The individual and global impact of copy-number variants on complex human traits
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
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2. Imputation of structural variants using a multi-ancestry long-read sequencing panel enables identification of disease associations;2023-12-22
3. Mechanisms of copy number variants in neuropsychiatric disorders: From genes to therapeutics;Current Opinion in Neurobiology;2023-10
4. GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data;Nature Genetics;2023-08-21
5. Copy-number variants as modulators of common disease susceptibility;2023-08-05
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