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419 results on '"Schleutker J."'

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1. Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases

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

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

4. Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score

6. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

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

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

9. 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).

10. KLK3 SNP-SNP interactions for prediction of prostate cancer aggressiveness.

11. Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer[Formula presented].

12. Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.

13. The CHEK2 variant C.349A>G is associated with prostate cancer risk and carriers share a common ancestor.

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

15. Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer

16. Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer

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

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

19. KLK3 SNP-SNP interactions for prediction of prostate cancer aggressiveness

20. Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study

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

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

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

24. The CHEK2 variant C.349A>G is associated with prostate cancer risk and carriers share a common ancestor

25. An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk

26. The CHEK2 Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor

27. 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)

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

29. 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)

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

31. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

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

33. Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/ BRCA2 mutation-negative breast cancer but not in other malignancies

34. Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies

35. 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).

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

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

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

39. 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).

40. 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).

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

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

43. Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma (vol 9, 3707, 2018)

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

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

46. Shared heritability and functional enrichment across six solid cancers

47. Genetic architecture of human plasma lipidome and its link to cardiovascular disease

48. Association analyses identify 31 new risk loci for colorectal cancer susceptibility

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

50. Shared heritability and functional enrichment across six solid cancers

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