Anders Kvist
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- 2019
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Mark
Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification
- Contribution to journal › Article
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Mark
Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study
- 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
- 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
- Contribution to journal › Article
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Mark
Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants : An ENIGMA report
- Contribution to journal › Article
- 2018
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Mark
Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication
- 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
- Contribution to journal › Article
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Mark
BRCAsearch : written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer
- Contribution to journal › Article
- 2017
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Mark
Cytohesin 1 regulates homing and engraftment of human hematopoietic stem and progenitor cells
- Contribution to journal › Article
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Mark
NF1-mutated melanoma tumors harbor distinct clinical and biological characteristics
- Contribution to journal › Article
