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Genome-wide copy number variation-, validation- and screening study implicates a novel copy number polymorphism associated with suicide attempts in major depressive disorder

2019-01-30

Abstract excerpt

<h4>Background</h4> The genetic basis of suicide attempts (SA) remained unclear, especially for the copy number variations (CNVs) involved. The present study aimed to identify the susceptibility variants associated with SA among major depressive disorder (MDD) patients in Chinese, covering both single-nucleotide polymorphisms and CNVs. <h4>Methods</h4> We conducted GWAS on MDD patients with or without SA and top...

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Literature Corpus work
a192afdf-d4c1-53a5-97e0-bcd42ee02348
DOI
10.1101/534909
Open publication

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Genome-wide copy number variation-, validation- and screening study implicates a novel copy number polymorphism associated with suicide attempts in major depressive disorderDOI 10.1101/534909
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