换一批Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
第一作者：
Soumya,Raychaudhuri
第一单位：
Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America.
作者：
医学主题词
脑(Brain);病例对照研究(Case-Control Studies);计算机模拟(Computer Simulation);DNA拷贝数变异(DNA Copy Number Variations);数据库, 遗传学(Databases, Genetic);基因缺失(Gene Deletion);基因(Genes);疾病遗传易感性(Genetic Predisposition to Disease);基因组, 人(Genome, Human);人类(Humans);模型, 遗传学(Models, Genetic);危险性评估(Risk Assessment);精神分裂症(Schizophrenia)
DOI
10.1371/journal.pgen.1001097
PMID
20838587
发布时间
2025-05-29
基金项目
K08 AR055688-03/AR/NIAMS NIH HHS/United States
K08AR055688/AR/NIAMS NIH HHS/United States
R01 HL087676/HL/NHLBI NIH HHS/United States
U01 HG004171/HG/NHGRI NIH HHS/United States
U01 DK062432/DK/NIDDK NIH HHS/United States
R01 DK064869/DK/NIDDK NIH HHS/United States
U01DK62432/DK/NIDDK NIH HHS/United States
R01DK083756-1/DK/NIDDK NIH HHS/United States
U01HG004171/HG/NHGRI NIH HHS/United States
K08 AR055688-04/AR/NIAMS NIH HHS/United States
K08 AR055688/AR/NIAMS NIH HHS/United States
G0800509/MRC_/Medical Research Council/United Kingdom
R01DK64869/DK/NIDDK NIH HHS/United States
R01 DK083756/DK/NIDDK NIH HHS/United States
- 浏览47
PLoS genetics
e1001097页
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