Singleton deletions throughout the genome increase risk of bipolar disorder.
Singleton deletions throughout the genome increase risk of bipolar disorder.
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DOI:
10.1038/mp.2008.144
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发表时间:
2009-04
影响因子:
11
通讯作者:
中科院分区:
文献类型:
--
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An overall burden of rare structural genomic variants has not been reported in Bipolar Disorder (BD), although there have been reports of cases with microduplication and microdeletion. Here, we present a genome wide copy number variant (CNV) survey of 1001 cases and 1034 controls using the Affymetrix SNP 6.0 SNP and CNV platform. Singleton deletions (deletions that appear only once in the dataset) more than 100 kilobases in length are present in 16.2% of BD cases in contrast to 12.3% of controls (permutation p = 0.007). This effect was more pronounced for age at onset of mania ≤ 18 years old. Our results strongly suggest that BD can result from the effects of multiple rare structural variants.
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通讯作者:
Daly, Mark J.
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通讯作者:
Sklar, P.
影响因子:
11
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Baum, A. E.;Akula, N.;McMahon, F. J.
通讯作者:
McMahon, F. J.
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通讯作者:
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通讯作者:
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