima I; Mori D; Yoshimi A; Aleksic B; Nawa Y; Toyama M; Furuta S; Yu Y; Ishizuka K; Kimura H; Arioka Y; Tsujimura K; Morikawa M; Okada T; Inada T; Nakatochi M; Shinjo K; Kondo Y; Kaibuchi K; Funabiki Y; Kimura R; Suzuki T; Yamakawa K; Ikeda M; Iwata N; Takahashi T; Suzuki M; Okahisa Y; Takaki M; Egawa J; Someya T; Ozaki N
    Transl Psychiatry; 2020 Dec; 10(1):421. PubMed ID: 33279929
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.
    Ishizuka K; Kimura H; Yoshimi A; Banno M; Kushima I; Uno Y; Okada T; Mori D; Aleksic B; Ozaki N
    Nagoya J Med Sci; 2016 Dec; 78(4):465-474. PubMed ID: 28008202
    [No Abstract]   [Full Text] [Related]  

  • 13. Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I.
    Jaijo T; Oshima A; Aller E; Carney C; Usami S; Millán JM; Kimberling WJ
    Mol Vis; 2012; 18():1719-26. PubMed ID: 22815625
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism.
    Li J; Zhao L; You Y; Lu T; Jia M; Yu H; Ruan Y; Yue W; Liu J; Lu L; Zhang D; Wang L
    PLoS One; 2015; 10(7):e0133247. PubMed ID: 26204268
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder.
    Chien WH; Chen CH; Cheng MC; Wu YY; Gau SS
    Int J Mol Sci; 2024 May; 25(10):. PubMed ID: 38791584
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.
    Yu Y; Lin Y; Takasaki Y; Wang C; Kimura H; Xing J; 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
    Transl Psychiatry; 2018 Jan; 8(1):12. PubMed ID: 29317596
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of
    Furuta S; Aleksic B; Nawa Y; Kimura H; Kushima I; Ishizuka K; Kato H; Toyama M; Arioka Y; Mori D; Morikawa M; Inada T; Ozaki N
    Nagoya J Med Sci; 2022 May; 84(2):260-268. PubMed ID: 35967956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Resequencing and association analysis of PTPRA, a possible susceptibility gene for schizophrenia and autism spectrum disorders.
    Xing J; Wang C; Kimura H; Takasaki Y; Kunimoto S; Yoshimi A; Nakamura Y; Koide T; Banno M; Kushima I; Uno Y; Okada T; Aleksic B; Ikeda M; Iwata N; Ozaki N
    PLoS One; 2014; 9(11):e112531. PubMed ID: 25393624
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
    Forsyth JK; Nachun D; Gandal MJ; Geschwind DH; Anderson AE; Coppola G; Bearden CE
    Biol Psychiatry; 2020 Jan; 87(2):150-163. PubMed ID: 31500805
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population.
    Egawa J; Watanabe Y; Shibuya M; Endo T; Sugimoto A; Igeta H; Nunokawa A; Inoue E; Someya T
    Psychiatry Clin Neurosci; 2015 Mar; 69(3):131-5. PubMed ID: 24836510
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.