Lv4
590 积分 2023-10-05 加入
Monoallelic loss-of-function variants in GSK3B lead to autism and developmental delay
3个月前
已完结
A common hub for sleep and motor control in the substantia nigra
3个月前
已完结
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
4个月前
已完结
The complex etiology of autism spectrum disorder due to missense mutations of CHD8
6个月前
已完结
Association between genetically predicted leisure and social activities and cardiovascular disease and other health outcomes
9个月前
已完结
An atlas of genetic correlations across human diseases and traits
10个月前
已完结
Leptin–dopamine interactions: unveiling the common link between type-2 diabetes and neuropsychiatric comorbidities
10个月前
已关闭
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