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164 related items for PubMed ID: 22253779

  • 1. Impact of the genome wide supported NRGN gene on anterior cingulate morphology in schizophrenia.
    Ohi K, Hashimoto R, Yasuda Y, Nemoto K, Ohnishi T, Fukumoto M, Yamamori H, Umeda-Yano S, Okada T, Iwase M, Kazui H, Takeda M.
    PLoS One; 2012; 7(1):e29780. PubMed ID: 22253779
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  • 7. Minor allele C of rs12807809 polymorphism in NRGN contributes to the severity of psychosis in patients with Schizophrenia in South Indian population.
    Sudesh R, Priyadarshini T, Preeti R, John S, Thara R, Mowry B, Munirajan AK.
    Neurosci Lett; 2017 May 10; 649():107-111. PubMed ID: 28389239
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  • 8. Influence of the NRGN gene on intellectual ability in schizophrenia.
    Ohi K, Hashimoto R, Yasuda Y, Fukumoto M, Yamamori H, Umeda-Yano S, Fujimoto M, Iwase M, Kazui H, Takeda M.
    J Hum Genet; 2013 Oct 10; 58(10):700-5. PubMed ID: 23903071
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  • 11. Polymorphisms in NRGN are associated with schizophrenia, major depressive disorder and bipolar disorder in the Han Chinese population.
    Wen Z, Chen J, Khan RA, Wang M, Song Z, Li Z, Shen J, Li W, Shi Y.
    J Affect Disord; 2016 Apr 10; 194():180-7. PubMed ID: 26828755
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  • 16. Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style.
    Rose EJ, Hargreaves A, Morris D, Fahey C, Tropea D, Cummings E, Caltagirone C, Bossù P, Chiapponi C, Piras F, Spalletta G, Gill M, Corvin A, Donohoe G.
    Br J Psychiatry; 2014 Feb 10; 204(2):115-21. PubMed ID: 24311551
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  • 20. The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia.
    Ohnishi T, Hashimoto R, Mori T, Nemoto K, Moriguchi Y, Iida H, Noguchi H, Nakabayashi T, Hori H, Ohmori M, Tsukue R, Anami K, Hirabayashi N, Harada S, Arima K, Saitoh O, Kunugi H.
    Brain; 2006 Feb 10; 129(Pt 2):399-410. PubMed ID: 16330500
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