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1. A pleiotropy scan to discover new susceptibility loci for pancreatic ductal adenocarcinoma

2. Host immune genetic variations influence the risk of developing acute myeloid leukaemia: results from the NuCLEAR consortium

3. A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

4. Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?

5. GWAS-Identified Variants for Obesity Do Not Influence the Risk of Developing Multiple Myeloma: A Population-Based Study and Meta-Analysis

6. Polymorphisms within Autophagy-Related Genes as Susceptibility Biomarkers for Multiple Myeloma: A Meta-Analysis of Three Large Cohorts and Functional Characterization.

7. Identification of novel genetic loci for risk of multiple myeloma by functional annotation.

9. Polymorphic variants involved in methylation regulation: a new strategy to discover risk loci for pancreatic ductal adenocarcinoma

11. Exploring the Neandertal legacy of pancreatic ductal adenocarcinoma risk in Eurasians

12. Polymorphisms in Transcription Factor Binding Sites and Enhancers as Pancreatic Ductal Adenocarcinoma Risk Factors

13. Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study

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

15. The Relative Importance of Auditor Characteristics Versus Client Factors in Explaining Audit Quality

17. Exploring the Neandertal legacy of pancreatic ductal adenocarcinoma risk in Eurasians

18. Polymorphisms in transcription factor binding sites and enhancers as pancreatic ductal adenocarcinoma risk factors

19. Association of genetic variants affecting microRNAs and pancreatic cancer risk

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

22. Lack of association of CD44-rs353630 and CHI3L2-rs684559 with pancreatic ductal adenocarcinoma survival

24. Genome-wide scan of long noncoding RNA single nucleotide polymorphisms and pancreatic cancer susceptibility

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

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

27. Lack of association of CD44-rs353630 and CHI3L2-rs684559 with pancreatic ductal adenocarcinoma survival

28. Polymorphisms within the TNFSF4 and MAPKAPK2 Loci Influence the Risk of Developing Invasive Aspergillosis: A Two-Stage Case Control Study in the Context of the aspBIOmics Consortium

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

30. Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival

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

32. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

33. Breast cancer risk factors and survival by tumor subtype: Pooled analyses from the breast cancer association consortium.

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

35. Genome-wide genediabetes and geneobesity interaction scan in 8,255 cases and 11,900 controls from panscan and PanC4 consortia.

36. Smoking modifies pancreatic cancer risk loci on 2q21.3.

37. Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078)).

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

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

40. Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk.

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

42. 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.

43. Expression quantitative trait loci of genes predicting outcome are associated with survival of multiple myeloma patients.

44. Association of Genetic Variants Affecting microRNAs and Pancreatic Cancer Risk

45. Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium

46. Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3

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

48. 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

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

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

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