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1. Common variants in breast cancer risk loci predispose to distinct tumor subtypes

2. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

3. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

4. Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

5. Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

6. Genome-wide association study of germline variants and breast cancer-specific mortality

7. Erratum: Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature communications (2019) 10 1 (431))

8. Shared heritability and functional enrichment across six solid cancers

9. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

10. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

11. PALB2, CHEK2 and ATM rare variants and cancer risk:data from COGS

12. Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21

13. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

14. BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

15. Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

16. Fine-mapping of the 1p11.2 breast cancer susceptibility locus

17. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

18. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

19. Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1

20. Prediction of breast cancer risk based on profiling with common genetic variants

21. A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

22. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

23. Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

24. Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

25. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

26. Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

27. Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

28. Refined histopathological predictors of BRCA1 and BRCA2 mutation status: A large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

29. 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

30. Exploring the link between MORF4L1 and risk of breast cancer

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