When rare meets common: burden and impact of rare genetic variants in primary psychiatric populations

当罕见遇到常见：初级精神病人群中罕见遗传变异的负担和影响

• 批准号: 365426
• 负责人: Sriretnakumar Venuja
• 金额: $ 7.65万
• 依托单位: Centre for Addiction and Mental Health (Toronto)
• 依托单位国家: 加拿大
• 项目类别: Studentship Programs
• 财政年份: 2016
• 资助国家: 加拿大
• 起止时间: 2016-10-01 至 2019-10-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=365426&lang=en
• 关键词: Bipolar Disorder; Copy Number Variants (Cnvs); Diagnostic Tools; Genetic Diseases; Major Depressive Disorder; Next-Generation Sequencing (Ngs); Psychiatric Disorders; Schizophrenia

Genetic diseases are individually rare but collectively common. Many genetic conditions can mimic mental health disorders and the psychiatric symptoms can be difficult to treat with regular medications. Most people are not aware that many genetic conditio

遗传性疾病在个体上很罕见，但在集体上很常见。许多遗传性疾病可以模仿精神健康障碍，精神症状可能难以用常规药物治疗。大多数人不知道许多遗传条件.