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- 2018
- Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
- 2016
- The BRCA1-Δ11q alternative splice isoform bypasses germline mutations and promotes therapeutic resistance to PARP inhibition and cisplatin
- Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
- BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
- No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
- 2015
- Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
- Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
- Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
- Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants
- 2014
- The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
- Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.
- Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study
- 2013
- Fine-Scale Mapping of the FGFR2 Breast Cancer Risk Locus: Putative Functional Variants Differentially Bind FOXA1 and E2F1
- Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
- 2012
- Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk