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- 2022
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Rare germline copy number variants (CNVs) and breast cancer risk
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- Contribution to journal › Article
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The diagnostic utility of DNA copy number analysis of core needle biopsies from soft tissue and bone tumors
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- Contribution to journal › Article
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
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- Contribution to journal › Article
- 2020
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Copy number variants (CNVs) : a powerful tool for iPSC-based modelling of ASD
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- Contribution to journal › Scientific review
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Genomic basis for RNA alterations in cancer
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- Contribution to journal › Article