精神分裂症(面向对象编程)
磁盘1
拷贝数变化
重要事件
精神分裂症的治疗
遗传学
分子遗传学
人类遗传学
三核苷酸重复扩增
生物
医学
精神科
等位基因
基因
抗精神病药
考古
基因组
历史
标识
DOI:10.1016/j.psychres.2022.114992
摘要
Rare structural variants have turned out to be the long sought for genetic variants of (relatively) high effect size for schizophrenia. Delineating the 22q11.2 microdeletion as the first molecular subtype of schizophrenia was a milestone in schizophrenia research, foreshadowing a more general role for rare copy number variation (CNV) in schizophrenia. The 22q11.2 microdeletion has a high effect size - one in every four individuals born with this deletion develops schizophrenia - and a relatively high prevalence for a rare condition. Discovery of this human genetic high-risk model for schizophrenia has shown how genetics can change clinical management, and also provide new opportunities for animal and cellular models. Further new findings indicate a role for tandem repeat expansion, other less complex rare variants, and collective background effects of common variants in the genetics of schizophrenia. Thus, the genetic architecture of schizophrenia is taking shape, with further advances on the horizon.
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