Anders Kvist
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- 2019
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Mark
Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study
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- Contribution to journal › Article
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Mark
Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes
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- Contribution to journal › Article
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Mark
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification
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- Contribution to journal › Article
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Mark
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants : An ENIGMA report
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- Contribution to journal › Article
- 2018
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Mark
BRCAsearch : written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer
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- Contribution to journal › Article
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Mark
Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication
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- Contribution to journal › Article
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Mark
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
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- Contribution to journal › Article
- 2017
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Mark
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility
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- Contribution to journal › Article
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Mark
Mutational and putative neoantigen load predict clinical benefit of adoptive T cell therapy in melanoma
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- Contribution to journal › Article
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Mark
Frequent miRNA-convergent fusion gene events in breast cancer
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- Contribution to journal › Article