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341 results on '"García-Closas M"'

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

2. 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

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

4. Rare germline copy number variants (CNVs) and breast cancer risk.

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

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

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

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

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

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

11. Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer

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

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

14. 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

15. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

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

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

18. Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement (Nature Reviews Clinical Oncology, (2020), 10.1038/s41571-020-0388-9)

19. Personalized early detection and prevention of breast cancer: ENVISION consensus statement

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

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

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

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

24. Shared heritability and functional enrichment across six solid cancers.

25. Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study

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

27. Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation

28. E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium

29. Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

30. Identification of nine new susceptibility loci for endometrial cancer

31. Body mass index and breast cancer survival: a Mendelian randomization analysis

32. Genetic modifiers of CHEK2∗1100delC-associated breast cancer risk

33. Body mass index and breast cancer survival

34. PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1

35. Reproductive profiles and risk of breast cancer subtypes

36. TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer

37. rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

38. Evidence that the 5p12 variant rs10941679 confers susceptibility to estrogen receptor positive breast cancer through FGF10 and MRPS30 regulation

39. RAD51B in familial breast cancer

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

41. Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

42. Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis

43. 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

44. SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival

45. Performance of automated scoring of ER, PR, HER2, CK5/6 and EGFR in breast cancer tissue microarrays in the Breast Cancer Association Consortium

46. Identification of novel genetic markers of breast cancer survival

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

48. Age-And tumor subtype-specific breast cancer risk estimates for CHEK2∗1100delC Carriers

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

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

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