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The Meaning of the Human Genome Project for Neuropsychiatric Disorders

机译:人类基因组计划对神经精神疾病的意义

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摘要

The past 3 years have witnessed a series of replicable, credible, and increasingly useful genetic discoveries in autism, schizophrenia, and bipolar disorder. I cannot emphasize enough the significance of this progress. Neuropsychiatric disorders are outsized contributors to global disease burden, yet treatment development has reached a near standstill. The problem is that the brain, with its myriad cell types and complex circuitry, represents such a difficult scientific frontier. Because genes play powerful roles in neuropsychiatric disorders, identification of causal variation could provide invaluable clues to their pathogenesis. Sadly, the genetic architecture of neuropsychiatric disorders is fiendishly complex, but unlike other areas of medicine wrestling with genetic complexity, psychiatry lacks objective phenotypic markers.
机译:在过去的3年中,在自闭症,精神分裂症和躁郁症中发现了一系列可复制,可信且日益有用的遗传发现。我不能足够强调这一进展的重要性。神经精神障碍是造成全球疾病负担的巨大因素,但治疗的发展已接近停滞。问题在于,具有无数细胞类型和复杂电路的大脑代表了如此困难的科学前沿。由于基因在神经精神疾病中起着强大的作用,因果变异的鉴定可以为其发病机理提供宝贵的线索。可悲的是,神经精神疾病的遗传结构异常复杂,但与其他因遗传复杂性而苦苦挣扎的医学领域不同,精神病学缺乏客观的表型标记。

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  • 来源
    《Science》 |2011年第6020期|p.1026|共1页
  • 作者

    Steven E. Hyman;

  • 作者单位

    Harvard University and Professor of Neurobiology,Harvard Medical School Boston, MA, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 02:53:54

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