Identifying rare genetic variants causing autism spectrum disorder via whole-genome sequencing

通过全基因组测序识别导致自闭症谱系障碍的罕见遗传变异

• 批准号: 300399
• 负责人: Xie Pingxing
• 金额: $ 9.83万
• 依托单位: McGill University
• 依托单位国家: 加拿大
• 项目类别: Fellowship Programs
• 财政年份: 2013
• 资助国家: 加拿大
• 起止时间: 2013-11-01 至 2016-11-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=300399&lang=en
• 关键词: Autism Spectrum Disorder; Bioinformatics And Biostatistics; Copy Number Variants; Rare Genetic Variants; Single Nucleotide Variants; Whole-Genome Sequencing

Currently, about 400,000 Canadians are living with autism spectrum disorder (ASD). The cost of providing lifetime care for each ASD patient is estimated to be $1.5 - 3.5 million. ASD is among the most heritable of all neuropsychiatric disorders, but its g

目前，大约有40万加拿大人患有自闭症谱系障碍（ASD）。为每位ASD患者提供终身护理的费用估计为150万至350万美元。ASD是所有神经精神疾病中遗传性最强的，但它的遗传性比其他疾病更强。