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- 2017
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Mark
Evaluation of polygenic risk scores for breast and ovarian cancer risk prediction in BRCA1 and BRCA2 mutation carriers
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- Contribution to journal › Article
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Mark
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing
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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
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Mark
Cytohesin 1 regulates homing and engraftment of human hematopoietic stem and progenitor cells
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- Contribution to journal › Article
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Mark
Abstract P1-07-17: The SCAN-B study: 5-year summary of a large-scale population-based prospective breast cancer translational genomics platform covering a wide geography of Sweden (NCT02306096)
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- Contribution to journal › Published meeting abstract
- 2016
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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
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Mark
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic
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- Contribution to journal › Article
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Mark
Genome-wide RNAi Screen Identifies Cohesin Genes as Modifiers of Renewal and Differentiation in Human HSCs
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- Contribution to journal › Article
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Mark
Aberrant activation of the PI3K/mTOR pathway promotes resistance to sorafenib in AML
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- Contribution to journal › Article
- 2015
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Mark
The Sweden Cancerome Analysis Network - Breast (SCAN-B) Initiative: a large-scale multicenter infrastructure towards implementation of breast cancer genomic analyses in the clinical routine.
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- Contribution to journal › Article