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No association with the neuregulin 1 haplotype to Japanese schizophrenia

Molecular Psychiatry volume 9, pages 126–127 (2004)Cite this article

SIR—Schizophrenia is a complex genetic disorder and has heritability of around 80%. The pathogenesis of the disease is hypothesized to be neurodevelopmental in nature based on reports of an excess of adverse events during the pre- and perinatal periods, the presence of cognitive and behavioral signs during childhood and adolescence, and the lack of evidence of a neurodegenerative process in most individuals with schizophrenia.1

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Authors and Affiliations

  1. Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, 470-1192, Aichi, Japan

    N Iwata, T Suzuki, M Ikeda, T Kitajima, Y Yamanouchi & N Ozaki

  2. Department of Psychiatry, Nagoya University Graduated School of Medicine, Nagoya, Japan

    M Ikeda & T Inada

Authors
  1. N Iwata
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  2. T Suzuki
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  3. M Ikeda
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  4. T Kitajima
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  5. Y Yamanouchi
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  6. T Inada
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  7. N Ozaki
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Correspondence to N Iwata.

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Iwata, N., Suzuki, T., Ikeda, M. et al. No association with the neuregulin 1 haplotype to Japanese schizophrenia. Mol Psychiatry 9, 126–127 (2004). https://doi.org/10.1038/sj.mp.4001456

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