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456 results on '"Daly MB"'

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1. Bilateral granulosa cell tumors: a novel malignant manifestation of multiple endocrine neoplasia 1 syndrome found in a patient with a rare menin in-frame deletion

2. Understanding the genetic complexity of puberty timing across the allele frequency spectrum

3. Use of risk-reducing surgeries in a prospective cohort of 1,499 BRCA1 and BRCA2 mutation carriers

4. A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

5. Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium

6. Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

7. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival.

8. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

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

10. Polygenic risk modeling for prediction of epithelial ovarian cancer risk (vol 30, pg 349, 2021)

11. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

12. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

13. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

14. Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling

15. Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

16. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

17. Recreational Physical Activity and Outcomes After Breast Cancer in Women at High Familial Risk

18. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

19. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

20. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

21. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021)

22. Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

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

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

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

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

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

28. A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

29. Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers (vol 22, 8, 2020)

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

31. Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers

32. Recreational Physical Activity Is Associated with Reduced Breast Cancer Risk in Adult Women at High Risk for Breast Cancer: A Cohort Study of Women Selected for Familial and Genetic Risk

33. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

34. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

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

36. Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium

37. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

38. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

39. Shared heritability and functional enrichment across six solid cancers

40. Two truncating variants in FANCC and breast cancer risk

41. Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

42. Benign breast disease increases breast cancer risk independent of underlying familial risk profile: Findings from a Prospective Family Study Cohort

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

44. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

45. Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk

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

47. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

48. Alcohol consumption, cigarette smoking, and familial breast cancer risk: findings from the Prospective Family Study Cohort (ProF-SC)

49. Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

50. Accuracy of Risk Estimates from the iPrevent Breast Cancer Risk Assessment and Management Tool

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