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

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
项目状态：
已结题
起止时间：
2016-10-01 至 2019-10-01
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

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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
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