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1. Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

2. Adult height is associated with increased risk of ovarian cancer: A Mendelian randomisation study

3. Adult height is associated with increased risk of ovarian cancer: A Mendelian randomisation study

4. rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology

5. RAD51B in familial breast cancer

6. Evaluating the ovarian cancer gonadotropin hypothesis: A candidate gene study

7. Adult body mass index and risk of ovarian cancer by subtype: A Mendelian randomization study

8. RAD51B in Familial Breast Cancer

9. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

10. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

11. Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA

12. Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

13. Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

14. Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC).

15. Identification of six new susceptibility loci for invasive epithelial ovarian cancer

16. Genome-wide significant risk associations for mucinous ovarian carcinoma

17. Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer

18. Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31

19. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

20. Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer

21. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

22. BRCA2 Polymorphic stop codon K3326X and the risk of breast, prostate, and ovarian cancers

23. Variants on the promoter region of PTEN affect breast cancer progression and patient survival.

24. RAD51B in Familial Breast Cancer

25. NTHL1 is a recessive cancer susceptibility gene.

26. New VOUS in CASK Gene Correlating with the MICPCH Phenotype.

27. Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D.

28. Recurrent moderate-risk mutations in Finnish breast and ovarian cancer patients.

29. rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology.

30. Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility.

31. Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study.

32. Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication.

33. FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population.

34. CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population.

35. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.

36. FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome.

37. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.

38. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer.

39. Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study.

40. Assessing the genetic architecture of epithelial ovarian cancer histological subtypes.

41. Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study.

42. RAD51B in Familial Breast Cancer.

43. No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

44. Screening of HELQ in breast and ovarian cancer families.

45. Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk.

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

47. Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer.

48. Shared genetics underlying epidemiological association between endometriosis and ovarian cancer.

49. Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk.

50. Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer.

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