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Your search keyword '"Maehle L"' showing total 242 results

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242 results on '"Maehle L"'

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1. Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.

2. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study.

4. Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction (Nature Genetics, (2021), 53, 1, (65-75), 10.1038/s41588-020-00748-0).

5. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.

6. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

7. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

8. Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

9. Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.

11. Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study

13. Risk reducing mastectomy: outcomes in 10 European centres

14. Screening for familial ovarian cancer: poor survival of BRCA 1/2 related cancers

15. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)

16. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

17. Correction to: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (Nature Genetics, (2018), 50, 7, (928-936), 10.1038/s41588-018-0142-8)

18. Germline variation at 8q24 and prostate cancer risk in men of European ancestry (vol 9, 4616, 2018)

19. Correction to: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (Nature Genetics, (2018), 50, 7, (928-936), 10.1038/s41588-018-0142-8).

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

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

22. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4).

23. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1).

24. Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci (Nature Genetics, (2018), 50, 7, (928-936), 10.1038/s41588-018-0142-8).

25. Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers.

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

27. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia (vol 9, 1340, 2018)

28. Large-scale transcriptome-wide association study identifies new prostate cancer risk regions (vol 9, 4079, 2018)

29. Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility (vol 8, 1892, 2017)

30. Shared heritability and functional enrichment across six solid cancers

31. Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)

32. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

33. Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers

34. Shared heritability and functional enrichment across six solid cancers

35. Publisher Correction: Shared heritability and functional enrichment across six solid cancers (Nature Communications, (2019), 10, 1, (431), 10.1038/s41467-018-08054-4)

37. Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

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

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

40. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition (vol 118, pg 266, 2018)

41. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

42. ANO7 is associated with aggressive prostate cancer

43. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.

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

45. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

46. Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

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

48. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition (vol 118, pg 266, 2018)

49. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

50. Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

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