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1. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

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

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

4. A KRAS variant is a biomarker of poor outcome, platinum chemotherapy resistance and a potential target for therapy in ovarian cancer

5. The association of polymorphisms in hormone metabolism pathway genes, menopausal hormone therapy, and breast cancer risk: A nested case-control study in the California Teachers Study cohort

6. Family history of haematopoietic malignancies and non-Hodgkin's lymphoma risk in the California Teachers Study

7. CCNE1 and survival of patients with tubo-ovarian high-grade serous carcinoma: An Ovarian Tumor Tissue Analysis consortium study

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

9. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.

10. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk.

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

12. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

13. Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score

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

15. Weight Gain and the Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers

16. Breast cancer risk after age 60 among BRCA1 and BRCA2 mutation carriers

17. Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer

18. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

19. Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects

20. 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

21. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

22. Polygenic hazard score is associated with prostate cancer in multi-ethnic populations

23. Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

24. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers

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

26. Common Susceptibility Loci for Male Breast Cancer

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

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

29. Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

30. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.

31. Polygenic hazard score is associated with prostate cancer in multi-ethnic populations

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

33. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

34. Identification of new breast cancer predisposition genes via whole exome sequencing

35. The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor

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

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

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

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

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

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

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

43. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)

46. Germline variation at 8q24 and prostate cancer risk in men of European ancestry (vol 9, 4616, 2018)

47. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (vol 9, 1340, 2018)

48. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (vol 9, 3707, 2018)

49. Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (vol 9, 4079, 2018)

50. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (vol 8, 1892, 2017)

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