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408 results on '"Orlow I"'

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

2. InterMEL: An international biorepository and clinical database to uncover predictors of survival in early-stage melanoma

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

9. A transcriptome-wide association study identifies novel candidate susceptibility genes for pancreatic cancer.

10. Association of Melanoma-Risk Variants with Primary Melanoma Tumor Prognostic Characteristics and Melanoma-Specific Survival in the GEM Study

11. Disease-Associated Risk Variants in ANRIL Are Associated with Tumor-Infiltrating Lymphocyte Presence in Primary Melanomas in the Population-Based GEM Study

12. Comparison of community pathologists with expert dermatopathologists evaluating Breslow thickness and histopathologic subtype in a large international population-based study of melanoma.

13. Differences in Melanoma Between Canada and New South Wales, Australia: A Population-Based Genes, Environment, and Melanoma (GEM) Study.

16. Genome-wide gene⇓diabetes and gene⇓obesity interaction scan in 8,255 cases and 11,900 controls from panscan and PanC4 consortia

17. Genome-Wide Gene-Diabetes and Gene-Obesity Interaction Scan in 8,255 Cases and 11,900 Controls from PanScan and PanC4 Consortia

18. Association of IRF4 single-nucleotide polymorphism rs12203592 with melanoma-specific survival.

19. No association between prediagnosis exercise and survival in patients with high-risk primary melanoma: A population-based study

20. MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort

21. Relationship of Chromosome Arm 10q Variants to Occurrence of Multiple Primary Melanoma in the Population-Based GEM Study

22. Alcohol and lung cancer risk among never smokers: A pooled analysis from the international lung cancer consortium and the SYNERGY study

23. Identification of nine new susceptibility loci for endometrial cancer

24. Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer

25. A risk prediction model for the development of subsequent primary melanoma in a population‐based cohort

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

27. Identification of nine new susceptibility loci for endometrial cancer.

28. The interaction between vitamin D receptor polymorphisms and sun exposure around time of diagnosis influences melanoma survival.

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

30. Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer

31. Identification of nine new susceptibility loci for endometrial cancer

32. Risk of Ovarian Cancer and the NF-? B Pathway: Genetic Association with IL1A and TNFSF10

33. A risk prediction model for the development of subsequent primary melanoma in a population‐based cohort.

34. Nevus count associations with pigmentary phenotype, histopathological melanoma characteristics and survival from melanoma

35. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

36. Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: Results from a large-scale collaboration

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

38. Variants in autophagy-related genes and clinical characteristics in melanoma: a population-based study

40. Cannabis smoking and lung cancer risk: Pooled analysis in the International Lung Cancer Consortium

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

42. Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer

43. Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration

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

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

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

47. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

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

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

50. Risk of ovarian cancer and the NF-kB pathway: Genetic association with IL1A and TNFSF10

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