Anders Kvist
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- 2019
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Mark
Long-term follow-up of HIV-2-related AIDS and mortality in Guinea-Bissau : a prospective open cohort study
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- Contribution to journal › Article
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Mark
Prevalence of BRCA1 and BRCA2 pathogenic variants in a large, unselected breast cancer cohort
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- Contribution to journal › Article
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Mark
Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification
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- Contribution to journal › Article
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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
- 2018
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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
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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
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
- 2017
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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
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
FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population
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- 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
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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
NF1-mutated melanoma tumors harbor distinct clinical and biological characteristics
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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
- 2016
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Mark
Multiregion whole-exome sequencing uncovers the genetic evolution and mutational heterogeneity of early-stage metastatic melanoma
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- 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
- 2015
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Mark
Molecular stratification of metastatic melanoma using gene expression profiling: prediction of survival outcome and benefit from molecular targeted therapy.
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- Contribution to journal › Article
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Mark
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
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- Contribution to journal › Article
- 2014
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Mark
The HER2-Encoded miR-4728-3p Regulates ESR1 through a Non-Canonical Internal Seed Interaction.
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- Contribution to journal › Article