4.8 Article

Copy-number variations associated with neuropsychiatric conditions

期刊

NATURE
卷 455, 期 7215, 页码 919-923

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NATURE PUBLISHING GROUP
DOI: 10.1038/nature07458

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资金

  1. The Centre for Applied Genomics
  2. Genome Canada-Ontario Genomics Institute
  3. Canadian Institutes for Health Research
  4. Canadian Institute for Advanced Research
  5. McLaughlin Centre for Molecular Medicine
  6. Canadian Foundation for Innovation
  7. Ontario Ministry of Research Innovation
  8. National Institutes of Health [HD055751]
  9. Children's Brain Research Foundation
  10. Jean Young and Walden W. Shaw Foundation
  11. Autism Speaks
  12. SickKids Foundation

向作者/读者索取更多资源

Neuropsychiatric conditions such as autism and schizophrenia have long been attributed to genetic alterations, but identifying the genes responsible has proved challenging. Microarray experiments have now revealed abundant copy- number variation - a type of variation in which stretches of DNA are duplicated, deleted and sometimes rearranged - in the human population. Genes affected by copy- number variation are good candidates for research into disease susceptibility. The complexity of neuropsychiatric genetics, however, dictates that assessment of the biomedical relevance of copy- number variants and the genes that they affect needs to be considered in an integrated context.

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