Targeted Sequencing of Genes Most Likely to Harbor Rare Causal Variants in Schizophrenia

被引：0

作者：

Dobbyn, Amanda ^{[1
]}

Feng, Claudia ^{[1
]}

Cheng, Esther ^{[1
]}

Moya, Emily ^{[1
]}

Rieder, M. K. ^{[1
]}

Johnson, Jessica ^{[1
]}

de Pins, Agathe ^{[1
]}

O'Donovan, Michael ^{[2
]}

Sullivan, Patrick ^{[3
,4
]}

Sklar, Pamela ^{[1
]}

Huckins, Laura ^{[1
,7
]}

Charney, Alexander ^{[1
,7
]}

Stahl, Eli ^{[1
,8
]}

机构：

[1] Icahn Sch Med Mt Sinai, Pamela Sklar Div Psychiat Genom, New York, NY 10029 USA

[2] Cardiff Univ, MRC Ctr Neuropsychiat Genet & Genom, Sch Med, Cardiff, Wales

[3] Univ N Carolina, Ctr Psychiat Genom, Chapel Hill, NC 27515 USA

[4] Karolinska Inst, Solna, Sweden

[5] SCHEMA Consortium, Mountain View, CA USA

[6] PGC Targeted Sequencing Study, New York, NY USA

[7] James J Peters VA Med Ctr, Mental Illness Educ Res Clin Care Ctr MIRECC, The Bronx, NY USA

[8] Broad Inst, Med & Populat Genet, Cambridge, MA USA

来源：

BIOLOGICAL PSYCHIATRY | 2020年 / 87卷 / 09期

关键词：

Schizophrenia; Rare Variants; Gene Burden; Targeted Sequencing;

D O I：

暂无

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

摘要：

引用

页码：S446 / S446

页数：1

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