BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

220 related articles for article (PubMed ID: 29317596)

  • 1. 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]  

  • 2. Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.
    Tarabeux J; Kebir O; Gauthier J; Hamdan FF; Xiong L; Piton A; Spiegelman D; Henrion É; Millet B; ; Fathalli F; Joober R; Rapoport JL; DeLisi LE; Fombonne É; Mottron L; Forget-Dubois N; Boivin M; Michaud JL; Drapeau P; Lafrenière RG; Rouleau GA; Krebs MO
    Transl Psychiatry; 2011 Nov; 1(11):e55. PubMed ID: 22833210
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Disease-associated GRIN protein truncating variants trigger NMDA receptor loss-of-function.
    Santos-Gómez A; Miguez-Cabello F; García-Recio A; Locubiche-Serra S; García-Díaz R; Soto-Insuga V; Guerrero-López R; Juliá-Palacios N; Ciruela F; García-Cazorla À; Soto D; Olivella M; Altafaj X
    Hum Mol Genet; 2021 Feb; 29(24):3859-3871. PubMed ID: 33043365
    [TBL] [Abstract][Full Text] [Related]  

  • 9. In-silico investigation of coding variants potentially affecting the functioning of the glutamatergic N-methyl-D-aspartate receptor in schizophrenia.
    Tsavou A; Curtis D
    Psychiatr Genet; 2019 Apr; 29(2):44-50. PubMed ID: 30664045
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exomic sequencing of the ionotropic glutamate receptor N-methyl-D-aspartate 3A gene (GRIN3A) reveals no association with schizophrenia.
    Shen YC; Liao DL; Chen JY; Wang YC; Lai IC; Liou YJ; Chen YJ; Luu SU; Chen CH
    Schizophr Res; 2009 Oct; 114(1-3):25-32. PubMed ID: 19665356
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders.
    Xing J; Kimura H; Wang C; Ishizuka K; Kushima I; Arioka Y; Yoshimi A; Nakamura Y; Shiino T; Oya-Ito T; Takasaki Y; Uno Y; Okada T; Iidaka T; Aleksic B; Mori D; Ozaki N
    Sci Rep; 2016 Jun; 6():27491. PubMed ID: 27271353
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A population-specific uncommon variant in GRIN3A associated with schizophrenia.
    Takata A; Iwayama Y; Fukuo Y; Ikeda M; Okochi T; Maekawa M; Toyota T; Yamada K; Hattori E; Ohnishi T; Toyoshima M; Ujike H; Inada T; Kunugi H; Ozaki N; Nanko S; Nakamura K; Mori N; Kanba S; Iwata N; Kato T; Yoshikawa T
    Biol Psychiatry; 2013 Mar; 73(6):532-9. PubMed ID: 23237318
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
    Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
    Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations of the glycine cleavage system genes possibly affect the negative symptoms of schizophrenia through metabolomic profile changes.
    Yoshikawa A; Nishimura F; Inai A; Eriguchi Y; Nishioka M; Takaya A; Tochigi M; Kawamura Y; Umekage T; Kato K; Sasaki T; Ohashi Y; Iwamoto K; Kasai K; Kakiuchi C
    Psychiatry Clin Neurosci; 2018 Mar; 72(3):168-179. PubMed ID: 29232014
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk.
    Demontis D; Nyegaard M; Buttenschøn HN; Hedemand A; Pedersen CB; Grove J; Flint TJ; Nordentoft M; Werge T; Hougaard DM; Sørensen KM; Yolken RH; Mors O; Børglum AD; Mortensen PB
    Am J Med Genet B Neuropsychiatr Genet; 2011 Dec; 156B(8):913-22. PubMed ID: 21919190
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; Arioka Y; Yoshimi A; Takasaki Y; Yu Y; Nakamura Y; Yamamoto M; Iidaka T; Iritani S; Inada T; Ogawa N; Shishido E; Torii Y; Kawano N; Omura Y; Yoshikawa T; Uchiyama T; Yamamoto T; Ikeda M; Hashimoto R; Yamamori H; Yasuda Y; Someya T; Watanabe Y; Egawa J; Nunokawa A; Itokawa M; Arai M; Miyashita M; Kobori A; Suzuki M; Takahashi T; Usami M; Kodaira M; Watanabe K; Sasaki T; Kuwabara H; Tochigi M; Nishimura F; Yamasue H; Eriguchi Y; Benner S; Kojima M; Yassin W; Munesue T; Yokoyama S; Kimura R; Funabiki Y; Kosaka H; Ishitobi M; Ohmori T; Numata S; Yoshikawa T; Toyota T; Yamakawa K; Suzuki T; Inoue Y; Nakaoka K; Goto YI; Inagaki M; Hashimoto N; Kusumi I; Son S; Murai T; Ikegame T; Okada N; Kasai K; Kunimoto S; Mori D; Iwata N; Ozaki N
    Cell Rep; 2018 Sep; 24(11):2838-2856. PubMed ID: 30208311
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.