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1. Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions

2. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

4. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

5. Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39

6. 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

7. Data from 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

8. Supplementary Table 3 from 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

9. Supplementary Table 2 from 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

10. Supplementary Table Legend from 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

11. Supplementary Table 1 from 9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association Consortium

12. Whole Exome Sequencing Study Suggests an Impact of FANCA, CDH1 and VEGFA Genes on Diffuse Gastric Cancer Development

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

14. Shared heritability and functional enrichment across six solid cancers

16. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

17. Association analysis identifies 65 new breast cancer risk loci

18. Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

19. Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants

21. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

22. Exome sequencing study of Russian breast cancer patients suggests a predisposing role for USP39

24. Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

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

26. A Splice Site Variant of CDK12 and Breast Cancer in Three Eurasian Populations

27. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

28. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

29. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

30. Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

31. Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom’s syndrome, is associated with breast cancer in Slavic populations

32. Breast Cancer Risk Genes - Association Analysis in More than 113,000 Women

33. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

34. Polygenic Risk Modelling for Prediction of Epithelial Ovarian Cancer Risk

35. Shared heritability and functional enrichment across six solid cancers

36. Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk.

37. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

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