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4. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

5. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

7. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

8. Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry.

11. PALLD mutation in a European family conveys a stromal predisposition for familial pancreatic cancer

14. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.

15. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores.

16. Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness.

17. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

18. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

19. The DNA sequence of human chromosome 21

22. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.

23. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.

24. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

25. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

26. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

27. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

31. Initial sequencing and analysis of the human genome

32. Abstract P3-09-04: Beyond CHEK2 in breast cancer: Search for additional moderately penetrant risk gene variants by analyzing the oligogenic disease course in CHEK2 mutation carriers

34. Expression map of the DYT3 critical region in Xq13.1

36. The DNA sequence of the human X chromosome

39. Chronic recurrent multifocal osteomyelitis (CRMO) : Evidence for a susceptibility gene located on chromosome 18q21.3-18q22

40. Initial sequencing and analysis of the human genome

41. DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements.

44. correction: The DNA sequence of human chromosome 21

49. A Splice site mutation in the methyltransferase gene FTSJ1 in Xp 11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9).

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