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- 2022
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Mark
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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Mark
Rare germline copy number variants (CNVs) and breast cancer risk
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- Contribution to journal › Article
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Mark
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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Mark
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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Mark
Inferring structural variant cancer cell fraction
(
- Contribution to journal › Article
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Mark
Genomic basis for RNA alterations in cancer
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- Contribution to journal › Article
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Mark
Comprehensive molecular characterization of mitochondrial genomes in human cancers
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- Contribution to journal › Article
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Mark
The landscape of viral associations in human cancers
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- Contribution to journal › Article
- 2019
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Mark
Genetic Imbalance Is Associated With Functional Outcome After Ischemic Stroke
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- Contribution to journal › Article
- 2013
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Mark
No association of primary Sjogren's syndrome with Fc gamma receptor gene variants
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- Contribution to journal › Article