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- 2020
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Mark
precisionFDA Truth Challenge V2: Calling variants from short- and long-reads in difficult-to-map regions
(2020)
- Working paper/Preprint › Preprint in preprint archive
- 2019
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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
Tumor Characteristics and Molecular Subtypes in Breast Cancer Screening with Digital Breast Tomosynthesis : The Malmö Breast Tomosynthesis Screening Trial
- Contribution to journal › Article
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Mark
Refinement of breast cancer molecular classification by miRNA expression profiles
- Contribution to journal › Article
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Mark
Detection of circulating tumor cells and circulating tumor DNA before and after mammographic breast compression in a cohort of breast cancer patients scheduled for neoadjuvant treatment
- Contribution to journal › Article
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Mark
Pre-operative plasma cell-free circulating tumor DNA and serum protein tumor markers as predictors of lung adenocarcinoma recurrence
- Contribution to journal › Article
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Mark
SVCurator: A Crowdsourcing app to visualize evidence of structural variants for the human genome
(2019)
- Working paper/Preprint › Preprint in preprint archive
- 2018
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Mark
Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study : experiences from re-contacting mutation carriers and relatives
- Contribution to journal › Article
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Mark
Minimizing inequality in access to precision medicine in breast cancer by real-time population-based molecular analysis in the SCAN-B initiative
- Contribution to journal › Article
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Mark
Abstract P3-02-02: Concordance between immunohistochemical and gene-expression based subtyping of early breast cancer using core needle biopsies and surgical specimens - experices from SCAN-B
- Contribution to journal › Published meeting abstract
