Åke Borg
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- 2017
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Mark
Frequent miRNA-convergent fusion gene events in breast cancer
- Contribution to journal › Article
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Mark
Somatic mutations reveal asymmetric cellular dynamics in the early human embryo
- Contribution to journal › Article
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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
- Contribution to journal › Article
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Mark
Clinical framework for next generation sequencing based analysis of treatment predictive mutations and multiplexed gene fusion detection in non-small cell lung cancer
- Contribution to journal › Article
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Mark
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population
- Contribution to journal › Article
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Mark
Metachronous and synchronous occurrence of 5 primary malignancies in a female patient between 1997 and 2013 : A case report with germline and somatic genetic analysis
- Contribution to journal › Article
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Mark
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
- Contribution to journal › Article
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Mark
Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers
- Contribution to journal › Article
- 2016
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Mark
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population.
- Contribution to journal › Article
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Mark
An integrated genomics analysis of epigenetic subtypes in human breast tumors links DNA methylation patterns to chromatin states in normal mammary cells.
- Contribution to journal › Article
