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30 results on '"Yannoukakos, D. (Drakoulis)"'

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

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

3. Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

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

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

6. Shared heritability and functional enrichment across six solid cancers

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

8. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

9. The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

10. The BRCA2 c.68‐7T > A variant is not pathogenic:a model for clinical calibration of spliceogenicity

11. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

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

13. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

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

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

16. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

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

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

19. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

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

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

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

23. Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

24. DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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

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

27. MicroRNA related polymorphisms and breast cancer risk

28. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

29. 19p13.1 Is a triple-negative-specific breast cancer susceptibility locus

30. Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 (CIMBA)

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