Dissecting the Contribution of Common Variants to Risk of Rare Neurodevelopmental Conditions

被引：0
|
作者：
Huang, Qin Qin [1 ]
Wigdor, Emilie M. [1 ,2 ]
Campbell, Patrick [1 ,3 ]
Malawsky, Daniel S. [1 ]
Samocha, Kaitlin E. [4 ]
Chundru, Kartik [1 ,5 ]
Warrier, Varun [6 ]
Young, Alexander Strudwick [7 ]
Hurles, Matthew E. [1 ]
Martin, Hilary C. [1 ]
机构：
[1] Wellcome Sanger Inst, Human Genet Programme, Hinxton, England
[2] Univ Oxford, Dept Paediat, Oxford, England
[3] Kings Coll London, Dept Genet, London, England
[4] Massachusetts Gen Hosp, Ctr Genom Med, Boston, MA USA
[5] Univ Exeter, Sch Med, Exeter, Devon, England
[6] Univ Cambridge, Dept Psychiat, Cambridge, England
[7] Univ Calif Los Angeles, Anderson Sch Management, Los Angeles, CA USA
来源：
BEHAVIOR GENETICS | 2024年 / 54卷 / 06期
关键词：
Neurodevelopmental disorders; Educational attainment; Cognition;
D O I：
暂无
中图分类号：
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号：
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要：
引用
收藏
页码：507 / 507
页数：1
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