跳至主要内容
临床试验/NCT00619437
NCT00619437Unknown不适用

Genetics of Schizophrenia

Sheba Medical Center1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2008年4月最近更新:
适应症

试验速览

阶段
不适用
入组人数
100
试验地点
1

研究概览

简要总结

Genetic etiology in schizophrenia is widely accepted. However, many chromosomal sites were shown to characterize the families of patients with schizophrenia. This is probably due to the high genetic heterogenity of this illness. Thus, it is important to investigate the genetic factor in relatively genetically homogenous populations. Many studies have indicate that Ashkenazy Jews show relative gentic homogenity. Indeed, the genes responsible for most Mendelian disorders of Jewish peoples have been identified. The study will apply genome-wide mutation screening methods to identify candidate allells in subjects of Ashkenazi Jewish ancestry with multiplex schizophrenia.

研究设计

研究类型
Observational
观察模型
Family Based
时间视角
Prospective

入排标准

年龄范围
18 Years 至 78 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Meet DSM-IV criteria for Schizophrenia;
  • At least one first-degree relative who Meet DSM-IV criteria for Schizophrenia;
  • Can sign the informed consent form.

排除标准

  • Patients suffering from terminal or incurabale disease;
  • Minors, incompetents

研究者

申办方类型
Other Gov

研究点 (1)

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