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1. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.

2. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

3. Genetic telecounseling: evaluation of efficacy and outcomes through the Genetic Counseling Outcome Scale (GCOS) questionnaire in a cohort of patients with a suspected melanoma susceptibility syndrome

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

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

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

7. Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.

8. Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

9. Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade.

10. Outcomes of a 3-Year Prospective Surveillance in Individuals at High Risk of Pancreatic Cancer.

11. Outcomes of a 3-Year Prospective Surveillance in Individuals at High Risk of Pancreatic Cancer

12. Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

13. Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA‐repair genes

14. Multiple facial angiofibromas: A manifestation of Frank‐ter Haar syndrome?

15. Supplementary Table 2 from Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

16. Data from Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer

17. Supplementary Tables 1-4 from Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

18. Supplementary Table 3 from Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

19. Supplementary Table 3 from Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer

20. Data from Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

21. Supplementary Tables 1-9 from Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

22. Supplementary Table 1 from Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer

23. Supplementary Table 2 from Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer

24. Supplementary Table 4 from Confirmation of 5p12 As a Susceptibility Locus for Progesterone-Receptor–Positive, Lower Grade Breast Cancer

25. Data from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

26. Data from 19p13.1 Is a Triple-Negative–Specific Breast Cancer Susceptibility Locus

27. Supplementary Methods, Tables 1-3, Figure 1 from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

28. Supplementary Tables 1-13 from 19p13.1 Is a Triple-Negative–Specific Breast Cancer Susceptibility Locus

29. Prevalence of Germline Mutations in Cancer Predisposition Genes in Patients with Pancreatic Cancer or Suspected Related Hereditary Syndromes: Historical Prospective Analysis

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

32. Abstract P3-18-16: Breast conserving surgery in BRCA-mutation carriers. A single Institution experience

33. FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor

34. Clinical genetic testing for familial melanoma in Italy: A cooperative study

35. Clinical and pathologic characteristics of BRCA-positive and BRCA-negative male breast cancer patients: results from a collaborative multicenter study in Italy

37. Evidence for a link between TNFRSF11A and risk of breast cancer

43. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

45. Additional file 8 of Exploring the link between MORF4L1 and risk of breast cancer

46. Additional file 7 of Exploring the link between MORF4L1 and risk of breast cancer

47. Additional file 16 of Exploring the link between MORF4L1 and risk of breast cancer

48. Additional file 5 of Exploring the link between MORF4L1 and risk of breast cancer

49. Additional file 9 of Exploring the link between MORF4L1 and risk of breast cancer

50. Additional file of Exploring the link between MORF4L1 and risk of breast cancer

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