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

页码：507 / 507

页数：1

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