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1. A PSA SNP associates with cellular function and clinical outcome in men with prostate cancer

2. Cluster effect for SNP–SNP interaction pairs for predicting complex traits

3. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease

4. NTHL1 is a recessive cancer susceptibility gene

5. Association between circulating inflammatory markers and adult cancer risk: a Mendelian randomization analysisResearch in context

7. Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen

8. KLK3 SNP–SNP interactions for prediction of prostate cancer aggressiveness

9. PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

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

11. Publisher Correction: Shared heritability and functional enrichment across six solid cancers

12. Sleep apnoea is a risk factor for severe COVID-19

13. Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

14. Shared heritability and functional enrichment across six solid cancers

15. Germline variation at 8q24 and prostate cancer risk in men of European ancestry

16. Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

17. AA9int: SNP interaction pattern search using non-hierarchical additive model set.

18. BioCPR–A Tool for Correlation Plots

19. Genetic association analysis of the RTK/ERK pathway with aggressive prostate cancer highlights the potential role of CCND2 in disease progression

20. Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families

21. Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility

22. Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

23. ShAn: An easy-to-use tool for interactive and integrated variant annotation.

24. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

25. SNP interaction pattern identifier (SIPI): an intensive search for SNP-SNP interaction patterns.

26. Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

27. New insights into the genetic etiology of Alzheimer's disease and related dementias

28. Supplementary Grant Support from Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

29. Supplementary Methods, Figures S1 - S3 from Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

30. Supplementary Tables S1 - S10 from Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

31. Supplementary Tables 2 - 5, Figures 2 - 3 from A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

32. Supplementary Table 1 from A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

33. Supplementary Figure 1 from A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

34. Supplementary Figure 1 from HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

35. Supplementary Table 2 from HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

36. Data from Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

37. Supplementary Figure 1 from Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

38. Data from HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

39. Supplementary Figure 3 from Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

40. Supplementary notes from Genome-Wide Association Study of Prostate Cancer–Specific Survival

41. Supplementary Table 5 from HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

42. Data from Synergistic Interaction of HOXB13 and CIP2A Predisposes to Aggressive Prostate Cancer

43. Supplementary Notes from Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

44. Supplementary Table 3 from HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

45. Supplementary Table 1 from HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

46. Supplementary Tables 1-8 from Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci

47. Supplementary data_310718 from Synergistic Interaction of HOXB13 and CIP2A Predisposes to Aggressive Prostate Cancer

48. Data from Genome-Wide Association Study of Prostate Cancer–Specific Survival

49. The variant rs77559646 associated with aggressive prostate cancer disrupts ANO7 mRNA splicing and protein expression

50. Transcripts of the Prostate Cancer-Associated Gene ANO7 Are Retained in the Nuclei of Prostatic Epithelial Cells

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