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367 results on '"Maehle, Lovise"'

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

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

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

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

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. Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS)

9. Lifestyle Factors and Breast Cancer in Females with PTEN Hamartoma Tumor Syndrome (PHTS)

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

13. 'It was an important part of my treatment': a qualitative study of Norwegian breast Cancer patients' experiences with mainstreamed genetic testing

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

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

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

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

19. Shared heritability and functional enrichment across six solid cancers

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

23. Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study

27. No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers

29. Germline PTEN mutations are rare and highly penetrant

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

31. BRCA1 and BRCA2 mutation spectrum - an update on mutation distribution in a large cancer genetics clinic in Norway

32. Runs of homozygosity and testicular cancer risk

33. Factors influencing ovulation and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

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

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

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

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

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

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

45. Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

49. Genome-Wide Linkage Analysis of 1,233 Prostate Cancer Pedigrees From the International Consortium for Prostate Cancer Genetics Using Novel sum LINK and sum LOD Analyses

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